Recently, I was playing a question-and-answer game with my partner, and one question that came up was, “What message would…
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
In a previous column, I spoke about some of the things that trigger a sickle cell crisis. This…
A sickle cell crisis is one of the main symptoms sickle cell patients face. However, just because we all…
Iron overload is a common side effect for sickle cell patients participating in blood transfusion programs. When this…
I turned 31 on Aug. 20, 2020. That’s 31 years as a sickle cell patient, and what a journey it…
Have you ever informed somebody of your diagnosis and found their response to be a little annoying? I often have.
Living in lockdown the past few months has been quite an experience. If you had asked me before the…
Whenever I meet new people and tell them I have sickle cell disease (and explain what it is), they often…
I recently was admitted to the hospital during a sickle cell crisis and because of suspected COVID-19. My…
Living with sickle cell disease, I rely on several medications and treatments for various situations. In general, I take medications…