Sick Cells
Philanthropy, 1012 14th STNW, , District of Columbia, Washington, 20005, United States, 1-10 Employees
Who is SICK CELLS
Sick Cells' mission is to elevate the voices of the sickle cell disease (SCD) community and their stories of resilience. In highlighting the grave disparities this community faces, we hop...
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Headquarters: 1012 14th STNW, Washington, District of Columbia, 20005, United States
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Date Founded: 2017
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Employees: 1-10
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Revenue: $1 Million to $5 Million
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Active Tech Stack: See technologies
Industry: Philanthropy
SIC Code: 6553
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Frequently Asked Questions Regarding Sick Cells
Answer: Sick Cells's headquarters are located at 1012 14th STNW, , District of Columbia, Washington, 20005, United States
Answer: Sick Cells's official website is https://sickcells.org
Answer: Sick Cells's revenue is $1 Million to $5 Million
Answer: Sick Cells's SIC: 6553
Answer: Sick Cells has 1-10 employees
Answer: Sick Cells is in Philanthropy
Answer: Sick Cells contact info: Phone number: Website: https://sickcells.org
Answer: Sick Cells' mission is to elevate the voices of the sickle cell disease (SCD) community and their stories of resilience. In highlighting the grave disparities this community faces, we hope to influence decision-makers and propel change. Sick Cells envisions that this narrative work will achieve the following: 1. Ignite public interest making sickle cell a public health concern 2. Humanize SCD, which is a relatively invisible disease that affects people of many races and ethnicities 3. Inspire the general public, who do not typically recognize their day-to-day encounters with SCD, to advocate for SCD 4. Influence policy makers, educators, employers, healthcare administrators and healthcare providers to act to improve treatment and care for the SCD population 5. Drive research and drug development which will lead to better treatments 6. Empower the sickle cell community, regardless of hemoglobin type, to share their stories and know that they are not alone Through these actions, we hope to improve the quality of life and care for people living with the most common genetic disorder by challenging current policy and shifting social norms.
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