A community leader in advocating for those affected by Sickle Cell, Rare Disease and those underserved in Nevada. Their vision will be achieved by bringing communities together through social events that provide support, community outreach, education, resources and awareness for Sickle Cell Disease and other disparities affecting marginalized communities.

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*We are currently partnering with Dreamsickle Kids Foundation, Inc., and are seeking additional community partners (individuals and organizations) to help in the expansion of our Association to better serve the unique needs of our target populations. If interested in being a community partner, please contact us via phone at 702-781-8008 and/or by email at glahnnia@bchwanv.org