One of my most memorable moments at the Naturalista Hair Show was when Nicole Melton said, “Dream big, start small!” 6 years ago, I started my blog and I have put a ton of effort into it and shed many tears. However, it still seems that I am still on the small end of the […]
Recap: The Naturalista Hair Show 2016 Read More »
The Biggest Story by Kevin Deyoung and illustrations by Don Clark is a fun book, audio and DVD set for kids. The illustrations are bright and interesting. Don uses geometric shapes to illustrate the Bible in a simple way. Viewers will see that the animations are basic, yet effective in getting the story across. The
The Biggest Story by Kevin Deyoung and a Giveaway Read More »
St. Jude Children’s Research Hospital is one of the institutions at the forefront of sickle cell disease (SCD) research. The hospital does clinical research at their facility in Memphis, TN. Then they transfer their findings to help healthcare professionals around the world offer better care to children and more hope for adults with sickle cell.
Hope For Adults with Sickle Cell #30forSickleCell Read More »
Ever wondered why I call my sickle cell awareness campaign #30forsicklecell? Well, September is Sickle Cell Awareness Month and it is 30 days long. Unfortunately, it seems that Sickle Cell only gains national attention for 30 days, and while I mainly run my campaign to raise awareness about sickle cell during the month of September,
Why #30forSickleCell? Sickle Cell Awareness Month Read More »
One of the largest sickle cell foundations is the Sickle Cell Disease Association of America. The goal of the SCDAA is “to advocate for and enhance our membership’s ability to improve the quality of health, life and services for individuals, families and communities affected by sickle cell disease and related conditions, while promoting the search
Tomorrow Sept 13th is the #SCDAA #SickleCell Twitter Party Read More »
Kyle’s story sheds light on the need for people living with sickle cell disorder to trust their doctor. Kyle was hospitalized over a thousand times. For many sickle cell patients, hospitalizations are inevitable. As a result, sickle cell patients and their families should research their medical professionals and find the best specialists who will give them the care
Do You Trust Your Doctor? #sicklecell Read More »
The long awaited, State of Sickle Cell Disease 2016 Report from the American Society of Hematology is now available. September is National Sickle Cell Awareness Month so I have made it my mission to stay in tune with the medical advances available to sickle cell patients. This is my first post of 30 this month
NEW State of Sickle Cell Disease 2016 Report #30forSickleCell Read More »
