Our mission is to #MakeSickleCellPopular, uniting communities and amplifying awareness to drive long-term change. Through education, advocacy, and addressing health disparities, we strive for equity and improved access to care for those impacted by Sickle Cell Disease and other Rare Diseases in Nevada. Together, we can create a brighter future for all affected individuals.
Our Vision is to stand as a beacon of hope and support for those affected by Sickle Cell Disease, Rare Diseases, and underserved populations in Nevada. We aspire to lead the community by fostering unity through impactful social events that offer not only support, but also outreach, education, resources, and awareness for Sickle Cell Dise
Our Vision is to stand as a beacon of hope and support for those affected by Sickle Cell Disease, Rare Diseases, and underserved populations in Nevada. We aspire to lead the community by fostering unity through impactful social events that offer not only support, but also outreach, education, resources, and awareness for Sickle Cell Disease and other disparities faced by marginalized communities. Through our unwavering commitment, we will create a more inclusive and equitable future for all.
SCD is a group of inherited red blood cell disorders. Healthy red blood cells are round, and they move through small blood vessels to carry oxygen to all parts of the body. In someone who has SCD, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle”. The sickle cells die early, which causes a con
SCD is a group of inherited red blood cell disorders. Healthy red blood cells are round, and they move through small blood vessels to carry oxygen to all parts of the body. In someone who has SCD, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle”. The sickle cells die early, which causes a constant shortage of red blood cells. Also, when they travel through small blood vessels, they get stuck and clog the blood flow. This can cause pain and other serious problems such infection, acute chest syndrome and stroke.
It is estimated that:
Your generous donation will help Dreamsickle Kids Foundation continue to #MAKESICKLECELLPOPULAR and help provide access to resources for children and families affected by Sickle Cell Diseas and all Rare Diseses in Nevada.
Stay Connected !
Sign up to hear from us about upcoming events, projects, and how you can help spread Sickle Cell Awareness!
Please feel free to reach out to us at anytime with questions, comments,corrections,blog ideas, partnership, and sponsorship opportunities. We love hearing from you!
6895 E. Lake Mead Blvd Suite 6 # 204 Vegas, Nevada 89156, United States
Open today | 09:00 am – 05:00 pm |
Dreamsickle Kids Foundation, Inc is a 501 ( C) 3 nonprofit registered in the state of nevada. tax id 82-4557748. Dreamsickle Kids Foundation, Inc 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
We are excited to announce that our popular Dream Juicing Workshops are back, and registration is now open! 🌟 This fun and informative event is designed for Sickle Cell patients and caregivers. Space is limited, so be sure to register early!
At the workshop, you'll enjoy raffles, delicious recipes, and tasty treats while learning about the benefits of juicing for improved health and wellness. Plus, each attendee will leave with a juicer to kickstart your juicing journey!
📍 Location: Provided upon confirmation of registration.
Click to Register!