Rare Disease Day and Myths and Misconceptions about Sickle Cell Anemia
Failed to add items
Sorry, we are unable to add the item because your shopping cart is already at capacity.
Add to basket failed.
Please try again later
Add to Wish List failed.
Please try again later
Remove from Wish List failed.
Please try again later
Follow podcast failed
Unfollow podcast failed
Rare Disease Day and Myths and Misconceptions about Sickle Cell Anemia
-
Narrated by:
-
By:
About this listen
Welcome back to another episode! Join Lucy as we discuss myths and misconceptions surrounding Sickle Cell Anemia, Rare Disease Day, and how you can support Sickle Cell Programs within your region, or even the American Sickle Cell Anemia Association. Creative and have sickle cell anemia? Send in 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!
What listeners say about Rare Disease Day and Myths and Misconceptions about Sickle Cell Anemia
Average Customer RatingsReviews - Please select the tabs below to change the source of reviews.
In the spirit of reconciliation, Audible acknowledges the Traditional Custodians of country throughout Australia and their connections to land, sea and community. We pay our respect to their elders past and present and extend that respect to all Aboriginal and Torres Strait Islander peoples today.