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#Women’sHealthResearch Matters

     As an individual or a group, there are lots of opportunities to be an advocate for healthcare equity and to make a true difference for women with TS. Advocacy takes many different forms, and your experience as an advocate can be tailored to your unique interests and skill sets. Legislative action is a […]

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card sale

Kick-Off the Holiday Card Auction

https://videos.files.wordpress.com/dBvVCDDe/winter-sale.mp4 PICK YOUR HOLIDAY CARD – WE MAIL IT FOR YOU! Looking for an easy way to support the Turner syndrome community and get ready for the holidays? The Turner Syndrome Greeting Card Sale is here! The variety of holiday cards for the autumn and winter holidays, including Halloween, Thanksgiving, Christmas, Hanukkah, and New Years.

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Teaming Up for TS: Thank You to the Dream Team of Donors!

     For Turner Syndrome Awareness Month in February, the LSU Women’s Basketball Team and their partners at Gordon McKernan Injury Attorneys organized the Playing for a Purpose fundraiser to support TS Awareness and share our mission, during which Gordon McKernan Injury Attorneys donated $20 to TSF for every point that players Angel Reese and Alexis Morris scored,

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Rally for Medical Research

Powerfully Impacting the TS Community: Legislative Advocacy

   There are many ways to get involved in awareness and work within the Turner syndrome (TS) community. Legislative advocacy is a very important part of that work, as it allows us to communicate directly with our federal, state, and local representatives who have the ability to officially proclaim awareness for TS. National awareness for

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Overcoming The Mental Mind Game

   The Turner Syndrome Foundation’s (TSF) My Story blog series highlights the experiences of individuals, families, and caregivers impacted by Turner syndrome (TS). Their stories have an incredible ability to inspire others and make a positive impact on the TS community. These serve the purpose of educating those who are unfamiliar with these types of

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Ways to support turner syndrome research

Register for TSRX to Help Science Know More About Turner Syndrome!

     The future of Turner syndrome research is in the hands of the patient community. The Turner Syndrome Foundation, in collaboration with Invitae Patient Insights Network (PIN), has established a TSRX PIN to assist the patient community in assisting the scientific community in creating an inclusive global data registry on TS; the biggest in

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Equity in Healthcare: How It Impacts Women with TS

Note: This post contains sensitive information about reproductive health that may not be appropriate for younger audiences. Everyone’s journey with TS is different. Please consult with your health care provider(s) for guidance regarding your unique health issues and appropriate treatments. TSF does not take a stance on medical treatments or provide medical advice. When seeking

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