SC Treatment Clinic Opens in Chicago
New sickle cell treatment clinic opens in Chicago
SC Treatment Clinic Opens in Chicago Read More »
New sickle cell treatment clinic opens in Chicago
SC Treatment Clinic Opens in Chicago Read More »
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
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
Sickle Cell Advocates & Activism Read More »
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
Sickle Cell Documentary Photo Collage Read More »
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:)
Minority Nurse Article Read More »
News research on blood stem-cell transplant reversing sickle cell disease in adults.
Blood Stem-Cell Transplant Regimen Reverses Sickle Cell Disease in Adults Read More »
Addendum: Anyone interested in sharing their story can followup on this. Shooting will be done in LA, and you will be flown in for the feature interview. Hope this helps! If interested, send an email to docprjtquery@demarfilms.net We are producing a feature length documentary on Sickle Cell Disease and those who live with it. Currently
More Info on the Sickle Cell Documentary Read More »
Okay, so ever since I wrote the Nicosan Woes post, I’ve gotten several people wanting to know what’s the new scoop on Xechem. I’ve kept my ears to the ground, and after emailing a few great Nicosan friends and supporters, have found out that things seem to be looking better and brighter for Nicosan. I
I came across this and thought someone might be interested. I’ve already sent in a request for more information (gotta do research for y’all first:) New and Engaging Documentary currently in Production seeks more cast members! Does someone you know or even yourself have Sickle Cell Disease? We are still seeking individuals and families willing
Sickle Cell Documentary Read More »