This blog focuses on the current available FDA-approved medications, promising therapies in clinical trials, and important questions patients should ask their doctors. It recognizes National Sickle Cell Awareness Month, showcasing the vital work of SCPASCC, advocating for education, community support, and access to care. Through compassionate guidance and practical insight, the post encourages readers to stay informed, get involved, and support lasting change in the sickle ce

Grassroots advocacy gives the sickle cell community strength and hope. This post shares how small acts of support like attending events, giving blood, or standing with a family, grow into powerful change. From awareness walks and press conferences to community blood drives, groups like SCPASCC show that everyone has a role to play in making voices heard and lives better.

A family discussing their health plan and reviewing an approval form with the help of a clinic nurse and staff member. Why This Matters...

Making sure you are covered for healthcare and prepared for any financial management for when necessary. Health insurance is supposed to...

Living with sickle cell disease brings a level of pain that many cannot imagine. These pain episodes, or crises, can come out of nowhere...

Teen and Caregiver Together in Waiting Room Accepting and Making Changes Getting older with sickle cell disease brings new challenges....

It's very important for a person with sickle cell to remain hydrated as much as possible. Why Food and Water Matter for Sickle Cell...

In the US, 1 in 13 African Americans and 1 in 100 Latinos have trait, not to mention - 1 in 333 whites born have the trait as well.

"Supacell" on Netflix raises awareness about Sickle Cell Disease, blending action with education and highlighting real challenges.