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
VIRTUAL Camp Cell-A-Bration
Camp Cell-A-Bration is a week-long camp for kids aged 6-14 with sickle cell disease. Many of our children with sickle cell disease have suffered strokes, jaundice, pain crisis, chronic blood transfusions, surgeries, acute chest syndrome, and damage to their internal organs. Although these children battle this life-threatening disease every day, we want to make sure they enjoy being KIDS!
Camp Cell-A-Bration will be held virtually this year from Monday, August 2nd, 2021 to Friday, August 6th, 2021.
This event has ended.
+myBinderRelated Content
-
people & placesHave A Heart for Sickle Cell Anemia FoundationThe Have A Heart for Sickle Cell Anemia ...
-
people & placesCrimsonBow Sickle Cell InitiativeCrimsonBow is a faith based non-governme...
-
news & eventsHow My Parents Set Me Up for Success in Sickle Cell ManagementMy parents knew they were carriers of th...
-
news & eventsSickle cell disease is complex on its own, but black men with the illness battle its stigmas and stereotypes tooDoctors didn’t expect Marqus Valen...
-
education & researchQualifying for Social Security Disability With Sickle Cell DiseaseIf you or your child has sickle cell ane...
-
news & eventsSickle Cell Disease Association of America, Inc. Hires New President & CEOThe Board of Directors for Sickle Cell D...
-
Community CenterSickle Cell UniteA place where those living with Sickle C...
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.