AngelmanSyndrome
1.1K posts
AngelmanSyndrome
@AngelmanIRE
Rare Disorder 1 in 20,000. Information & support for families, caregivers & service providers. Collaborate with international scientists to advance treatments.
Ireland เข้าร่วม Temmuz 2011
404 กำลังติดตาม1.1K ผู้ติดตาม
We are kindly beneficiaries of Saturdays gala ball. As a lot of our families are also supported by Jack & Jill all funds raised will be helping our children. Please support our fundraising goals which will be ensuring our participation in exciting... gofundme.com/6urdyao?pc=ot_…
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Gentle reminder - Sunday IAD family meet up in playground. Closest entrance is the one on Whitechurch road - parking etc. Main entrance takes you closer to Market, coffee shops.
All welcome 1-3. visitdublin.com/see-do/details…
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Hi can you take time to vote for Angelman uk film which the very talented lotti fox has made. A quick register to vote then scroll down charities to Angelman uk. That’s it. facebook.com/angelmansyndro…
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Delighted if we help support a great night where ASI will benefit as well. facebook.com/angelmansyndro…
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350,000 EURO FOR RESEARCH ON ANGELMAN SYNDROME
Call for Applications for Research Grants into Angelman Syndrome
Deadline 4th January 2019
Angelman Syndrome is a rare neurogenetic disorder, resulting from the loss of function of a single gene,... angelmanalliance.org
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For latest summary of alliance research kindly put together by Annette in more family friendly terms see web site - angleman.ie angleman.ie
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Best of luck to Annette Kent one of our board members - wishing you all sunshine. facebook.com/angelmansyndro…
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