Connective Tissue Disorders/Ehler Danlos, the ECM and Chronic Issues - MCAS, CIRS, POTS, CFS, IBS, Dystonias, Pain, Proprioceptive Disorders, ETC.!

Gaby

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Connective tissue plays an integral role in keeping things "together" in a cohesive way, and it is composed primarily of an extracellular matrix (literally meaning the matrix outside the cell) and a number of cells like the fibroblasts, adipocytes, macrophages, mast cells, and leukocytes.

Specialized connective tissues include adipose, cartilage, bone, blood, and reticular tissues which are essential for the body's structure and function. Connective tissue is found in between other tissues everywhere in the body, including the nervous system. Most types of connective tissue consists of elastic and collagen fibers, ground substance and cells. Blood and lymph are a specialized fluid connective tissue. All are immersed in the body water.

The vast inclusion of connective tissue, also known as conjunctive tissue, explain how disorders at this level like in Ehler Danlos syndrome include so many conditions: Mast cell activation syndrome (MCAS) (basically allergies on steroids everywhere and because of anything), postural orthostatic tachycardia syndrome (POTS), chronic fatigue syndrome (CFS), irritable bowel syndrome (IBS) (there's permanent leaky gut because of the laxity of the conjunctive tissue), chronic inflammatory response syndrome (CIRS), dystonias (trembling of the body or certain parts of the body specially after an effort or exercise), severe anxiety and agoraphobia, generalized pain (specially in tendons and around muscle joints and often without signs of arthritis or arthrosis), repetitive subluxations and luxations (all the joints "crack" or dislocate), bleeding tendencies (gums, bruises, hematomas, heavy menstruation which can be confused with endometriosis, etc), propensity to have cysts in body organs and subcutaneous fatty nodules, sleeping disorders like restless leg syndromes and decreased deep sleep cycles, proprioceptive disorders where your sense of self in space doesn't work due to an anomaly of the sensors in all your connective tissue.

This list is not inclusive, but a start and I think it's useful to see certain problems from the point of view of the extracellular matrix (ECM) or connective tissue because it helps us to think more holistically (with our "right brain") as opposed to seeing everything by systems, molecularly, analytically, etc.

Because of the complexity and inclusivity of the conjunctive tissue, and how it affects so many people (i.e. COVID long resembles a lot Ehler Danlos issues since the spike protein is spiking the connective tissue), I decided to open a thread and revise this subject with everyone. I already did a LOT of research, but I figure I should share the articles, excerpts and the like as time permits because I think that most people will find it interesting or useful. Others can chime in. I hope to post all the above problems as it relates to conjunctive tissue disorders, highlighting what is sorely missing in the Anglosphere, as there are certain fields almost exclusive to certain European countries.

For instance, the proprioceptive problems are at the base of most problems in conjunctive tissue disorders as sensors at this level are anomalous because of the laxity of the conjunctive tissue, leading to multiple problems in itself. It's not the joint hypermobility that leads to pain or problems, but the proprioceptive issues in conjunction with the joint hypermobility that leads to problems. There are populations with over 50% joint hypermobility that don't have any health issues or major problems, they're just flexible. On the other hand, there are acquired infectious diseases that lead to joint hypermobility, like bartonellosis.

It can be said, that people with proprioceptive problems within the context of a connective tissue disorder have a somato-psycho disease and not the other way around, i.e. not a psychosomatic disease. Because the postural sensors don't work, people with this problem can't fully "land" into their bodies or ground per se. The postural sensors in the retina don't work well and these are directly linked to neural fibers in the brain's amygdala, leading then to anxiety. There are postural sensors in the ears, in the soles of the feet, in the manducatory system (leading then to temporomandibular joint issues). Their posture is permanently incorrect despite their best efforts, and they are known to be clumsy, displaying the "sign of the door", that is, they stumble against walls or doorknobs because they miscalculate the proportion of their body in space as they walk around.

I was thinking the other day that this forum is full of nutrient, molecular, psychological, physical and many other therapies, yet for me, treatment of proprioceptive problems don't figure prominently in this forum. I hope to bring more awareness into the subject, along with anybody else willing.

Within the context of my Ehler Danlos, I now wear prisms to correct my proprioceptive deficits in my peripheral retina, compressive garments when I work out, and proprioceptive insoles. Within the first 10 seconds of wearing my prisms glasses, I felt grounded and the constriction in my chest eased up a couple of notches, I also felt tension in my temporomandibular joint easing. I felt like I had a procaine infusion (neural therapy) in my vein! That is, totally chilled out. And I can concentrate better now. This is only with the prisms!

I also hope to review here the most complex region of the human genome, which is the RCCX gene cluster on chromosome 6, located in the major histocompatibility complex (MHC) class III region. Problems at this level can explain why so many people, usually very gifted and empathetic, have autoimmune disease, conjunctive tissue disorders and psychological susceptibilities. As a curiosity for forum members, this cluster contains a big chunk of the "ALU repeat" referenced in this session:


It is now known that there are pieces of DNA within a gene that are not translated into protein. These intervening sequences, or INTRONS, are somewhat of a mystery, but appear to be a very common phenomenon."

Now, is this thing they are talking about, these INTRONS, are these the core that you were talking about?

A: In part.

Q: What about this ALU repeat with over 300,000 copies of the same base pair sequence. What is it?

A: Tribal unit.

Q: What is a tribal unit?

A: Sectionalized zone of significant marker compounds.

Q: What does this code for?

A: Physiological/spiritual union profile.


Q: Could you define "tribal" for me?

A: You define.

Q: What does the rest of the DNA code for that is not coding for structural genes. What else can it be doing?

A: Truncated flow.

Q: Truncated flow of what?

A: Liquids.
All for now, as I said, as time permits 😅
 
The internal structure of the human body and its relationship with external elements.

Gaby said:
Most types of connective tissue consist of elastic and collagen fibers, ground substance and cells. Blood and lymph are a specialized fluid connective tissue. All are immersed in the body water.
------------------------------------
Water and blood among other fluids is a basis of body structure. There, sugar levels are transferred into liquids, and depending on the amount, they can be lower or higher, resulting in an imbalance in the levels of that substance: glucose/sugar, which is the cause of diseases such as diabetes, which has become a nightmare for millions of people around the world.

My question is: SUGAR, as an element in its natural state, is transformed by an external element, fire, to convert it into HONEY, which is a different state from the original matter (sugar). Does this not alter or modify the harmful elements contained in sugar, or do those elements continue despite having passed through the fire element and undergone an obvious transformation?

Another transformation must occur with blood when it comes into contact with the air element. Or are the components of blood (liquid, cells, blood cells, etc.) not altered upon contact with the components of air or another external element?

.
 
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Thank you Gaby for opening the thread, there are some somatopsychic symptoms listed above that i'd recognize in myself.

I definitely can relate to the below part 100%:

I also hope to review here the most complex region of the human genome, which is the RCCX gene cluster on chromosome 6, located in the major histocompatibility complex (MHC) class III region. Problems at this level can explain why so many people, usually very gifted and empathetic, have autoimmune disease, conjunctive tissue disorders and psychological susceptibilities
Could it be that, hypothetically speaking, the members of a soul group, as they're progressing in their path, would share similar "genetic disorders" that actually are just a manifestation of something else, ie, the proof of their interconnectedness as a tribal unit?

Just some thoughts.
 
It is now known that there are pieces of DNA within a gene that are not translated into protein. These intervening sequences, or INTRONS, are somewhat of a mystery, but appear to be a very common phenomenon."

Now, is this thing they are talking about, these INTRONS, are these the core that you were talking about?

A: In part.

Q: What about this ALU repeat with over 300,000 copies of the same base pair sequence. What is it?

A: Tribal unit.

Q: What is a tribal unit?

A: Sectionalized zone of significant marker compounds.

Q: What does this code for?

A: Physiological/spiritual union profile.


Q: Could you define "tribal" for me?

A: You define.

Q: What does the rest of the DNA code for that is not coding for structural genes. What else can it be doing?

A: Truncated flow.

Q: Truncated flow of what?

A: Liquids.
One and two echoes of this session:
(L) It's getting to be regular. Okay, now... I printed out some session extracts from a few years back because I started thinking about them in relation to trying to find some answers to certain questions that I'm going to get to in a minute. The first one is from September 23rd, 2000. I was asking about DNA and about INTRONS and so forth:

(L) Well, I think that obviously "tribal" means physiological spiritual union profile, and that that may have something to do with what we were talking about at a previous session when we asked about Caesar's soul group. Physiological spiritual union profile would be what defines what tribe you belong to, but it's a spiritual tribe and not necessarily specifically physical. You can grow into it according to some criteria... “graduate” was the term used. Am I correct here about a tribal group being like a soul group? Is that an accurate way of putting it?

A: Very close.

Q: (L) Is there anything that can get me closer?

A: In some cases there is also a supersensory component.

Q: (L) What is a supersensory component?

A: Externally driven mutation.

Q: (L) Externally driven by what?

A: Most often by the occupying soul itself.

Q: (L) So are you saying that if a soul selects a body or gets a close frequency match to a body that it wants to use, that it can also modify that body for its own purposes if it needs to and if the DNA match isn't quite to its taste or purposes?

A: Yes.

Q: (Andromeda) So our souls can cause mutations?

A: Yes.

Q: (Perceval) Does that happen pre-birth?

A: No, it can happen once the soul is seated and as needed.

Q: (L) So, what are some of the processes that can effect this in a physical way?

A: Diet is one. Also "arrangement" to contract the needed sickness.

Q: (Pierre) So you contract a sickness because the soul wants to learn something and experience something, and it's through this sickness that this learning will occur?

A: No. The soul and its helpers wants to trigger DNA modification!

Q: (L) They're saying no, that it's far more pragmatic. Okay, next question... I'm never going to get to my questions that I have! [laughter] Okay, when you say, "the soul and its helpers", what the heck are the soul's helpers?

A: Tribal unit members both in the body and out.

Q: (L) So if you're a member of a tribal unit, you are in a way connected via DNA connections or signals or frequencies with your other tribal members, whether they are incarnated or not? Is that what we're saying here?

A: Pretty much; no man is an island!

Q: (L) Okay, now, let me get back to my questions. In the rest of this session excerpt I have here, I asked:


(L) And then I gave up, because I was absolutely and completely clueless about where they were going, and I said I'd have to research it. And then, after I gave up on that line, I asked:


(L) So this takes us back to what they were just saying a minute ago about the soul being able to change DNA itself, or with its tribal unit helpers; that is, you can change your DNA through "Mind through central nervous system connection to higher levels." Now then, going back to this little bit right here about the naturally bonding combination, "the most efficient conductor of chemical compounds for low-wave frequency charge." Well, in another session they made the remark that DNA was a superconductor, and that DNA could also have a core of light. Now, what just happened to make me start thinking about all this was that there was an article:


(L) So, liquid DNA... What we have here is a little bit of a confirmation of what the C's were saying way back when, that DNA can turn from a solid to a liquid – the truncated liquid reference in the context of genetic engineering - to infect a cell. But we also know that DNA can also produce beneficial changes. The likelihood is that we have DNA that infected us at some point in time. It truncated the flow of some other DNA that's in our cells already there, but it isn't doing anything because it's been blocked by an infection that inserted introns of blockages. The possibility exists, I am surmising, that at some point in time, this could be changed or reversed possibly - probably - virally. Now, am I on to something here?

A: Oh indeed! The times ahead will be most interesting especially if the network both expands to the full tribal unit strength, and many others take the initiative to move up to the next stair step.

Q: (L) So, in a sense, what you're saying is that there is a need for the network to expand as in connecting chakras and so forth which is probably what helps with these “helper” things described a few minutes ago. When people are connected, they can help each other, both in and out of the body to make DNA changes and changes in their whole system. So, that's important. Also, people need to graduate when they get these DNA changes going on in their bodies that are helped by their helpers because of their connecting chakras because the network has strength. Does that make sense, everybody?

(Pierre) More members, and...

(L) And more involved, more doing.

(Chu) Not necessarily quantity, though. Because it says strength.

(Perceval) Well, that's the question: What is the full tribal unit strength?

(L) Does that means quantity, and/or quality?

(Data) Or both?

A: Both.

Q: (Pierre) So when you reach this critical mass, it means you can have this influence, you can have this soul group influence on all the members and trigger these changes?

(L) Is that what you're saying here?

A: Yes!

Q: (L) When the tribe reaches critical mass, it'll start changing people's DNA.

(Pierre) We'll start to change, and grow arms, and tentacles, and extra eyes... [laughter]

(Perceval) And fur!

(Kniall) Pierre, you can hold four tools at once!

(Chu) And if many others move up to the next stair step, that leaves more room for new people to come up.

(L) So, it's very, very important if people want to make this transition to be like the wise virgins: keep the faith, and keep doing, keep putting one foot in front of the other day after day even though they don't see any immediate benefits for themselves. Is that what we're getting to here?

A: Yes.

Q: (L) Okay.

(Perceval) Does the full tribal unit strength have anything to do with Gurdjieff's mention of 200 people?

A: Close enough.

Q: (L) And there was something else I wanted to ask that you guys made me think of... I had something, and it slipped out of my brain. I'm having a senior moment... OH! Is this full tribal unit strength capacity kind of what you meant way back when when you talked about "broader receivership capability", that it's not simply restricted to an individual, but that it's like creating a net that is kind of like an array of antennas that...

(Perceval) The signal received is spread throughout the array...

A: Yes yes yes!

