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Donations Available Until 6th July 2022
Adam
1y
€10
Marcus &am
1y
€50
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Thank you for taking the time to visit my fundraising page on iDonate.ie
As most of you know our 18 year old son Roan has suffered from a post viral illness since the age of 12.
He was diagnosed in 2018 with ME/CFS (Myalgic Encephalomyelitis) and since then he has not been able to go to sch...
Thank you for taking the time to visit my fundraising page on iDonate.ie
As most of you know our 18 year old son Roan has suffered from a post viral illness since the age of 12.
He was diagnosed in 2018 with ME/CFS (Myalgic Encephalomyelitis) and since then he has not been able to go to school or sit his Senior Cert Exams in Midleton CBS Secondary School and has had to give up hurling with Midleton GAA and all activities he once enjoyed and remains mostly house bound.
For those who had to experience lockdowns or illness during covid restrictions most people now have returned to their "normal" lives again.
For people with ME/CFS and their carers a life of lockdown continues.
Without organisations such as the Irish ME/CFS Association we would have very little support or understanding as unfortunately we dont have many medical professionals aware of this illness.
Im taking part in the "Blue Sunday Tea Party for ME" on Sunday May 15th 2022 as a way of helping raise awareness of ME/CFS and raise money for the worthy charity The Irish ME/CFS Association. This is an online virtual tea party and we'd love to see any photos you share on the day with blue cups, blue plates or blue icing on your cakes or even blue hair if you wish!!! 💙💙💙
I've chosen to fundraise for Irish ME/CFS Association . All funds raised here will go directly to this great cause. I hope you can help me by donating whatever you can.
Simply click the Donate button above. All donations are processed securely. You can also share my page using Share options below. This is a great way to show your support. Many Thanks for your support.
Yvonne Ger Roan and Adam
From Adams own money, the best brother anyone with ME could wish for xxx
We’ll done Yvonne, fantastic work for a great cause
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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) 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
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