Our sweet son Arthur was born with a venous malformation on his foot. Since birth, we’ve been working closely with specialists at the Cincinnati Children’s Hospital to monitor and manage his care. While we are grateful for the wonderful doctors there, we want to make sure Arthur has the very best chance for a healthy and thriving future.

This fall, we have been given the incredible opportunity to travel to New York to meet with Dr. Nassiri, one of the top vascular specialists in this field, through the Vascular Birthmark Foundation Super Clinic. This visit will give us a second opinion on Arthur’s treatment plan and connect us with families and children who share similar diagnoses, which is both rare and encouraging.

We are raising funds to help cover the cost of travel, lodging, meals, and other medical expenses. Any contribution, no matter the size, will go directly toward supporting Arthur’s journey to receive the best possible care.

Arthur is the brightest light in our lives, and we are so hopeful about what this next step could mean for his future. Thank you for reading, sharing, and supporting us along the way it truly means the world.

Anyone who is curious or has questions about his diagnosis and current treatment plan please feel free to reach out. I would love to inform you and spread awareness about this vascular anomaly.