Turner Syndrome FoundationArchives
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If you have not already, now is the time to subscribe to our newsletter! You won’t miss a thing when you receive this monthly update on what we’ve been up to. It will keep you up-to-date on events, research initiatives,…
Read MoreLessons Learned in Research
In celebration of the ten year anniversary of receiving her PhD, TSF Director of Research, Danielle Moore, shares the lessons and insights she’s learned as a medical and scientific researcher. Celebrating Lessons in 15 Years of Scientific and Medical Research…
Read MoreResearch Opportunities
Research is a team effort. The more people that are on the team, the more effective research can be. It is important for all women, girls, and family members affected by Turner Syndrome to contribute to clinical trials in order…
Read MoreRally for Medical Research
Advocating for Turner Syndrome is very easy: Put on a good pair of shoes, meet up with the group and tell your story! Join us at Capitol Hill on September 12-13th and meet legislators to raise awareness and advocate for…
Read MoreRutgers University Study on the Epidemiology of TS
Rutgers Student Studies Health Concerns in Turner Syndrome For MPH Project Veronia Hanna, Rutgers University Masters of Public Health student, chose to study Turner Syndrome for her practicum poster presentation, a final project required for Masters of Public Health candidates….
Read MoreSurvey Parent Perspectives on Delivery of Diagnosis
Survey – Sex Chromosome Aneuploidies: Parent Perspectives on Delivery of Diagnosis You are invited to participate in a research study that focuses on the experience parents have had while receiving a diagnosis of a sex chromosome aneuploidy (SCA) for their…
Read MoreRally for Medical Research
2017 Rally for Medical Research Turner Syndrome Foundation representatives attended the 2017 Rally for Medical Research this September in Washington, DC. The meetings and reception were held in the Grand Hyatt Hotel and on Capitol Hill. Aligning with advocacy…
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