
Sickle Cell Medical Advocacy Inc
Our mission is to advocate for transformative and quality healthcare for Sickle Cell patients. At Sickle Cell Medical Advocacy a medical advocate virtually accompanies a patient with Sickle Cell disease into the hospital/ER during a pain crisis. The advocate provides information for Sickle Cell crisis management to healthcare providers. Sickle Cell Medical Advocacy (SCMA) was created by Sickle Cell patients for Sickle Cell patients. Our mission is to advocate for transformative and quality health care for sickle cell disease (SCD) patients. Founded in 2021 by Simone Uwan MD, a physically disabled, retired physician living with SCD and teaching authority in the SCD community, SCMA is the only nonprofit to take a nationwide approach to medical advocacy and patient education. SCMA trains volunteers nationwide and pairs them with SCD patients. Advocates virtually accompany patients to the emergency department/hospital to respectfully advocate for them, to improve patient health care outcomes. They also serve as a resource to health care providers who are not familiar with the updated treatments or management of the disease.

ICO
872303319
3299
X (Twitter)
71
Address
Orlando
Welcome | SCMA About Us Resources Testimonials Helpline Shop Contact More Welcome to SCMA. Register for Sickle Cell Healthcare Navigator course Message from our founder celebrating our FIRST anniversary. 2022 Thank you to our sponsors FSCDR Vertex and Pfizer. Our Mission Sickle Cell Medical Advocacy Inc.
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✨ The Navigator Course officially kicked off yesterday and it’s not too late to join us. This training equips advocates, caregivers, and warriors with the tools to confidently navigate the healthcare system, stand up for patients in the hospital, and create real change in sickle cell care. 📚 Be part of the class and gain the skills to make an impact where it matters most.
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