Dreamsickle Kids is committed to education and recognize it's importance to SCD and Rare Disease patients and their caregivers. Every year we will be providing scholarships to at least one patient,sibling, parent ,or caregiver that is in pursuit of higher education. Understanding the lack of medical providers that serve SCD patients and those with knowledge of Rare Disease, we will also be giving a scholarship to a medical student that studies hematology, oncology, or Rare Diseases. We will also provide a scholarship to a student in Public Health as it is also important to have community advocates working towards better health outcomes for communities. *Scholarship limits may vary, recipients will be randomly chosen by the Dreamsickle Kids board of directors.
Bone Marrow Transplant ( BMT) and Blood Donation are very important to the SCD and Rare Communities , many SCD patients receive chronic transfusions to maintain their quality of life. Currently , BMT is the only viable cure for SCD. We are committed to educating the community on how simple registering as a BMT donor or donating blood to help save lives.
This program provides FREE activities for children from 0 to 17 . This program allows children and siblings time to relax with activities that are fun and informative, our Annual Warrior Drive is currently our biggest event geared towards celebrating children impacted by SCD and Rare Diseases.
Dreamsickle Kids Loves to partner with national and local organizations. Here is a complete list of our current partnerships. If you or your company is interested in partnering with Dreamsickle please email your inquiry to firstname.lastname@example.org . We look forward to hearing from you.
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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