Office: 63, Sardarkunj Society, Bahai Centre, Shahpur, Ahmedabad - 380001, Gujarat, India Clinic (OPD): Indukak Ippcowala Seva Sansthan / Health & Care Foundation (Polio Foundation), Nr. Pavansut Society, Opp. Rajvadu, Behind Sun Flower School, Jivrajpark, Ahmedabad - 380051, Gujarat, India Clinic Timings: Every Saturday, 12:30 PM to 3:00 PM bsshah_associate@yahoo.com
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About

About Us

IntroductionThe Indian Muscular Dystrophy Society (IMDS) is a voluntary, non-profit organization supported by dedicated scientists, concerned citizens, and clinicians. The settlor of the trust is Advocate Mr. Bharat Shantilal Shah, who conceptualized the noble thought of detection, treatment, and rehabilitation of Muscular Dystrophy patients.The mission is to develop an advanced research institute where inherited dis...

About Organization

Introduction

The Indian Muscular Dystrophy Society (IMDS) is a voluntary, non-profit organization supported by dedicated scientists, concerned citizens, and clinicians. The settlor of the trust is Advocate Mr. Bharat Shantilal Shah, who conceptualized the noble thought of detection, treatment, and rehabilitation of Muscular Dystrophy patients.

The mission is to develop an advanced research institute where inherited diseases can be prevented, diagnosed, and treated.

Organization History

This society was founded by Shri Bharat S. Shah (Advocate) and Smt. Neela B. Shah (Advocate). Their young children were suffering from this disease, and the foundation of the society was laid with the aim of giving a ray of hope to patients suffering from the same condition.

The trust is established by the Managing Trustee Shri B. S. Shah, Advocate, and nurtured by Managing Trustee (Clinical) Dr. J. J. Mehta. It is supported by reputed neuro-physicians, pediatricians, physicians, and orthopedicians of the city and state.

The trust is registered under the Bombay Public Charitable Trust Act (Registration No. E-7420, Ahmedabad) and holds an 80-G Income Tax Exemption Certificate.

Vision & Mission

Our Mission

To prevent, diagnose, treat, and rehabilitate Muscular Dystrophy patients (person/child) suffering from this disease. To develop a network of NGOs to create awareness about this disease amongst the public. To create awareness amongst doctors, paramedical staff, and those associated with the medical field.

Our Objects

  • To establish and/or acquire and maintain a research center and a hospital with ultra-modern facilities for Muscular Dystrophy patients.
  • To establish and support professorships and services connected with muscular dystrophy science, medical science, or pharmaceutical science.
  • To establish and maintain hospitals, rest houses/hostels, and provide boarding and lodging to needy and deserving students receiving education/training in relevant medical sciences.
  • To provide monetary assistance to schools, colleges, universities, and institutions imparting education in Muscular Dystrophy science.
  • To promote education and learning in medical (Muscular Dystrophy) and allied branches.
  • To establish, maintain, and/or support libraries or reading rooms affiliated with educational institutions connected with Muscular Dystrophy or pharmaceutical sciences.

Our Activities

  • To combat Muscular Dystrophy disease.
  • To support worldwide research through grants and fellowships for physicians and scientists in hospitals and universities in India and abroad.
  • Drug development and research on potential therapeutic agents that may arrest or reverse disease progression.
  • Genetics studies of defects implicated directly or indirectly in neuromuscular diseases.
  • Fundamental research on nerve and muscle, including muscle function, regulation, regeneration, biochemical changes, and nerve–muscle interaction.
  • Support research programs on individual or institutional bases.

Patient & Community Support

Our trust provides diagnostic, therapeutic, and rehabilitation assistance, including follow-up care. Support includes:

  • Monetary aid/subsidies for walkers, body-jackets, leg braces, wheelchairs, orthopedic shoes, motorized hospital beds, and repairs.
  • Aids for day-to-day needs (heel/elbow protectors, specialized urinals, bedpans, raised toilet seats, communication devices, suction machines for aspiration, etc.).
  • Social service counseling and support for clinic examinations and laboratory tests.
  • Carrier screening projects supported through DNA diagnosis; genetic counseling and family screening.
  • Occupational and respiratory therapy (including yoga and supportive therapies) by experts.
  • Transportation support for appointments at clinics or sponsored clinics, and sponsored services for fitting braces and orthopedic devices.
  • Camp programs for young patients (ages 6 to 21) with trained staff, nurses, doctors, and volunteers.
  • Professional educational programs to increase awareness among physicians, nurses, and therapists; support for scientific meetings and training.
  • Support for accessibility and mobility initiatives for people with disabilities, and assistance to procure community resources.
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