
Phelan-McDermid Syndrome Foundation
@phelan_mcdermid
Official site of the Phelan-McDermid Syndrome Foundation. We support families and fund research. #PMS #PMSF #raredisease #specialneeds #pmsfad
ID: 96217004
https://www.givingchallenge.org/organizations/phelan-mcdermid-syndrome-foundation 11-12-2009 22:08:20
2,2K Tweet
1,1K Followers
560 Following

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29 February 2024 is Rare Disease Day. Raising awareness for patients, families and carers around the world that are affected by rare diseases. #RareDiseaseDay
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@quantpsychiatry
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The keys to survival…smiling, sharing , caring and listening…
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Asociación Síndrome de Phelan McDermid España
@phelanmcdermid
Nuestra misión es mejorar la calidad de vida de las personas afectadas por el síndrome de Phelan-McDermid. 📲 Dona por Bizum: 02019
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Parent group raising awareness of #22q Working toward integrated care for 22qDS & individually rare collectively common #RareDiseases. Tweets AnneL CHY 17647
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@autismbrainnet
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Cambridge Rare Disease Network (CamRARE)
@camraredisease
making #rarediseases an everyday conversation bsky.app/profile/camrar…
RARE Revolution Magazine
@rarerevolutionm
Digital magazine giving a voice to those affected by rare conditions and the charities that support them. Contact us: [email protected]
Phelan Lucky
@phelanlucky2213
A campaign benefiting the Phelan-McDermid Syndrome Foundation in honor of our son, Jack.
Rareminds
@raremindsuk
Specialised mental health and wellbeing services for the rare disease community. bit.ly/rarementalheal…
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EmilyCartoons.com
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Pediatric Epilepsy Research Consortium
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Sadie Zawisza
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Laura Cristescu
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Entré para ver de qué iba ésto de la marea fucsia y me quedé 💜
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Kelsie Adams
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🔬 Scientist, Promoter Designer & Co-founder of Re:Pair Genomics in Toronto. Develop gene therapy for epilepsy, Dravet Syndrome, and rare genetic disorders.
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Phelan-McDermid_Portugal
@pms_portugal
Visamos a defesa e promoção dos direitos e interesses das pessoas com a síndrome Phelan-McDermid e as suas famílias perante a sociedade em geral.