Google
Trusted Resources: News & Events
Latest announcements and gatherings
Camp Sickle Stars
Camp Sickle Stars is the only camp in the state of Mississippi that is exclusively for children with Sickle Cell Disease. MS Sickle Cell Foundation funds Camp Sickle Stars through various fundraisers and donations. The camp is free to all children between the ages of 6-14 and transportation is available for those who need it.
Date:
June 17-20, 2020
+myBinderRelated Content
-
Annual Sickle Cell Disease and Thalassaemia Conference (ASCAT) 2022The Annual Scientific Conference on Sick...
-
The Sickle Cell Association of New Jersey’s 10th Annual Statewide Sickle Cell Disease SymposiumOur goal is to improve and expand patien...
-
COVID-19 Outcomes Among Individuals With Sickle Cell Disease by IASCNAPA – WebinarLearning Objectives: • Understand how...
-
A Conversation With a Twist: Mental Health and Sickle Cell DiseaseOur goal is to help raise awareness abou...
-
Inaugural Event, World Cord Blood Day 2017, Highlights Non-Controversial Source of Stem CellsWorld Cord Blood Day (November 15th) wil...
-
Coronavirus Preparedness for People With Chronic Diseases – WebinarEvent Date: Mar. 13, 2020 Event...
-
Current Advocacy Work in Sickle Cell Disease: The Global PerspectiveJoin the Global Alliance of Sickle Cell ...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.