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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.
Michael's Cause – Fighting Duchenne Muscular Dystrophy
Fighting Duchenne Muscular Dystrophy
CARE-NMD: Improving care for Duchenne muscular dystrophy
Improving care for Duchenne 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.
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.
Harrisons Fund
Charity dedicated to fighting Duchenne Muscular Dystrophy
Jett Foundation | Home
Empowering families. Fighting Duchenne muscular dystrophy.
Author: Aug 5
Dystrophy Annihilation Research Trust – Aspiring to achieve Total Annihilation of Muscular Dystrophy
Aspiring to achieve Total Annihilation of Muscular Dystrophy
Spinraza Muscular Dystrophy
Spinraza Muscular Dystrophy,SMA Clinical Trials,Spinal Muscular Atrophy Therapy,Spinal Muscular Atrophy Treatment
Homepage - Emflaza (deflazacort)
PRESERVE WHAT MATTERS TO YOUR CHILD AFFECTED BY DUCHENNE MUSCULAR DYSTROPHY
TimothyGriff.in
A certified inhabitant of The Universe living with FSH muscular dystrophy.
Author: Timothy Griffin Timmargh
Home | STC4Duchenne
STC is running the marathon in april for Duchenne Muscular Dystrophy
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.
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Life science company focused on solving Duchenne muscular dystrophy
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.
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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.
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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
Home - Progena
Progena is a Swiss Duchenne Foundation for patients with Duchenne muscular dystrophy, their families, doctors, therapists.
The Romito Foundation -
The Romito Foundation - Striving to improve the quality of life of those living with Duchenne Muscular Dystrophy
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Sarepta Therapeutics – Duchenne.com
Visit Duchenne.com to learn about Duchenne Muscular Dystrophy (DMD) symptoms, testing, genetics, and resources.
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
Timothy Griffin (Timmargh)
A playing card collecting, science fiction absorbing, certified inhabitant of The Universe living with muscular dystrophy.
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
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Muscular Dystrophy Association a 10 year tradition of Hans getting rubber chickens signed by sports heroes for Justin.
Muscular Dystrophy Association
MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research.
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.
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!
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.
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.
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.
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
Enrique Brandan home web page. Enrique Brandan Laboratory
Enrique Brandan web page. Brandan Laboratory is concentrated to study skeletal muscular dystrophies. Process of fibrosis and function of proteoglycans.
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
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
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
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.
Music Player
Alex Hosking, a singer songwriter from Adelaide. Alex has just released her debut album 'WISH'
Academy of Applied Epigenetics
In Memory of Joshua Dubcak - Muscular Dystrophy - Why Jerry Lewis was fired - Dr. Joel Wallach - Marvin Ropp - Youngevity - Colloidal Minerals - Selenium - Donations
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.
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Stem Cell Therapy Hospital & Centre In Delhi India - StemCellCareIndia
StemCellCareIndia is a Stem Cell Therapy Centre in Delhi, India; provides treatment of muscular dystrophy, multiple sclerosis, spinal cord, Stem Cell Therapy
Home | Crann Centre Ireland
Our services are focused on, but not limited to, people who have Spina Bifida, Hydrocephalus, Muscular Dystrophy, Cerebral Palsy, Childhood ****, Spinal Cord Injuries, and their families.
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.
Aged Care Service, Massage Therapy, Muscular Dystrophies Therapy Sydney
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Call: +91-9370000380 - Dr. Sagar Jawale for Stem Cell Therapy in India - Risk-Free and Effective Treatment | Contact Us for Muscular Dystrophy and Kidney Failure Therapy/Treatment India to avoid muscular, kidney, diabetes and various other serious problems
Author: Stem Cell Therapy India Diabetes; Kidney Failure; CP - Dr. Sagar Jawale
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.
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.
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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.
CP- Innovation - Compassion - Purpose, Green Bay, WI
Serving persons of all abilities including those with cerebral palsy, als, muscular dystrophy, multiple sclerosis, autism, and other special needs. Leaders in caring, personalized and progressive solutions for a fully inclusive community.
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Dystrophy.ir Dystrophy Iran 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.
Nerve MD | Natan Shaoulian MD| Neurology Muscular Dystrophy and Neuropathy Institute
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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.
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Save Our Sons Duchenne Foundation: SOS
– sosdf
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FSMA Hong Kong
To help in the relief of hardship and suffering of patients afflicted with Spinal Muscular Atrophy (SMA) and their family members.
Home - LGMD Awareness Foundation
ABOUT US LGMD Awareness Foundation, Inc. is a 501(c)(3) non-profit advocacy organization dedicated to globally raising awareness of the rare neuromuscular conditions known as limb-girdle muscular dystrophy (LGMD). In collaboration with other LGMD foundations, our focus is to provide curated educational information and resources for the LGMD community and public. By increasing
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Home
ABOUT US LGMD Awareness Foundation, Inc. is a 501(c)(3) non-profit advocacy organization dedicated to globally raising awareness of the rare neuromuscular conditions known as limb-girdle muscular dystrophy (LGMD). In collaboration with other LGMD foundations, our focus is to provide curated educational information and resources for the LGMD community and public. By increasing
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