Supacell, the innovative British sci-fi drama series created by Rapman (Andrew Onwubolu), has captivated audiences with its unique blend of superpowers and real-world issues. One of the most compelling aspects of the show is how it addresses sickle cell disease (SCD) and its genetic inheritance. Through its characters and storylines, Supacell provides an engaging and informative look at how SCD can be passed down through generations.
What is sickle cell?
Sickle cell disease (SCD) is a group of inherited red blood cell disorders. The most common form is sickle cell anemia. This condition is characterised by red blood cells that assume an abnormal, rigid, sickle shape. These sickle-shaped cells can block blood flow, causing pain and organ damage, and they break down prematurely, leading to a constant shortage of red blood cells (anemia)
How the show highlights sickle cell
Common Symptoms of sickle cell
When Dione, Michael’s fiancée, notices his eyes turning yellow, she tries to determine the cause. During her research, she discovers that the yellowing could be due to jaundice.
What is Jaundice?
Jaundice is a medical condition characterised by the yellowing of the skin and the whites of the eyes. This yellow discoloration occurs due to an excess of bilirubin, a yellow pigment produced during the normal breakdown of red blood cells.
In reality jaundice is a common sign and symptom of sickle cell disease.
Family Dynamics
Through its narrative, Supacell subtly educates viewers about how sickle cell disease can pass down generations. The five people with superpowers all have one parent who had sickle cell. In the series it is discovered that ‘Supa cell’ is a mutation of sickle cell. This mutation gives the five individuals special superpowers.
The show delves into the dynamics of families affected by sickle cell disease. It explains how parents who are carriers (each having one sickle cell gene and one normal gene) have a 25% chance of having a child with sickle cell disease, a 50% chance of having a child who is a carrier, and a 25% chance of having a child with no sickle cell genes. These probabilities are woven into the narrative, helping viewers understand the genetic risks and implications.
The reality of living with sickle cell
Throughout the show, we witness Michael’s (Tosin Cole) mother struggling with sickle cell. She is shown in severe pain on the hospital bed, while Michael desperately tries to get the nurses’ attention to help her.
Life changing treatment for sickle cell
In the program, Michael talks with senior nurses and the head of London’s first sickle cell treatment center about his mother’s treatment. However, the head of the center is not what she appears to be – no spoilers, you have to watch the show! Michael’s mother is reluctant because staying at the center would be very expensive, but Michael is determined to do whatever it takes for her care.
In May 2024, it was announced that a new treatment for sickle cell disease, Voxelator, will be made available across the UK following a successful patient-led campaign. Previously, UK health regulators had rejected Voxelator last summer, which was disappointing for the 17,500 patients with the disease in the UK.
This is the first sickle cell treatment to be approved by the National Institute for Health and Care Excellence for regular use in the NHS. Patients using Voxelator have reported significant improvements in their quality of life, such as less pain and more energy. However, the rollout is still in its early stages, and it remains to be seen whether this drug can fully treat sickle cell disease.
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How can we raise more awareness for sickle cell?
Lobby for Policy Changes
Advocate for policies that support sickle cell research, improve healthcare services, and provide better insurance coverage for those affected. Engage with local and national representatives to promote legislative action.
Participate in Awareness Campaigns
Join national and international sickle cell awareness campaigns. Participate in events like World Sickle Cell Day (June 19th) to show solidarity and raise awareness.
Host Educational Workshops and Seminars
Organise events at local schools, community centres, and healthcare facilities to educate people about sickle cell disease. Provide information about the genetic basis of the disease, symptoms, treatment options, and the importance of early diagnosis.
Donate Blood if you can!
I know the thought of doing this is scary but imagine how terrifying it is to be living with a genetic condition that has no official cure yet.
One of the most critical treatments for sickle cell patients is blood transfusion. These transfusions can relieve pain, prevent strokes, and improve the overall quality of life for those affected. However, the need for blood is constant and urgent.
Visit www.blood.co.uk on more information about how donating blood works!
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Supacell excels in raising awareness about sickle cell disease through its thoughtful integration of the condition into a compelling sci-fi narrative. By providing representation, educating viewers, breaking stigmas, and sparking conversations, the series plays a crucial role in bringing attention to sickle cell disease.
As entertainment continues to be a powerful tool for social change, Supacell sets a precedent for how media can contribute to health awareness and advocacy.
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