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Yvonne's Fundraiser for Irish ME/CFS Association

Fundraising For Irish ME/CFS Association
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The Irish ME/CFS Association is a volunteer-led organisation, run by people with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)

Irish ME/CFS Association

The Irish ME/CFS Association is a volunteer-led organisation, run by people with Myalgic Encephalomy...

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After several years of illness, our 14 year old son was diagnosed in 2018 with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). Currently, he is based at home full-time and unable to attend school. Some of the many symptoms he has include constant stomach pain,migraine, Irritable Bowel Syndrome,tired and weak muscles and chronic fatigue. He has gone from being an active sporty teenager to being confined to his home and even a short walk is too much for him right now.

There is no proper diagnosis for ME/CFS. There is no treatment. There is no cure. We need to support organisations like the...

RT @IAforME: Today we are sharing Krista's story from Australia https://t.co/X5FkSwVhH1 You should follow @EmergeAus one of our IAFME mem…

Sat Dec 15 23:58:27 - 0 Favorite

RT @TomKindlon: "Keeping your ticker [heart] in top-notch condition will help prevent illnesses that could exacerbate your M.E. symptoms. O…

Sat Dec 15 23:58:21 - 0 Favorite

RT @TomKindlon: "In this regular feature, Rose opens the pages of her diary to provide a frank insight into a life affected by severe M.E."…

Sat Dec 15 23:58:16 - 0 Favorite

RT @TomKindlon: "Studying with a chronic illness isn’t easy. Student and Welfare Officer at Durham University, Lorna Reeve, shares her advi…

Sat Dec 15 23:58:12 - 0 Favorite

RT @TomKindlon: "Dear Doctor: Diabetes and M.E. Our medical advisor, Dr Gregor Purdie, answers a reader's question about type 2 diabetes an…

Sat Dec 15 23:58:04 - 0 Favorite

RT @TomKindlon: I remember an Irish woman with ME and #diabetes telling me she was advised to walk daily around a nearby lake, a walk that…

Sat Dec 15 23:57:58 - 0 Favorite

RT @TomKindlon: "Many family members & friends might not consider themselves to be carers – but looking after someone with #MyalgicE makes…

Sat Dec 15 23:57:54 - 0 Favorite

RT @TomKindlon: "When you have M.E., friendships can be difficult to maintain – particularly if you’re housebound. Here, we look at how to…

Sat Dec 15 23:57:50 - 0 Favorite

RT @PlzSolveCFS: Were you able to catch the Jarred Younger SMCI Webinar? Watch it now on our Youtube page: https://t.co/iuihw4r0FA as Dr. Y…

Sat Dec 15 15:33:15 - 0 Favorite

RT @anitavandenbeld: 800,000 Canadians suffer from ME/FM, a debilitating medical condition that limits the ability to perform daily activit…

Sat Dec 15 15:32:10 - 0 Favorite
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Supporters

1
08-12-2018

Joe Heffernan

Thanks very much Joe ! Greatly appreciated! Yvonne xx
08-12-2018
50.00

About the Cause

Irish ME/CFS Association
The Irish ME/CFS Association is a volunteer-led organisation, run by people with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and their families. We work to help improve matters for those affected by ME/CFS in whatever way we feel we are able to, given our resources. Over the years we have organised meetings with international speakers and screenings of documentaries on ME/CFS in many venues around the country. We strive to raise as much awareness and understanding as possible of ...