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Thinking of our Angelman Syndrome community as we celebrate joy, strength, advocacy, incredible beauty, connection, action, remembrance and always, always hope on this International Angelman Day.

#IAD #AngelmanDay #InternationalAngelmanDay

When Genetics Becomes Personal: Rare Disease, Family, and Genomic Medicine - Reflections from a Centre for Personalised Medicine Research Fellow - cpm My name is Sally Sansom. I’m a Research Fellow within the Centre for Personalised Medicine at St Anne’s College, and I’m also in the final year of my PhD within the Health Economics Research Centre at...

(2/3) Ahead of #InternationalAngelmanDay (15 Feb), we are sharing a written version of Sally’s talk here for anyone interested in how genomics is reshaping rare disease diagnosis and care, and why robust evidence and careful evaluation remain essential

cpm.ox.ac.uk/when-genetic...

Concord Monitor The Concord Monitor is a Pulitzer Prize winning daily newspaper and website located in the capital city of New Hampshire. The Concord Monitor is Central NH's dominant media with more than 70 percent h...

Read more about Allison and Amy in the Concord Monitor: concordmonitor.com/angelman-
syndrome-rare-genetic-disorder-governor-proclamation-news-Concord-59431451
#AngelmanSyndrome #InternationalAngelmanDay #AngelmanSyndromeAwareness #RareDiseaseMonth #DisabilityAdvocacy

Today is #InternationalAngelmanDay!

I love working with this patient population and am so proud to be part of a specialty clinic to support patients with #AngelmanSyndrome and #Dup15q.

youtube.com/shorts/3LE2k...

#AngelmanDay2025 #Medsky #NeuroSky #PsychSky

It's #InternationalAngelmanDay. Let's spread the word, raise awareness & create a more inclusive world. 🌎💙

#angelmanday2025 #AngelmanSyndromeAwareness #AngelmanStrong #angelmansyndrom