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: Tanielle Randall
It was not until their daughter was born five years ago with SCD that Tanielle Randall and her husband found out he was a carrier of the disease. Two years later, she would discover that her second child had the disease. But Randall quickly decided she had to “emotionally move past the fact that my children have this illness and start being proactive and the best parent I could be.” So she dug in, learning everything she could, and eventually joined the board of the Kids Conquering Sickle Cell Disease Foundation. Now, in addition to holding down a full-time job while caring for her daughters, Randall offers resources and advice to other families who are on a similar journey.
Related Content
-
education & researchSickle Cell Disease in Children: Care InstructionsSickle cell disease turns normal, round ...
-
people & placesAzizi ColemanAzizi Coleman is the Clinical Research P...
-
education & researchStrategies to Avoid the FluIt’s cold and flu season and the usual...
-
people & placesSickle Cell Foundation of MinnesotaSickle Cell Foundation of Minnesota (SCF...
-
people & placesPat Corley, RNPat Corley is a retired nurse coordinato...
-
news & events8th Annual Leadership Summit and General Assembly of Patients, Caregivers & CBOsThe Sickle Cell Consortium (SC3) announc...
-
people & placesSupporters of Families With Sickle Cell DiseaseSupporters of Families with Sickle Cell ...
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.