Warriors for Sickle Cell Awareness! I love it! I have been a spokes person, advocator, poster model for the New York Blood Center and QSCAN trying to spread SC awareness for over the past 20+ years. Doing it all by myself feels Tireing & also Defeating becus one person with the disease is surely not Loud enough nor can one person do it alone. Every other disease out their has a National Foundation and research heing done that gives HOPE to a Better quality of life. Sickle Cell has been around for way over 100 years now and still there is No Cure, NO FORM OF TREATMENT, THERE IS NOOO PILL, NO MEDICINES, & NO PATCH AS OF YET THAT WILL HELP IMPROVE THE QUALITY OF LIFE, GIVE HOPE THAT A CURE IS AROUND THE CORNER OR ANYTHING like that! WE ARE DIEING EVERYDAY BY THE THOUSANDS AND YET IT HAS STILL NOT BEEN LISTED AS A CAUSE OF DEATH. But I know oh too well that it does kill you. I have lost way too many friends to this scary disease. YET AS WARRIORS WITH THIS DISEASE WE ARE ALL FIGHTERS IN OUR OWN RIGHT. SICKLE CELL MIGHT EFFECT EACH PERSON DIFFERENTLY YET, WE ALL FEEL LIKE WE ARE SOME HOW RELATED BECAUSE WE ALL SHARE THE SAME FIGHT AND WE SHARE THE SAME INNER FEARS, WE ALL SUFFER FROM THE SAME PAIN AND WE ALL KNOW OH TOO WELL THE SOUNDS OF A SICKLERS CRIES AND FUSTRATIONS. Please help me and my other Warriors spread Sickle Cell Awareness. Please help us get the balls rolling or the hope of finding a cure. September is National Sickle Cell Awareness Month. Please help us to make a difference. Calling, all, Warriors, come out and playa!
Posted on: Fri, 29 Aug 2014 11:49:15 +0000
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