Lessons from the Ehlers-Danlos Syndrome Community
Fascinating - all the many helpful approaches that exist - and people diagnosed with PD are not referred to them!!! It is a kind of murder. In fact, so many do die, and before dying, lose so much of the possibility of their lives.
Thank you Gary. The issues are in our tissues, as they say! I hadn't come across the body braid and the way it is described does resonate with me. I look forward to hearing more about your experience. I know so many people with fibromyalgia. Perhaps body braid could offer an opportunity for a group to trial it.
I'd be interested in trying it, also mucuna. Diagnoses of EDS & FMS... basically a world of pain!
Gary, I'm glad that you're getting some positive results from using the Body Braid. Thank you for sharing about this.
I love this ❤ thank you.
It reminds me of my early research, 2 decades ago, after I learned my son has a large genetic deletion which includes almost every disease known to mankind if mutated. I wanted to understand what he was lacking and how to prevent disease. Once I learned how to ask good questions I found the one common denominator in most of them is glutathione deficiency. I connected as many common denominators as I could, had many tests done on his blood, feces and hair. This is how I planned my sons supplements and vegetables I cold press juiced for their enzymes and nutrients.