Rare Diseases, Health, Education, Lifestyle, Livelihood, Environment, Rural Development

Power In Me
Claim This Podcastby Power In Me Foundation
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Podcast Overview
Rare Diseases, Health, Education, Lifestyle, Livelihood, Environment, Rural Development
Language
🇺🇲
Publishing Since
11/14/2020
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Recent Episodes

July 11, 2025
Talk On Life With NMOSD With Rare Warrior Rashmi
<p>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. </p><p>The following episode is focused on living a life with a rare disease “<strong>NMOSD (Neuromyelitis optica spectrum disorder)</strong>” with <strong>Rare Warrior Ms. Rashmi</strong>. 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.</p><p>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. </p><p>You Can Follow Power In Me Foundation on Our Social Media Handles too. </p><p>1. Linkedin- <a href="https://www.linkedin.com/company/power-in-me-foundation/?viewAsMember=true" rel="ugc noopener noreferrer" target="_blank">https://www.linkedin.com/company/power-in-me-foundation/?viewAsMember=true</a></p><p>2. Instagram- <a href="https://www.instagram.com/powerinmefoundation/" rel="ugc noopener noreferrer" target="_blank">https://www.instagram.com/powerinmefoundation/</a></p><p>3. Youtube- <a href="https://www.youtube.com/@powerinmefoundation" rel="ugc noopener noreferrer" target="_blank">https://www.youtube.com/@powerinmefoundation</a></p><p>4. Facebook- <a href="https://www.facebook.com/Powerinmefoundation/" rel="ugc noopener noreferrer" target="_blank">https://www.facebook.com/Powerinmefoundation/</a></p><p>ForVolunteering, Pro Bono Work and Membership with our Organization you can emailus at <a href="mailto:mpowerinme@gmail.com" rel="ugc noopener noreferrer" target="_blank">mpowerinme@gmail.com</a> andContact at +91-8851537816.</p><p>#powerinmefoundation #rarediseases #podcast #NMOSD #nervedisorder #rarewarrior #rashmi #ngo #socialawareness #resource #rarediseaseawareness </p><p>#india #delhi #mumbai #bhopal #pune #hyderabad #kolkata #usa #england #australia </p>

May 25, 2025
Talk on discovery of Perinatal Lethal Serpinopathy With Dr. Shagun Agarwal, NIMS, Hyderabad
Manoj Kumar Singh interviews Dr. Shagun Agarwal about her team's discovery of Perinatal Lethal Serpinopathy, a novel rare disease, and the importance of early detection and genetic counseling.

December 7, 2024
Talk with Chocolate Entrepreneur Shifa Saeed | Low Investment Business| Podcast|Homemade Chocolates
Power In Me Foundation's National President Manoj Kumar Singh talks to chocolate entrepreneur Shifa Saeed about her low-investment, homemade chocolate venture Melts and shares tips for starting a successful chocolate business.
18 total episodes available
Recent guests on Power In Me
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Dr Shagun Agarwal
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Frequently asked questions
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- What is Power In Me?
- How often does this podcast release new episodes?
This podcast updates weekly.
- Where can I listen to this podcast?
This podcast is available on 6 platforms including Apple Podcasts, Spotify, and more. You can also use the RSS feed directly.
- Does this podcast accept guests?
Yes, this podcast regularly features guests.
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