Subscribe to our blog In this post, Lori, a mother of a woman with Turner Syndrome (TS), details two awareness and fundraising events she organized and how she has pivoted to virtual activities since then. My Motivation People ask me why I fundraise for the Turner Syndrome Foundation (TSF). I do it not only to help […]
Why I Fundraise: Ideas for In-person and Virtual Fundraisers Read More
February is Turner Syndrome Awareness Month! We want to let you know how you can get involved and make a difference by raising awareness of Turner Syndrome. Each and every person’s efforts to spread the word about Turner Syndrome has an impact on future research, health care, and resources for the community. Awareness Month 2021
Awareness Month 2021: YOU Can Make a Difference Read More
Written by Elizabeth (Liz) Rivera, Turner Syndrome Foundation (TSF) intern and blog post writer. TSF’s newest volunteer endeavor, the Awareness Committee, has started full speed ahead on its first project, a video project called The Questions Campaign. The Awareness Committee aims to raise awareness of Turner Syndrome (TS), but what does that mean? Why Awareness
Awareness Committee Video Project Increases Awareness of Turner Syndrome Read More
Written by Elizabeth (Liz) Rivera, Turner Syndrome Foundation intern and blog post writer. Struggling with finding ways to make a positive impact in your community? Through grassroots activism and legislative advocacy for Turner Syndrome, we can all make a difference! Grassroots Activism Through grassroots activism and legislative advocacy, we can help implement solutions to benefit
Grassroots Activism for Turner Syndrome: YOU Can Make a Difference! Read More
February is Turner Syndrome Awareness Month
Help Us Raise Awareness in Every State! Read More
February Awareness Month is almost here, and we have prepared so many ways for you to join us in making change. Raising awareness happens all year, but February is a special time for us to focus our efforts and work together! We have created a packet for you to download that explains many Awareness Month
Awareness Month Involvement Packet Read More
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
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
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
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