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Jacqueline Blair

Jacqueline's Raising Awarness For ME/CFS/PVFS Conditions

Fundraising for ME Association
£396
raised of £100 target
by 21 supporters
Donations cannot currently be made to this page
Biomedical research into M.E.is seriously underfunded. We need to do more if we are to learn how and why this cruel illness starts - how to test for it or treat it, or better still, how to cure it.

Story

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.

About the campaign

Biomedical research into M.E.is seriously underfunded. We need to do more if we are to learn how and why this cruel illness starts - how to test for it or treat it, or better still, how to cure it.

About the charity

ME Association

Verified by JustGiving

RCN 801279
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.

Donation summary

Total raised
£395.96
+ £27.50 Gift Aid
Online donations
£395.96
Offline donations
£0.00

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