Raising funds to help Kinley's family offset the costs as they travel to New York and Italy for a new, groundbreaking treatment for Kinley's venous malformation!

Kinley's story: Kinley was born with a rare venous malformation impacting her neck, airway, mouth, tongue, and major blood vessels in her chest. To date, Kinley has had 22 surgeries and procedures under anesthesia to treat her venous malformations. During the course of her treatments, Kinley has dealt with blood clots, pain, severe sleep apnea, airway issues, and bleeding issues associated with her condition, as well as the pain and risks associated with her many surgeries.

Despite all this, Kinley continues to be a ray of sunshine. She is the apple of her medical team's eye, an amazing artist and dancer, and a spunky little girl. She is the bravest person we know!

In April of 2026, Kinley's mom became aware of a groundbreaking new treatment available to those suffering with complex venous malformations. This treatment is only being offered in Italy and will require Kinley to travel to meet the doctor in charge of this new treatment in New York. Kinley and her family will then fly to Italy for an extended stay for her treatment, recovery, and follow-up. This treatment would give Kinley a childhood not overshadowed by constant painful medical interventions and risky procedures.

Thanks to other venous malformation parents and patients who have also gone through this incredible procedure, we have a rough estimate of how much this treatment will cost for Kinley. This treatment will be life-changing for our wonderful Kinley and her amazing family. Please consider sharing Kinley's story, and thank you for being part of her journey!

For more information on Kinley's journey, follow along on Facebook, Instagram, and TikTok!

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