Q: (L) Okay.

(PoB) This full tribal unit strength that affects progress and changes DNA and so on, does it happen progressively, or is it like yes or no?

(L) You mean like on or off?

(PoB) Yes.

A: Critical mass much involved.

Q: (L) So you have to hit a critical mass before it switches.

(Andromeda) So it's more like on/off.

(L) I would say there are SOME individual cumulative things, but the big changes depend on critical mass.

A: Yes.

Q: (L) So we can each be working on ourselves individually with diet, cold therapy, with our networking, with getting rid of our emotional baggage, learning how to get along, etc. But all of that is really just kind of like preparatory for a phase transition?

A: Yes.

Q: (Pierre) And how many percent of this full tribal strength have we reached right now? [laughter]

A: Not enough obviously.

Q: (PoB) Will we know when we reach it?

(Perceval) Yeah, Pierre will grow a tentacle.

A: You will know indeed!

Q: (L) Alright.

(Chu) "Not enough" is the new percentage measurement.

(Andromeda) We have missing members of our family that we need to find!

(L) Okay, another question I had about this DNA study was that it says:


(L) Now, we're doing these dietary changes and this cold therapy and so forth. I'm wondering if that is going to change our normal body temperature by changing some DNA which will then enable a different temperature-related INTRON or something in the body to activate or deactivate the blockage? Is this kind of temperature-related?

A: Yes.

Q: (L) So, there is more to this temperature thing than meets the eye. Well, the thing I noticed is that I am more cold tolerant. Also, the heater in my body seems better... Well, obviously it goes together. It's almost as though exposing oneself to cold actually heats you up.

(Perceval) Yeah, it's a reaction from the body to a cold environment.

(L) So whatever it is, I conjecture that it activates at a higher normal body temperature.

(Perceval) Well, does cold adaptation increase your core body temperature?

A: Ultimately, yes.

Q: (Pierre) By how much?

A: A degree or two.

Q: (Pierre) Like when you're sick.

(Perceval) Which might be deadly to specific viruses... It might be beneficial for keeping bad things away.

(L) It definitely might. That might be one of the activating effects of the...

(Perceval) If there are so many viruses around, they've probably adapted to the human body temperature. They've been around human beings for so long that they've adapted to living in humans and they do their thing at human body temperature. But if it's higher, they don't work so well.

(Pierre) At 39 degrees C, most of them die.

(L) So, if you have a higher body temperature, not only could you be activating some good DNA inside of you, you'd definitely be cutting off the access of the evil viruses.

(PoB) Like a constant fever.

A: Yes.

Q: (Perceval) It's kind of interesting because you'd think that's a natural function of being in a cold environment all the time. Like simulating being an Eskimo... Maybe with Eskimos their body temperature also drops a lot so it equalizes somehow. But, people doing cold adaptation who are not in super cold environments, maybe it would make it easier to increase the body temperature. But only periodically.

(L) Yeah.

(Andromeda) I woke up twice last night feeling like I had a fever.

(L) I can feel the heater effect come on at odd times. All of a sudden, I feel like I'm having hot flashes again!

(Andromeda) I feel hot like I want to get into the cold pool, which is weird for me!

(L) So, that covers that. Okay, in a previous session I was asking a question... And I asked about the... Um... I was asking about the EE program, and they said:


(L) So obviously EE is part of this hooking up with your tribal unit and your helpers. But this, "receivership capability and also capacity" thing is what I wanted to get to. And then I wanted to go to lists of questions from the forum, and you interrupted:
And:
(L) Well, on an adjacent topic to DNA, I would like to know why I feel... Um... compelled or obsessed by my genealogy database. [laughter] I'm embarrassed to talk about it because it's taken SO much time, and yet it's like I WANT TO KNOW!

A: Keep in mind that there is a certain power transmitted by awareness of ancestors.

Q: (L) How can there be power transmitted by awareness of ancestors? They're dead, first of all. Second of all, maybe those that had the potential have reincarnated and would be living other lives in other places. Or they'd be floating around in 5th density or whatever dead ancestors do...

(Artemis) Well, in a roundabout way, it's almost like knowing about your past lives.

(Andromeda) Yeah.

A: Yes

Q: (L) So, knowing past lives is helpful. Knowing ancestors is helpful. Well, the ancients believed that if you remembered your ancestors, they helped you. If you didn't take care of them or you forgot about them, they could bring bad luck on you. Can it? [laughter]

A: Something like that. You can help to heal some things and draw strength via your DNA antennae which, you must remember, is also their DNA antennae.

Q: (Andromeda) Makes sense.

(Chu) You inherited their receivers.

(Andromeda) And you can learn things from their experiences thereby.

(Pierre) You were wondering about how you relate to them. They're dead, they're far away. Sharing the same DNA antennae, if we are connected via DNA to an information field, and you have other people with similar DNA connected to a similar part of the field, and time really doesn’t exist on other planes, then you can access these kinds of memories or information shared by ancestors...?

A: Exactly.

Q: (Pierre) Wow.

(Joe) There's also epigenetics...

(L) I keep saying that reading all this early American history tells me why Americans are the way they are. They are completely messed up. But then, so is everybody else!! It's terrible.

(Chu) Epigenetics is only about this life, right?

(L) Oh no! Oh no! Your parents can have methylation that gets passed on to you. All kinds of weird stuff can happen. You just would not believe it. So in other words, we're back to ancestor worship! [laughter]

(Artemis) Get some incense and a shrine!

(Pierre) Is one of the reasons for the importance of the cult of ancestors this relation to the information field via DNA?

A: Yes. They went a bit far with it and forgot why it was important.
Also this little compiled discussion:
Click on zak.

Within the context of my Ehler Danlos, I now wear prisms to correct my proprioceptive deficits in my peripheral retina, compressive garments when I work out, and proprioceptive insoles. Within the first 10 seconds of wearing my prisms glasses, I felt grounded and the constriction in my chest eased up a couple of notches, I also felt tension in my temporomandibular joint easing. I felt like I had a procaine infusion (neural therapy) in my vein! That is, totally chilled out. And I can concentrate better now. This is only with the prisms!
I'm really glad you've found an anchor that can help you navigate through these tumultuous oceans inside you.

Recently I came across a link to products that I'd tried and put on hold for a while.
Maybe you've already heard of it, and I don't know if it would be of any use (and as you say there are a lot of solutions in this Forum, and sometimes this is not just enough, we still have to keep networking again and again for the common good.) , but in any case here's the link to the functional status correctors:
Qu'est-ce que le CEF ?..
 
Recently I came across a link to products that I'd tried and put on hold for a while.
Maybe you've already heard of it, and I don't know if it would be of any use (and as you say there are a lot of solutions in this Forum, and sometimes this is not just enough, we still have to keep networking again and again for the common good.) , but in any case here's the link to the functional status correctors:
Qu'est-ce que le CEF ?..

Your link doesn’t work, zak.

Here is a link to one of the product pages for those Functional State Correctors (FSC).
I’ve never tried one of those and haven’t done any research either.
 
I thought to continue with the Ehler Danlos classification and diagnostic tools as it's conceived today to illustrate the completely myopic and left-brain dominance that pervades this field nowadays, which has reduced conjunctive tissue disorders to the area of rare genetic diseases in complete discordance to objective reality.

The Cs summarized the gist of it perfectly in the Session March 1, 2025, as follows:
Q: (L) Can you tell me the genetic mutation?

A: No. There are several interactive genes. And to some extent it can be mitigated by up or down regulation.
Q: (Joe) Does their cluster of symptoms have a medically known name or syndrome attached to it?

A: Not as such. But close to Gaby's syndrome. There are many conditions that are specific to the individual. Your science likes to group them for definitive diagnosis when that is not always possible or accurate.

Q: (L) So there can be theoretically as many conditions as there are people, thanks to that wonderful process called genetic recombination.
One of this forum's recommended readings is "Making Sense of Genes" by Kampourakis Kostas (2017) where he illustrates through various well known "genetic diseases" how complex the entire thing is:
[...] a so-called monogenic disease is rather complex and cannot be explained on the basis of mutations on a single gene alone. [...] there is really no single "gene for" any of these diseases, as well as that having the disease does not necessarily support the inference to the existence of a "gene for" it. The reason for this is not only that mutations in several other DNA sequences except for the main gene affect the disease, but also that a variety of disease phenotypes may exist even for people with the same genotype.
[...] the common distinction between "simple" and "complex" or "monogenic" and "multifactorial" characters or disease is an oversimplification. Whereas it is certainly the case that some characters and some diseases are strongly associated with one gene, other DNA sequences may also be involved in their development. In addition, it is possible that within the main gene numerous variants exist that have a variety of phenotype outcomes. Therefore,
[...] variation within a single gene can result in very different phenotypes, that phenotypes cannot be accurately predicted from genotypes even in cases of monogenic characters and disease, and that several genetic and nongenetic factors may also have a contribution to the respective phenotypes. Therefore, even monogenic characters and disease had better be considered as complex ones, too, even if they are less complex than others. This conclusion makes the idea of a single "gene for" a character or disease untenable.
[...] But even at a theoretical level, the idea of "genes for" makes no sense conceptually. "Gene for" talk is about the attribution of characters and diseases to DNA, even though it is not DNA that is directly responsible for them. [...] it is proteins of different kinds that directly affect characters and diseases.
Therefore, it would make more sense to state that a person has a defective conjunctive tissue, and not that a single gene is directly responsible for this disease. Despite the fact that these are "101 Genetics" for high school or even primary school teachings, you'll find the so-called experts in every field reducing everything to myopic impossible standards, preferring to attribute a condition to a single gene or genes rather to the affected protein or tissue.

If many genes produce or affect the production of a protein that in turn affects a disease, it makes no sense to identify one gene as the gene responsible "for" this disease.

Keeping in mind the above, now let's take a look at the following classification made by "the best of experts":

brave_screenshot_www.uptodate.com.png
The above gives the impression that they have everything figured out. It also gives a false sense of security to a person with type 3 Ehler Danlos Syndrome (EDS) because it makes them think that they don't have the vascular kind. As if an affliction of the conjunctive tissue could be reduced to only the conjunctive tissue of your joints and nowhere else in the body. In objective reality, the above simply doesn't exist. All people with type 3 EDS can have arterial aneurysms in their bodies, despite the fact that they are considered as NOT having the vascular EDS. And this is because there's conjunctive tissue in the arteries as well. The vascular form gene (COL3A1) is often absent in people who have had vascular complications, and there are those who have this vascular gene who never manifested any problems at all in their arteries.

We can find even more problems with the diagnostic tools for EDS. The body has 350 joints, and the main EDS screening test comprises only joint hypermobility fixed in a five out of nine-point success test, attributed to Beighton. The test is often poorly performed and fails to take into account the fact that 55 joint complexes make up human biomechanics, and that examining a few of them is highly insufficient to assess joint hypermobility. Moreover, Beighton's choice of joints is particularly poor as he skipped altogether the shoulders and hips which are key for daily living and often afflicted, while including the knees and the ability to touch the ground without bending your knees. Due to the fact that bilateral hamstring retraction is prevalent among people with EDS, often starting in childhood, knees and the spine maneuver are often negative for the test. Let's have a look:

opinions-on-the-beighton-scoring-system-v0-IdKbbgVsgDpLq2v0WGSBxyGK9Bp0a7Y03uXlXAsExN8.webp

When I discovered the score, I had 9 out of 9. The maneuvers contracted my hamstrings and by the time I visited a doc for an official diagnosis other than myself, the knees were negative, negating me proprioceptive garments for them (more on proprioception in a future post). At least the orthopedist who took my measurements asked me if I wanted my knees included.

That's one side of the story. The other side of the story is that some people with EDS have hypermobility only in one joint or a few joints, which don't have to be the ones described in the Beighton score. Still others had hypermobility in the past, but no longer in the present, yet they're afflicted with various systemic health problems related to their connective tissue anomaly.

Moreover, this score gives high emphasis on joint hypermobility, which is the least of the problems in people with EDS. It poses no problem at all to have all joints cracking or moving in extreme, impossible positions. Often, the cracking of all joints and hyperextension maneuvers are therapeutic for someone with EDS (unless it triggers hamstring retraction and pain). The problem comes from the hypermobility in conjunction with the proprioceptive problems at the level of the connective tissue - where the receptors that inform your body's position, movement and force don't work well. This leads to pain and fatigue, along with other factors related to conjunctive tissue anomalies.

People can be very good at yoga, having very extremely hypermobile joints, and have no health problems at all. The combined problem of hypermobility and proprioceptive issues due to the conjunctive tissue problem, leads to a propensity to luxations and subluxations, pain, and even dystonias. And people with little hypermobility can have a lot of dystonias too, due to an anomaly of proprioception at the level of the conjunctive tissue. As we revise in a future post the symptoms and health problems in people with conjunctive tissue disorders, we'll understand better the functions and physiopathology of conjunctive tissue disorders.

Proprioceptive problems in EDS opened diagnostic and therapeutic venues. It also revealed precautions for people who overlooked this problem in daily practice. For instance, it is highly discouraged to give chiropractic or osteopathic cervical maneuvers to people with EDS, as the tissue constituency is different and can't inform the therapist of how much force has to be applied in the maneuver. The tissues are "soft" and there are cases of carotid artery dissection after a cervical maneuver. Often, as I can attest, a deep fascia neck massage made with great force can exacerbate pain and all systemic symptoms of EDS.

