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Editorial – Doctor Care: My Rights Were Wronged!
I thought I had dealt with everything that one person had to go through, until the day I made the decision to express my concerns about my doctor care. Continue reading →
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Poetry Corner: Forever Present
Mortality is my reality Built on a hereditary technicality Forever to be carried through this adventure of living Removal of blinds Continue reading →
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Show Sickle Cell Patients Love this Valentine’s Day
While African-Americans comprise nearly 13 percent of the US population, less than one percent are blood donors.” Continue reading →
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Blood Donations and Sickle Cell Anemia
people of color currently donate less than one percent of the country’s blood supply. Continue reading →
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Living With Sickle Cell: ‘I Don’t Know What It Means to Be Without Pain’
It’s World Sickle Cell Day, and we’re taking a look at the chronic pain and regular hospitalizations that are the reality for many suffering from sickle cell disease. RE-post By: Allison KeyesPosted:...
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