This year I thought I would keep it really simple and stress free. Yet involving as many ME sufferers as we can from all over the world .

I can't do much at the moment so what better way to still get involved by asking for donations for having a Pyjama party 🎉
All you need to do is put on your best pjs take a picture and post it on FB/Twitter/Instagram with the #MEPyjamaParty..
Let's see if we can get it trending all over the world on 12th May 2017 .
Ask friends and family to sponsor you any amount from £1 to £1000 and help us raise money and awareness.

Join this page and let's see how big our ME Pyjama Party can be .
I will share more social media pages soon x x

ME needs awareness raising all over the globe the more people who get involved then the louder our voice becomes .

I have severe ME , which has me bedridden . My Husband and Daughter are now my career . Life is tough , really tough .

Personally I want to make a difference because of my latest medical support which the DWP sent me a copy of it stated and I quote " The Available evidence suggests improvement is unlikely in the longer term."

My prognosis from them reads " I advise that work is unlikely in the longer term." 

Do you have any idea of how that feels , I am only 39 ! ME has taken everything from me . This year already I have been diagnosed with something else on top of ME which is De Quervains syndrome , having painful injections into both wrists was not fun . This illness takes and takes , if you try and fight back it punishes you for it .   I am not alone. 

Health care professionals needs to be educated in order to treat us with dignity.

I support the ME Association because of all they have done for me . They have been my friends when I felt I had none , they offered me help and advice and they gave me strength to try and make a difference even if it is a small one .

 Please help us to support people with ME and their families.ME (Myalgic Encephalopathy), or Chronic Fatigue Syndrome, blights the lives of 250,000 people in UK today. The smallest exertion can floor them; their joints and muscles ache unbearably; restful sleep eludes them; and ‘brain fog’ clouds their thinking. It changes lives drastically – disrupting study; making work impossible; and straining family relations to breaking point. Many sufferers cannot leave their homes. There is no known cure. Please help us to help them.