The Sickle Cell Blog
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Request a Warrior For Your Event. Living with Sickle Cell Posts feature topics on work, school, travel, life, diet and all other coping strategies with sickle cell. We are what we eat after all. Love and Sex All questions about sickle cell, love, sex and relationships are explored here. Videos Videos related to sickle cell.
Tampa Area Sickle Cell Support Group. We are a resource for information regarding sickle cell anemia awareness in the Tampa Bay area. We meet monthly the second Saturday of each month. Our goal is to inform the public and patients with sickle cell as well as their families. Tuesday, July 13, 2010. Tuesday, June 8, 2010. UN Declares World Sickle Cell Day. Sickle Cell and Brain Function. I was shocked by this.
Portland, Oregon, United States. Feel free to read archived posts. they are pretty interesting as well. I would also appreciate any comments you may have in whatever arena. The more the merrier! View my complete profile. Michelle Obama on Love and Relationships. Why Do People Play Games? If I would .
Wednesday, February 29, 2012. When I Was A Blogger. I decided to go bouncing through the blogging world one day and thought, why not blog too? Posted by Adventures In Waitressing. Wednesday, September 15, 2010. Not sure if some of you have heard of this or not, but some restaurants do their best to help out charities and such. Usually it is, but tonight was an exception. What sucks the most is that .
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The Sickle Cell Blog. This blog will chronicle the wonderful, poignant and fun filled days of living, loving and surviving with sickle cell anemia. My illness does not define me- -I define my illness. This is my story. Sunday, May 16, 2010. This blog was the beginning of a beautiful chapter in my life, and I dont think I have the heart to ever close it down. But as of today, I will no longer be posting on here. I will be posting to the brand spankin new Sickle Cell Warriors. I hope to see you on there!CONTENT
This web page sicklecellblog.blogspot.com states the following, "This blog will chronicle the wonderful, poignant and fun filled days of living, loving and surviving with sickle cell anemia." We saw that the webpage said " My illness does not define me- -I define my illness." It also said " Sunday, May 16, 2010. This blog was the beginning of a beautiful chapter in my life, and I dont think I have the heart to ever close it down. But as of today, I will no longer be posting on here. I will be posting to the brand spankin new Sickle Cell Warriors. I hope to see you on there!."SEEK SIMILAR DOMAINS
Pain and the experience of SCD. In the Hospital and Other Healthcare Settings. What Is Bone Marrow? Am I A Candidate? How do I become an advocate for SCD? NIH Center of Excellence. What is Comprehensive Care? What care should you expect? In the Emergency Room.
Community Based Sickle Cell Project. Welcome to Brookdale University Hospital and Medical Center.
The Sickle Cell Cares Foundation was established in January of 2013 by Kellyn George as an initiative to address the lack of awareness about the Sickle Cell Disease in Dominica. With continued efforts of the foundation and its volunteers, we can make a positive difference in the lives of individuals and families living with sickle cell disease. Thank you for your support. Sign in to your account.
A nonprofit corporation working to cure sickle cell disease. The Sickle Cell Cure Foundation, Inc. Thus, all donations to the Foundation are tax-deductible.