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: Community Center
Online groups, photo galleries and blogs
Sickle Cell Disease isn’t Laughable, But It Has a Comedic Ambassador — Kier “Junior” Spates
Mr. Spates believes in living a full life with this disease instead of feeling sorry for himself. He understands that there will be times in which he’ll feel extremely bad, but he also knows that in a few days he’ll be better again. During his childhood, he was told that he wouldn’t live past the age of 11. However, he refused to comply with the doctors’ restrictions and limitations. In high school, he participated in football and track & field. Mr. Spates’ family instilled a powerful belief in him at a young age that the disease wouldn’t prevent him from living. It’s this determination, resilience, and courage that propelles him throughout his life.
Related Content
-
news & eventsU.S. Government Awards Missouri Researcher $4.3 Million to Study Sickle Cell in Teens, AdultsThe National Institutes of Health (NIH) ...
-
news & eventsPfizer and National Newspaper Publishers to Raise Awareness About Sickle Cell DiseasePfizer and the National Newspaper Publis...
-
people & placesArrey Echi Agor NdakawArrey Echi Agor Ndakaw is the Interim Vi...
-
Community CenterLiving With Unpredictable Pain: A Sickle Cell Disease StoryGrowing up, Vismel Marquez wanted to joi...
-
education & researchSickle Cell Disease: Tipping the Balance of Genomic Research to Catalyse Discoveries in AfricaThe completion of the Human Genome Proje...
-
education & researchConditions screened by stateWhile all states require newborn screeni...
-
Community CenterDarryl Watkins Stays Positive in Spite of Sickle Cell DiseaseDarryl Watkins has the HbSS variant of s...
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.