This post underscores the concept put forward by Prof. Claude Hamonet, someone I consider as "the Last of the Mohicans" in terms of being able to think like a Master in EDS research (as opposed to an Emissary to quote "The Master and its Emissary" by Iain McGilchrist). And that is: there is no such thing as 15 types of EDS, but just ONE. There's ONE type of EDS and this one syndrome has several clinical manifestations that can vary in severity thanks to the wonderful process of genetic recombination, as Laura so beautifully put it in the session quoted above.

Other than EDS, this means that anyone having a conjunctive tissue disorder can have several clinical manifestations due to genetic recombination. It ain't no single gene that is responsible for something as complex as the connective tissue and extracellular matrix.

Despite the fact that this post heavily emphasizes EDS, it illustrates very well why conjunctive tissue disorders generally don't come to the attention of the average person. EDS is relegated to a rare genetic disease, which by definition is 1 in 2000 or 1 in 1500 individuals, depending on the country. However and for EDS alone, research suggests that 3% of any given population is affected, which makes it the opposite, not rare at all.
 
Let's bring up a few concepts that a lot of people can relate or know about : COVID Long and fascia.

In some research, fascia and connective tissue are used interchangeably. For practical purposes, it's the same, also because it makes the subject of connective tissue less esoteric and more materialistic.

Due to the materialist focus of this reality, we think of fascia as a very mechanical thing. For most people, the importance of fascia is reduced to getting a good massage in order to feel better. Yet, fascia is intimately interconnected with the neurological system, opening the door to understanding how the entire body is regulated. But in reality, fascia is not only related with the neurological system.

Fascia has it all, and this might be true in ways we don't understand as we develop tools to study it better. It has nerves, blood vessels, lymphatics, hormones, peptides, neurotransmitters. It is considered like a bodyguard or "watchman" as it is the depository of information from within and without.

People with fascia issues have pain, fatigue, brain fog, allergies, chronic inflammation, autonomic nervous system issues, etc.

I once thought that the autonomic nervous system was the most unrecognized system in Western medicine, but now I think that the connective tissue takes the price. It explains why conventional practitioners were so unprepared to deal with fibromyalgia and chronic fatigue syndrome, relegating them to the field of "it's all in your head" or "just get over with it". And it is the reason why most health practitioners have no idea what Ehler Danlos syndrome is or involves. Ignorance in the field of connective tissue still reigns supreme, despite growing awareness efforts.

Just as cell membranes (cell "mem-brain") are known to be of critical importance for the cell itself to the point that some consider it the cell's real brain, similarly fascia or connective tissue have "mem-brain" like properties for everything that it connects and encapsulates. And, there is connective tissue connecting absolutely everything. In the simplest of terms, it's the connecting interface of the muscles/joints, hormones, and the autonomic nervous system. Yet, this will not quite cover the implications. For those interested, here's some knots and bolts fascinating background information:


Fascia surrounds, supports and protects every nerve, muscle, blood vessel, and organ in the body, and is abundantly innervated (7, 8). Fascia is estimated to house over 250 million nerve endings (8), with sensory neurons outnumbering motor neurons 9:1 in some regions (9). Fascia houses 25% more nerve endings than skin, and 1,000% more than the collective innervation of muscle, so fascia could very well be considered our richest sensory organ (7, 8).
Fascial integrity is paramount to movement, bodily sense, hormonal, autonomic and neurovascular regulation, and purposeful interaction with our environment. For movement and locomotion, fascia regulates posture (2), force transmission (10), strength generation (11), elastic recoil (12), proprioception (1), exteroception, and interoception (13). Fascia also regulates lymphatic efficacy (14), protection of delicate neural and vascular elements and organs (4), thermoregulation, inflammatory and immune responses (15), wound healing (16), hormonal production and secretion (adrenaline, estrogen, insulin, thyroid hormones, oxytocin) (17, 18), and venous return (19). Fascia plays a critical role in the transmission of neurotransmitters, namely serotonin, dopamine, GABA, and acetylcholine (17, 20). The regulation of peripheral resistance arteries by interfacing fascial tissue is essential for control of blood pressure, and for the increase in blood flow to the central nervous system and the heart under stress conditions (21). Alterations in the superficial fascia can also reciprocally lead to lymphedema/lipedema, which in turn may exacerbate suboptimal health of superficial fascia (22). Fascial morphology is initially determined by embryological and early childhood development (23), and undergoes perpetual adaptation across the lifespan in response to functional demand. Fascia is constantly evolving, both dependent on and modulating sustained postures, repetitive movement, quantity of motion, load (24), stress, strain, hydration (25), pH, temperature (23), neurotransmitters, and hormones (26).
The fundamental components of fascial tissue are primarily specialized cells, collagen fibers, elastin fibers, and an extracellular matrix (ECM): (2).

Cells provide the metabolic properties of the fascial tissue.

• Collagen and elastin fibers provide mechanical strength.

• ECM (also known as the ground substance) provides plasticity and elasticity.
Fascial cell types include fibroblasts, fasciacytes, adipocytes, macrophages and mast cells (27), undifferentiated mesenchyme cells, chondroblasts, chondrocytes, osteoblasts, and osteocytes (28). ECM contains hyaluronan (hyaluronic acid; HA), glycosaminoglycans (GAGs), water and ions (2). GAGs create an osmotic imbalance, which enables the ECM to attract up to 1,000 times its own weight in water (29). This hydrophilic quality of proteoglycans (glycoproteins that contain GAGs) is responsible for maintaining the volume of the extracellular matrix, which is constrained by the surrounding collagen fibers (30). The capacity for ECM to attract up to 1,000 times its weight in water is particularly important, because fascia is the “arena” in which localized acute inflammation and edema occurs (30).
Fascia evolves almost exclusively from the mesodermal layer during embryological development (23). Embryos first develop cerebrospinal fluid and fascia, then the remaining body systems and structures form within this “endless web” of fascia (23, 31). Fascia facilitates “a true continuity throughout our whole body” (2), and has been referred to as the “organ of form” (32), and “the architect of human movement” (22)

Those with Sjogren Syndrome, systemic lupus erythematous, polyarthritis and COVID long have acquired connective tissue disease.
Though the picture is clearer when you study symptoms and signs of those with hereditary connective tissue disorders such as Ehler Danlos: there are dislocations of joints, tendons and nerves. There's neck instability, oral/manducatory issues, IBS, dysautonomia, stomach acid reflux, diverticulosis, POTS (postural orthostatic tachycardia syndrome), "onion-skin" scarring, easy bruising, lymphedema, chronic fatigue syndrome, chronic pain of the "tearing apart" kind, pelvic organ prolapses, mast cell activation syndrome, severe anxiety, and higher odds of ADHD, etc.

A lot of the above will resonate to those with COVID Long, which is an acquired connective tissue disorder, even when the focus nowadays is at a molecular/spike protein level.

There is constant strain and effort just to lead a "normal" life, regardless of your weight. Swimming pools are very soothing to people with connective tissue disorders, especially if the chlorine won't trigger the mastocytes (allergies) or the temperature is perfect as people with these disorders have dysautonomia (they're either heat intolerant or cold intolerant, or both, even when thyroid function is perfect which often is not the case).

There's an entire universe of receptors located at the level of the connective tissue, which science doesn't even attempt to quantify. Broadly speaking, there are mechanoreceptors, thermoreceptors, proprioceptors, pain receptors, and chemoreceptors based on the information they receive.

Mechanoreceptors alone are classified in tactile, proprioceptors, and baroreceptors which serve different functions in the body. Just in the human skin alone, there are mechanoreceptors holding names of their discoverers like Merkel’s disks, Meissner’s corpuscles (for touch and low-frequency vibration), Ruffini endings (detect stretch, deformation, and warmth), and Pacinian corpuscle (for transient pressure and high-frequency vibration). A fifth type of mechanoreceptor, Krause end bulbs, are found only in specialized regions and they detect cold.

Professor Hamonet, a doctor specialized in physical and rehabilitation medicine, reports how a person, in denial of having Ehler Danlos, ruptured the popliteal artery in his knee while practicing sports, requiring emergency bypass surgery. This person did not break the artery only because he was fragile and hypermobile, but because the receptors at this level didn't inform him that the stretch was beyond what his tissue could literally support. He just kept going, whereas in a normal person the receptors will signal "stop!". A simple elastic knee brace could have prevented the disaster.

The compression, provided in specialized elastic braces, palliate the lack of appropriate receptor function at the level of the connective tissue. Which is why compressive garments are a key to treatment, even though they often trigger mastocytosis due to the pressure the garments apply at the tissues, leading to urticaria and allergies (Darier sign) and bruising due to capillary breakage in soft tissues. For some, urticaria and bruising is the least of the problems when it comes to incapacitating symptoms.

According to Hamonet, kinesiotape serves the same function for those who can't tolerate compressive garments, the kinesiotape proving much needed proprioceptive information, other than the other benefits for which they are known:

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Proprioception, meaning the sense of self-movement, force, and body position in space, is a field that science is only starting to understand. Proprioceptive signals, from receptors in the connective tissue all over the body, are transmitted to the nervous system where they have to be integrated with other incoming signals coming from sensory organs to create this sense of self in space.

People with problems at the proprioceptive level are bodily stupid. They stumble against the handle of doors when they go through them, against people, corners, stuff falls from their hands easier, etc. Paradoxically, when they're in movement, their proprioception works better or even better than average, so they can be great dancers, martial artists, etc. Provided that luxations, pain and fatigue don't bring their career to an abrupt end...

This is why Ehler Danlos syndrome is often riddled with contradictory symptoms and signs depending on the context. Another curiosity, even though they can be crippled by fatigue and pain, they often display what it's called the Madonna's sign, which is that they seem 10 or 20 years younger than their real age because of the proprioceptive and/or connective tissue anomalies at the level of their face and body. Professor Hamonet likes to call it the sign of the Gioconda (Mona Lisa or Lisa del Giocondo), because her mysterious smile reminded him of Ehler Danlos patients and their difficulty for expression due to connective tissue anomalies.

We finish with more proprioceptive trivia:


Proprioceptive feedback derives in large part from specialized mechanoreceptive organs in skeletal muscle. Extensive anatomical and physiological analysis have revealed two types of muscle receptors: muscle spindles and Golgi tendon organs7. Muscle spindle (MS) mechanoreceptors are considered the main drivers for the sense of limb position and movement (kinesthetic sense)

The Golgi organ, is a proprioceptor at the level of the connective tissue, providing information for an inhibitory reflex in order to prevent too much tension on the muscles or tendons. The reflex is called the Golgi tendon reflect or inverse stretch reflect, and it partially explains why people with acquired or hereditary connective tissue disorders have pain or tension at the musculoskeletal joints. The Golgi organ doesn't really quite work properly.
 
This post is a translation of a questionnaire developed by Dr Hamonet and his team, based on thousands of Ehler Danlos patients. It helps people to get oriented as to what a typical conjunctive tissue disorder entails. Consultations for these problems are often impossible to breach during a normal doctor's time, especially if it's a practice where consulting for more than 30 minutes is beyond the possibility. This is one of the reasons why the delay in making a diagnosis for a hereditary conjunctive tissue disorder such as Ehler Danlos is of approximately 20–25 years.


Five factors, according to our clinical observations of over 7,000 cases, strongly influence the expression of symptoms: female hormones (manifestations are clearly more marked in women), trauma (obvious and often lasting aggravation after a road accident, fall or surgery), infections (including COVID), intense motor activity without breaks, and climatology (beneficial effect of hot, dry weather, negative effect of damp cold), with some patients choosing to move to a sunnier region.
Diagnosis is based on clinical manifestations, usually in the absence of genetic testing, the grouping of which makes it possible to affirm, with certainty, the hereditary nature of the disease, based on the presence of identical cases (even incomplete ones) in the family. Diagnosis of certainty by electron microscopy is possible at the University of Louvain in Belgium, but curiously is not practised in other countries.

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Four other points are worth noting; they help to consolidate the diagnosis rather than destroy it, as is all too often the case: the great variability of symptoms in the same person, the negativity of imaging studies (MRI, CT scans) contrasting with the intensity of painful manifestations (abdomen, uterus, joints), the great variability from one person to another in the same family (even in homozygous twins), the unpredictable nature of the evolution, which is not always in the direction of aggravation, even under the effects of age, with frequent improvement after the menopause.

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During childhood

1. Did you frequently had :
-... ear infections? yes no
-... tonsillitis / sinusitis? yes no
-... bronchitis ? yes no
-... asthma attacks? yes no
-... sprains? yes no
-... bruises? yes no
-... nosebleeds? yes no
-... Wounds (knees, forehead, hands, other...)? yes no
-... migraines? yes no
2. Did you have severe stomach pains? yes no
Were you constipated? yes no
3. Were you out of breath (especially when climbing stairs)? yes no
Were you often tired? yes no
4. Were you clumsy (bumping into door frames, table corners, dropping objects, tripping, falling...)? yes no
5. Did you have any difficulties at school? yes no
Were you easily distracted? yes no
6. Were your feet (and/or hands, nose, ears) cold? yes no
7. Did your joints ache (shoulders, wrists, hands, knees...)? yes no
8. Were you very flexible (putting one foot behind your head, sucking on your big toe, doing a facial splits)? yes no

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Background

1. At what age did symptoms become more pronounced and troublesome (disabling)? ______ years
2 Have you had any major accidental trauma(s)
(falls, sports accidents, road accidents)? yes no
What kind? (Specify)
At what age(s)?

