Subscribe to our blog Brooke Caron and her mom, Kathy, are veteran volunteers of the Turner Syndrome Foundation! They’ve been successful in raising awareness of TS, even getting Turner Syndrome Awareness Month declared in their home state of Maine. Now they’re getting creative with their awareness efforts with a new podcast, The Butterfly Pod! I […]
TS Podcast: The Butterfly Pod Read More
Do you know all of the ways your employer can support TSF? Learn about them here (you may even get a day off to volunteer)!
Subscribe to our blog The eXemplarY Kids Clinic of Cedars-Sinai in Los Angeles, CA is a multidisciplinary clinic for children with X & Y chromosome variations. We spoke with Dr. Schweiger, Director of Pediatric Endocrinology and Co-Director of the Clinic, to learn how this center cares for girls with Turner Syndrome. What kind of specialized
TS Care Center: eXemplarY Kids Clinic Read More
Manasquan Bank is a sponsor of the Turner Syndrome Autumn Retreat!
Manasquan Bank Sponsors Turner Syndrome Camp Weekend Read More
TSF was pleased to be a part of the 2018 PENS Conference!
TSF at the 2018 PENS Conference Read More
Subscribe to our blog What is the TD Bank Affinity Program? The TD Bank Affinity Program is designed to help support non-profit organizations at no cost to its members or supporters. TD Bank makes an annual contribution to Turner Syndrome Foundation based on the average balance in all members’ accounts. Checking, savings, money market, CD, and retirement
TD Bank Affinity Program Read More
Subscribe to our blog Know the signs. Change a life. For more than a decade, the median diagnosis age for Turner Syndrome has been 15 years old. This is a problem. In the best possible situations, Turner Syndrome girls are diagnosed at birth or even earlier. Life-changing interventions for Turner Syndrome generally begin in infancy
Share: Turner Syndrome PSA Read More
Subscribe to our blog One of the greatest joys of work at the Turner Syndrome Foundation is hearing stories of people getting involved across the nation to make a difference. On February 5, a wonderful Turner Syndrome parent and advocate, Dana, and her daughter, Carly Joy, went before the Pennsylvania State Senate on behalf of
Legislative Advocacy in PA Read More
Subscribe to our blog We have been running our campaign to gain signatures on a letter to legislators for a few weeks now and have recieved great feedback! We’d like to further stress how simple it is to sign on to this legislative advocacy, yet how much of an impact your support can have. Our
The importance of writing to your legislators Read More
Subscribe to our Newsletter
