I have just come across a fantastic website, ME Research UK, which despite countless internet searches through my M.E. years, I have never heard of before.
ME Research UK is a national UK charity funding biomedical research into Myalgic Encephalomyelitis (ME) or Chronic Fatigue Syndrome (CFS). They aim to commission and fund high-quality scientific (biomedical) investigation into the causes, consequences and treatment of ME and also have a mission to 'Energise ME Research'.
Their website contains lots of useful information including research publications, support groups and useful links. You can register to receive e-mail updates on new additions to their website and also to receive their newsletter. You can make donations and sign up to become a friend of ME Research UK. They've also got some great Christmas cards which you can order by downloading a PDF flyer from the site and all profits go to ME Research UK.
The charity has helped produce the book Shattered: Life with M.E. by Lynn Michell.
This website is definitely worth a look and I will be putting in my order for some Christmas cards very shortly







