Phoenix Rising tells QMUL: release the PACE trial data
Mark Berry, Acting CEO of Phoenix Rising, presents the Board of Directors’ open letter to Queen Mary University of London (QMUL) urging them to release the PACE trial data, and hopes that other non-UK organisations will join British charities in the same request...
Discuss the article on the Forums.

Inflammation in Lyme / CFS / FM presentation by Dr Horowitz

Discussion in 'Other Health News and Research' started by cigana, Oct 12, 2013.

  1. cigana

    cigana Senior Member

    Messages:
    897
    Likes:
    625
    UK
    Lotus97 likes this.
  2. Lotus97

    Lotus97 Senior Member

    Messages:
    2,018
    Likes:
    469
    United States
    I watched part of that video so far and we got Dr. Horwitz's book out of the library. Also, the first two Lyme doctors we've looked up both say they studied under him.

    One thing I'm wondering is that he said the pain is migratory. But my pain tends to occur in specific areas and it gets worse with more use. I've been trying a collagen protocol and also supplements for inflammation. I'm not really sure what to do. Right now it's worse in my hands, but other times it's been worse in other parts of my body. I've also tried medications for nerve pain and I'm taking the high dose of methylcobalamin. I'd really like to know what's causing the pain. He mentioned low dose Naltrexone (LDN) which I know some of the people on Phoenix Rising have been taking. I think I'm going to try that next because hopefully it will help with inflammation. Besides pain I've been having depression on and off for the past year which I think is from inflammation. I've actually had depression for a lot longer, but it was somewhat under control with my medication until recently.
     
  3. Valentijn

    Valentijn Activity Level: 3

    Messages:
    10,818
    Likes:
    24,204
    Amersfoort, Netherlands
    I think Lyme and ME/CFS are different illness, albeit with a significant overlap. PEM is not part of Lyme. I think it's most likely that Lyme, like other infections, can lead to ME/CFS. Getting rid of the Lyme might or might not resolve the ME/CFS.
     
    Last edited: Jan 29, 2014
    SOC likes this.

See more popular forum discussions.

Share This Page