FDA: ‘Elevidys Gene Therapy Will Continue to Be Used in Ambulatory DMD Patients’
In a statement Monday, it said the FDA's swift action eliminated a problem with Sarepta, allowing Elevidys to return to the market without another safety study as had been feared.
Read MorePotential Upcoming New Gene Therapies for Duchenne Muscular Dystrophy
The results of new gene therapy studies for Duchenne muscular dystrophy disease will be watched by curious eyes in 2025.
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Next Generation Exon Skipping Therapies Developed for the Treatment of DMD
Next generation exon skipping therapies for Duchenne Muscular Dystrophy (DMD) represent a promising area of research aimed at addressing the underlying genetic mutations that cause the disease.
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We Call on Health Ministries and Pharmaceutical Manufacturers to Take Action on DMD
We call on all health ministries around the world and manufacturers of DMD treatments approved by the FDA and EMA to take action.
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DMD WarrioR’s Turkish Representative Shares His Views on Elevidys Gene Therapy
We spoke to DMDWarrioR's Turkiye Representative about his perspective and concerns regarding Elevidys gene therapy. We also received surprising information about DMD studies in Turkiye.
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Is Elevidys Cost Worthy? Clinical Trials Review of Elevidys Gene Therapy
Is Elevidys Effective and Cost Worthy Compared to Clinical Trials?
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Why Isn’t Roche Applying Marketing Authorization in Every Country for Elevidys Gene Therapy?
If you are wondering when Elevidys gene therapy will come to your country, this article may help you get an idea.
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What is Duchenne Muscular Dystrophy?
Duchenne Muscular Dystrophy (DMD) is a genetic disorder that affects thousands of families worldwide. It primarily impacts boys, causing muscle degeneration and weakness over...
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Genetic Causes of Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (DMD) is rooted in the intricate world of genetics, specifically emanating from changes in a single gene known as the Dystrophin...
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Does My Child Have Duchenne Muscular Dystrophy (DMD)?
When parents ponder the question, “Does My Child Have Duchenne Muscular Dystrophy (DMD)?” they often find themselves grappling with a whirlwind of emotions as...
Read MorePotential Upcoming New Gene Therapies for Duchenne Muscular Dystrophy
The results of new gene therapy studies for Duchenne muscular dystrophy disease will be watched by curious eyes in 2025.
Read MorePotential Upcoming New Gene Therapies for Duchenne Muscular Dystrophy
The results of new gene therapy studies for Duchenne muscular dystrophy disease will be watched by curious eyes in 2025.
Read More
About our Mission
Many people in the world do not know what Duchenne muscular dystrophy is. Because only one in every 5,000 boys gets this disease. However, families and their surroundings whose children struggle with this disease have to live with the stress of this disease every day. We call them DMD Warriors.
DMDWarrior.com was established to raise awareness of this disease worldwide, facilitate access to treatments, and ensure that treatment costs are affordable.
What is our purpose?
One in every 5,000 children in the world is born with DMD, and many families only realize their child has the disease when they are 3-4 years old. FDA-approved treatments for DMD are too expensive for families to afford. Our goal is to reduce treatment costs and have the costs covered by the government.
Ease of Access to Treatments
In many countries, DMD treatments are not available, and families incur huge costs for travel abroad.
Reducing Treatment Costs
Treatments for DMD are very expensive, and it is nearly impossible for families to cover these costs themselves.
Raising Awareness on Social Media
We do not want any child to die. If you also want to find a solution to this situation, follow us on social media.