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CARE-NMD: Improving care for Duchenne muscular dystrophy
Improving care for Duchenne muscular dystrophy
Parent Project Muscular Dystrophy (PPMD) | Fighting to End Duchenne
Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
Duchenne UK - Bringing an end to Duchenne muscular dystrophy
Duchenne UK is the leading UK charity for Duchenne muscular dystrophy. We're going further and faster than ever before to find effective treatments for DMD.
Jesse's Journey | Duchenne Muscular Dystrophy | Canada
Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5,000 boys.
Joining Jack - Join Jacks' fight against Duchenne Muscular Dystrophy
Jack has Duchenne Muscular Dystrophy, DMD. There is no cure at the moment. We're raising money to fund research to find effective treatments
Duchenne Muscular Dystrophy Foundation (Duchenne SpierDystrofie Stichting) - Home
WE are so glad that you visit this site of DUCHENNE MUSCULAR DYSTROPHY. This is a registered Humanitarian FOUNDATION located in the country of SURINAME SOUTH AMERICA. WE are here to help you and your loved ones to have HOPE as you face the challenges in
VISION-DMD – Designed to ensure a timely & cost-effective **** development for Duchenne muscular dystrophy
Designed to ensure a timely & cost-effective **** development for Duchenne muscular dystrophy
Alex's Wish | fundraising charity for Duchenne Muscular Dystrophy
Alex’s Wish is a charity set up to eradicate Duchenne Muscular Dystrophy, an aggressive form of Muscular Dystrophy that affects 1 in every 3,500 boys born and results in total paralysis. Established by Emma and Andy Hallam (parents to Alex) in late 2012, Alex's Wish helps raise vital funds to help bring about new treatments and ultimately a cure for this devastating condition.
Spinraza Muscular Dystrophy
Spinraza Muscular Dystrophy,SMA Clinical Trials,Spinal Muscular Atrophy Therapy,Spinal Muscular Atrophy Treatment
Annual Sam's Night to End Duchenne - Benefiting PPMD
Sam's Night is an opportunity to help raise funds to benefit the research programs of Parent Project Muscular Dystrophy, and to fight to end Duchenne.
Muscular Dystrophy Australia Muscular Dystrophy Assoc
Muscular Dystrophy Australia (MDA) the one stop shop for information and support for people living with neuromuscular diseases.
Author: Boris M Struk
Muscular Dystrophy | Neuromuscular Condition | Spinal Muscular Atrophy
Muscular Dystrophy NSW - Helping our muscular dystrophy community build strength and reach potential. Contact us today to find out more.
Harrisons Fund
Charity dedicated to fighting Duchenne Muscular Dystrophy
Jett Foundation | Home
Empowering families. Fighting Duchenne muscular dystrophy.
Author: Aug 5
Welcome to Duchenne and You - Duchenne and You
This website provides educational resources to support healthcare professionals recognise the early signs and symptoms of Duchenne Muscular Dystrophy.
Welcome to Take on Duchenne - Take on Duchenne
This website provides educational resources to support healthcare professionals recognise the early signs and symptoms of Duchenne Muscular Dystrophy.
Finding a cure for Duchenne | Caring for Duchenne | CureDuchenne
CureDuchenne is the global leader in research, patient care and innovation for improving & extending the lives of children with Duchenne muscular dystrophy.
Facioscapulohumeral Muscular Dystrophy Info - Treatment - FSHD Society
Get Involved in the fight to cure FSHD muscular dystrophy. Newly or recently diagnosed? Please contact us to - Volunteer - Join - Donate.
What is Duchenne? • World Duchenne Awareness Day
On September 7, we raise global awareness for Duchenne and Becker Muscular Dystrophy, two rare muscle wasting conditions. Join us! 🎈
Author: Worldduchenne
Other sites like michaelscause org
Muscular Dystrophy Association
MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research.
Dystrophy Annihilation Research Trust – Aspiring to achieve Total Annihilation of Muscular Dystrophy
Aspiring to achieve Total Annihilation of Muscular Dystrophy
Indian Association of Muscular Dystrophy Solan | Symptoms | IAMD
Muscular dystrophy is a progressive neuromuscular genetic disorder. Know more about its initial symptoms & what indian association of muscular dystrophy does to provide relief.
¿Qué es Duchenne?
¿Qué es Duchenne?. Duchenne y tú es un espacio dedicado a las personas que conviven con la distrofia muscular de Duchenne.
Author: Admin
Home Page 1 - Pietro's Fight
Help Pietro fight Duchenne Muscular Dystrophy (DMD). Join us in learning more about this disease that affects 300,000 children worldwide and donate to help fund the fight for a cure. This is our mission of love and our fight for a cure!
Home - Action Duchenne
Formed in 2001 Action Duchenne was the first national charity dedicated to supporting those living with Duchenne muscular dystrophy (‘DMD’). Our work to date has seen over £10m invested in ground-breaking research, educational programmes and campaigns.
2nd Gene Therapy for Muscular Disorders Summit | April 2022 | Home
The 2nd Gene Therapy for Muscular Disorders Summit will focus on overcoming the challenges of developing genetic therapies targeting muscular disorders, including Duchenne Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, Pompe Disease and X-Linked Myotubular Myopathy.
