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Blood, Sweat, Cells: The Power of Peer Support
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Content provided by The Heart of Gold Sickle Cell Foundation of NOVA and Valerie Bey. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Heart of Gold Sickle Cell Foundation of NOVA and Valerie Bey 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://ppacc.player.fm/legal.
Blood, Sweat, and Cells: Real Talk about SCD is a podcast that provides in-depth, educational information about sickle cell disease (SCD). Each episode features interviews with patients or family members, doctors, and researchers who share their insights and experiences living with and treating this chronic condition. Our primary aim is to educate and advocate for patients with SCD and help them live their best quality of life.
We all want to take charge of our health, and with new technology, there are more tools than ever to help us manage it. But sometimes, the greatest gains come from something more human: connection. For people living with chronic health conditions like sickle cell disease, the healthcare system can sometimes feel impersonal and focused solely on the physical aspects of the illness.
In this episode, we're diving into a vital aspect of well-being that goes beyond medical charts and treatment plans: the power of peer support. We'll explore how connecting with others who understand your journey can make a profound difference in living with sickle cell disease. Guests: Donisha Holley, Social Worker and Support Group Organizer from the Inova Adult Sickle Cell Center, and Sickle Cell Warrior Sunday Coleman.
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