By Karen Stokes Elodie Ontala Babongui is a beautiful, educated woman that has a great job and is engaged to be married next year. The day I met her she was full of energy. That was a good day. Unfortunately, every day is a question mark concerning her health, living with sickle cell disease. “I […]
Ask Dr. Kevin: Out with the Old, In with a New Understanding to Improve SCD Care
By Dr. Kevin Williams (Chief Medical Officer, Pfizer Rare Disease Unit) The “Ask Dr. Kevin” series is brought to you by Pfizer Rare Disease in collaboration with the National Newspaper Publishers Association (NNPA) to increase understanding of sickle cell disease. With National Sickle Cell Awareness Month just next month, I’ve been thinking a lot about […]
Patients, Health Professionals Observe World Sickle Cell Day
By Stacy M. Brown (NNPA Newswire Contributor) It’s been 100 years since sickle cell disease (SCD), a hereditary blood disorder, was first discovered. And, according to health experts, it’s no secret that an alarming number of children and adolescence have died, and the condition remained in the province of pediatrics. Known as “the silent killer,” […]
Ask Dr. Kevin: Understanding Clinical Trials and Sickle Cell Disease in the Black Community
By Dr. Kevin Williams (Chief Medical Officer, Pfizer Rare Disease Unit) This article is the third installment in the “Ask Dr. Kevin” series, brought to you by Pfizer Rare Disease in collaboration with the National Newspaper Publishers Association (NNPA) to increase understanding of sickle cell disease. Clinical trials are critical to bringing new medicines to […]
Pfizer Officials Call For Blacks to Participate in Sickle Cell Disease Clinical Trials
By Joan H. Allen NNPA News Wire Contributor June 19, 2016 marks World Sickle Cell Day. In a desire to help create a greater awareness of sickle cell disease (SCD) and increase their efforts to find a cure, Pfizer invited members of the Black Press to meet and discuss with key members of their rare […]