S.C. Gov. Henry McMaster has declared Oct. 22 as Vascular Anomalies Awareness Day. His proclamation provides an opportunity to bring awareness and begin discussions about vascular anomalies and other rare vascular conditions.

Jasmine Simmons, who has vascular malformations, played a vital role in establishing this important day for our state. Jasmine, a 12-year-old middle school student from Lancaster, has taken up this important cause as a way to raise awareness and help others navigate the medical challenges that come with having the rare condition.

Jasmine, the author of “Jasmine’s Journey: A Story of Overcoming Obstacles,” has been on a mission to raise awareness about the group of disorders called vascular anomalies, which affect both children and adults. Vascular anomalies occur when veins or arteries form abnormally. Some vascular anomalies like hemangiomas are very common and easily treated. Most hemangiomas are visible on the surface of the skin. However, there are other rare disorders called vascular malformations that are less common and often hard to diagnose. Individuals who have these rare disorders often experience severe pain and physical disfigurement. 

As in Jasmine’s case, some of the rarest vascular malformation disorders are often misdiagnosed, which leads to delays in treatment. Delays in medical care can contribute to additional health concerns, as well as issues with positive physical and emotional development. Raising awareness of these rare conditions is Jasmine’s goal.