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To educate society about genetic disorders being preventable
To create awareness amongst youth about inherited disorders
To create awareness about pre -marital genetic counselling and testing to avoid birth of children with serious genetic disorders
In the 1850s, descriptions of boys who grew progressively weaker, lost the ability to walk and died at an early age became more prominent in medical journals. In the following decade, French neurologist Guillaume Duchenne gave a comprehensive account of 13 boys with the most common and severe form of the disease. It soon became evident that the disease had more than one form and that these diseases affected people of either sex and of all ages.
Satisfied Donors
To Live Is The Rarest Thing In The World, Most People Just Exist
Every Parent happy to see their New born child ran should happy. And they enjoy their life smoothly And They dance when Musician play the Music.
In rare disease like Muscular Dystrophy new born children of growing children are not moving their body or parts of the body because of they are physical disorder and as this diseases is progressive they couldn’t dance when music is playing.
IMDS founder trustee Mr.Bharat Shah suffered and victim of their two late young sons. Have Duchene Muscular Dystrophy. They learnt from experience by different incident from the society have founded INDIAN MUSCULAR DYSTROPHY & RESEARCH CENTRE(IMDS) with the aim of giving a Ray of Hope to the victim patient and their family .In the year 1989 And Registered before the public charitable commissinior vide registration No.7420. AHMEDABAD AND ALSO EXAMPTED UNDER SECTION 80G OF INCOME TAX