Did symptoms worsen after the accident(s)? yes no
3. What medical diagnoses were made or evoked before Ehlers-Danlos disease was suspected?

4. Have you had any operations? yes no
If yes, please give details of operations and dates:

yes no
5. Are there other people in your family with
symptoms similar to yours? yes no
If yes, who?

6. Any other information you would like to provide:
Current data

1. Pain
1.1. Do you have frequent pain in or around your joints (back, shoulders, elbows, hands, hips, knees, feet)? yes no
1.2. Do you experience pain (cramps, twists, tears, etc.) in your muscles (neck, thighs, calves, hands, feet)? yes no
1.3. Do you have violent pains (in fits and starts) in your stomach? yes no
1.4. Do your ribs hurt? yes no
1.5. Is your skin very sensitive? yes no
1.6. Are your periods very painful? yes no
1.7. Do you suffer from migraines? yes no
Circumstances of onset of pain :

How do you relieve them?
Current data
1.Pain
1.1. Do you have frequent pain in or around your joints (back, shoulders, elbows, hands, hips, knees, feet)? yes no
1.2. Do you experience pain (cramps, twists, tears, etc.) in your muscles (neck, thighs, calves, hands, feet)? yes no
1.3. Do you have violent pains (in fits and starts) in your stomach? yes no
1.4. Do your ribs hurt? yes no
1.5. Is your skin very sensitive? yes no
1.6. Are your periods very painful? yes no
1.7. Do you suffer from migraines? yes no
Circumstances of onset of pain :
How do you relieve them?
4.Mobility - Movement control
4.1. Do you experience dizziness (being drawn forward, backward, sideways or turning, or feeling that the scenery around you is turning or tilting) when you move from lying to standing or when you tilt your head? yes no
4.2. Do you experience involuntary jerking movements? yes no
4.3. Do you have tremors? yes no
4.4. Do your legs jerk when you fall asleep? yes no
4.5. Do you have muscle twitches (face, thighs, etc.)? yes no
4.6. Do you often twist your ankles, fingers, knees? yes no
4.7. Do your joints crack? yes no
4.8. Do you have joint blockages (back, neck, limbs, jaws...) yes no
4.9. Do you have joint dislocations? (shoulders, elbows, wrists, fingers, jaws...) yes no
4.10. Are you clumsy (bumping into door handles or corners of furniture, dropping objects)? yes no
4.11. Do you have difficulty lifting your arms? yes no
4.12. Do you have difficulty writing? yes no
4.13. Do you have difficulty standing? yes no
4.14. Do you have difficulty sitting? yes no
4.15. Do you have difficulty getting up? yes no
4.16. Do you have difficulty walking? yes no
4.17. Do you have difficulty running? yes no
4.18. Do you have any falls? yes no
4.19. Do you have difficulty styling your hair? yes no
4.20. Do you have difficulty putting on your clothes? yes no
4.21. Do you have difficulty cutting bread? yes no
4.22. Do you have difficulty pouring yourself a drink? yes no
4.23. Are your joints very mobile (little finger turning, hyperextension of elbows and knees, excessive shoulder mobility, etc.)? yes no
5.The skin
5.1. Is it fine and transparent (you can see the veins through it)? yes no
5.2. is it soft to the touch (“baby skin”, velvety)? yes no
5.3. Is it fragile (easily flayed, poorly healing, the site of early stretch marks -in childhood- or numerous stretch marks, stretchable on the neck or face)? yes no
5.4. Do you easily feel electric discharges (car door, shopping trolley, contact with a person (“electric kiss”)? yes no
6.Bleeding
6.1. Do you bruise easily at the slightest shock? yes no
6.2. Do you have frequent and abundant nosebleeds? yes no
6.3. Do your gums bleed when you brush your teeth? yes no
6.4. Do you have heavy periods? yes no
6.5. Do wounds bleed a lot and for a long time? yes no
6.6. Are veins fragile when blood is drawn, with significant bruising (“Miget's sign”)? yes no
7.Aberrant reactions of the vegetative system (“dysautonomia”)
7.1. Are you cold? yes no
7.2. Do you sweat profusely (head and upper body sweating at night, clammy hands, sweaty feet, armpits)? yes no
7.3. Do you have temperature rises, even in the absence of infection? yes no
7.4. Do you have “hot flushes”? yes no
7.5. Are your feet (hands, nose, ears) cold? yes no
7.6. Do you have accelerated pulse (palpitations)? (at rest, the pulse may be 40 or 50) yes no
7.7. Do you have low blood pressure? yes no
7.8. Do you experience dizziness or even brief loss of consciousness when rising from a chair or bed?
8. Digestive tract, abdomen
8.1. Do you have a bowel movement every day? yes no
If no, every __________ days.
8.2. Are you bloated? yes no
8.3. Do you swallow crookedly? yes no
8.4. Do you have trouble swallowing? yes no
8.5. Do you have acid reflux from the stomach? yes no
8.6. Do you have hernias (externalization of a piece of intestine through the stomach wall) in the stomach area (around the umbilicus, at the bottom of the stomach, just above the thigh)? yes no
8.7. Have you had surgery on your stomach? yes no
9. Mouth and teeth
9.1. Do you have jaw pain? yes no
9.2. Do your jaws lock or dislocate? yes no
9.3. Is your mouth dry? yes no
9.4. Are your gums sore? yes no
9.5. Do your teeth break? yes no
9.6. Do your teeth move? yes no
9.7. Have your teeth grown out of alignment? yes no
10. Bladder-Perineum
10.1. Can you go a whole day without having to urinate? yes no
10.2. Do you have urgent urges to urinate, or even occasional bladder weakness? yes no
10.3. Do you have prolapse? yes no
10.4. Have you had any urinary infections? yes no
11. Hearing-Phonation-Olfaction
11.1. Are you bothered by noise? yes no
11.2. Do you have a very fine ear (can you hear “little noises” that others can't)? yes no
11.3. do you have a musical ear? yes no
11.4. Are you a musician? yes no
11.5. Do you have voice deafness (weak voice, loss of voice)? yes no
11.6 Do you have difficulty hearing, especially if there is noise or voices around you? “Sign of hubbub” yes no
11.7. do you sing well? yes no
11.8. Do you hear spontaneous noises inside your ears (tinnitus)? yes no
11.9. Do you have a keen sense of smell? yes no
12. Vision
12.1. Are you short-sighted? yes no
12.2. Are you astigmatic? yes no
12.3. Do you experience visual fatigue (reading, screen) even with your glasses? yes no
12.4. Do you see double? yes no
12.5. Are you bothered by light? yes no
12.6. Are your eyes irritated? yes no
13. Breathing, lungs, bronchi
13.1. Do you suffer or have you suffered from bronchitis? yes no
13.2. Do you have episodes of respiratory “blockage”? yes no
13.3. Are you short of breath? Staircase sign" yes no
14. Genital life, sexual life, pregnancy, childbirth
14.1 Do you have sensory difficulties during sexual relations? yes no
14.2. Have you had any miscarriages? yes no
14.3. Have symptoms diminished during pregnancies? yes no
14.4. Were deliveries difficult? yes no
15. Cognitive and learning functions, emotionality
15.1. Do you have memory problems? yes no
15.2. Do you have attention problems? "Yes No
15.3. Do you have difficulty concentrating? yes no
15.4. Do you have a good sense of direction? yes no
15.5. Are you emotional? yes no
Appendix
Some simple, highly significant signs
(put a cross if the sign is present)

Door sign:
Knocking door frames or hanging door handles.

Door sign (or caddy sign):
Receiving an electric shock when opening a car door or pushing a caddy = thin, highly conductive skin.

Sock (or hot water bottle) sign:
Wearing socks at night to sleep = dysautonomia with cold feet = dysautonomia with sensation of cold feet.

Staircase sign:
Shortness of breath due to lack of respiratory control = malfunction of mechanoreceptors in lower limbs.

Miget's sign:
Significant ecchymosis in the elbow crease when blood is drawn; described in Alexandre Miget's thesis on Ehlers-Danlos (Paris, 1933), in which he first associated Ehlers and Danlos to name this disease with numerous clinical forms, which he wrongly labelled a syndrome.

Gorlin's sign:
Possibility of touching the tip of the nose with the tip of the tongue, indicating the absence or stretchability of the tongue frenulum.

Sign of the hubbub:
Difficulty hearing what a speaker is saying when several people are talking next to each other or in a noisy environment.

Coq à l'âne sign:
Switching easily from one subject to another.
The questionnaire has been expanded by the various societies to review each joint specifically and to evaluate better dysautonomia. Also, a section for mast cell activating syndrome has been added:
1. Referral to mast cell disorders
1.1. After showering, do you experience
- redness yes no
- itching yes no
- fatigue yes no
1.2. Do you have frequent abdominal pain
- frequent yes no
- very intense yes no
- accompanied by episodes of diarrhea yes no
1.3. Do you have any food intolerances? yes no
If yes, which ones?

1.4. Do you suffer from hives? yes no
1.5. Do you have rhinitis? yes no
1.6. Have you had conjunctivitis? yes no
1.7. Have you had asthma or pseudo-asthma? yes no
1.8. Have you had angioedema? yes no
If yes, do you know the cause?
Mast cells are usually reactive in conjunctive tissue disorders, releasing mastocytes and histamine and other inflammatory molecules in the presence of foods like strawberries, citrus foods, gluten and dairy, but also fish, contrast media and medications such as opioids, morphine, tramadol, etc. I'll review this later subject separetely.

So the above is a standard questionnaire to orient people in their conjunctive tissue state of health, but it also serves as an initial questionnaire for anyone suspecting of having EDS.
 
I also hope to review here the most complex region of the human genome, which is the RCCX gene cluster on chromosome 6, located in the major histocompatibility complex (MHC) class III region. Problems at this level can explain why so many people, usually very gifted and empathetic, have autoimmune disease, conjunctive tissue disorders and psychological susceptibilities. As a curiosity for forum members, this cluster contains a big chunk of the "ALU repeat" referenced in this session:
It's time to review this because this has shown up in some people's genetic reports. I hope that the 101 genetics review above will help to put the information into perspective. Or as the Cs say, it's the soul that counts!

Courtney Snyder, a holistic, functional and environmental psychiatrist, provides a down to earth explanation:


Basically there’s a cluster of genes that are inherited together, they each can mutate easily and because they're big players, if they do have a mutation, they can make people vulnerable to wide range conditions and symptoms.

That these genes are inherited as a block as opposed to being inherited separately, doesn’t mean a mutation in one causes a mutation in all. There does, however, seem to be a high rate of co-inheritance of mutations in two of the genes - the gene that relates to hypermobility and the gene that relates to an impaired hormonal stress response that can result in chronic physical or mental illness in large part due to the mast cell activation it causes.

The genes in question are the RCCX gene cluster on chromosome 6, located in the major histocompatibility complex (MHC) class III region:

AdobeStock_94412309-e1546468554932.jpg

Notice how Class III is embedded between Class II and Class I. Some might remember Class II as related to several autoimmune diseases. A brief overview:


Comprising four key genes—C4, CYP21A2, TNXB, and RP1—the RCCX locus is notable for its high degree of variability, including copy number variations (CNVs) and modular arrangements. These genetic variations contribute to phenotypic diversity but also predispose individuals to a range of diseases, from autoimmune disorders to connective tissue and endocrine conditions.

[...] The RCCX complex is composed of repeating tandem modules, with each module containing:
  • C4 (Complement component 4): A critical component of the immune system, playing a role in the classical complement pathway. The C4 gene exists in two isoforms, C4A and C4B, which differ slightly in function but both contribute to immune defense. Variability in the copy number of these isoforms has been linked to autoimmune diseases such as systemic lupus erythematosus (SLE).
  • CYP21A2 (Cytochrome P450 21-hydroxylase): Essential for cortisol and aldosterone biosynthesis. Mutations in CYP21A2 cause congenital adrenal hyperplasia (CAH), one of the most common genetic endocrine disorders.
  • TNXB (Tenascin-X): Encodes an extracellular matrix glycoprotein that contributes to tissue elasticity and integrity. Variants and deletions in TNXB are implicated in hypermobile Ehlers-Danlos syndrome (hEDS), where tissue fragility and joint hypermobility are hallmark symptoms.
  • RP1 (STK19 pseudogene): A gene with unclear function, likely a relic of evolutionary changes to the region.
The variability in the RCCX locus stems from its repetitive modular architecture. Unequal crossing-over events during meiosis can generate CNVs, leading to duplications, deletions, or hybrid modules. These rearrangements influence gene dosage and function, impacting traits and disease risks.

Additionally, the linkage to HLA alleles within the MHC means that RCCX variability may have indirect effects on immune responses, potentially exacerbating predispositions to conditions like type 1 diabetes, multiple sclerosis, and inflammatory bowel disease.