The Speak Foundation - Limb Girdle Muscular Dystrophy
Established in 2008, The Speak Foundation is the first patient led organization to help those living with Limb Girdle Muscular Dystrophy and other forms of NMD.
Author: The Speak Foundation
Mayopathys Home - Muscular Dystrophy Ayurvedic Treatment Home in Tamilnadu
Mayoapthys Home - Muscular Dystrophy Ayurvedic Treatment Home To provide 100% cure and to make the people come to us for Muscular Dystrophyt reatment, Paralysis or Cerebral palsy
Author: Mayopathys Home - Muscular Dystrophy Ayurvedic Treatment Home
Homepage - Emflaza (deflazacort)
PRESERVE WHAT MATTERS TO YOUR CHILD AFFECTED BY DUCHENNE MUSCULAR DYSTROPHY
Home | STC4Duchenne
STC is running the marathon in april for Duchenne Muscular Dystrophy
Home - Progena
Progena is a Swiss Duchenne Foundation for patients with Duchenne muscular dystrophy, their families, doctors, therapists.
Home • Solid Biosciences
Life science company focused on solving Duchenne muscular dystrophy
Muscular Dystrophy | Laughing At My Nightmare, Inc. | United States
Laughing At My Nightmare is a 501(c)3 nonprofit dedicated to providing equipment to those living with muscular dystrophy and teaching students that all people deserve kindess and respect, regardless of their differences.
Aged Care Service, Massage Therapy, Muscular Dystrophies Therapy Sydney
Mega Therapy providing aged care service, massage therapy, relaxation massage, and Muscular Dystrophies Therapy Sydney. Contact us today to avoid problems with your health tomorrow.
Save Our Sons Duchenne Foundation: SOS
– sosdf
Save Our Sons is the peak body for Duchenne muscular dystrophy in Australia. We have focused our energy and fundraising efforts toward finding a cure. Open Monday To Friday. Donate Online. Founded In 2008. Highlights: Founded In 2008, Donation Option Available.
The Romito Foundation -
The Romito Foundation - Striving to improve the quality of life of those living with Duchenne Muscular Dystrophy
News - Zack Heger Foundation
The Zack Heger Foundation is an organization dedicated to raising money for finding a cure for Duchenne Muscular Dystrophy. We are part of the The Duchenne Alliance
Sarepta Therapeutics – Duchenne.com
Visit Duchenne.com to learn about Duchenne Muscular Dystrophy (DMD) symptoms, testing, genetics, and resources.
Willkommen auf MD-Duchenne - „Fight for the cure“
Wir sind eine Gruppe von Betroffenen, die an der Erbkrankheit Muskeldystrophie vom Typ Duchenne erkrankt ist.
What else michaelscause.org alternative websites
Nerve MD | Natan Shaoulian MD| Neurology Muscular Dystrophy and Neuropathy Institute
The Neurology Muscular Dystrophy and Neuropathy Institute, headed by Doctor Natan Shaoulian, The Nerve MD. USC trained, Dr. Shaoulian is a board certified Neurologist subspecializing in neuromuscular disorders. Located in Beverly Hills California
The Diagnosis and Management of Duchenne Muscular Dystrophy
Consortium.AI
Consortium.AI - the joined force to apply the latest advances in AI to discovery of novel small molecules for the Duchenne Muscular Dystrophy (DMD) and other rare orphan diseases.
Catabasis
Our mission is to bring hope and life-changing therapies to patients and their families affected by rare diseases, and our primary focus is Duchenne muscular dystrophy.
Little Hercules Foundation » Little Hercules Foundation
Little Hercules Foundation was founded by three moms, two of which have sons living with Duchenne muscular dystrophy. We are working to raise money to fund groundbreaking research that will save this current generation of boys.
Only Watch - the official website
Only Watch is a biennial charity auction of luxury timepieces made by the finest watchmakers for research into Duchenne Muscular Dystrophy. Only Watch is an event organised by Association Monégasque contre les Myopathies.
Home - Duchenne Parent Project España
Únete al #DesafíoDuchenne para poner fin a la Distrofia Muscular de Duchenne y Becker. Y que saltar, levantarse o correr dejen de ser un reto diario para nuestros niños. Quiero donar bajar +2.000.000€ en Investigación invertidos en la promoción y financiación de proyectos de investigación Apoyo Psicosocial a los afectados y sus familias para mejorar …
Common Cause - Fighting to Uphold the Values of American Democracy
Common Cause is an organization fighting for an accountable government, equal rights/opportunities/representation and empowering voices to be heard.
Michael Bornhütter: Stuntman - Actor - Fight Choreographer
Michael Bornhütter: Stuntman, Actor und Fight Choreographer
Michael Bornhütter: Stuntman - Actor - Fight Choreographer
Michael Bornhütter: Stuntman, Actor und Fight Choreographer
Step Up For Mental Health - To Educate. Fight Causes. Change minds on Mental Health.
To Educate. Fight Causes. Change minds on Mental Health.
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