Dreamsickle Kids will be sharing daily tips to assist SCD Advocates in understanding and navigating local and federal legislative bodies to better advocate for long term policy change that will benefit the SCD Community. We welcome all legislative questions and will provide the best answers available.
Dreamsickle Kids Executive Director , Gina Glass, will be sharing best practices in legislative advocacy which led Nevada to a SCD bill (AB254), SCD proclamations, and much more!
Do you reside in Nevada? Would you like to attend the 8th Annual Warriors Convention (virtual)? If so send us an email with " Warrior Convention Scholarship" in subject line and we will provide a special code to attend the convention FREE! *Subject to availability*
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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