<div>The final episode of 1 in 20000 touches upon the legal rights of rare disease patients. In this conversation with Advocate Ashok Agarwal, who practices in the Delhi High Court, we get a glimpse of the distance India still has to go on securing a life of dignity for them.</div><div>
<br><em>For more stories like this, you can listen on </em><a href="http://www.sunoindia.in/"><em><a href="http://www.sunoindia.in">www.sunoindia.in</a></em></a><em>. Also follow us on </em><a href="https://www.facebook.com/sunoindia.in"><em>Facebook</em></a><em>, </em><a href="https://twitter.com/SunoIndia_in"><em>Twitter</em></a><em> or </em><a href="https://www.instagram.com/sunoindia.in"><em>Instagram</em></a><em>.</em>
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8: Awaiting Change

There are more than 7,000 documented rare conditions in the world. While there is no known cure for some conditions, where there is a cure (or maintenance through medicines is possible), the cost of medication is exponentially high to bear. This podcast will focus on the status of rare conditions in India, which has been talked about very little in Indian society. It will be a one-of-its-kind attempt in India to document the gamut of challenges and achievements of people with rare conditions and will open a constructive dialogue on what can be done. This is important because an estimated 1 in 20 Indians are affected by a rare disease. The series will bring out the human face behind rare conditions – the patients, the families, caregivers, doctors, activists and geneticists working to improve life for people with rare conditions.