Top 26 alternative sites to jessesjourney.com
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.
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 - 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.
Muscular Dystrophy News Home - Muscular Dystrophy News
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Sarepta Therapeutics | Biopharmaceutical Company for Rare Diseases
We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
CARE-NMD: Improving care for Duchenne muscular dystrophy
Improving care for Duchenne muscular dystrophy
Michael's Cause – Fighting Duchenne Muscular Dystrophy
Fighting 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.
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
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.
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.
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
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
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.
Muscular Dystrophy Association
MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research.
Sarepta Therapeutics – Duchenne.com
Visit Duchenne.com to learn about Duchenne Muscular Dystrophy (DMD) symptoms, testing, genetics, and resources.
The French Muscular Dystrophy Association (AFM-Téléthon)
AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling disease
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.
Other sites like jessesjourney com
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!
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.
Cure HHT - The Cornerstone of the HHT Community
HHT disease is a genetic blood vessel disorder that affects 1 in 5,000 people - 90% of whom are undiagnosed. Our mission is to find a cure for HHT.
Parkinson India | Parkinson’s Disease Information and Treatment in India
Parkinson’s disease is a progressive disorder of the nervous system that affects movement. It is estimated that 1 million people have Parkinson’s disease in India. Understand it better with this Parkinson's disease guide.
Author: Redbull
Williams Syndrome | Information, support, personal stories, research | WS Australia
Williams syndrome (WS) is a genetic condition that is present at birth and can affect anyone. It is characterized by medical problems, including cardiovascular disease, developmental delays, and learning disabilities. It affects 1 in 10,000 people worldwide and occurs equally in both males and females and in every culture.
Home Page - Project Alive
We Believe a Cure Is Within Reach Hunter Syndrome (MPS II) is a rare genetic disease that affects less than 500 boys in the United States. These boys are missing an enzyme used to break down cellular waste. When that waste builds up, it leads to progressive damage throughout their little bodies. Some never develop speech, … Continue reading "Home Page"
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Voiture Conseil -
Author: VoitureConseil