KMDA spearheaded the introduction of the Sickle Cell Disease Treatment Centers Act of 2024, aiming to improve access to comprehensive care. The organization also played a key role in organizing the inaugural Sickle Cell Summit led by the U.S. Secretary of Health, which brought together over 400 participants to discuss critical next steps for sickle cell care. Additionally, KMDA was appointed to the CDC’s Sickle Cell Data Collection national team, contributing to essential data-driven policy improvements.
Charity is a dynamic and forward-thinking charity donation organization committed to making a positive impact on communities around the world.
Advocate for increased funding for research, treatment, and comprehensive healthcare services for sickle cell patients.
Establish specialized treatment centers and improve healthcare access for underserved communities.
Promote sickle cell as a national public health priority.
Support training for healthcare providers.
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Founder & Executive Director
Chief Medical Officer
Director of Community Outreach
Volunteer Coordinator
At KMD Advocacy Center, we believe that the power of compassion and generosity can drive transformative change for those affected by sickle cell disease. Your support is crucial in helping us advance our mission and make a meaningful impact on the lives of individuals and families in need.
Contribute financially to support our advocacy, research, and community programs.
Join our campaigns to promote legislative changes and increased funding for sickle cell care and research.
Contribute financially to support our work increasing the federal investment, equity in treatment and care, as well as accurate data to guide investments in programs.
