In India, a large number of people have been diagnosed with Limb Girdle Muscular Dystrophy (LGMD) disease, which is one of the rare disease, but now it is very common in India as no one raises voice for the upliftment of medicine, Where top reputed doctor has said. There is "NO CURE and PROPER TREATMENT" in India even outside India.

My brother - Ritesh Dubey, 26 years old only at the end of January 2020 he has been diagnosed with LGMD. My brother's condition is getting worse day by day. What more should we do for my Brother, so that his illness does not increase further.

My question is to the government as well as the doctors that why till now NO Medicine has come for this disease? Why are these people playing with people's lives? Do they have no importance in their family? and why should they take it lightly just because no one in their house is suffering from this disease. REDICULOUS!

The Government should see when the medicine will come to cure this disease. The Government should at least focus on people and their Basic Health Facilities.

I also urge people to be aware and raise their voice for Basic Health Facilities which they should get and if they do not get it then bring this issue to the attention of the concerned people so that it can be provided to us. I urge everyone to help us achieve a better, brighter future and encourage us to speak up for our basic needs. Please sign this petition so that people affected by Muscular Dystrophy can live their lives like others again. To be free from the fear of such rare disease.

Consider my petition on an urgent basis.Is there any hope of recovery of My Brother?Any hope when a proper cure or medicine will arrive?