ME CFS FREE

Talk to your friends or contact them through Facebook, Twitter or other social media and encourage them to support ME/CFS. You may have other symptoms like problems with thinking. Research in New Zealand shows that ME/CFS affects peoples lives as severely as Parkinsons Disease and Multiple Sclerosis. Like any illness, there is a continuum of severity - some patients are bedbound and others able to function day-to-day. Any kind of activity often makes your symptoms worse. ME/CFS is a chronic illness whereby overwhelming fatigue is often triggered by even minimal exertion.

Sleeping problems occur along with extreme fatigue that doesnt get better with rest. You might consider making a donation to her work by clicking on the following PayPal button or the link below it.ДЈ. Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disease that causes you to feel so ill that you cant do your normal activities. Our work with the scientific, medical, and pharmaceutical communities. Nancy Klimas who is one of the leading scientists in the world for medical research into ME/CFS. The Solve ME/CFS Initiative (Solve M.E.) is a non-profit organization that serves as a catalyst for critical research into diagnostics, treatments, and cures for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid and other post-infection diseases. Consider making a donation in any amount you can afford for ME/CFS medical research. Take personal responsibility for our own health and do whatever you can to support ME/CFS medical research. Send email and letters to your representatives in congress (find their contact info at ) and demand that they take steps to increase funding for ME/CFS by National Institute of HealthДў. Clearly, we need to demand more of our government.ДЄmong the steps you can take to support your own well-being from the ravages of ME/CFS:ДЎ. as prostate cancer, multiple sclerosis, breast cancer and muscular dystrophy which collectively receive $1,168,000,000 in N.I.H. This, in spite of the fact that ME/CFS afflicts almost as many people in the U.S. The total cost of the National Institute of Health ME/CFS projects for fiscal year 2017 was a paltry $7 million.

YouвЂ™ll find us interesting, informative and supportive. To learn more about servere fatigue, ME/CFS (aka: chronic fatigue syndrome) and related conditions please refer to our open-access website.

Our membership roster is not shared with any other organization nor used for any commercial purpose.

ME CFS FREE

Membership in our ME-CFSCommunity is FREE and VERY PRIVATE. To facilitate the free and open exchange of information between those who know the most about the true impact of the affliction and are the most affected by it. The mission of the ME-CFSCommunity website is to help members move beyond the challenges of the disease. The ME-CFSCommunity is a private community reserved for those individuals from around the world who wish to learn from, and directly communicate with, those who are affected by ME/CFS and related conditions.ДЄccess to this website beyond the Home page is limited to MEMBERS ONLY to protect their privacy.

Me cfs