08/24/2026
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Family’s like the Pedrick family are who we run and walk for. today we are highlighting a special kiddo from the birthmark community meet Walker. His family just joined the Miles For Vascular Anomalies Run walk Club. Please take a moment to read his inspiring story.
Walker is a silly and energetic 2 and a half year old. He was born with a vascular malformation and a mosaic BRAF gene mutation, an extremely rare condition that causes rapid vascular tumor growth on his face, eyelid and scalp.
In just two short years, Walker has undergone 11 surgeries to remove over 18 bleeding tumors and has trialed 6 different medications in the search for effective treatment. He now takes daily oral cancer medication, which thankfully has prevented new tumors from developing for the last 10 months.
While most toddlers are busy exploring the world, Walker is courageously facing challenges that no child should have to endure.
Despite everything, he continues to show us what strength, resilience, and joy truly look like.
We are sharing Walker’s journey to raise awareness and help others learn about vascular anomalies.
Next year, we will travel to Italy for a promising new treatment, needleless electrosclerotherapy, which can treat the affected tissue directly and hopefully allow Walker to come off daily oral cancer medication.