
The Adventures of Team Sean
@teamsean24_gib
Hi 🌎 I’m Sean & this is the story of my family’s Angelman Syndrome journey #TeamSean #AngelmanSyndrome #ForwardAlwaysForward #Forever24
ID: 1360266613602328577
https://youtu.be/Vr6EscdZWas 12-02-2021 16:37:08
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AngelmanSyndromeFdn
@angelman
Angelman Syndrome Foundation advances the awareness and treatment of Angelman Syndrome through education, information, research and support.
FAST
@cureangelman
Dedicated to finding a cure for Angelman syndrome, to bring practical treatment into current medical practice as quickly as possible.
Paula Evans
@contactpaula
#cureangelman - let's do it!
Angels On Earth -AOE
@asangelsonearth
OUR MISSION: B4 long... EVERYONE will know what Angelman Syndrome is! We provide stylish clothing & jewelry to promote Angelman Syndrome awareness. #AOEGEAR
Dup15q Alliance
@dup15q

AngelmanSyndrome
@angelmanire
Rare Disorder 1 in 20,000. Information & support for families, caregivers & service providers. Collaborate with international scientists to advance treatments.
angelman-asa
@angelmanasa
La asociación Síndrome de Angelman es una entidad sin ánimo de lucro para el soporte, asesoramiento e información, en el conocimiento de este síndrome.
Angelman Vietnam
@angelmanvietnam
Angelman Syndrome Organization in Vietnam was born to raise awareness and treatment of Angelman Syndrome through propaganda and information.
angelmanuk
@angelmanuk
UK charity(1021882) run by and for those affected by the genetic condition Angelman Syndrome and interested professionals.Our patron is director Gareth Edwards.
Int Angelman Day
@intangelmanday
- Raise awareness - Mobilise people, encourage fundraising - Promote research & educational resources - Remember those with AS who are no longer with us
Wayne Tunbridge
@gib1wayne
The Chronicles of Wibble, proud retired RGP officer & Gibraltarian 🇬🇮#ForwardAlwaysForward #MentalHealthAwareness #Wibble #TeamSean #AngelmanSyndrome
Fighting Angels
@fightangelman
Fighting Angels Foundation, Inc. is a charitable organization dedicated to support and awareness of the rare neuro-genetic disorder Angelman Syndrome.
Angelman Argentina
@angelmanarg
Somos una asociación sin fines de lucro que agrupa a familias/amigos de personas afectadas por el Síndrome de Angelman. #AngelmanArgentina #SindromeDeAngelman
Angelman Syndrome
@angelsyndaware
This is an awareness page for Angelman Syndrome. Please feel free to also 'Like' my Facebook page: facebook.com/angelmansyndaw…
Future Footprints
@ffce_australia
We aim to teach children with disabilities to reach beyond what is expected; motivating them to improve, to achieve and to gain independence.
Terry Jo Bichell
@tjbichell
Politics and Science, in equal measure. Rare disease biomarkers and outcomes specialist. DCDP Exec Comm at large.
AFSA
@angelmanafsa
Association Française du Syndrome d'Angelman
AngelmanAcademy
@angelmanacademy
We provide carefully curated resources, community connections and expert taught courses for all who love and work with individuals with Angelman Syndrome.
DEE-P Connections
@dee_pconnection
Connecting families with severe developmental & epileptic encephalopathies to information, resources and each other
AngelmanSyndromeAustralia
@angelmansyndro3
Improving the lives of people living with Angelman syndrome and their families through support, networking, advocacy, education and promoting research
FAST ESPAÑA - Foundation for Angelman Syndrome
@fast_spain
FAST ESPAÑA - Foundation for Angelman Syndrome Therapeutics
[email protected]
@possabilitiesgi
PossAbilities Gibraltar - Gibraltar’s Special Educational Needs support facility Reg. Charity 340
Angelman Syndrome
@dup15qawareness
This account is being used for a school project.
Angelman Biomarkers
@angelmanbiomark
Official twitter for A-BOM: Angelman Biomarkers & Outcomes Measures Alliance #angelman #biomark #ABOM
Fast Italia Cureangelman.it
@cureangelmanit
ONLUS💌🔬