SWAlexander
Senior Member
- Messages
- 2,077
Hi Martin, I listen to the podcast with Mark. Very confirming. Thank you.
https://open.spotify.com/episode/7JBo0ARMOzBbFk1bds0R9n?si=eAZMDp23RXC3fy1yK9YnSQ&nd=1
Mark, compared to the millions, has a very good Doctor. Mark also mentions, as many can confirm, that some meds can help temporarily which would confirm my previous suspicion the core problem lies in the Cerebrospinal fluid (CSF), or in the spine/bones/bone mark where corpuscles are produced.
Listen to what different meds Mark has tried and didn´t work or only temporarily strengthen my belief that there is genetic methylation.
In my opinion, the only way to find a bio-marker is, if 23andme would get involved by comparing genes from 1000 ME/CFS patients to find a common marker.
https://open.spotify.com/episode/7JBo0ARMOzBbFk1bds0R9n?si=eAZMDp23RXC3fy1yK9YnSQ&nd=1
Mark, compared to the millions, has a very good Doctor. Mark also mentions, as many can confirm, that some meds can help temporarily which would confirm my previous suspicion the core problem lies in the Cerebrospinal fluid (CSF), or in the spine/bones/bone mark where corpuscles are produced.
Listen to what different meds Mark has tried and didn´t work or only temporarily strengthen my belief that there is genetic methylation.
In my opinion, the only way to find a bio-marker is, if 23andme would get involved by comparing genes from 1000 ME/CFS patients to find a common marker.