1 month ago
This campaign is closed and is not accepting further donations
If you'd like to support Hope 4 ME & Fibro Northern Ireland, please view their charity page.
![](/images/fundraising/91a95918-3ddf-4f3d-b4b2-1325a60e38c5/xl.jpg)
![Hope 4 ME & Fibro Northern Ireland](/charity/13170/images/homepage/logo-md.jpg?20220420100618)
Total raised so far
£5,148.00 Online donations +£660.00 Gift Aid See breakdown
Recent donations
1 month ago
Laura Caldwell
2 months ago
Kerrie Mcilmoyle
+ £6.25 Gift Aid
An incredible team effort for this very worthy cause.
2 months ago
James from Limavady Health Centre
2 months ago
Phil & Mel
+ £5.00 Gift Aid
Well done team, keep up the good work
2 months ago
Aaron
+ £2.50 Gift Aid
Good effort all
2 months ago
James Mc Vicar
Goodman Oran
2 months ago
Lynne
Well done the Walton gang
2 months ago
Fran Mcstravick
+ £5.00 Gift Aid
You're making a difference
2 months ago
Dallas Family
About us
An all volunteer, not for profit charity offering support to all patients, carers, family members and friends of patients suffering from M.E., Fibromyalgia and Long Covid. Raising awareness, providing educational events for healthcare providers and lobbying for specialist NHS services in Northern Ireland.
Roe Valley Sprint Triathlon
Event date: Saturday 18th May
Thanks to the Walton family and friends who are taking part in Triangle Triathlon Club, Roe Valley Spirit Marathon, to raise vital funds for the charity,
Myalgic encephalomyelitis (ME/CFS), is a serious, chronic, complex, and systemic disease associated with neurological, immunological, autonomic, and energy metabolism dysfunction (Institute of Medicine, 2015). Individuals with ME/CFS experience a range of symptoms including significant impairment in function, post-exertional malaise, sleep impairment, cognitive issues, pain, orthostatic intolerance, flu-like symptoms, sensory intolerance, gastrointestinal and genitourinary issues.
Post-exertional malaise (PEM) is the hallmark of the disease in which even trivial amounts of activity result in a prolonged exacerbation of symptoms and a further reduction in function.
There is no effective treatment nor cure.
The charity is campaigning for specialist M.E. services in Northern Ireland, we provide CPD certified education courses for healthcare providers and offer support, and information for patients and their family members.
Please watch the short video below to learn more about this severely debilitating disease.
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