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| FAST (Foundation for Angelman Syndrome Therapeutics)
FAST España es una fundación, sin ánimo de lucro, creada por familias españolas con hijos afectados por el Síndrome de Angelman, con la finalidad de concienciar a la comunidad española y trabajar juntos por promover el desarrollo de terapias que propicien la cura y llevar el tratamiento a la práctica médica, actual, lo más rápido posible.
FAST (Foundation for Angelman Syndrome Therapeutics) in Canada
Learning that your loved one has Angelman syndrome can be scary and overwhelming, but hope is here. FAST’s sole mission is to cure Angelman syndrome and, with our partners around the world, we are getting closer every day. Five gene therapy strategies are in development to treat Angelman syndrome. Your donation to FAST Canada helps fund all of them.
Author: Gerardo
FAST (Foundation For Angelman Syndrome Therapeutics) - Home
FAST is committed to assisting individuals living with Angelman syndrome to realize their full potential and quality of life.
Author: Gerardo Duenas
Angelman Syndrome Foundation | Welcome
Angelman Syndrome Foundation
Author: Angelman Syndrome Foundation
Angelman Syndrome News Home - Angelman Syndrome News
No Description.
Author: Theme Templates
Angelman syndrome Research
Angelman Syndrome Ireland
Angelman Syndrome - UK Support, Education and Research Trust - Angelman Syndrome
UK Support, Education and Research Trust
Fynn-Fuchs Angelman Syndrom
Angelman-Syndrom, auch Happy-Puppet-Syndrom genannt
Author: Fynn Fuchs
Aaliyah – Leben mit dem Angelman-Syndrom
Norsk forening for Angelmans syndrom
Angelman Syndrome Greece I Hellas I Official Site -
Angelman Syndrom Julia Della Rossa - juliadellarossa
Behinderung, Gendefekt, Entwicklungsverzögerung, Angelman Syndrom, geistig behindert, körperlich behindert
Yannick Otzelberger – Besonders normal – Leben mit dem Angelman Syndrom
Author: Mama
Irlen Syndrome Foundation
Visit the post for more.
Noonan Syndrome Foundation
The Noonan Syndrome Foundation: created to help support, educate, & advocate for and on behalf of all those who have bee affected by Noonan Syndrome.
Therapeutic Guidelines Foundation | Therapeutic Guidelines
Therapeutic Guidelines Foundation is a philanthropic foundation that promotes the quality use of medicines and supports the creation and dissemination of independent therapeutic information. Through its grants, the Foundation seeks to advance health care, treatment and medical knowledge through research, education and creation or dissemination of information in low resource settings. Since 2016, the Foundation... Read more »
Welcome to Loeys-Dietz Syndrome Foundation Canada | Loeys-Dietz Syndrome Foundation Canada
Central Pain Syndrome Foundation -
Other sites like cureangelman org au
Home - Dravet Syndrome Foundation
Your Content Goes Here More News Dravet Syndrome Foundation is a non-profit organization dedicated to aggressively raising research funds for Dravet syndrome, a rare and catastrophic form
Author: Admin
Shwachman-Diamond Syndrome Foundation
What is SDS? Shwachman Diamond Syndrome (SDS) is a rare blood disorder that affects the pancreas, bone marrow, and skeleton, but other organs may also be affected.
Loeys-Dietz Syndrome Foundation
Our purpose is to provide information about what Loeys-Dietz Syndrome is and give hope to those impacted by the condition. We hope that you will find medical information and personal support to assist you and your family on your journey with Loeys-Dietz Syndrome. Learn more about our foundation and
False Memory Syndrome Foundation
The False Memory Syndrome Foundation is a 501(c)(3) organization founded in March, 1992 to seek the reasons for the spread of the false memory syndrome, to work for ways to prevent the spread of the false memory syndrome, and to aid those who were affected by the false memory syndrome and bring their families into reconciliation.
Welcome « Stevens Johnson Syndrome Foundation
Stevens Johnson Syndrome Foundation
Barth Syndrome Foundation : Home
Kiwanis Down Syndrome Foundation
Indian RETT Syndrome Foundation
Home - Williams Syndrome Foundation
Reye's Syndrome | National Reye's Syndrome Foundation | United States
In 1974, the National Reye's Syndrome Foundation, a children's health advocacy organization, was incorporated as a 501(c)3 charity, with a mission to eradicate the incidence of Reye's Syndrome. The Foundation does not receive, nor seek, government funding, and relies on the generosity of donors for support of all progr
Gould Syndrome - COL4A1 - COL4A2 genes - Gould Syndrome Foundation
Gould Syndrome Foundation a 501(c)3 Nonprofit, exists to provide hope and help to children and adults with the Ultra Rare Disease, Gould Syndrome; affecting COL4A1 and COL4A2 genes.
Author: Jselser
Angelman Syndrome Association of WA – Providing support in Western Australia since 2007
Our mission is to support, inform, educate, network, and advocate for families with a child with Angelman Syndrome
Home - Angelman
Angelman Brasil
A associação Angelman Brasil tem como objetivo prestar apoio e informações aos familiares de portadores da Síndrome de Angelman no Brasil, bem como a profissionais e técnicos de saúde, investigadores e demais interessados
Angelman's Notary
Angelman e.V.
