Consult India’s Best Ayurvedic Doctor For Muscular Dystrophy Treatment
AyurVAID Hospitals is now a part of Apollo Hospitals Group.
Progressive weakness and loss of muscle mass are generated by a class of diseases known as Muscular Dystrophy or Duchenne Muscular Dystrophy.
AyurVAID has pioneered evidence-based, award-winning decision Ayurveda-based protocols for Muscular dystrophy treatment. Following the fundamental principles of Ayurveda, our physicians perform an in-depth assessment of the key symptoms and health factors of each patient to diagnose the root causes around your diet, individual constitution, lifestyle, work pattern, and genetic predisposition.
Based on the assessment, we arrive at the optimal Ayurveda Muscular dystrophy treatment (DMD Treatment) protocol for Samprapti Vikhatan or breaking the etiopathogenesis, considering the extent of disease progression, risk factors, your constitution (prakriti), and the disease prognosis. This approach bridges the gap between the patient’s individualistic factors and the standard treatment protocols thereby making the therapy effective and safe.Our whole person-centric approach will help you regain your happiest and healthiest state of life. Our rehabilitation specialists will also give you advice on ergonomics, nutrition, and lifestyle changes to help you better manage Muscular dystrophy
AyurVAID is India’s 1st Ayurveda hospital to be accredited by NABH (National Accreditation Board for Hospitals & Healthcare Providers), Quality Council of India.
This condition can cause a hard time running, walking, or jumping. As the disease progresses, it can affect a child's heart and lungs. One of the common forms of muscular dystrophy is DMD.
The second most common muscular dystrophy whose symptoms can appear anytime between the ages of 5 and 60. Often the males are more likely to get impacted. This ailment affects the hip, thigh, and shoulder muscles and ultimately the heart.
The third common type of muscular dystrophy that affects the muscles in the face, shoulder blades, and upper arms. The symptoms of this condition tend to appear before the age of 20.
Emery-Dreyfuss muscular dystrophy, Limb-girdle muscular dystrophy, Myotonic dystrophy, and Oculopharyngeal muscular dystrophy are the various rare found types of muscular dystrophy.
Genetic mutations and differences induce most conditions of muscular dystrophy. One or both parents may pass an impaired gene to their child even if the parent is not affected by the condition. Therapies that are physical and occupational strengthen and stretch muscles. These therapies can help to retain function and range of motion.
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