Lily's fundraiser for ME Association

Lily Anderson is raising money for ME Association
Donations cannot currently be made to this page

London to Brighton 2025 · 15 June 2025 ·

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

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.

My Mother, is one of the many people who suffer with ME. She had to see 30 specialists before getting a diagnosis, many of whom had no idea what it was or how to treat it. She has been suffering with ME for over 20 years.

I am taking part in the London To Brighton Bike ride 2025 to raise money for this Charity, To help reduce misinformation and Stigma around the illness as well as more funding to study ME/CFS and help develop better care plans and support for those who suffer from it.

Please help me, to help them.

Donation summary

Total
£655.00
+ £117.50 Gift Aid
Online
£655.00
Offline
£0.00

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