Addison was diagnoised with Turner Sydrome in 2012 at the age of 4. Most people have not heard of Turner Syndrome until someone they knew loses a baby or is diagnosed with TS. TS is a rare chromosomal disorder. Only about 1% of babies with TS survive to live birth. The Turner Syndrome Society of Minnesota chapters mission is create awareness, promote research and provide support for all families touched by Turner Syndrome. Specifically, we work to promote awareness, create friendships, and provide financial assistance to help defray medical expenses, hearing aid costs, and offer scholarships. 

Our largest fundraiser of the year is the Turner Syndrome Walk, which will be held on Saturday, September 7, 2019 in Plymouth MN. I hope that you will thoughtfully consider a contribution to our walk. All donations small or large will help the Turner Syndrome Society of Minnesota promote awareness, research, and provide support.