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: News & Events
Latest announcements and gatherings
Health or education? The daily dilemmas of a student with sickle cell anaemia
Every student feels the pressure of assessments, deadlines and attending classes. But most don’t face the daily dilemma that I do living with sickle cell anaemia: do I settle for lower grades because the hard work needed to achieve the highest standards may result in me becoming sick?
After hundreds of hospital visits and a double hip replacement before the age of 21, I know as well as anyone that living with sickle cell anaemia is challenging. But if I were given the choice to cure it, I would have to decline.
Related Content
-
Community CenterSickle Cell Mommies ClubThis is a place for moms with children w...
-
Community Center‘Every Time It’s A Battle’: In Excruciating Pain, Sickle Cell Patients Are Shunted AsideAmy Mason had toughed it out for hours o...
-
education & researchSickle Cell Disease: Reducing the Global Disease BurdenSickle cell disease has been largely an ...
-
news & eventsSickle cell patients in UK survey, especially those 16 to 20, voice problems with care and pain relief givenIn a survey, patients across the...
-
education & researchPediatric to Adult Transition in Sickle Cell Disease: Survey Results From Young Adult PatientsBackground/Aims: We surveyed sickle cel...
-
people & placesKwamie Lassiter FoundationThe mission of the Kwamie Lassiter Found...
-
Community CenterA Sickle Cell Warrior Survival Story— Timi Edwin“When I was 10, I was flogged by a tea...
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.
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.