The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research - Home - The Cute Syndrome Foundation
Learn more about The Cute Syndrome Foundation and the SCN8A Epilepsy and PCDH19 Epilepsy Research we fund
Utah Down Syndrome Foundation : Home
Author: John M Simmons
Mal de Débarquement, Debarkation Syndrome | MdDS Foundation
Mal de Débarquement, Disembarkment or Debarkation Syndrome is a disorder that leaves patients with a constant feeling of movement, as if on a boat. The MdDS Foundation advocates for and seeks treatments to end the suffering from MdDS. Learn more!
Author: MdDS Foundation
The National Fragile X Foundation | Fragile X Syndrome
The NFXF serves all those living with Fragile X, including awareness, research, and community for individuals and families at all stages of life.
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Home - Phelan-McDermid Syndrome Foundation
Improving lives affected by Phelan-McDermid Syndrome Join Donate Newly Diagnosed International DataHub Upcoming Events Resource Library It is the mission of the Phelan-McDermid Syndrome Foundation to improve the quality of life of those affected by Phelan-McDermid syndrome worldwide by providing family support, accelerating research, and raising awareness. Latest News & Blog Post We are Phamily […]
Welcome to M S F A | Moebius Syndrome Foundation Africa (MSFA)
Homepage | International Rett Syndrome Foundation
Author: Kassie Morell; Mom; Kaylie age 4
Proteus Syndrome Foundation - Support and Education
The Proteus Syndrome Foundation's goals are Supporting / Educating Families of individuals living with Proteus Syndrome, public education, research funding
Pallister-Killian Syndrome Foundation of Australia
Pallister-Killian Syndrome Foundation of Australia
Author: Catch Themes
Smith-Magenis Syndrome Research Foundation
Barth Syndrome Foundation of Canada - Home
Restless Legs Syndrome Foundation Blog
Support for those affected by restless legs syndrome (RLS). For more info visit www.rls.org.
Author: Restless Legs Syndrome Foundation
Home - Moebius Syndrome FoundationMoebius Syndrome Foundation | Home for the Moebius Community
Home - Welcome to the Post-Finasteride Foundation - The Post-Finasteride Syndrome Foundation
Angel Water: R2 Donated to Angelman Syndrome awareness for every bottle of water sold
Angel Water: R2 Donated to Angelman Syndrome awareness for every bottle of water sold
Twin to Twin Transfusion Syndrome (TTTS) Foundation
The TTTS Foundation provides immediate and lifesaving support to families, medical professionals and caregivers dealing with TTTS.
Mowat-Wilson Syndrome Foundation | Official Website
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Author: Marcia Smith
Australian POTS Foundation – Postural Orthostatic Tachycardia Syndrome
News | Down Syndrome Inclusive Education Foundation
Author: Lasith Madurasinghe
Alport Syndrome Foundation - Hope, Action, Support
Alport Syndrome Foundation is a patient-led non-profit dedicated to improving the lives of those affected by Alport Syndrome.
Lynch Syndrome Hereditary Cancer Foundation | AliveAndKickn
Hereditary cancer foundation, lynch syndrome, non-profit, patient advocacy organization, colon cancer, endometrial cancer, genetic mutation, AliveAndKickn AliveAndKickn is a patient advocacy organization for individuals and families with Lynch syndrome hereditary cancer genetic mutations.
Down Syndrome Research Foundation | DSRF UK
The DSRF UK Is A National Charity Formed By Parents Of Down’s Syndrome Children Who Want Greater Emphasis Placed On Medical Research.
Author: Down's Syndrome Research Foundation
Inicio - Angelman Argentina
Suomen Angelman-yhdistys
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Home | The Angelman Network
NOT A DRY EYE Foundation - Dry Eye Syndrome Information
Learn About Dry Eye, MGD, Blepharitis and More. Symptoms, Causes, & Treastments. A 501(c)3 Non-Profit Organization Founded by Patients.
Cure Sanfilippo Foundation | Accelerating a cure for Sanfilippo Syndrome
Our mission: Advocate for and fund research directed towards a cure and treatment options for children with Sanfilippo Syndrome (MPS III).
Author: Katie Walton
APS Foundation of America, Inc. | Antiphospholipid Syndrome - APS
FNMS Home Page | The Foundation for Nager and Miller Syndromes
The Foundation for Nager and Miller Syndromes (FNMS) is an international support group dedicated to helping those affected by these two similar and extremely rare, genetic conditions which involve moderate to severe **** and limb anomalies, but do not usually affect intellect.
Global Down Syndrome Foundation | Research, Care, Education, Advocacy
The Global Down Syndrome Foundation is dedicated to improving the lives of people with Down syndrome through research, medical care, education and advocacy.
Home Page - Koolen-de Vries Syndrome Foundation | KDVS
Koolen-de Vries Syndrome Foundation's mission revolves around Awareness, Education and Research. Learn more about the syndrome, research and upcoming events
Supporting Families who have Children and Adults with Smith-Magenis Syndrome - Smith-Magenis Syndrome Foundation UK
Help us support a fulfilling future for everyone living with Smith-Magenis syndrome We want to bring more families together, provide education and awareness training, and sponsor research into SMS. But we can’t do it without your help. We are the Smith-Magenis Syndrome (SMS) Foundation UK, and we support families who have children and adults with …
ASA – Asociación del Síndrome de Angelman
Todo aquello que te ayude a ti, ayudará a tu hijo Hazte Socio Todo aquello que te ayude a ti, ayudará a tu hijo Hazte Socio 670 909
Author: ASA-angelman
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