Frequently Asked Questions (FAQ's)
There is currently no universal cure for muscular dystrophy. Treatment focuses on managing symptoms, preserving function, slowing progression where possible, and addressing complications
There is no single treatment that is best for every patient. Management depends on the type of muscular dystrophy, genetic cause, age, symptoms, disease stage, and overall health.
Yes. Patients can access specialist evaluation, medication management, physiotherapy, rehabilitation, respiratory care, cardiac monitoring, orthopedic care, genetic counseling, and other multidisciplinary services in India.
DMD management may include corticosteroids, physiotherapy, respiratory care, cardiac monitoring, orthopedic management, rehabilitation, genetic counseling, and selected disease-specific therapies depending on the patient’s clinical and genetic profile.
Genetic testing can identify disease-causing variants and help confirm or classify certain types of muscular dystrophy. The specific test depends on the suspected condition and clinical findings.
Children can receive specialized pediatric neurology, rehabilitation, respiratory, cardiac, orthopedic, and genetic care depending on their diagnosis and clinical needs.
There is no fixed cost. Expenses depend on diagnosis, investigations, medications, rehabilitation, specialist consultations, and other medical requirements.
An initial online medical-record review or consultation may be possible before travelling to India, depending on the healthcare provider and clinical requirements.
