Our mission | To #MakeSickleCellPopular by increasing awareness, educating, and advocating for long term changes for the SCD population of Nevada to improve Equity and access to care for those affected by SCD and other Rare Diseases while also addressing health disparities. |
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Needs | We do not have any specific needs at this time. Contact us to explore possible ways we could work together |
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How you help |
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About us | The purpose of the organization is to increase Awareness, celebrate, educate and support families impacted by Sickle Cell Disease and now all Rare Diseases in Nevada, while also educating medical providers and the community on the affects of this debilitating disease. Dreamsickle Kids partners with many organizations and individuals to elevate Sickle Cell Awareness in the state of Nevada and across the United States. Being the pioneer of advocacy for this rare disease in Nevada, Dreamsickle Kids has been tasked with bringing more information and awareness to Nevada to ensure that the Silver State accounts for the needs of all of its citizens, including the small Sickle Cell population. |
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What people say |
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