Current Stanford / Dr Montoya / Dr Bonilla ME/CFS Treatment Protocol (November 2017)

[XenForo]

I think MCAS is showing up more and more in patients with MECFS. That's what I'm reading and hearing from inside the medical field.

I recently got back from seeing the Center for Complex Diseases in Mountainview CA and the doc there is having me do a bunch of mass cell tests.

 

[Diwi9]

That is my understanding, that MCAS is autoimmune.

My guess, is that MECFS will be eventually discovered to be an immune illness also, with dysregulation at both ends -- meaning the patient has both an under-active immune system and over-active immune system (autoimmune).

Did you see today's thread with the hypothesis by Jonas Blomberg? http://forums.phoenixrising.me/inde...toimmunity-and-me-an-explanatory-model.57761/

 

[Suffering Succotash]

Did you see today's thread with the hypothesis by Jonas Blomberg? http://forums.phoenixrising.me/inde...toimmunity-and-me-an-explanatory-model.57761/

Thank you for that. Interesting to read. I predict that the exhaustion suffered by MECFS patients will be discovered to be a cell mitochondria autoimmune illness -- the immune system attacks the mitochondria and disrupts the energy production cycle, the ATP --> ADP energy synthesis.