Sickle Talk: Running the Shores feat. Bianca Griffin

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Sickle Talk: Running the Shores feat. Bianca Griffin

Utter Randomness with Lulu

20 minutes 1 second

1 year ago

Sickle Talk: Running the Shores feat. Bianca Griffin

September is National Sickle Cell Awareness Month.

Welcome back to another episode, where we speak with our first guest, Bianca Griffin, President and Spokeswoman of the Jack and Jill Erie Shores Chapter. On September 8th, the Erie Shores Chapter and the American Sickle Cell Anemia Association will be holding a 5K Run/Walk, Running the Shores, where we honor the memory of the late founder of the ASCAA, Dr. Edgar B. Jackson, Jr. We will also be spreading awareness and education about sickle cell anemia during this inaugural event.

Learn more about Jack and Jill Erie Shores Chapter ⁠here ⁠and ⁠here⁠.

Subtitles Coming Soon!

Creative and have sickle cell anemia? Send your artwork, photographs, stories, and more to sickletalk@ascaa.org. Your art could be featured in an episode! Sickle Talk is owned and operated by the American Sickle Cell Anemia Association and funded by viewers and listeners like you. Thank you! Support our organization by donating ⁠here ⁠or by buying t-shirts, hoodies, or mugs ⁠here⁠! For More Information: Website: www.ascaa.org Follow Us! Facebook Instagram Twitter (X) Threads Spotify iHeartRadio Amazon Music Podcasts The American Sickle Cell Anemia Association is a 501(c)(3) nonprofit in Cleveland, Ohio. Since 1971, ASCAA has tested, counseled, and assisted individuals, families, and the population at risk of Sickle Cell Anemia. ASCAA is affiliated with multiple major hospitals in our local area, including, but not limited to, Cleveland Clinic Foundation, Cleveland Clinic Children's Hospital, University Hospital, MetroHealth Hospital, Rainbow Babies and Children, and local clinics and community centers. Mission Statement: ASCAA is a comprehensive health organization whose mission is to connect with families, inspire hope, and improve their quality of life. We are ultimately working to create a world without sickle cell disease. Disclaimer: All information is merely for educational and informational purposes for sickle cell anemia. It is not intended as a substitute for professional advice. Please seek medical advice from an appropriately qualified and licensed physician. Should you decide to act upon any information given, you do so at your own risk. While we have verified the information to the best of our abilities, we cannot guarantee that there are no mistakes. We reserve the right to change this policy, which will be promptly updated. To ensure you are up to date with the latest changes, we advise you to visit this page frequently.