The feature below is brought to you by The Crescent Cell, an organization that is in the running to receive a See Beautiful Grant. For more information about all of our giving initiatives, please click here. To learn more about The Crescent Cell, please visit their website page: here. Faces of Sickle Cell Strength. The light was dim. The heavily conditioned air of the room contrasted the humid August heat. Although the afternoon was still, through a wooden door, a piercing cry filled the air. In the clinical room beyond the wooden door, the agonizing pain from a ten year old boy met no relief from the healthcare providers' voices of reassurance. As I sat down to take pain medication for myself, I reflected on the young child’s experience. The long days dragging into the night, the pain, the tears, the isolation, were all too familiar. Even with a ten year difference, the treatment options for what we were both going through had made little progress. It is the unfortunate fate that over 100,000 people in the United States, including the ten year boy and myself, are forced to face everyday. We are bonded through blood by a simple genetic mutation called sickle cell disease. All through my life, I did my best to hide the effects of sickle cell. You can’t tell someone has it just by appearance, so it becomes manageable to hide. Just as the condition is deemed “the forgotten disease,” I, like many sickle cell warriors, became invisible. I did my best to avoid what causes the debilitating pain episodes: dress warm, stay hydrated, try to avoid stress and exhaustion. When the pain did happen, I would disappear for days to weeks at a time. I would go from being bedridden to re-entering the world as if nothing happened. I was doing whatever I could to fight sickle cell without people knowing I actually had it. Finally, I committed to what I knew all along: the best way to truly ignite change was to publicly speak out.
Written by: Omonike Oyelola, Director
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