How COVID Affected Me With Sickle Cell Disease
The peak of the COVID-19 pandemic was a crazy time for us all. Right now, it feels like a period that didn’t happen ....
Dunstan Nicol-Wilson is from London, England, and was diagnosed with the “invisible disorder” sickle cell anemia from birth. Nicol-Wilson has a BSc in bioscience and an MSc in public health (global health). He has spent his career in research governance and is now a clinical project manager. In addition, he is also a freelance columnist and mentor. Nicol-Wilson began advocating for sickle cell anemia in 2018 through various talks, columns, and community outreach. He hopes his advocacy will raise awareness for sickle cell and blood donation, encouraging others to share their stories. Outside of work and advocacy, he loves to travel, try new experiences, and spend time with friends and family. He can be contacted via Instagram and LinkedIn.
The peak of the COVID-19 pandemic was a crazy time for us all. Right now, it feels like a period that didn’t happen ....
I've often counted myself unlucky to carry this unsurmountable pain caused by sickle cell disease. This journey, at times, has felt so isolating ...
Sickle cell was never taught or spoken about in my school. When I tried to explain what was happening to the other kids, no one knew what I was talking about ....
I choose to accept myself for myself and live a life I want to live without the shackles of what society thinks. I’m on a journey of embracing my true self ...
I wish people knew what sickle cell disease was instantly like other conditions, but that isn't the reality, which can lead to mistreatment or misdiagnosis ...
I had a mixed experience going to school with sickle cell disease. Sickle cell meant I missed more school days than I would have liked ...