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Tilo & Tane Dietzig’s Cycle from Swansea, Wales to Hüfingen, South Germany

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

Please help us to support people with ME and their families.

We know two young girls whose lives have been massively impacted by ME and POTS and are aware that this affects so many more young people across the UK.

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.

Help Bec Dietzig

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Donation summary

Total
£1,308.35
+ £273.75 Gift Aid
Online
£1,308.35
Offline
£0.00

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