I was unwell for a week in August. It began with deep lethargy. After about two days of that,…
Mary Shaniqua
Mary Shaniqua is a sickle cell patient (HbSS) living in the United Kingdom. She was diagnosed with sickle cell at 18 months old and uses "Shaniqua’s Sickle Chronicles" to narrate her experiences, to educate healthcare professionals, as well as empower and embolden other sickle cell patients. Mary Shaniqua is committed to raising awareness of sickle cell and its impact, with an aim to educate non-haematological specialist healthcare workers and the general public more widely on the life of a sickle cell patient.
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Articles by Mary Shaniqua
I have a difficult time knowing when I’m not feeling well apart from when I have a severe illness. That…
I recently watched a film on Netflix called “Strain,” which depicts the life of a child with sickle cell…
When a sickle cell patient mentions a crisis, most people think of a painful, vaso-occlusive crisis. I can understand…
Today is my birthday. When I was born, the life expectancy of sickle cell patients in the U.K. was 10…
People often tell me that I make living with sickle cell disease look easy. It is not. Whenever people make…
Most COVID-19 restriction laws were lifted in England on July 19. This includes mask requirements, social distancing rules, work-from-home…
One of the many stereotypes of British people is that we can be extremely reserved. In many places in the…
World Sickle Cell Day is upon us tomorrow, June 19. Following are memories that illustrate sickle cell’s ugly grip…
One of the most annoying things about sickle cell disease is that a hospitalization can occur with very short notice.