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
DanceBlue inspired UK alumnus to study and fight health disparities
Jordan McDowell, a 2014 alumnus of the University of Kentucky, has always been interested in the ways having a child with a chronic illness affects families. Part of this interest comes from his own experience with sickle cell disease.
McDowell knows first-hand the experiences and difficulties a child with a chronic illness can have when transitioning from their parents’ care to a new environment like college. As a child, McDowell was diagnosed with sickle cell disease, a severe hereditary form of anemia in which a mutated form of hemoglobin distorts the red blood cells into a crescent shape which can block blood flow and cause severe pain.
+myBinderRelated Content
-
videos & visualsThe vibrant, subversive art of 17-year-old Panteha Abareshihttps://www.youtube.com/watch?v=xjbkLPfQ...
-
news & eventsMARAC Advisory Statement: COVID-19 UpdateAugust 26, 2021 — The Sickle Cell Dise...
-
news & eventsSCDAA Partners With Phi Beta Sigma FraternityThe Sickle Cell Disease Association of A...
-
videos & visualsConnect with the sickle cell community on the SMART social wallhttps://www.youtube.com/watch?v=JObAMmnn...
-
people & placesNetwork of Rare Blood Disorder OrganizationsThe Network of Rare Blood Disorder Organ...
-
people & placesSickle Cell Data Collection ProgramThe Sickle Cell Data Collection (SCDC) p...
-
news & eventsKNOWvember Webinar: A grandparent’s voice – Advocacy and support for chronic pain familiesWhile parents are often the prim...
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.