It's Dr. Meglathery, having Ehler Danlos herself, who has connected the dots and invited people to do more research on the subject. She developed mast cell activation (MCAS), postural orthostatic tachycardia syndrome (POTS), raised intracranial pressure, chronic fatigue syndrome (CFS) and other conditions within the context of her hereditary conjunctive tissue disorder. According to her experience and research:

I believe that the RCCX Theory solves some of medicine and psychiatry's greatest mysteries. The RCCX Theory explains the co-inheritance of a wide range of overlapping chronic medical conditions in individuals and families (EDS/hypermobility, autoimmune diseases, chronic fatiguing illness, psychiatric conditions, autism, etc.). It explains the underlying pathophysiology of chronic fatiguing illnesses with so many overlapping features (EDS-HT, CFS, Chronic Lyme Disease, Fibromyalgia, toxic mold, Epstein Barr Infection, MCAS, POTS, etc.). And finally, it reveals the gene which I believe confers a predisposition toward brilliance, gender fluidity, autistic features, and stress vulnerability, as well as the entire spectrum of psychiatric conditions (other than schizophrenia which can be co-inherited).
Please understand that I am NOT saying that everyone with these diagnoses fits in this group; rather I am saying that in many families, a cluster of these diagnoses will be found and I believe that those families are likely to contain the gene mutations I discuss. For example-you may see a family with a member, often female, diagnosed with or suspected to have Ehlers-Danlos Syndrome, Hypermobility Type (EDS-HT), postural orthostatic tachycardia syndrome (POTS) and mast cell activation syndrome (MCAS). Then in the extended family, you may find autoimmune diseases, i.e. multiple sclerosis, cutting and eating disorders, "possible bipolar disorder," gender fluidity, a highly successful and innovative genius, someone with chronic fatigue syndrome (CFS) or fibromyalgia (FM), someone with severe post-traumatic stress disorder (PTSD) and someone else with bouts of psychosis. The children who are more scrutinized in this day and age, may be diagnosed with attention deficit disorder (ADD), sensory processing issues plus or minus Asperger's Disorder (I know, I know, not in the DSMV:>)). And the kicker, these issues may be found on both sides of the family because I believe that we are attracted to each-other. There is a characteristic psychological profile (CAPS) which goes with this: sensitive, emotional, often gifted and we tend to surround ourselves with others who share these traits.) The degree of hypermobility ranges from none to severe in this family and correlates with the degree of musculoskeletal involvement (joint pain/dislocations/surgeries required to stabilize joints) and orthostasis/"dysautonomia," but not with the other "sick" symptoms which tend to develop later in life only in some, mostly women but not always. Many will react strongly to stress. If this sounds like your family (albeit a dramatic version), I am writing this for you.
Over time, it has become clear to anyone who frequents the chronic illness forums, sees patients with an open mind or keeps up with the literature in this field that there seems to be a frequently disabling epidemic involving a large number of syndromes/symptoms/diseases with overlapping symptoms affecting mainly young, vibrant, talented people (predominantly women) and if you look, many, but not all, have joint hypermobility (double jointedness, ligament laxity). These are (to name a few and I'm probably leaving some out inadvertently):

Ehlers-Danlos Syndrome, Hypermobility Type (EDS-HT)
Chronic fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME)
Fibromyalgia (FM)
Chronic Lyme Disease, Gulf War Syndrome, Toxic Mold/Biologic Illness
Mast Cell Activation Syndrome (MCAS)
: histamine intolerance, migraines, diarrhea, sinus pain, burning eyes, syncope, distractibility, brain fog, irritability, interstitial cystitis, hyper-adrenergic POTS, etc., depending on location of the mast cells
Postural Orthostatic Tachycardia (POTS), Dysautonomia, Orthostatic Intolerance, Low Blood volume
Pain Syndromes: Neuropathic Pain Syndromes/Chronic Regional Pain Syndrome/Myofascial Pain Disorder/Frequent Dislocations/Dysmenorrhea/Chronic Headache/Migraines/Interstitial Cystitis/Vulvodynia/Temporomandibular Joint Disorder (TMJ)
GI Syndromes: Irritable Bowel Syndrome/Cyclical Vomiting/Gastroparesis/Food Intolerance/Gut dysbiosis/Candida overgrowth/Leaky Gut Syndromes/Malabsorption Syndromes
Raised Intracranial Pressure Conditions: Pseudotumor Cerebri/Benign Intracranial Hypertension/Posterior Reversible Encephalopathy/Acquired Chiari Malformation
Neurological Issues: Neuropathies/Pain Syndromes/Uncoordinated Swallow/Vertigo/Central Apnea/Sleep Paralysis/Dysautonomia/Seizure-Like Episodes/Dystonia/Narcolepsy/White Matter Lesions/Small Fiber Polyneuropathy (Erythromelalgia)/Restless Leg Syndrome/Brain Anatomic Abnormalities (big Amygdalae-fear and emotional center; small anterior cingulate; chiari malformation, hydrocephalus)
Mitochondrial Disorders
Immune Dysregulation:
Combined Variable Immunodeficiency (CVID)/IgA deficiency/fungal infections/recurrent HSV infections/no colds for years, severe bacterial infections, inability to clear strep/Epstein Barr/mycoplasma/chlamydia/candida, dysbiosis, small intestinal bacterial overgrowth, multiple sclerosis (MS), autoimmune disorders-classic and non classic, i.e. mixed connective tissue disorders/eosinophilic disorders, high TGF beta/inflammatory conditions (endometriosis, etc.), Chronic Inflammatory Response Syndrome (CIRS)
Psychiatric Issues: Psychiatric Conditions due to Dysautonomia (Panic/Anxiety)/ADD/Hyperfocus/Autistic Wiring/Sensory Processing Disorders/Psychosis/Schizophrenia/Chronic Illness: Stress and Loss/PTSD/Mood Disorders (Bipolar/Unipolar)/Chronic Insomnia/Generalized Anxiety Disorder/Obsessive Compulsive Disorder/Phobias/Obsessive Compulsive Personality Disorder/Paranoid Disorders/Emotional Dysregulation/Compulsive Behaviors
Hormonal Disorders: Sex Hormone Disorders-Cystic Ovaries, Acne, Water +/- Fat Associated Weight Gain, Breast and Tissue Swelling, Fertility issues, Hot Flashes/Night Sweats; Adrenal Gland Issues: Adrenal Fatigue, Addison's, High/Low Cortisol, Low Aldosterone; Pituitary Hormone Abnormalities-ACTH, TRH-Mediated Thyroid Disorders; Autoimmune Hormonal Issues (i.e. Hashimotos's Thyroiditis), etc...
GU/Renal Issues: Fibromuscular Dysplasia, Diabetes Insipidus, Interstitial Cystitis, Vesicoureteral Reflux
Misc.: Extreme Temperature Dysregulation (Dysautonomia or not), Multiple Chemical Sensitivity, High Adrenaline/Noradrenaline (also called norepinephrine) States, Erythromyalalgia, Raynaud's, Livedo Reticularis, Evidence of Poor connective tissue integrity (dislocations, bruising, bleeding, petechaie, calcific aortic valves, Mitral Valve Prolapse, etc), Dry eyes, Tinnitis, Subcutaneous Adipose Disorders (Lipidema, Dercum's Disease), Left Handedness, Gender Fluidity (LGTB, lack of traditional gender roles),
Perhaps: Medullary Sponge Kidney, Pyroluria, disorders of copper and zinc regulation, Early Onset Parkinson's Disease
I believe that many cases of these overlapping medical issues/diseases/syndromes/symptoms result from just a few mutated genes which tend to travel together in contiguous (side by side) mutations in the only part of the human genome where that can happen, the RCCX module. In other words, these mutations mix and match to produce different patterns of these conditions within families, dependent on the severity of the mutation, the amount of stress involved (e.g. the CYP21A2 mutation) and the presence of other mutations which can enhance or decrease the overall severity of illness. This is why these conditions occur in a high rate in hypermobile folks but hypermobility is not necessary to go down this path.
I think her observations are very astute. The above does seem to occur within families, although not always.

Provided all that can possibly go wrong, having a hereditary connective tissue disorder is not your worst case scenario, considering the above. If it makes you more aware to connect the dots, more empathetic and sensitive, it might be the price to pay.

Professor Hamonet describes another sign of Ehler Danlos patients, which is that despite all the fatigue and pain and other incapacitating symptoms, they're often first in their class. Their awareness, insight and capacity to pay attention, is above average.

Although efforts have been made to pair up autism with Ehler Danlos, the fact remains that Ehler Danlos individuals are very empathetic, gravitating to roles and jobs where they can help others, in direct contradiction with autistic definitions. This "urge to help others" tendency is noted also by Hamonet, after evaluating thousands of patients.

For some people, inability to make direct eye contact is more related to anxiety and proprioceptive problems, where they can feel and sense everything without the appropriate boundaries. Hamonet also noted how the only system not affected in Ehler Danlos is the neurological system. The seemingly neurological issues: dystonias (trembling), neuropathic-like pain and bigger amygdalas and anxiety, comes from the proprioceptive defects and inappropriate connective tissue, not the brain per se. The brain only wires according to stress signals which can then later affect the mind and temperament of the individual, and the size of the amygdala. Connective tissue anomalies surrounding the brain (meninges) can give rise to Chiari-like problems, but it's not the brain at fault, but the surrounding connective tissue.

Autistic children may be hypermobile, benefiting often from the same treatment (compressive garments) as with Ehler Danlos individuals. There's a clear contrast of those clearly autistic and those who, despite everything, make it their aim to connect and serve others. I suspect that the autism vs not-autism, might have to do with this session:


(L) Is there some telepathy going on with these kids?

A: Yes

Q: (aragorn) Are these abilities a direct result of their condition?

(L) That is, they are autistic, right?

(aragorn) Yeah.

(L) Is it a direct result of their condition?

A: No.

Q: (aragorn) Did they just happen to inherit certain genes?

A: No. Modified in the womb.

Q: (L) Modified by who? By who?

A: 4D STS. Who else?

Q: (aragorn) Do most autistic non-speakers have these abilities?

A: A large number, yes. But genetic modification is problematic.

Q: (L) Why is the genetic modification problematic?

A: If ensouled that can modify the modifications.

Q: (L) Are you suggesting that not all of them are ensouled?

A: Yes.

Q: (L) So if they're not ensouled, if they're like OPs, then the genetic modification works. Is that it?

A: Yes.

Q: (Joe) Why are they modified in the womb by 4D STS to have these abilities? What's the point of modifying them?

A: Preparation for coming changes.

Q: (Joe) They'll turn them into minions.

(aragorn) The non-physical place, The Hill, where these non-speakers say they meet regularly to communicate sounds a lot like a locus in fifth density. Is this an accurate assessment?

A: No. Abducted to 4D.

Q: (aragorn) Many of the non-speakers talk about teachers coming to them at night to teach various things like new languages. One said she had learned Hebrew from a rabbi, and another said he had learned Egyptian hieroglyphics from a God. Who or what are these teachers?

A: Typical abduction experiences.

Q: (L) So they're being abducted by aliens and taught stuff.

(Niall) Presumably their parents were...

(Joe) It is very similar to the UFO lore about abductions and impregnating... the Cs have talked in previous sessions about creating a new race, and all that kind of stuff. But is the fact that they're autistic a function of the genetic modification, or is their autism a function of something else?

A: Accessibility portal.

Q: (Gaby) So do these children have a soul or not?

(L) We already covered that. They said if they're ensouled, it can modify the modifications. But if they are OPs, the modifications hold.

(Joe) Did we ever ask what the general cause of autism in kids is?

(L) What is the general cause of autism?

A: Vaccines.

Q: (L) So in other words, a large number of kids are being made autistic by vaccines, which then makes them susceptible or accessible to 4D STS. Is that it?

A: Yes.

Q: (T.C.) The funny thing is... I've just been thinking about that over the last minute or two, and the problem is that these kids were tampered with whilst still in the womb, and vaccines are obviously given after the kids are born. So it must be a different method.

(L) Yeah, so...

(irjO) I've got a follow up question: If they have a soul and that can modify the modifications, can they connect with the STO side?

A: Yes.

Here's how Dr. Meglathery puts up the mental issues:


I posit that a child carrying a CYP21A2 mutation has the same brain as a child raised in adverse circumstances, with enlarged limbic structures (amygdala), wired-in dysautonomia and primed connections in the limbic and neuroendocrine systems. This is a brain wired for danger, (CAPS, CYP21A2 Associated NeuroPsychiatric Spectrum). With increased threat detection and enhanced stress response comes some gifts, if present in moderation: enhanced empathy (ability to read emotions in others), sensory sensitivity, superior pattern recognition/information processing, times of intense hyperfocus/obsession/special interests and unusual abilities (often in music, arts or abstract thinking) . With any stress (even minimal trauma), the threat response circuits are reinforced and epigenetic changes can further strengthen these connections, creating PTSD-like wiring and reactions. These stress-induced/primed circuits in the brainstem and limbic system can be associated with the emergence of bursts of emotional dysregulation, dysautonomia, motor and sensory syndromes (hallucinations, dystonia, catatonia, cataplexy, non-dermatomal sensory symptoms, non-epileptic seizures, etc.) and inappropriate states of consciousness (fight/flight, freeze, shutdown).
She doesn't highlight the proprioceptive problems, which can exacerbate emotional dysregulation and explain non-epileptic seizures at a physiological level, but still, very good points above.

In short, this is a vulnerable cluster gene, which has some part of the "ALU repeat" referenced in the first post in this thread, which is related to "truncated flow". Technology nowadays can't study it in any detail. Though some people might have the tenascin-X gene anomaly showing on 23 and me, then you know that the cluster was affected within your family.

The congenital adrenal hyperplasia (CAH) co-existing with Ehler Danlos due to genetic recombination within this genetic cluster might explain the gender fluidity issues in Ehler Danlos patients. They're just kind of flooded with male hormones at a very early stage (in case of the co-existence of the CAH gene cluster).

