EventsNewsSeizure First Aid – from Epilepsy Ireland1 month ago** SIGN UP WITH YOUR EMAIL TO GET ZOOM LINK: ** https://mailchi.mp/c9dbbeea9d7c/4ebtn5da0wOur friends over at Epilepsy Ireland are providing a…
EventsNewsIAD 2025 is Coming And we’re Lighting Up BLUE!1 month agoIreland Turns Blue for International Angelman Day February 15 On Saturday 15 February, prominent landmarks in Ireland and around the…
FundraisingRun with ASI – Clontarf Half Marathon Nov 20245 months agoJoin Us for the Clontarf Half Marathon & 5 Mile Run in Support of Angelman Syndrome Ireland! This November, we…
NewsOur Community In The MediaIrish Times – For patients and parents of people suffering from rare ailments, struggling for better is a fight worth taking6 months agoFor patients and parents of people suffering from rare ailments, struggling for better is a fight worth taking Joan Johnston…
NewsOur Community In The MediaColin Farrell Starts Foundation in Honor of Son with Angelman Syndrome as He Opens Up About Their Life7 months agoAngelman Dad Colin Farrell opened up about life with his son James in this beautiful interview with People magazine Original…
FundraisingOur Community In The MediaIn the News: Kerry community walk a great success!8 months agoThis weekends Irish Independent featured one of our wonderful Angelman families from Kerry. Little RóRó inspired over 250 people to…
EventsSummer Picnic 20248 months agoJoin us at Clonfert Farm & Mini-zoo this July 21st at 12pm for a family picnic. There’s plenty to keep…
NewsOur Community In The MediaPodcast: Crystal talks to Ulysses Neuro about life with Angelman Syndrome2 years agoIn this episode, hosts Ciara and Clare speak with mam Crystal to discuss life with her 3 year old son…
NewsOur Community In The MediaIrish Examiner – Families of children with rare diseases wait three years for genetic counselling2 years agoFamilies of children with rare diseases wait three years for genetic counselling Families are waiting up to three years for…
NewsOur Community In The MediaVideo – Jack & Jill and the Johnstons2 years agoMeet Joan Johnston, who is Mum to Leo, aged five. Leo was diagnosed with Angelman Syndrome just three weeks before…
NewsOur Community In The MediaPodcast: Danielle Cullinan Opens Up About Her Daughter’s Angelman Syndrome3 years agoDanielle Cullinan talks on the Everymum podcast about her daughter Claras diagnosis, the journey to getting a diagnosis and parenting…
NewsOur Community In The MediaRadio – mother of a boy with Angelman Syndrome has said his diagnosis was discovered thanks to an “on the ball” consultant.5 years agohttps://www.newstalk.com/news/without-diagnosis-think-youre-problem-mother-son-angelman-syndrome-praises-consultant-840584 The mother of a boy with Angelman Syndrome has said his diagnosis was discovered thanks to an “on the…