South Central PA Sickle Cell Council, Dwayne Golden
19 episodes
1 month ago
"SCD Stories" a podcast dedicated to amplifying the voices of individuals and families affected by Sickle Cell Disease and other health disparities.
Each episode features powerful conversations with individuals who have experienced the challenges of living with Sickle Cell Disease firsthand, as well as experts in the field who are working to advance research, treatment, and care for those living with chronic illnesses and health disparities.
Through these stories, we aim to shed light on the often-overlooked experiences of those living with Sickle Cell Disease and other health disparities, while also exploring strategies for resilience, self-advocacy, and community building.
Join us on this journey as we seek to inspire hope, promote awareness, and cultivate empathy for those living with chronic illnesses and health disparities.
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"SCD Stories" a podcast dedicated to amplifying the voices of individuals and families affected by Sickle Cell Disease and other health disparities.
Each episode features powerful conversations with individuals who have experienced the challenges of living with Sickle Cell Disease firsthand, as well as experts in the field who are working to advance research, treatment, and care for those living with chronic illnesses and health disparities.
Through these stories, we aim to shed light on the often-overlooked experiences of those living with Sickle Cell Disease and other health disparities, while also exploring strategies for resilience, self-advocacy, and community building.
Join us on this journey as we seek to inspire hope, promote awareness, and cultivate empathy for those living with chronic illnesses and health disparities.
In this episode of the SCD Stories podcast, the guest, Allan Pratt, talks about his book "Hope and Destiny," which aims to educate patients, families, and clinicians about sickle cell disease. The book was inspired by a lack of services for sickle cell patients in 1985, and Pratt, who is also the Director of Admissions for Emory University's preventative medicine PA department, got involved as a physician assistant at the 24-hour sickle cell unit that was established at Grady Hospital. The speakers discuss the importance of education about sickle cell disease, advancements in medical treatments, and the role of nurse practitioners and physician assistants in improving patient care. They recommend resources for physicians who want to learn more about sickle cell disease and emphasize the importance of genetic testing to know one's status regardless of skin color. The stigma surrounding sickle cell disease should be looked past, and proper education and understanding should be promoted.
SCD Stories
"SCD Stories" a podcast dedicated to amplifying the voices of individuals and families affected by Sickle Cell Disease and other health disparities.
Each episode features powerful conversations with individuals who have experienced the challenges of living with Sickle Cell Disease firsthand, as well as experts in the field who are working to advance research, treatment, and care for those living with chronic illnesses and health disparities.
Through these stories, we aim to shed light on the often-overlooked experiences of those living with Sickle Cell Disease and other health disparities, while also exploring strategies for resilience, self-advocacy, and community building.
Join us on this journey as we seek to inspire hope, promote awareness, and cultivate empathy for those living with chronic illnesses and health disparities.
