Doing Muscular Dystrophy Treatment Since 2024
Doing Muscular Dystrophy Treatment Since 2024
India’s Best Treatment Center for “Muscular Dystrophy”
What Is Muscular Dystrophy?
Muscular dystrophy is a group of diseases that make muscles weaker and less flexible over time. It is caused by a problem in the genes that control how the body keeps muscles healthy. For some people, the disease starts early in childhood. Others don’t have any symptoms until they are teenagers or middle-aged adults.
Symptoms
For most types of muscular dystrophy, symptoms start to show up in childhood or in the teen years. In general, children with the condition: Fall down often Have weak muscles Have muscle cramps Have trouble getting up, climbing stairs, running, or jumping Walk on their toes or waddle
Questions for Your Doctor
You’ll want to find out as much about your child’s condition as you can to learn how they can stay as healthy as possible. You may want to ask: What kind of muscular dystrophy do they have? Do they need any more tests? Do we need to see any other doctors? How will the disease affect their life? What kinds of treatments are available? How will they make them feel? What can I do to keep their muscles strong? Are there any clinical trials that would be good for them? Will my other children get muscular dystrophy?
Featured News
Breakthrough gene therapy offers hope for Duchenne muscular dystrophy
A new gene therapy treatment for Duchenne muscular dystrophy shows promise of not only arresting the decline of the muscles of those affected by this inherited genetic disease, but perhaps, in the future, repairing those muscles.
A Boy With Muscular Dystrophy Was Headed For A Wheelchair.
Puspender life has been an incredible journey, filled with determination and a strong…
Sarepta’s Duchenne gene therapy fails to meet primary endpoint in pivotal trial
Sarepta Therapeutics said Monday afternoon that its gene therapy for Duchenne muscular dystrophy…
Since 2024. has been transforming the lives of Muscular Dystrophy & other Neuromuscular disorders-affected families. I
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