Welcome to The Invizibles! The second episode of our Exploring the Invizible series is with Sneha Dave, founder of the Health Advocacy Summit and Crohn’s and Colitis Young Adults Network. Sneha was diagnosed with Ulcerative Colitis when she was 6 and as she grew up, she noticed that there were limited resources available for young adults learning how to advocate for themselves. She started the Health Advocacy Summit to fill that gap and provide much-needed resources for the chronic illness community. Enjoy and don't forget to thumbs up and subscribe! MORE OF THE INVIZIBLES 💞 Instagram » https://www.instagram.com/theinvizibl... Facebook » https://www.facebook.com/theinvizibles Twitter » https://twitter.com/TheInvizibles Website » https://www.theinvizibles.org/ CHECK OUT HEALTH ADVOCACY SUMMIT & CCYA 🧬 HAS Website: https://www.healthadvocacysummit.org/ HAS Instagram: https://www.instagram.com/healthadvocacysummit/ HAS Twitter: https://twitter.com/HA_Summit CCYA Website: https://www.ccyanetwork.org/ CCYA Instagram: https://www.instagram.com/ccyanetwork/ CCYA Twitter: https://twitter.com/CCYANetwork Sneha’s Instagram: https://www.instagram.com/snehadave98/ Sneha’s Twitter: https://twitter.com/snehadave98 We are dedicated to raising awareness for invisible illnesses, including chronic, rare, and mental health issues. Our founder, Rebecca Nadler, was diagnosed with an autoimmune disease over 5 years ago, and she launched The Invizibles to help educate the public about the hundreds of millions of people that live with an "invisible" condition. Our Mission: Here at The Invizibles, we seek to foster a more inclusive community for people struggling with invisible illnesses while raising awareness for their conditions. We highly value health and wellness and want to alleviate the daily challenges that patients and caregivers face by raising funds for translational research focused on invisible illness.

Welcome to The Invizibles! The first episode of our invisible illness interview series is with Claire Barrow, founder of the app RareGuru. Claire was diagnosed with Hypophosphatasia, a rare genetic bone disease, in 2019 and created RareGuru as a resource for rare and chronic disease sufferers to have throughout their diagnosis journey and beyond. Enjoy and don't forget to thumbs up and subscribe! Rare with Claire Spotlight on The Invizibles » https://www.instagram.com/tv/CGHrsZqDWZw/ MORE OF THE INVIZIBLES 💞 Instagram » https://www.instagram.com/theinviziblesorg/ Facebook » https://www.facebook.com/theinvizibles Twitter » https://twitter.com/TheInvizibles Website » https://www.theinvizibles.org/ CHECK OUT RAREGURU 🧬 App: https://apps.apple.com/app/id1497253264 Instagram: https://www.instagram.com/rareguru/ Facebook: https://www.facebook.com/rareguru Website: https://rareguru.com/ We are dedicated to raising awareness for invisible illnesses, including chronic, rare, and mental health issues. Our founder, Rebecca Nadler, was diagnosed with an autoimmune disease over 5 years ago, and she launched The Invizibles to help educate the public about the hundreds of millions of people that live with an "invisible" condition. Our Mission: Here at The Invizibles, we seek to foster a more inclusive community for people struggling with invisible illnesses while raising awareness for their conditions. We highly value health and wellness and want to alleviate the daily challenges that patients and caregivers face by raising funds for translational research focused on invisible illness.