Turner Syndrome FoundationCategory: Supporter
Celebrating TSF’s Volunteers
April is National Volunteer Month! As the month comes to a close, we want to highlight some of our amazing volunteers. TSF is primarily volunteer-led. We are grateful for the individuals who generously offer their time and talent to advance…
Read MoreHow To Call Government Officials Like A Pro
Calling your local government officials is a great way to spread awareness of your cause and fight for actionable change, but many people may not know how to do it, or why. This article will tell you everything you need…
Read MoreHappy Employee Appreciation Day
Happy Employee Appreciation Day! At TSF, a nonprofit, we’re lucky to have many wonderful student employees that help us positively impact the TS community daily. TSF Student Employee Stories Ameka Yawson Ameka Yawson has been working at the Turner Syndrome…
Read MoreYou Are Enough (It’s a Girl Thing)
February is Turner Syndrome (TS) Awareness Month, and the Turner Syndrome Foundation (TSF) has several awareness and educational activities throughout the month. One of them is a blog hop and cardmaking challenge (see more information below). As a woman with…
Read MoreWho Are the TSF Awareness Committee?
All throughout February we’ve been talking about the TSF Awareness Committee, and you may be wondering, who are they and what do they do? You might even be thinking, “that sounds really cool, how can I get involved?” Today we…
Read MoreHigh School Club Raises Awareness of Turner Syndrome
When a group of high school students approached us to volunteer in fall of 2020, we were excited and inspired by their interest in making a difference! Today we would like to share the accomplishments of the club members as…
Read MoreMake Your Voice Heard!
“I have Turner Syndrome and it took a very long time to diagnose my condition. I would greatly appreciate any representation this community is given.” Shaylie, Oregon For February Awareness Month, Turner Syndrome Foundation launched a petition to advocate for…
Read MoreWhy I Fundraise: Ideas for In-person and Virtual Fundraisers
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…
Read More2020 in Review
As a TS patient, I’ve been longing for a community and resources to access the information and community I’ve been craving. TSF has given that to me 10-fold as I began joining their online forums, volunteer on their Awareness Committee…
Read MoreFrom 1938 to 2020: It’s Time for Change
Did you know that Turner Syndrome (TS) was first discovered in 1938? It might be hard to believe, given that, after 80 years, there is still a lack of awareness, research, and support for the TS community. Take a look…
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