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Total raised so far

£4,008.00 Online donations +£532.50 Gift Aid See breakdown

Recent donations

10 hours ago

Michelle Mcelhinney

£20.00

+ £5.00 Gift Aid

Well done team Waltons on highlighting the lack of funding and research in ME

2 days ago

Kieran Doherty

£10.00

Thinking of James and best of luck to both teams

2 days ago

Joyce, Alison, Edward and family

£50.00

+ £12.50 Gift Aid

Very best of luck to you all! We’ll be thinking of you!! Xx

3 days ago

Anonymous

£20.00

+ £5.00 Gift Aid

4 days ago

Aaron Bell

£20.00

4 days ago

Lisa

£10.00

4 days ago

aaron campbell

£10.00

The lack of research and treatments and general attitude towards this illness from medical professionals is a scandal. Things need to change!!

6 days ago

Cara McLaughlin

£20.00

+ £5.00 Gift Aid

1 week ago

Erica Lawrence

£20.00

1 week ago

Paul and Brenda Mullan

£10.00

30 pounds total

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.

Charity number: CT58352

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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