Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Dreamsickle Kids Foundation
4660 South Eastern AvenueLas Vegas, Nevada
United States
Email Phone Web
Dreamsickle Kids Foundation is the 1st Sickle Cell Organization in Nevada. Created in 2018 by mother and Executive Director Gina Glass. Gina witnessed firsthand the lack of knowledge and resources for people affected with Sickle Cell in Nevada. From her personal experience, Dreamsickle Kids was birthed. 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 effects 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.
Related Content
-
65th American Society of Hematology (ASH) Annual Meeting & ExpositionThe 65th ASH Annual Meeting and Expositi...
-
UT Southwestern Medical CenterUT Southwestern Medical Center is a lead...
-
Lifespan Comprehensive Sickle Cell CenterThe Lifespan Comprehensive Sickle Cell C...
-
‘Every Time It’s A Battle’: In Excruciating Pain, Sickle Cell Patients Are Shunted AsideAmy Mason had toughed it out for hours o...
-
Sickle cell disease: when to transfuseHello. I am Dr Mary Hulihan, a health sc...
-
TCD with Transfusions Changing to Hydroxyurea (TWiTCH): Hydroxyurea Therapy As an Alternative to Transfusions for Pr...Transcranial Doppler (TCD) screening in ...
-
10th Annual Sickle Cell Disease Therapeutics Conference – VirtualThe Annual Sickle Cell Disease Therapeut...
+myBinder