DISCLAIMER
The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.compose your message
message sent
email sent successfully
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
Related Content
-
videos & visualsShine the Light on Sickle Cell – Webinarhttps://www.youtube.com/watch?v=IIG0UUO5...
-
news & eventsAnnual Sickle Cell Road Race/WalkThe Sickle Cell Foundation of Georgia, I...
-
news & eventsThe 12th Annual International Conference on StigmaThe 12th Annual International Conference...
-
news & eventsNational Sickle Cell Advocacy Day 2020 — Sickle Cell Disease Association of America – CANCELEDPlease join the Sickle Cell Disease Asso...
-
news & eventsCamp New Hope 2022Camp New Hope is a seven-day; six-night ...
-
news & eventsSickle Cell & Me: Survivor Discussion with Clarisse H. (Sickle Cell Survivor)The Lambda Epsilon Sigma Chapter of Sigm...
-
videos & visualsFacebook Live: Stem Cells and Sickle Cell Diseasehttps://www.youtube.com/watch?v=IPzNx8i_...
send a message
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.
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.