The hidden face of M.E is when you can't see me

Ellen Adby is raising money for ME Association
Donations cannot currently be made to this page

The hidden face of M.E is when you can't see me · 3 May 2018

The ME Association campaigns hard to get ME recognised as a severe neurological illness. Our helpline provides essential information and support to adults and children who have ME/CFS, and to their families and carers. We also fund biomedical research into the physical nature and causes of ME/CFS.

Story

I am going to be posting something about my journy with M.E/CFS on social media each day 7th may - 13th may. Which is M.E awareness week 2018.

I have had M.E/CFS  for about 3 1/2 years now, it has been a rocky journy. With plenty of ups and downs, mostly i am on the up right now, but have had afew blips recently.

It was two years ago, i woke up one morning and found i could no longer hold my own weight. I couldn't walk. Slowly i have regained this ability with lots of rest, a walking stick and wheelchair.

M.E can hit anyone young or old; it is something you never expect to happen to you. It feels like one big nightmare that you can't escape. Try being bound to your bed in a darkend room, for weeks maybe even months at a time. See how it feels. Definatly not fun...

Donation summary

Total
£70.00
+ £17.50 Gift Aid
Online
£70.00
Offline
£0.00

Charities pay a small fee for our service. Learn more about fees