Search results

I do some work on their website. That was a link to an old page that is now taken down. They just updated their Resources page to this https://www.omf.ngo/resource-center/ I would definitely suggest that the best way to be included would be to contact them.

I don't usually post but am a long time patient and advocate. I feel like this needs to be recognized. 50 ME/CFS researchers got together to discuss their findings and OMF sponsored the event. Dr. Ron Davis made this statement at the recent Community Symposium sponsored by OMF. (my bolding)...

Yes, I had that problem with both the Charge and the Mio. I would have loved to wear the monitor regularly but it felt like I was getting arthritis in the arm that had it on. The pain increased over time. I read of many accounts on the internet about people having that same sensitivity. Somebody...

Does anyone know what the placebo was? It seems that since Rituximab is given via an IV, the placebo was probably saline. I personally respond very well to saline and wish I could find a doctor to prescribe it for me regularly (although I know that Dr. Edwards has claimed that there would be no...