People with connective tissue disorders do seem to be more psychic. They are also reported to have more spirit attachments, until they work otherwise. That is why some come across as so negative or totally crazy. But as I mentioned elsewhere in the forum:

An analogy can be said about the conjunctive tissue in the brain's interface with the information field, in a sense. It's also permeable or leaky. And as we are in 3D service to self (STS), the main influence by default, unless it's consciously chosen against with knowledge and being, is negative because we are aligned with 4D STS by default. Sure, there will be service to others (STO) elements, and that depends mostly on each individual's inner nature. But our state of affairs in this realm is service to self (STS).[...]

That doesn't mean it's negative from the get-go. Perhaps some hEDS can just be more open to non-material realms. For instance, reading about polysomnography papers in hEDS to see sleep disturbances, the two cases whose results were available for free without being behind a paywall, reported seeing shadows in the bedroom of the hospital where they slept. Those shadows perhaps are always there, influencing everybody, and no one can ordinarily see them. I used to see shadows when I was little, and I knew that they were not supposed to be there. As a little kid, it just gave me extra awareness about the reality around me.

I think when people with hEDS develop healthy boundaries and a sense of self, they can be immune from service to self energies from higher realms or from parallel dimensions. Mitigating incapacitating symptoms in hEDS will help a long way with this process. Hyperbaric oxygen therapy, a diet that doesn't trigger inflammatory reactions and adapted exercise can go a long way. By consciously aligning yourself with creative STO forces, the STS influences lose their power.
 
All very interesting! Thank you, Gaby.
My hyper-mobility (mild) seems to come and go year to year. Relatively stiff right now.
I'm a big fan of KT Tape for managing related hand instability issues, which can be (occupationally) painful.
Don't really agree that (extreme) hyper-mobility isn't a big deal, as it can be in weight-bearing foot stability.
Lycra is wonderful for skin/soft tissue/vascular support, especially later in life when propensity to conditions like chronic leg edema and venous insufficiency can wreak havoc. I have the hardest time to convince patients at risk for such to begin even light compressive therapy. I'm working mostly in elder-care facilities now, where I see complications of these issues all the time. Remarkably, they're usually not painful.
Off-topic:
American healthcare model seems to $trongly align with problem management rather than problem prevention. Exception seen in prevention of Diabetic Foot Ulcers/amputation prevention programs, which have been really helpful. A lot of federal arm-twisting being done these days to force PCPs to do foot health examinations.

I've been trying to get hold of some of that elastic mono-filament used in Herman Miller Aeron Chairs. It is manufactured in Greensboro, NC, not too far from here. No luck yet, as they seem to be more interested in industrial-size sales. I have in mind to experiment with it on a domestic finer gauge knitting machine to create a fabric for compression and maybe even a new type of foot suspension/support model. So many possibilities...

Wondering if there are any reported issues of RF exposure with collagen/whatever integrity? Are we seeing a recent uptick in such problems?
 
Regarding compressive soft tissue support with RF protection, I'm thinking it might be interesting to try to core-spin a bombyx silk fiber around an elastic monofilament, then machine knitting compression garments with that type of yarn. Zips could make them easier to don and doff.
Personally, I feel a lot better when wearing "strong" underpinnings. Perhaps these help with hypotensive issues, like frequently needing a bit of Trendelenburg position after a shower and getting dizzy on up-elevator trips.

Here's a short video on core-spinning yarn. I have in mind a finer-diameter yarn than this for my project, and also use of a more organized type of silk filament (pure bombyx fibers), which could then be plied for better filament wear.
 
Let's review the subject of allergies and mast cell activation disorder, the kind of affliction that leaves you in total dysfunction for daily life. Many might have heard "histamine intolerance" instead.

In MCAS or mast cell activation disorder, mast cells are reactive when they shouldn't be, releasing their contents (degranulating) when they shouldn't necessarily.

Mast cells originate from stem cells in the bone marrow, and then pass into the bloodstream as “progenitors” and finish their maturation process in connective tissue, particularly the skin, but also in the mucous membranes of the digestive, respiratory, ear, nose and throat tracts, and the urogenital mucosa.

Mast cells are sentinels, they protect us from possible aggression.

They provide immune defense, they protect us against tumor proliferation, they promote wound healing, they contribute to fibrosis processes and angiogenesis. These are all good things.

When mast cells are stimulated, they release locally and eventually into the bloodstream, substances they have synthesized, including histamine, heparin, prostaglandins, leukotrienes, platelet activation factor, angiotensin converting enzyme, proteolytic enzymes, cytokines, chemokines, tumor necrosis factor alpha.

The problem comes when they degranulate when they shouldn't or when they're hyperreactive, as it's often the case in connective tissue disorders.

Then, there's a lot of inflammation, both localized - lungs, digestive tract, urinary bladder and genitals, skin, eyes, nose throat. And generalized - lot of retention of liquids, you're literally miserable with brain fog, fatigue, but also pain.

In the skin there might be redness, warmness, urticaria, dermographism and Darier's sign (provocation of characteristic redness and edema by rubbing a skin lesion), you can write your name in your skin!

In the digestive tract there's colics, pain, diarrhea and/or constipation, nausea, vomiting, bloating, flatulence, belching. Digestive pain can lead a person to the emergency room.

At the cardiovascular level there are palpitations, vasovagal reactions, low blood pressure, anaphylactic reaction, postural tachycardia or dysautonomia.

At the level of the musculoskeletal system there are all types of joint, bone, muscle and/or tendon pains. These pains may be entirely due to the mastocytosis activation disorder.

At the urogenital tract level there's frequent urination (> 6 per day), urinary burning sensations, interstitial cystitis, libido disorders.

At the level of the lung and ear-nose-throat tracts there's cough, respiratory issues, conjunctivitis and sinusitis.

At the neurological and psychological level there's pathological fatigue, sleep disorders, headaches, dizziness, mood disorders such as unusual sadness, anxiety, irritability, concentration and memory difficulties.

Notice how MCAS resemble COVID19 Long and Ehler Danlos Syndrome. They're practically interchangeable, and this is because the problem is at the level of the extracellular matrix, fascia and/or conjunctive/connective tissue.

Infamous triggers for MCAS include:
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Common food triggers are gluten and dairy, nuts, chocolate, fish, smoked meats or fish, strawberries, pineapple, kiwis, and literally ANY spicy food. Which is why a carnivore diet is so healing for people with extracellular matrix dysfunction or connective tissue anomalies.

For more food for thought, I'm quoting functional practitioner Michael McEvoy, who works with clients afflicted with conjunctive tissue disorders, which has sparked his interest in the importance of the extracellular matrix:

you start to realize that we have spent a tremendous amount of time looking at all of the intricate pathways inside of the cell, the genomics, even the mitochondria, cell membrane dynamics, go on and on and on forever about all that stuff. But we have to appreciate that the cell does not exist in an isolated state. Our cells literally are existing in a truly holistic environment with its extracellular space.
that extracellular matrix is comprised of a lot of different things. It’s comprised of what is referred to as the matrisome or basically the network of connective tissue and collagen fibers, but it’s also comprised of the lymphatic vessels which run through the connective tissue, and all of the tributaries in the lymphatic system.
The extracellular matrix also will include in it immunological factors. For example, mast cells and macrophages are highly concentrated in the extracellular matrix, coordinating different immunological responses. The extracellular matrix is integral to the function and behavior of the cells in many different important ways. The extracellular matrix controls the lifecycle of the cell, modulates and influences the behavior of the cell, modulates and influences how growth factors are utilized. And that may be one of the most interesting and important parts of the matrix function, is its ability to regulate growth factors. And we know that there’s about 15 to 20 growth factors of the body that are modulated by the extracellular matrix glycoproteins.
Well, the symptom profile of Ehlers-Danlos syndrome usually involves far more than hyperlaxity of the joints. It involves usually a complex dysregulation, a multi-system atrophy, a comorbidity, its comorbidity meaning multi-symptom, multi-disease, multi-everything going on. Very common symptoms in EDS and in individuals that think they have or might have EDS include some of the stuff that I’ve already mentioned such as the tissue hypoxia, extremely weak extremities or extremely weak muscle tone, muscle function, motor function has been reduced. The oxygen saturation of the tissues may be lower. Individuals may suffer from postural orthostatic tachycardia. They may suffer from mass cell activation disorder. They may suffer from chronic fatigue or they’ve been diagnosed with CFS/ME. They may have autoimmune disease. They may have lupus or RA or even history of that in the family. They may have CAH, congenital adrenal hyperplasia. They might have problems with blood clotting, which is rapid in the EDS community. They may have endometriosis or PCOS, very common among individuals with hypermobility. These are very common things that you start to see coexisting with this disease phenotype.
one of the largest concentrations of mast cells, which are basically a type of immune cell that release histamine as well as other chemical mediators, these mast cells are found in extraordinarily high concentrations in the connective tissue of the extracellular matrix. And they have a dual function.

So a lot of us hear about mast cell activation disorder, mast cell activation syndrome, of which there is just chronic histamine intolerance, and then histamine intolerance eventually became MCASin a very short period of time now people are calling it MCAS, it’s no longer histamine intolerance. But the point is is that these mast cells have dual functions. They don’t only degrade and release histamine and serotonin and other mediators, they are also part of the regenerating and rebuilding phase of the matrix. But the mast cells are in a communicative kind of crosstalk with the cells that produce the extracellular matrix constituents called fibroblasts. You can think of the fibroblast cells as spiders, I like to think of them as spiders, and the matrix is the web that gets spun out from these fibroblasts.

And so when you have matrix dysregulation, when you have mast cell activation disorder you have some type of matrix involvement that’s going on. You have something that’s taking place that’s causing these mast cells to shift from a balanced state or a state of repair and regeneration to granulation and degradation. So we have to look at more causal factors. We know that environmental toxins can play a tremendous role in matrix dysregulation because of the fact that the glycosaminoglycans – and forgive me for keeping just brambling on – but the glycosaminoglycans which are one of the major constituents of the extracellular matrix, they’re often referred to as GAGs. The GAGs are negatively charged, they’re sulfated, and so a negatively-charged anion is going to attract positively-charged cations. And it’s been speculated for decades that positively-charged trivalent cationic metals like aluminum and mercury and cadmium, aluminum having a triple valent plus charge, are going to bond to the sulfate tails of the extracellular matrix glycosaminoglycans, causing potential autoimmune and/or immunological and/or inflammatory innate immune responding kinds of effects.

So Stephanie Seneff, the MIT scientist who’s done a tremendous amount of research publishing with [inaudible 00:26:09], was speculating based upon the overwhelming amount of evidence that the Monsanto chemical glyphosate from the ground up chemical … The glycine of the connective tissue is being replaced by glyphosate, they’re very, very similar in structure. And then all of her research kind of goes deeper into investigating these possible autoimmune effects because the metalloproteinases and the matrix can’t break down the glyphosate protein link bonds and so you’ve got all kinds of different problems going on.
So when you have matrix dysregulation it has a systemic effect, not necessarily just a localized effect. When your mast cells are degranulating in your forearm and you’re itching like mad, that is having a direct effect on receptors in the brain, that is having a direct effect on the hypothalamus and the HPT access and the ability for certain hormones to be released. We know that the release of cortisol is going to have an effect on the matrix. We know that the release of estrogen and progesterone are also going to have an effect on the matrix. Different concentration gradients are going to have an effect on the matrix. The status of a person’s hydration is going to affect the matrix. The exposure of different light is known to affect the matrix. We know that near infrared light increases collagen synthesis. We know that near infrared light attracts water to the connective tissue. We know that the extracellular matrix is very similar in its effects that if you look at the matrisome, if you look at the tunnel-like structures that the extracellular substance is comprised of, it’s remarkably similar to Dr. Gerald Pollack’s description of exclusion zone water in which you have these lipophilic tubules that are ejecting protons and are creating a highly negative charge to maintain this water fluid concentration gradient and hydration gradient. That’s happening in the extracellular matrix and all the work in ’80s and ’90s show that, even before Pollack.

So what we’re after here is a truly more holistic way of understanding pathology, of understanding physiology and how really the matrix is an organ. I don’t know if anyone realizes this, but the interstitium was just recognized as an organ system just weeks ago. Well, the interstitium is basically a bunch of spaces filled inside of the extracellular matrix, part of the extracellular matrix. I would argue that the organ system is everything that’s around the interstitium. But the interstitium has these polysaccharides and jellylike polysaccharides and proteins. Well, polysaccharides are the basic substrate or the source of all these glycosaminoglycans that make up the collagen and the connective tissue.
 
Midwestern Doctor has an interesting dot-connecting article on hypermobility, Manganese, zeta potential and structured water, venous integrity, and the vaxx. The last part is behind a paywall, so I can't link it here as I don't have access and I think it may be against forum rules.


Story at a Glance:

•Ligamentous laxity is found to be commonly associated with a variety of complex illnesses, and is frequently seen in patients who have an increased sensitivity to their environment.

•A variety of unrecognized (and often treatable) factors in the modern environment have caused ligamentous laxity to become much more common in recent years.

•A novel hypothesis that explains many of the unusual complications of the COVID-19 vaccines is that they trigger a collapse of the iliac veins in susceptible persons (e.g., those with ligamentous laxity and a corresponding weakness of the tissue lining the vessels). This, in turn, causes a variety of complications including micro-clots and mast cell activation syndrome.

•Many of the agents which significantly injure patients (e.g., vaccines) partially do so by causing the fluids in the body to clump together. This directly impairs the circulation within the body and indirectly impairs it by removing the repulsive force which prevents weakened vessels from compressing.

