Talk On Life With NMOSD With Rare Warrior Rashmi
Impossible d'ajouter des articles
Échec de l’élimination de la liste d'envies.
Impossible de suivre le podcast
Impossible de ne plus suivre le podcast
-
Lu par :
-
De :
À propos de ce contenu audio
Power In Me Foundation is a National Trust with CSR1, 80G and 12A certification. We are dedicated for the welfare of rare disease patients and their families. Power In Me is the official podcast of Power In Me Foundation that is aimed tocreate awareness and to be a resource for professionals and common people in understanding rare diseases and other health related information in an easy way.
The following episode is focused on living a life with a rare disease “NMOSD (Neuromyelitis optica spectrum disorder)” with Rare Warrior Ms. Rashmi. This episode aims to create awareness about this rare disease in the society and help in the early detection of the condition for timely intervention/treatment.
Manoj Kumar Singh, National President of Power In Me Foundation talks to Ms. Rashmi on her journey with NMOSD from the day it was diagnosed till today with her daily challenges. She even talks about her life’s aspirations.
You Can Follow Power In Me Foundation on Our Social Media Handles too.
1. Linkedin- https://www.linkedin.com/company/power-in-me-foundation/?viewAsMember=true
2. Instagram- https://www.instagram.com/powerinmefoundation/
3. Youtube- https://www.youtube.com/@powerinmefoundation
4. Facebook- https://www.facebook.com/Powerinmefoundation/
ForVolunteering, Pro Bono Work and Membership with our Organization you can emailus at mpowerinme@gmail.com andContact at +91-8851537816.
#powerinmefoundation #rarediseases #podcast #NMOSD #nervedisorder #rarewarrior #rashmi #ngo #socialawareness #resource #rarediseaseawareness
#india #delhi #mumbai #bhopal #pune #hyderabad #kolkata #usa #england #australia
Vous êtes membre Amazon Prime ?
Bénéficiez automatiquement de 2 livres audio offerts.Bonne écoute !