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
The Warrior Series
After a recent stint in the hospital, I began researching documentaries and photo series about sickle cell. Disappointed by what I found – sad stories, stories that narrow in on the pain and, stories that tell how there is no cure; I decided it was time for a different narrative. One of strength, hope and joy. People living with sickle cell often call one another warriors. So I contacted my closest warrior friends and began discussing what it means to be a Sickle Cell Warrior.
Being born with Sickle Cell Anemia has its ups and downs. This disease has humbled me, and through that humility I’ve developed a better spiritual relationship with GOD. My image represents a fighter who wins.
Related Content
-
Community CenterBrandi Abernethy: Nursing Student, Patient, Single MomWhen she was growing up in St. Petersbur...
-
videos & visualsIsaac Singleton: Sickle Cell Freehttps://www.youtube.com/watch?v=a5mMgnuz...
-
Community CenterWarren rapper draws influence from sickle cell diagnosisSeventeen-year-old Ja’Vionte “Tae Mo...
-
news & eventsCelebrating Nurses’ WeekNurses’ week takes place between Thurs...
-
Community CenterChronically FearlessChronically Fearless blog welcomes all w...
-
videos & visualsSickle Cell Patient Finds a Better way of Living Through Apheresishttps://www.youtube.com/watch?v=BSTUaeFz...
-
Community CenterToday’s Faces of Sickle Cell Disease: Tanielle RandallIt was not until their daughter was born...
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.