A program for children with SCD or Rare Diseases from age 0 to 13. The Dream Kids program allows children to learn about their illness and taking care of their health while having fun doing what any child would love to do.
The Dream Scholarship is for those affected by SCD and other Rare Disease, their siblings and parents looking to achieve a higher education. The Dream Scholarship is also available to medical students in Nevada as well as Public Health students as an incentive to advocate and practice in the field of hematology, oncology, genetic, and Rare Diseases.
* Scholarship amounts may vary from year to year with a minimum of $500*
This program works to educate those in the community about the importance of blood and bone marrow donation , which can be very essential to the quality of life for people with SCD and other Rare Diseases. Education and awareness of its importance is achieved through workshops and health fairs throughout Nevada.
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.
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