Dreamsickle Kids Foundation is the 1st Sickle Cell Organization in Nevada. Created in 2018 by mother and Executive Director Gina Glass. Gina witnessed first hand 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 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. With the passing of AB254 this past June, the state is on the path to do just that.
Dreamsickle Kids Foundation provides many types of support not listed, please contact us via phone or email for more information on the available assistance we can provide to families impacted by Sickle Cell or Rare Diseases.
Permission to use the Dreamsickle Kids Foundation name or logo in any variation, is subject to the terms and conditions expressly agreed upon in writing with approval from the Dreamsickle Board of Directors. Unauthorized use is prohibited and subject to legal ramifications.
Copyright © 2018 DREAMSICKLE KIDS - All Rights Reserve
Powered by GoDaddy Website Builder