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
How My Parents Set Me Up for Success in Sickle Cell Management
My parents knew they were carriers of the sickle cell trait before I was born, so they made an effort to find out if I had the disease during the prenatal stages of my mother’s pregnancy. Once they found out I had it, plans and preparations were made to ensure they knew how to be effective caregivers from the moment I was born.
My parents certainly tried their best to make sure they kept me as healthy as possible. There are quite a few things that I remember them encouraging me to do from a very young age.
The anthem of my childhood: “Tito, drink water!” Even though I didn’t fully understand what the importance of drinking water was, I just knew I had to do it and I never really questioned it. Drinking enough water is important for all people with sickle cell because it promotes healthy blood circulation and reduces the chance of a sickle cell crisis.


Related Content
-
news & events2019 Annual Sickle Cell Symposium – Sickle Cell: Past Present and FutureDRAFT Agenda 5:00pm Registration, netwo...
-
videos & visualsDr. Freda Gives the 411 on Sickle Cell Diseasehttps://www.youtube.com/watch?v=_aMrRu7R...
-
people & placesThe Heart of Gold Sickle Cell Foundation of Northern VirginiaIt is our mission to serve as an advocat...
-
people & placesHands of Hope -Sickle Cell Awareness FoundationHands of Hope- Sickle Cell Awareness Pro...
-
Community CenterSickle Cell Disease isn’t Laughable, But It Has a Comedic Ambassador — Kier “Junior” SpatesMr. Spates believes in living a full lif...
-
people & placesLisa M. RoseLisa M. Rose is the Curriculum Developer...
-
Community CenterSickle Cell Aid FoundationSickle Cell Aid Foundation is a register...
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.