Sickle Cell Patient Dies in Bahrain:(

To all my sickle cell warriors in other countries, my heart goes out to you. I know that we mostly talk about the care in the US, and I know that at times, the care in other places can be even more difficult than what we have over here. Wherever you are, whatever your struggle,…

Read More

Sickle Cell News

Medical researchers are developing a new surveillance system to determine the number of patients diagnosed with a family of inherited blood disorders known as hemoglobinopathies, including sickle cell disease, thalassemias, and hemoglobin E disease. The National Heart, Lung, and Blood Institute (NHLBI) of the National Institutes of Health is funding the four-year pilot project, which…

Read More

Sickle Cell Advocates & Activism

Hello fabulous warriors! Okay, everyone here has gotten something from the sickle cell online community in one way or another. Now here is your chance to participate and help others with knowledge the same way you have been helped. Remember, we are the only ones that can change the way the world views sickle cell…

Read More

Sickle Cell Documentary Photo Collage

Project Hemoglobin S December 17 at 1:13am Report Our Documentary needs faces! We have a collage we’re featuring in our film of Sickle Cell Survivors! If you would like to have your picture featured in our film during our collage of Sickle Cell Survivors Contact Us! We’d Love to have you! Let the world know…

Read More

Minority Nurse Article

Here is the Minority Nurse article I got featured in last year. It’s titled Providing Culturally Competent Sickle Cell Care. So I guess now you know my real name:)

Read More

American Society of Hematology Conference

I know it’s probably late for anyone to travel there, but if anyone is in New Orleans…this conference just might be for you ~ by the American Society of Hematology. I thought you and Sickle Cell Can Kiss My A** readers might be interested in learning about some of the cutting-edge medical research directly impacting…

Read More