•In this article, I will discuss how manganese plays a critical role in ligamentous strength and our preferred protocols for repairing ligamentous laxity.


Note: over the last month, individuals who’ve been injured by the COVID vaccine reached out to me to share the earlier version of this article was very insightful for them. As such, I felt it was important to revise it so more could learn about this concept (likewise why I recently published another article discussing what creates fluid motion in the body).

Frequently, a treatment which works very well for one patient will fail to help (or harm) a patient with a very similar issue. In turn, a critical aspect of medicine is being able to recognize the unique differences between patients so you can best determine what treatment fits best for each patient and what dose is the most appropriate for each patient. Unfortunately, in “standardized medicine” (where everyone follows treatment algorithms) there is no single approach which helps all patients, and as such, protocols and dose are decided upon which will overall fit the most number of people, but simultaneously fail many others (which is a major reason individuals quit conventional care and seek out alternatives).

Note: the art of selecting the correct dose (and the perils of our current approach to it) are discussed here.


Constitutional Archetypes​

Fortunately, while this task seems impossible (as the basics of medicine are complicated enough), there are a variety of tricks that make the process much easier. One is a recognition of “constitutional archetypes” where individuals share a cluster of similar traits. This concept (discussed further here) is very useful, as once you become familiar with an archetype and you spot indicators of it in someone, it then becomes possible to identify to predict many other characteristics of that individual.

In medicine, I find one of the most helpful archetypal frameworks to be the three Gunas (from Hinduism), which posits that three primordial energies exist that individuals can be composed from:

Sattva, which has qualities including “goodness, calmness, harmonious.”

Rajas, which has qualities including “passion, activity, and movement.”

Tamas, which has many qualities including “ignorance, inertia, laziness.”
Note: Sattva in many ways mirrors Vatta, and to a lesser extent the ectomorph type. Rajas in turn pairs with Pitta and mesomorphs while Tamas pairs with Kapha and endomorphs.

From a medical standpoint, Tamasic patients tend to have a general thickness, heaviness and solidity to them, while Sattvic patients tend to have a more light and ephemeral quality to them. Each in turn has a very different response to medical therapies. Tamasics typically tolerate and often only respond to forceful interventions (e.g., many of the standard medical therapies) whereas Sattvic’s respond very poorly to aggressive therapies and instead need gentle ones to coax their health back (which are often energetic in nature like acupuncture)—something which often does virtually nothing for Tamasic patients.

Put differently, Sattvics are often recognized as being much more sensitive to environmental toxins and harmful medications (e.g., many of them refer to themselves as canaries in reference to the birds miners used to monitor for toxic gases in coal miners as they would be affected much sooner than the miners and that we should be taking their medical injuries as a warning sign many of the substances we are being exposed to are not safe). Likewise, Sattvics frequently need much lower doses of medications, but unfortunately often instead are overdosed because standardized medicine only uses the dose that best fits the entire population (which as I discuss here, is inevitably the wrong dose for many).

Note: COVID vaccine injuries disproportionately affected the Sattvic archetype.

Throughout my life, I’ve known more Sattvics than I can count, and one of the things I’ve always found immensely unfair is that most people cannot relate to the struggles they face (e.g., many, including some of their doctors, think they are “crazy” or “hypochondriacs”) or how sensitive they are to many things around them most never even notice.

As such, I’ve made one of the missions of this Substack to bring attention to their situation. At the same time however, I’ve always wondered “why is this constitution so sensitive?

Ligamentous Laxity​

At this point, I often immediately recognize the sensitive patients by their presence, their psychological demeanor and their body shape. For instance, one of the frequent physical traits I associate with this archetype is a distinct pattern of movement (which is often graceful) that I believe results from laxity in their ligaments.

Since the ligaments stabilize the joints of the body by constraining their maximum range of motion, once the ligaments weaken, their laxity (looseness) frequently causes the maximum range of motion of the joint to increase.



Individuals with ligamentous laxity have certain advantages. For example, they are normally much more flexible (e.g., they can stretch their body much further), and often become dancers because of the mobility afforded to their body.

Conversely, ligamentous laxity also creates a variety of issues for those patients. The most common one is that since their body uses the ligaments to stabilize itself when a force enters it, once the ligaments weaken, things will frequently shift inside the individual more than they should in response to those forces.

For example, individuals with ligamentous laxity tend to be more susceptible to developing chronic injuries from car accidents or other physical traumas. Likewise, their joints “pop” easily, but if they get forceful adjustments to reset the position of their bones, the bones will often go back out of place (since the stability which would otherwise maintain that structure is lacking).
Note: I have seen numerous patients with ligamentous laxity that had far too many forceful adjustments that eventually created issues for them. This normally occurs either because the repeated adjustments (performed due to the patient’s pain rapidly returning after each adjustment) further weakened their ligaments or because the weakened joint exceeded its expected range of motion during a thrust and the bones of the joint ended up in a position which created other issues for the body.

Similarly, individuals with ligamentous laxity (especially when it is significant) tend to develop a variety of issues that are ultimately treated with surgery. Unfortunately, due to being more “sensitive” and having an impaired ability to heal following the surgery, they frequently suffer significant complications from those surgeries—which sadly leads to even more surgeries (e.g., there are many stories of this in the Ehlers-Danlos syndromes [EDS] support groups).
Note: since ligaments are composed of collagen, impaired collagen production often gives rise to ligamentous laxity. Likewise, since collagen production is needed to heal from surgeries, individuals with impaired collagen production have greater difficulty recovering from surgery.

Ligamentous laxity can also create a variety of other issues throughout the body (e.g., all sorts of gastorintestinal problems). One of the least appreciated consequences of hypermobility is that the body depends upon ligamentous tension for proprioceptive feedback (knowing where the body is in space), and as a result, once the ligaments become lax, hypermobile patients lose some of the general awareness that allows us to subconsciously navigate through the world.

For example, EDS is known to be associated with impaired balance and an increased likelihood of falling. However, it’s much less appreciated that this lack of proprioceptive feedback can give rise to a general sense of anxiety because the ground does not feel as stable below one’s feet—something which is difficult to appreciate unless one has experienced it directly (e.g., I’ve met people who easily survived a major earthquake but were psychologically disturbed for years after as a result of them briefly losing their sense of the ground which they had always previously taken for granted).

What Causes Ligamentous Laxity?​

A variety of processes can cause ligamentous laxity. Frequently, a combination of these are at work (e.g., someone with a pre-existing weakness in a ligament is more likely to have something injurious to a ligament create a chronically lax ligament).

Physical Injuries​

Ligamentous weakness is frequently caused by a chronic injury to a ligament (or an injury which did not properly heal). For example, when the ankle is injured from a sprain, the ligament that keeps the ankle from turning inwards gets damaged, predisposing us to an unstable ankle and future ankle injuries until the ligament is repaired and strengthened.



Pharmaceutical Injuries​

In addition to physical injuries, biochemical injuries can also occur. This is best known to occur following the use of anti-inflammatory medications. For example, NSAIDS like Ibuprofen (which are typically the go to for “treating” sports injuries) in addition to reducing the discomfort of an ankle injury also weaken the ligaments (as by suppressing the inflammatory process it also suppresses the healing process).

This results in sprains that are treated with NSAIDs often being predisposed to future injuries (since the stability given to the joint by those ligaments is partially lost until something like a regenerative therapy is given to repair that ligament)—which in the case of ankle sprains is something I and colleagues frequently see in our patients.

One of the most common therapies given to treat joint pain are injected steroids, which, by being powerful anti-inflammatories, are often initially effective in making the patient feel better. Unfortunately, injected steroids are also weaken ligaments at the site where they are injected, particularly when they are given multiple times. Since joint inflammation (and pain) often is a result of improper joint stabilization by a ligament (leading to the joint being worn down by inappropriate pressures), this treatment approach results in patients needing more and more injections as their ligaments further weaken.
Note: this is also a common issue for those with chronic neck or back pain and unfortunately often results in them often “needing” to get a surgery to stabilize the spine—which often makes things even worse (that subject and alternative approaches to treating spinal pain are discussed here and here). One of the particularly frustrating things about this situation is that DMSO can be used for many of the same injuries and chronic pains the ligamentous destroying drugs are used for, but rather than further weaken them, DMSO often repairs the ligaments (along with often being far more effective at resolving the patient’s condition).

Additionally certain more toxic pharmaceuticals can also weaken the ligaments. For instance, beyond steroids, I have also frequently observed this after the someone suffers an injury from a more toxic pharmaceutical (e.g., this is well known to occur from fluoroquinolone antibiotic like ciprofloxacin but I’ve also seen it after an accutane injury).

This I believe results from the fact that the body is continually rebuilding and remodeling its structural tissues to meet the needs of the environment. For example, the bones depend on the weight of gravity to signal growth, so when astronauts are in space for prolonged periods of time, their bones significantly weaken (and may break once they return to Earth’s gravity) unless the astronauts also do special exercises in space.

In addition to bones, the collagen of the body also continually rebuilds and remodels itself. Since collagen production is an energy intensive process, if the mitochondria get injured (which fluoroquinolone antibiotics are notorious for doing), over time the connective tissue in the body will also weaken until it fails as a result of it no longer being able to accommodate a previously manageable force input (e.g., sudden tendon ruptures are very common after fluoroquinolone usage).

Constitutional Predispositions.​

EDS and Marfan Syndrome are the two classic medical conditions that are associated with ligamentous laxity. Both of these conditions are considered to be rare diseases, with EDS being estimated to affect between 1 in 5000 to 1 in 100,000 patients (depending on its severity and the source of the estimate), while Marfan Syndrome is estimated to affect 1 in 5000 patients.
Note: One recent paper found that the prevalence of diagnosed EDS was 1 in 500 and many believe it is even more common (e.g., I’ve met dozens of people who have appear to have EDS or an EDS-like syndrome).

In addition to EDS, there is also a self-explanatory condition known as “generalized joint hypermobility,” (GJH) which is found to affect around 12.5% of the population and predisposes them to musculoskeletal pain and injury. At this point I suspect that both this condition and EDS are under-diagnosed and that a spectrum exists between overt EDS and GJH.

Functional Predispositions​

It some cases you can watch a ligamentous laxity rapidly onset within the body. The most classic example results from the hormone relaxin (released during pregnancy), which weakens the ligaments of the body so that the pelvis becomes able to stretch and accommodate the birthing process. Because of this increased hypermobility, pregnant women become more predisposed to physical injuries (and developing musculoskeletal pain from the weight their baby).
Note: other hormones the female body secretes counteract the effects of relaxin, especially once the pregnancy is complete, and in turn, those with pre-existing hormonal imbalances are significantly more susceptible to musculoskeletal issues both during and after a pregnancy. Likewise, having pre-existing hormonal imbalances (due to the ligamentous weakness they create) can make women much more susceptible to musculoskeletal issues, particularly after menopause.

In my eyes the most important functional predisposition of ligamentous integrity is nutritional status. While a variety of things can affect ligamentous integrity, we’ve found the often forgotten metal manganese (Mn) plays one of the most important roles. In turn, it is extremely common to find people who:

•Live in areas with lower manganese levels in the soil also appear to have higher rates of ligamentous laxity.

•Have ligamentous laxity that gradually improves when they appropriately take manganese for a prolonged period.

•Have a predisposition to ligamentous laxity (e.g., EDS or a hypermobility syndrome) be tipped over the edge by a manganese deficiency, and likewise have patients with existing hypermobility significantly improve from manganese supplementation.

Since manganese deficiency is such a common issue now, we’ve put a lot of thought into why we see it so frequently. Presently, we have four leading explanations:

•First, the topsoil has been heavily depleted of essential minerals by our modern farming practices. This creates a variety of issues (and likewise significant improvements are seen in the plants grown in remineralized soil and in the humans who consume those plants).

•Glyphosate (Roundup), a toxic but widely used herbicide, has a high affinity for chelating (trapping) certain minerals, once of which is manganese. Because of this, I believe the continually increasing levels of glyphosate in the environment have contributed to the current widespread deficiency of manganese.

•Bacteria require iron for their metabolism (and in turn one of the defensive mechanisms the body has to stop an infection is to sequester iron so bacteria cannot reproduce). The bacteria which causes Lyme disease has an unusual adaptation, which to my knowledge is unique in nature (which raises interesting questions about where Lyme came from). It uses manganese instead of iron, which thereby protects it from that defense mechanism, and we have long suspected it also causes individuals infected with the bacteria (including those with “silent” infections) to become manganese deficient.

•Mineral absorption is intrinsically linked to the acidity of the stomach (as acid is needed to chelate minerals that are tightly bound to plants), so deficient stomach acid (especially in the setting of nutritionally depleted soil) may predispose one to a manganese deficiency and hypermobility.
Note: in many cases, hypermobile patients have a variety of emotional sensitivities and varying degrees of psychiatric instability. Some of these patients have remarkable responses to targeted trace mineral supplementation (particularly for anxiety or feeling “ungrounded”). This observation in turn has led me to suspect an inability to obtain sufficient minerals from the diet (e.g., manganese) plays a key role in hypermobility.

Lastly, the relationship between manganese levels and hypermobility can also be seen in animals. For example, a study (inspired by the observation manganese deficiency correlated with weak antlers that were more likely to break) supplemented half of the deer with manganese and showed those deer had thicker and stronger antlers compared to the ones which did not receive manganese.

