Artwork

Content provided by Dhanya Varma. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Dhanya Varma or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
Player FM - Podcast App
Go offline with the Player FM app!

Dhanya Ravi talks to Dhanya Varma about living with Brittle Bone disease and the challenges that she has faced inorder to live an empowered life.

43:36
 
Share
 

Manage episode 433128904 series 3453927
Content provided by Dhanya Varma. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Dhanya Varma or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Dhanya Ravi, India's Locomotor Disability Ambassador at Purple Fest 2023, was born with Osteogenesis Imperfecta (OI) also known as brittle bone disease. This rare genetic disease makes her known as the country's "glass woman". Despite her condition, she has achieved remarkable feats, including receiving State and National awards and speaker at two TEDx and Josh Talk events. She works as an executive at Enable India, Dhanya has participated in numerous webinars for college students and corporations, where she has discussed topics such as inclusivity, mental health, and social responsibility. She has spoken to over 10000 people worldwide and has been an active contributor to the disability sector for over a decade, inspiring many differently abled individuals to pursue their goals. Dhanya is actively mobilizing and sensitizing people about OI, rare diseases, and the disability community in India and the USA, working in collaboration with various non-profit organizations (NGOs). She advocates for a more inclusive society and strives to raise awareness. about rare genetic conditions. Dhanya manages Aasmaan Foundation Trust, an in-house NGO that assist people with disability to live a dignified life. She loves to volunteer her time in audio reading for individuals with visual impairments and fulfills the Vital role of a mentor for special parents. Over the past 3 years, her trust has distributed over 8 lakh powered wheelchairs, connected prospects for education and hosted two social awareness events. Her life stories and experience meeting people worldwide through the Disability Awareness and Advocacy Program have earned her many testimonials. Dhanya's life message and mentorship have empowered women and youth in the community to live a life of independence. 29th Feb is rare diseases day. Osteogenesis Imperfecta is a rare disease. We are happy to bring forth this conversation to you.

  continue reading

57 episodes

Artwork
iconShare
 
Manage episode 433128904 series 3453927
Content provided by Dhanya Varma. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Dhanya Varma or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Dhanya Ravi, India's Locomotor Disability Ambassador at Purple Fest 2023, was born with Osteogenesis Imperfecta (OI) also known as brittle bone disease. This rare genetic disease makes her known as the country's "glass woman". Despite her condition, she has achieved remarkable feats, including receiving State and National awards and speaker at two TEDx and Josh Talk events. She works as an executive at Enable India, Dhanya has participated in numerous webinars for college students and corporations, where she has discussed topics such as inclusivity, mental health, and social responsibility. She has spoken to over 10000 people worldwide and has been an active contributor to the disability sector for over a decade, inspiring many differently abled individuals to pursue their goals. Dhanya is actively mobilizing and sensitizing people about OI, rare diseases, and the disability community in India and the USA, working in collaboration with various non-profit organizations (NGOs). She advocates for a more inclusive society and strives to raise awareness. about rare genetic conditions. Dhanya manages Aasmaan Foundation Trust, an in-house NGO that assist people with disability to live a dignified life. She loves to volunteer her time in audio reading for individuals with visual impairments and fulfills the Vital role of a mentor for special parents. Over the past 3 years, her trust has distributed over 8 lakh powered wheelchairs, connected prospects for education and hosted two social awareness events. Her life stories and experience meeting people worldwide through the Disability Awareness and Advocacy Program have earned her many testimonials. Dhanya's life message and mentorship have empowered women and youth in the community to live a life of independence. 29th Feb is rare diseases day. Osteogenesis Imperfecta is a rare disease. We are happy to bring forth this conversation to you.

  continue reading

57 episodes

Tous les épisodes

×
 
Loading …

Welcome to Player FM!

Player FM is scanning the web for high-quality podcasts for you to enjoy right now. It's the best podcast app and works on Android, iPhone, and the web. Signup to sync subscriptions across devices.

 

Quick Reference Guide