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Total raised so far

£3,678.00 Online donations +£482.50 Gift Aid See breakdown

Recent donations

6 hours ago

Stef&Tom

£5.00

+ £1.25 Gift Aid

20 hours ago

Ellen Grant

£50.00

Well done Waltons, a great cause. A beautiful family, hope you get some answers and James some relief soon x

yesterday

Anne Marie Kelly

£10.00

+ £2.50 Gift Aid

Thinking of you James

yesterday

Peter and Sharon Jack

£50.00

+ £12.50 Gift Aid

yesterday

Shane McCafferty

£10.00

yesterday

Anonymous

£50.00

Something to help you reach your target - well done the Waltons!

yesterday

Gavin Connolly

£20.00

Donating in the name of my son Gavin who has been living with ME for 10yrs now. Thoughts of our family are with you James and with your family. We're involved with Predator Tri Club do your story strikes a cord!

yesterday

Siobhan Archibald

£30.00

+ £7.50 Gift Aid

yesterday

Debra McGonigle

£50.00

+ £12.50 Gift Aid

For James and all the Walton Family

yesterday

Heather McLaughlin

£30.00

+ £7.50 Gift Aid

Best of luck team Walton.

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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