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Team A.S.A.P. is a nonprofit organization composed of sickle cell warriors, sickle cell trait carriers, caregivers, and those who have a passion to see a change within the sickle cell community.
ASAP GOES TO TALLAHASSEE TO CHANGE SICKLE CELL LAWS
On February 2, 12-year-old Shamar, an A.S.A.P. (Advancing Sickle Cell Advocacy Project) Junior Advocate, stood before the Florida Senate Health Policy Committee and courageously shared his personal testimony in support of SB 844. Speaking with wisdom and confidence far beyond his years, Shamar became a powerful voice for sickle cell warriors across Florida, helping lawmakers better understand the real challenges patients face when seeking treatment. His advocacy demonstrated that young people can create meaningful change and showed the impact of empowering the next generation to speak up for their communities.
Shamar's testimony was part of a broader movement that has now led to a historic victory for the sickle cell community. Beginning July 1, 2026, Florida's new law, CS/SB 844, will require healthcare practitioners who prescribe controlled substances to complete continuing education that includes training on pain management for patients with sickle cell disease. The legislation addresses a longstanding concern among patients who have often faced misunderstanding, stigma, and barriers to receiving appropriate pain treatment during medical crises.
For individuals living with sickle cell disease, this new requirement represents more than a policy change. It is a step toward greater compassion, improved clinical understanding, and equitable care. Patients like Steven Moody have spoken about the frustration of being perceived as drug-seeking when they are simply seeking relief from severe pain. By ensuring healthcare providers receive specialized education, the law aims to improve treatment outcomes and build trust between patients and medical professionals.
The passage of this legislation is a testament to the power of advocacy, education, and lived experience. Organizations like Advancing Sickle Cell Advocacy Project (A.S.A.P.) have worked tirelessly to elevate the voices of sickle cell patients and families, and young leaders like Shamar are helping write a new chapter in that story. His courage before the Senate serves as a reminder that one voice, regardless of age, can help influence policy, change perceptions, and improve the lives of countless individuals across Florida.

BETTER EXISTS PRESENTS:
A J. SNOW DOCUMENTARY
YOU LOOK FINE
A Free Movie Screening
UPCOMMING EVENTS
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