The ME Association

Playing Nice With NICE

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  From Dizzy Girl Writes.   In view of my last blog post, I have decided to email NICE to talk about my experiences of having ME under the current guidelines and to raise my concerns about their panel. The latest tweets I’ve seen suggest that their panel for the review of guidelines for treating […]

Flu Vaccination And M.E. (2018-19)


By Dr Charles Shepherd – 12 September 2018   Seasonal flu (also known as influenza) is a highly infectious illness caused by several types of flu virus. It spreads rapidly through small infected droplets that are coughed or sneezed into the air by an infected person. Even people with mild or no symptoms can infect other people. […]

ME Connect Helpline


Whereas this site is new and is still coming together, we will never pretend that we can be manned 24/7 to give help when maybe it’s needed.  There are other national ME sites that are more established that might be able to provide you a service when you most need it.  The ME Association has […]

Two major sponsors throw their weight behind the next ME/CFS research conference | Newcastle, 13-14 October 2015


‘WE’RE DELIGHTED TO HAVE THE SUPPORT OF THE WELLCOME TRUST AND ARTHRITIS RESEARCH UK’ People with M.E. need better treatment and support. This can only be achieved through increasing the quality of research; by coordinating a stronger collaborative approach to stimulate more research through bringing in expertise from outside the field and supporting early stage […]

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