So sorry to hear of your loss of your precious daughter. I have been totally disabled by ME/CFS for 15 years from age 50 on and at least I had 50 good years before being afflicted including being able to be the father of two to mostly healthy children.
I don’t know why heartless trolls pounce on ME/CFS threads to mock sufferers or to this day even my own PCP still tells me I am “just depressed” when the literature is clear that ME/CFS is clearly a neuro/immune disease, just as multiple sclerosis was before it became recognized as a “genuine” illness.
I am sure that the same mockers that are here now on this thread mocking CFS sufferers would have been mocking multiple sclerosis sufferers 30 years ago as having an imaginary illness without even reading the thread article showing the latest MRI evidence from Stanford U.
Dr. Montoya at Stanford heads up the neuroimmune clinic at Stanford dedicated to treating ME/CFS and I am being treated at a similar clinic at NOVA U. heare in South Florida.
Free Republic CFS thread trolls who love to mock those of us with ME/CFS need to get up to date on the medical research which proves that people with REAL ME/CFS are often found be severely immune compromised and have lots of opportunistic infections of viruses.
Hey, have you ever looked into the possibility of Lyme Disease infection? It’s an insidious disease that can mimic many other diseases, and diagnosing it can be difficult without a doctor well-versed in the subject