Note: manganese is often considered to be a toxic element (as it is associated with the neurological issues that follow chronic exposure to welding gas). I always thought this was strange as manganese is a necessary cofactor for numerous critical enzymes in the body (e.g., some of those within the mitochondria). Presently, I believe this is because the toxic form of manganese (e.g., that found in welding gas) is Mn³⁺, whereas the form that helps people found in the dietary supplements (and that typically tests well for patients) is Mn²⁺. In turn, I suspect that for some reason, Mn³⁺ impairs the function of essential enzymes that depend upon Mn²⁺. Alternatively, a hypothesis has been put forward (with data to support it) that manganese, while essential, also becomes toxic at high doses.

Ligamentous Laxity and Vaccine Injuries​

There has been a longstanding observation in the integrative field that ligamentous laxity correlates with a predisposition to vaccine injuries. Likewise, a lot of readers have shared this observation with me after I broached this subject. For example, this comment was left by one reader:



Prior to COVID, the HPV vaccine Gardasil was considered by many to be the most dangerous vaccine released upon the general population (a strong case could also be made that it was either the original DPT vaccine or the original smallpox vaccine, however by the time Gardasil emerged, those atrocious vaccines had mostly faded into memory).

Gardasil caused a variety of debilitating conditions (e.g., constant fatigue, cognitive impairment, a variety of autoimmune conditions and widespread neurologic dysregulation—things also frequently seen after the COVID-19 vaccination). At some point, holistic physicians began noticing patients (particularly women) with existing ligamentous laxity were much more likely to develop Gardasil injuries (and in turn a few researchers proposed genetic variations to account for this).

At the time, I assumed this correlation was due to:

•Individuals with ligamentous laxity also being more likely to be the more sensitive patients.

•Ligamentous laxity having a longstanding association with mast cell disorders, a condition which makes one hypersensitive to a variety of substances (e.g., drugs or vaccines).
Note: mast cell disorders are frequently observed to emerge in patients who develop COVID-19 vaccine injuries.

However, last year I learned of a novel hypothesis put forward by one of the leading doctors treating COVID-19 vaccine injuries which tied a lot of things together.

Iliac Vein Compression​

The edited (condensed) twelve minute version of his presentation can be viewed here:


Dr. Jordan Vaughan’s key points (and my comments on them) are as follows:

•Many of the debilitating complications of the COVID-19 vaccine appear to result from the iliac vein (which governs venous return from the legs and pelvis) becoming compressed and its blood supply becoming significantly obstructed (which in turn gives rise to numerous characteristic symptoms that can be recognized once one knows to look for them). More importantly, this compression can often onset quite suddenly and patients remember the exact moment that compression occurred.

•The blood flow obstruction created by an iliac vein compression appears to cause a variety of conditions which could be analogized to “putrid blood,” such as blood clots throughout the body and mast cell activation syndrome.
Note: over a century ago, quite a few of the early pioneers in the medical field also noted that compression of the iliac region predisposed patients to a variety of illnesses they commonly attributed to the blood or lymph in the pelvis “fermenting.”

•A condition known as May-Thurner syndrome affects slightly over 20% of the population. In it, the (high pressure) right common iliac artery overlies and compresses the (low pressure) left common iliac vein against the lumbar spine



Normally, individuals with this syndrome do not notice it, but it some cases it can predispose them to unexpected blood clots (due to venous return being obstructed).

•Dr. Vaughan believes that the (well-documented) damage the spike protein causes to walls of the blood vessels weakens the iliac vein enough that pressure from the iliac artery can cause it to collapse. In turn, he has collected compelling radiography to prove it.




•If an iliac vein compression is treated with anticoagulation, this typically improves the symptoms of it, but once the anticoagulants are stopped, the symptoms return (as the source of the clotting has not been addressed). For this reason, iliac vein compressions are often treated with stenting, which Dr. Vaughan reports frequently significantly benefits patients.

Once I heard Dr. Vaughan’s lecture, I realized his hypothesis tied together many observations I’d made over the years and likewise explained many of the successes I had come across in vaccine injured patients after manual therapists after working on a patients hip socket either intentionally or unintentionally had partially (or fully) decompressed the iliac vein and created a dramatic “inexplicable” improvement in the patient’s condition.

The Hidden Life of Water​

In many ways, the primary purpose of a scientific model is to create the worldview that nature is fully understood and has been “mastered,” when in reality, it often has a degree of complexity which greatly exceeds what any model can accurately encapsulate. In turn, as you begin to really look into phenomena, you’ll gradually notice inconstancies that upend the entire model.

As such, I’ve tried to draw attention to the fact water has a variety of unique properties that help explain many of life’s mysteries.

Liquid Crystalline Water​

For example, I’ve written about the discovery that water ( H2O), when exposed to ambient energy source (particularly infrared) and a polar surface, will displace some of its hydrogen atoms and begin forming a hexagonal lattice of H3O2 molecules, and enter a fourth phase of matter between being a liquid and solid where it behaves like a liquid crystal.

This property is immensely consequential in biology, as much of the water within living organisms (due to them having many polar surfaces it can form from) is in this phase. For example, in a recent article, I highlighted that the hydrogen ions being displaced creates an energy gradient which allows life to transform ambient energy sources in the environment into something that can be harvested to fuel life (e.g., by creating spontaneously flows within the body).

Another critical property of this 4th phase of water is that it expands, resists compression or penetration, and is virtually frictionless when two layers of it slide against each other (in a manner virtually similar to what is seen when a skater skis on ice). This serves many critical functions for the body. For example, in the blood vessels, by having a continuously regenerating lining of H3O2 coat the inside of them, it protects them from being worn down and damaged by all the blood flowing through (while simultaneously providing a lubricating surface that allows the blood to freely flow through the vessel). Likewise, many of the joints (e.g., the knees) are lined by polar surfaces that promote the formation of this water and contain viscous proteins that further promote the formation of this water, all of which then creates a frictionless weight bearing mechanism between the bones that does not get worn down by the forces continually exerted against it.

Note: here I discuss in much more detail how liquid crystalline water creates the structure and stability of the body.

Zeta Potential​

Another concept I’ve emphasized throughout this publication is zeta potential, which quantifies the electrical charge difference between colloidal particles in the liquid they are suspended within (and applies to most fluids systems in nature). This is because like charges repel each other, so when a sufficient amount of matching charges are present (which in nature are almost negative due to liquid crystalline water creating a negatively charged layer on what it coats), the particles in the solution will resist outside pressures (e.g., gravity or attracting charges) to clump together and instead stay dispersed. Conversely, when insufficient zeta potential is present, they will clump together, with the clumps becoming larger and larger as the zeta potential declines.



In the body, if this happens, red blood cells will clump together, eventually forming microclots which can cause either acute illness, or more commonly chronically debilitating illnesses. In turn, we believe this process underlies many chronic illnesses as agents that are well suited for restoring it often create dramatic improvements in health (which numerous readers here have reported) while conversely agents that are well suited for disrupting it (e.g., aluminum, the spike protein, and dangerous microbes such as malaria) can often cause a myriad of challenging illnesses.

Note: other fluids in the body (e.g., cerebrospinal fluid or lymph) will also clump together if their zeta potential is disrupted.

Interwoven Vessel Integrity​

Because the body is so interconnected, it is often quite challenging to break it into separate pieces (which every model has to do). For example, there is a huge overlap between liquid crystalline water and zeta potential, so as one worsens, the other often does too and as one improves, the other often improves (discussed further here).

One of the key things to understand about both of these is that they allow the blood vessels to resist compression, as throughout the body liquid crystalline water creates the incompressible units that create the inherent expansion of the body and likewise, the mutually repelling charges in water (with a sufficient zeta potential) also prevent compression from occurring. Finally, the vessels themselves have an inherent tissue strength that allows them to resist compression, which in most cases can compensate for a partial impairment of the other two.

However, as these fail, it begins becoming possible for compressive forces to collapse the veins. Since hypermobility weakens the lining of the blood vessels, in practice, we find hypermobile patients have a reduced ability to tolerate impairments of the physiologic zeta potential or the liquid crystalline water within it (as the strength of the blood vessel linings can no longer adequately compensate for a loss of the expansive forces within the vessels), and as such, they often far more frequently pass a critical zeta potential threshold where issues immediately follow.

Similarly, both of these also directly influence the integrity of the lining of blood vessels. For example, in addition to liquid crystalline water (if present) providing the layer that protects the blood vessels, the blood supply for the larger vessels, the vasa vasorum is quite narrow and hence easily obstructed by zeta potential induced microclots (which disproportionately affect the smallest vessels), at which point the lining of the vessels was repeatedly observe to desquamate (fall off, allowing the deeper areas to get damaged). Likewise, many of the agents which impair the physiologic zeta potential (e.g., pathogenic bacteria or the COVID spike protein) also frequently damage the lining of the blood vessels.

Because of all of this, I hence believe the increased susceptibility to blood vessel compression and the myriad of symptoms blood flow obstructions can create helps to explain why hypermobile patients are so sensitive to certain toxins (e.g., many microbial ones) which adversely affect the physiologic zeta potential. Likewise, I believe many of the dramatic improvements certain patients see (e.g., those with COVID vaccine injuries) result from critical blood flow obstructions reopening.

To further illustrate the interconnectedness of these processes:

•In addition to stenting the iliac vein (to reopen it) other dramatic improvements have also been observed with venous stenting. For instance, for years patients with multiple sclerosis (a condition which has been found to be 10-11 times as common in EDS patients) have experienced significant benefit from stenting their jugular veins open (thereby improving the venous drainage of toxins from their head). Likewise, before this technique was restricted I heard many stories of individuals with other complex disorders (e.g., fibromyalgia and lyme disease) significantly improve following stenting of their jugular vein.

•Many of the challenging chronic neuroimmune illnesses that are associated with both poor circulation and mast cell activation syndrome (e.g., Lyme disease and mold toxicity) also have unique characteristics that directly impair zeta potential. In turn, we frequently find that attempts to treat these diseases don’t go well unless something is also done to mitigate their adverse effects on zeta potential (especially within the lymphatic system).

Zeta Potential Destroying Vaccines​

To “work,” Gardasil (the HPV vaccine) used an adjuvant which dramatically impaired the physiologic zeta potential. In turn, once the vaccine hit the market, a wide range of injuries were reported from it, including many new autoimmune disorders, a variety of circulatory impairments and it triggering mast cell activation syndrome.

As it happens, those are also the exact same issues that were found from the COVID vaccines (another vaccine which is highly damaging to the physiologic zeta potential)—and as I hope this article has shown, there is a rational basis for that link.

Note: Besides the HPV vaccine and COVID vaccines I believe the vaccines which most effectively disrupted the physiologic zeta potential (and all created significant illness) were:
The original smallpox vaccine.
The anthrax vaccine
The now banned DTwP (we use the DPaT now and ship DTwP to the third world).

As such, I now believe a key reason why I often see so much improvement in venous circulation after treatments are provided (e.g., for a COVID vaccine injury) to restore the zeta potential of the body is because doing so “re-expands” the compressible vessels of the body (including those within the lymphatic system).

In short, these concepts illustrate how interconnected the body is and how a weakness in one area can often predispose to a severe complication from something others would be relatively unaffected by. For example in addition to this concept we also noticed that COVID vaccine injuries would disproportionately affect areas of pre-existing injuries or inflammation (e.g., chronic arthritis or an old scar)—indicating that most of the body could tolerate the stress the COVID vaccine placed on the body, but the weaker areas could not—much in the same way the vessels can no longer tolerate a loss of the expansion within the fluids.

Note: a similar pattern of the disease first appearing in areas of pre-existing weakness is also seen in Lyme disease (another chronic inflammatory disease that adversely affects the physiologic zeta potential).


Repairing Ligamentous Laxity​

In a previous article, I share my perspectives on neck and back pain, emphasizing essentially that the root cause of those issues are rarely addressed and instead people are routinely given extremely dangerous drugs or surgeries to “fix” that pain—even though, sadly they often just make it worse. In the second part of the series, I shared some of my perspectives on how to treat spinal pain.

A key foundation of that approach is that it’s necessary to restore the strength of the ligaments in the spine, as its ligaments stabilize it and prevent the joints from grinding each other down (at which point they become inflamed, lose their mobility and hurt). Unfortunately, the approach medicine uses to address this, injecting steroids into the joints to reduce the inflammation, in many ways is the worst thing you can do because steroids damage ligaments, and thus it’s quite common to see people who receive steroid injections for back pain progress to needing (often disastrous) spinal surgeries—something I believe in part is motivated by how incredibly lucrative those surgeries are.

Note: as you might guess, individuals with ligamentous laxity (e.g., EDS patients) frequently end up being subjected to harmful spinal surgeries, and in that article, I shared a few tragic cases of this happening.

In the final part of this article, I will discuss how many of the same approaches we use for other issues in the body (e.g., manganese protocols for spinal issues) can also be used for individuals with ligamentous laxity to strengthen their ligamentous integrity (which in addition to repairing the musculoskeletal system ofter creates a myriad of unexpected benefits).
 
Well this just summed up my life, I answer yes to most of the questions and statements. Symptoms increasing as I get older. Not only can I suck my toes (been a while since last I wanted to) but I can wrap my feet around my head, I’m always in pain, seemingly intolerant to everything, tried every trick, detox, supplement, remedy, support etc in the book with no relief, multi system failure but no one can find anything wrong with me… all of the mental stuff, physical and psychic stuff…. The whole banana. Except a few tiny bites .

It’s good to have a probable answer.

Thanks Gaby and everyone who contributed info here. Looks like beef is the answer…. and manganese …


 
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