When living with a condition like sickle cell disease, effective communication between different hospital departments and the patient is…
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’ve shared that I’m on a blood transfusion program as part of my sickle cell treatment. There…
In my previous column, I shared that I’d contracted what I think was food poisoning, which led to dehydration and,…
I was recently hospitalized for a sickle cell crisis. You see, I’d planned to go to dinner with a…
Health-related stigma, as I discussed in my last column, is not the only stigma that afflicts those with…
Living with sickle cell disease means dealing with constant fatigue and painful vaso-occlusive crises. These symptoms can impede…
In a previous column, I gave a brief overview of my family’s experience with sickle cell disease. Both…
In recent columns, I have written about why knowing your genotype is imperative when planning a family, as well…
Living with sickle cell disease is no easy feat. At 32, I still struggle to understand my body and…
If you haven’t already, I would recommend you get your genotype tested. Sickle cell is an inherited disease. This…