Rare Disorder 1 in 20,000. Information & support for families, caregivers & service providers. Collaborate with international scientists to advance treatments.
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... https://t.co/Lbt6u8joG0
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. https://t.co/AWXR8Hxhb1
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. https://t.co/yeZxvuyof7
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,... https://t.co/tGYLpq6ysE
For latest summary of alliance research kindly put together by Annette in more family friendly terms see web site - https://t.co/ywDL8kTH6g https://t.co/K6r0nzyTyP
Emails asking for us to keep your details and send you updates making their way. I appreciate everyone has full inboxes but its the EU law and we have to make contact.
Replies appreciated and required.