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
458 Tweets
1,9K Followers
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Wayne Tunbridge
@Gib1Wayne
The Chronicles of Wibble, proud retired RGP officer & Gibraltarian 🇬🇮#ForwardAlwaysForward #MentalHealthAwareness #Wibble #TeamSean #AngelmanSyndrome[email protected]
@possabilitiesgi
PossAbilities Gibraltar - Gibraltar’s Special Educational Needs support facility Reg. Charity 340DEE-P Connections
@DEE_Pconnection
Connecting families with severe developmental & epileptic encephalopathies to information, resources and each otherFighting Angels
@fightangelman
Fighting Angels Foundation, Inc. is a charitable organization dedicated to support and awareness of the rare neuro-genetic disorder Angelman Syndrome.Angelman Biomarkers
@AngelmanBiomark
Official twitter for A-BOM: Angelman Biomarkers & Outcomes Measures Alliance #angelman #biomark #ABOMAFSA
@AngelmanAFSA
Association Française du Syndrome d'AngelmanAngelmanAcademy
@AngelmanAcademy
We provide carefully curated resources, community connections and expert taught courses for all who love and work with individuals with Angelman Syndrome.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. #AOEGEARAngelman Vietnam
@AngelmanVietnam
Angelman Syndrome Organization in Vietnam was born to raise awareness and treatment of Angelman Syndrome through propaganda and information.Angelman Argentina
@AngelmanArg
Somos una asociación sin fines de lucro que agrupa a familias/amigos de personas afectadas por el SÃndrome de Angelman. #AngelmanArgentina #SindromeDeAngelmanangelman-asa
@angelmanasa
La asociación SÃndrome de Angelman es una entidad sin ánimo de lucro para el soporte, asesoramiento e información, en el conocimiento de este sÃndrome.Int Angelman Day
@IntAngelmanDay
- Raise awareness - Mobilise people, encourage fundraising - Promote research & educational resources - Remember those with AS who are no longer with usPaula Evans
@contactpaula
#cureangelman - let's do it!Terry Jo Bichell
@TJBichell
Politics and Science, in equal measure. Rare disease biomarkers and outcomes specialist. DCDP Exec Comm at large.Fast Italia Cureangelman.it
@CureangelmanIt
ONLUS💌🔬Dup15q Alliance
@dup15q
AngelmanSyndromeAustralia
@AngelmanSyndro3
Improving the lives of people living with Angelman syndrome and their families through support, networking, advocacy, education and promoting researchFuture 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.Angelman Syndrome
@AngelSyndAware
This is an awareness page for Angelman Syndrome. Please feel free to also 'Like' my Facebook page: https://t.co/jTyNGqbfx0Angelman Syndrome
@DUP15QAwareness
This account is being used for a school project.FAST ESPAÑA - Foundation for Angelman Syndrome
@FAST_SPAIN
FAST ESPAÑA - Foundation for Angelman Syndrome TherapeuticsAngelmanSyndrome
@AngelmanIRE
Rare Disorder 1 in 20,000. Information & support for families, caregivers & service providers. Collaborate with international scientists to advance treatments.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.FAST
@cureangelman
Dedicated to finding a cure for Angelman Syndrome, to bring practical treatment into current medical practice as quickly as possible.AngelmanSyndromeFdn
@angelman
Angelman Syndrome Foundation advances the awareness and treatment of Angelman Syndrome through education, information, research and support.