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
Today’s Faces of Sickle Cell Disease: Marqus Valentine
When Marqus Valentine went to junior college, he serendipitously took a film class, fell in love with the medium, and decided to use it to document his daily struggles with SCD, which have been lifelong. He posted his musings online and eventually turned them into a mini-documentary. It was his way of honoring the many friends he’d lost to the illness—and it led to his co-founding, with his sister Ashley Valentine, of Sick Cells. It is an organization that encourages the sickle cell community to influence public policy and awareness by sharing their own stories.
Marqus Valentine’s dedication has grown—he personally appeared before a Food and Drug Administration (FDA) panel to lobby for sickle cell drug development, and last year made a successful pitch for approval of the drug Endari (L-glutamine oral powder).
Related Content
-
news & eventsWalks, Blood Drives Among Activities Marking Sickle Cell Awareness MonthFrom walks to blood drives, a host of ac...
-
people & placesJames R. Clark Memorial Sickle Cell FoundationThe James R. Clark Memorial Sickle Cell ...
-
videos & visualsSickle Cell Disease – The ‘Invisible’ Illnesshttps://www.youtube.com/watch?v=OXFWezTx...
-
people & placesSickle Cell Support Society of NigeriaWith its current population at 167 milli...
-
news & eventsReadout From the First Lady’s Roundtable on Improving the Lives of Americans Living With Sickle Cell DiseaseFirst Lady Melania Trump and the Health ...
-
people & placesAdrienne ShapiroAdrienne is a fourth generation of mothe...
-
Community CenterWarren rapper draws influence from sickle cell diagnosisSeventeen-year-old Ja’Vionte “Tae Mo...
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.