Turner Syndrome FoundationArchives
Deep Learning Could Lead to Earlier Turner Syndrome Diagnosis
As part of its mission to support the Turner Syndrome (TS) community, the Turner Syndrome Foundation (TSF) is committed to making earlier diagnosis a reality. Early diagnosis means that TS patients and their caregivers can better prepare for any related…
Read MoreInternational TS Treatments
Intro Much of the Turner Syndrome Foundation’s (TSF) focus is on helping individuals with Turner Syndrome (TS) manage their health challenges. However, with the pandemic highlighting the power of spreading awareness and sharing research to overcome global health challenges, we…
Read MoreElectronic Health Records Enhance Turner Syndrome Diagnosis
As part of its mission to support the Turner Syndrome (TS) community, the Turner Syndrome Foundation (TSF) spreads awareness of earlier diagnosis. Early diagnosis means that TS patients and their caregivers can better prepare for any related medical issues and…
Read MoreTSF Celebrates National Disability Employment Awareness Month
October is National Disability Employment Awareness Month. It is a time to celebrate the contributions of those with disabilities, including people with chronic conditions like Turner Syndrome (TS), who may have other physical or cognitive disabilities. The Turner Syndrome Foundation…
Read MoreA Guide to Common Challenges of Elementary Schoolers with Turner Syndrome
School can be difficult for many students, but especially if they have a chronic condition. This article will address the common challenges of elementary schoolers with Turner Syndrome (TS) and how to help them overcome them.. Disclaimers: Caretakers, this article…
Read MoreHow To Open a Conversation About Turner Syndrome Diagnosis
One of the most challenging aspects of Turner Syndrome (TS) is knowing when and how to approach the TS diagnosis conversation. Whether you are a parent/caregiver or patient, read on to learn more about when and how to have this…
Read MoreMy Story: What I’ve Learned as an Angel Mommy
Chelsea Patterson is a make-up artist and blogger from Michigan. Since losing her unborn baby, Noa, to Turner Syndrome (TS)-related complications, she has been on a mission to spread awareness of TS and support other angel mommies. Below is the…
Read MoreEnvironmentally Friendly Ways To Promote TS Awareness & Fundraise
You can help members of the Turner Syndrome (TS) community and protect the environment at the same time. Learn more about environmentally friendly ways to promote TS awareness and how to support the Turner Syndrome Foundation (TSF), while also doing…
Read MoreWhen to Share the Turner Syndrome Diagnosis?
In this post, we explore perspectives on when to share the diagnosis of Turner Syndrome with a child. This post is an update of an article published by TSF, based on a 2006 research study. Some personal perspectives shared within…
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…
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