In 2018, my child was diagnosed with an inter-muscular venous malformation. Initially, our family was not able to find proper treatment, or doctors with extensive knowledge. Thankfully, we came across VBF on social media.
The Vascular Birthmarks Foundation has been pivotal and life changing in the treatment and eradication of our daughters recently diagnosed medical condition. My goal as a parent is to help spread the word to other parents and patients, as well as those around me to help bring awareness and education.
Our family loves being part of the VBF community!