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

[worldbridger]

Wrote an intro on this subject here:

Ehlers-Danlos Syndrome Shines Light on Our Most Sensory Organ

Connective Tissue Disorders Also Key to Understanding 'Miracle Cures'

healthmatrixnet.substack.com

https://twitter.com/x/status/1964432332351578315

Alternative practitioners, who have mastered non-mainstream treatments to deal with problems at the level of the connective tissue and its relation to the autonomic nervous system, witness miracle cures every day.

They have learned to expect "action at a distance" and have understood why throughout the decades.

I once believed that the autonomic nervous system was the most unrecognized system in Western medicine, but now I think connective tissue (or fascia) takes that position.

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.

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, fascia/connective tissues have "mem-brain" like properties for everything that they connect with and encapsulate.

Understanding Ehler Danlos Syndrome is a lesson in understanding connective tissue.

Learning about miracle cures developed 100 years ago by physiologists can teach us a lot about the connective tissue and the autonomic nervous system. For more information, see: Ehlers-Danlos Syndrome Shines Light on Our Most Sensory Organ

Does Marcaine works too, or does it have to be Procaine?

 

[Gaby]

What seems to help me to keep in check some of these symptoms is watching my diet, exercising almost daily (very important) also, taking B complex, B1, Omega 3 and Mind+ helps a lot.

It seems to me that you have conjunctive tissue disorders that stemmed from after the COVID-19 era. Long COVID really brought some of the experience that EDS or fibromyalgia patients have to a large segment of the population. I was puzzled to see that people were puzzled that they had fatigue after a viral infection. I sometimes joked with some of my patients, "welcome to my world and how I felt for my entire life".

EDS have very specific clinical signs that can be identified upon physical examination, including hypermobile joints and atrophic scars, piezogenic papules on the feet, etc. EDS is really something you're born with, and there are already signs and symptoms throughout childhood.

Does Marcaine works too, or does it have to be Procaine?

For neural therapy, only procaine and lidocaine will do. It has to do with their chemical properties, half life, their structural signature, etc.

Procaine is way preferable than lidocaine.

 

[worldbridger]

It seems to me that you have conjunctive tissue disorders that stemmed from after the COVID-19 era. Long COVID really brought some of the experience that EDS or fibromyalgia patients have to a large segment of the population. I was puzzled to see that people were puzzled that they had fatigue after a viral infection. I sometimes joked with some of my patients, "welcome to my world and how I felt for my entire life".

EDS have very specific clinical signs that can be identified upon physical examination, including hypermobile joints and atrophic scars, piezogenic papules on the feet, etc. EDS is really something you're born with, and there are already signs and symptoms throughout childhood.


For neural therapy, only procaine and lidocaine will do. It has to do with their chemical properties, half life, their structural signature, etc.

Procaine is way preferable than lidocaine.

I tried this 8 years ago, only doctor in Sweden that does this, but he only uses Marcaine, maybe the reason it didn't work. Procaine is not available or not registered in Sweden anymore.