Turner Syndrome FoundationArchives
Welcome Back Advocacy Coordinator, Liz Carmines!
TSF is happy to welcome Liz Carmines back to the team as Advocacy Coordinator! In this role, Liz will be working one-on-one with YOU to connect you with an opportunity to take action and raise awareness. Liz spent the past…
Read More10 Ways to Raise Awareness after February
Awareness Month is a unique opportunity to call on legislators, the media, industry leaders, and more to pay attention and take action! But, it doesn’t mean we stop our efforts when February ends. In order to bring about real change,…
Read MoreSign the Awareness Petition
Advocacy is the path to obtaining the support and services you need. As an advocacy organization, we understand that gaps exist in certain areas of Turner Syndrome care, legislation, and more. However, with your help, we can raise awareness to…
Read MoreMy Story: “It’s Rewarding to Help Others”
A Turner Syndrome Advocacy Volunteer Shares Her Story My name is Kym and I was diagnosed with Turner Syndrome at 16 years old. I was born the youngest of six with my twin brother in 1971. Growing up I showed…
Read MoreMeet Doreen: Mother & Advocate
My husband Gary and I were married for 4 years, the proud parents of Paul, almost 2 years old, and pregnant with Olivia, when we received a call from our OBGYN with our amniocentesis test results. When I replied, “What…
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 MoreKeep February Awareness Going!
Since February has been deemed Awareness Month for Turner Syndrome, it is the time of year we always look forward to. February is an opportunity to take extra strides in passing along information about Turner Syndrome to our connected community…
Read MoreMeet our Advocacy Coordinator, Liz Carmines
Turner Syndrome has the potential to affect anyone in some way, so raising support for the disorder is everyone’s responsibility.
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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