As many of you know, I am currently in my fourth year of medical school and dream of becoming a pediatric dermatologist. Throughout this journey, I’ve had countless memorable experiences, but one particular patient interaction stands out:
Earlier this year, I met a remarkable teenage girl while shadowing in clinic. She was vibrant and chatty, sharing stories about her school life, future travel plans, and her recovery progress after cancer treatment. But as she removed her wig for the physical exam, her demeanor completely changed. The bright smile faded, her eyes lowered, and she began to fidget with her thumbs. In that moment, it felt like I was seeing a different person altogether.
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Hair loss is a common side effect of cancer treatment. Unfortunately, it is also one of the most distressing. While it is typically temporary, up to 1 in 7 childhood cancer survivors never fully regrow their hair, leaving them with bald patches or hair thinning long after their treatment ends. I’ve seen how persistent hair loss can have a devastating impact on a child’s self-esteem, identity, and social life. Although wigs and hair extensions can help, they are often prohibitively expensive, costing hundreds to thousands of dollars and rarely covered by insurance.
This is why I am running to increase awareness and improve care for children with persistent hair loss after cancer treatment. Many people are unaware that treatments exist for this type of hair loss and believe they must simply accept it. We need to work on educating patients and doctors on recognizing and treating this distressing condition.
The funds we raise will go towards creating educational materials on hair loss for patients and doctors, and covering treatment for patients who cannot afford it.
Thank you for your support in making a difference!
