Determined to make a difference in the lives of individuals with Turner Syndrome through education, research and support, I founded this organization to advocate for a randomly acquired and complex condition affecting women. Precious lives, families and communities are struggling for answers.
As the Program Development Coordinator for Turner Syndrome Foundation, I listen to the needs of the women in our community and watch industry trends to create programs that assist in fulfilling TSF’s mission. To ensure program success, I collaborate with colleagues to develop funding proposals, resources, and marketing materials. Outside of the office, I’ve volunteered at TSF events and ran a half marathon and 5K for Team TSF. Being a part of TSF gives me a first-hand view into just how great an impact this organization makes in the Turner Syndrome community, and I am happy to give back in any way that I can!
In the role as Talent & Communication Coordinator, I share the excitement of advocacy opportunities with individuals and companies to encourage support for the important objectives of the Turner Syndrome Foundation. Creating new alliances for a greater awareness, allows me to understand the personal or professional commitment of our talented volunteers. It is my goal to align each with a meaningful way to give back and get involved. There is an opportunity here for everyone.
I believe that personal connections are an important part of implementing effective solutions to social issues, and will continue to utilize every effort to make the health of Turner Syndrome patients a priority in our society. Liz is currently abroad for two-years with Americorps.
Danielle E. Mouta
I am currently a senior in the field of health studies working on a team to establish deeper connections in the medical field to improve clinical care outcomes for patients with Turner Syndrome. While working at the Turner Syndrome Foundation, I hope to see how the initiatives I support can make a positive impact in raising awareness and improving lives for those with TS.
Jonah is a student at Monmouth University majoring in Chemistry with a concentration in Biochemistry. Jonah is also a part of the pre-med program, and is pursuing a career in the medical field. He is working on a team to establish deeper connections in the medical field to improve care outcomes. His goal as a member of the foundation is to help raise awareness about Turner Syndrome, and support the initiative to improve the lives of those affected by Turner Syndrome.
I graduated as a Neuroscience major from Drew University in the spring of 2017 and I am going to apply to medical school in the 2018 cycle. The more I learned about Turner Syndrome, the more I understood the need for advocacy, research, and support. At the Turner Syndrome Foundation, I know I am contributing to all three of these goals by volunteering. As a volunteer at the foundation, I have the honor of learning the stories of those affected by Turner Syndrome, and attempt to connect them to the resources they need.
I have run 6 full marathons including a 50 mile ultramarathon, while giving back to the community by volunteering with running charities such as Achilles International and Team for Kids. I have also overcome 3 knee surgeries, and hope to inspire others with any kind of setback that accomplishing your goals is possible.
Veronia S. Hanna
Masters of Public Health | Rutgers, The State University of New Jersey
Alyssa M. Dennis
Hi my name is Alyssa I am 27. I was diagnosed with Turner Syndrome at birth. I am currently a medical assistant at a university affiliated OB-GYN. The mission of the Turner Syndrome Foundation is inclusive and welcomes all to participate in patient outreach to increase education and facilitate support to all young girls and women with Turner Syndrome. It’s highly important that our families know we are here to help, communicate, and bring comfort to them through these efforts. It is a rewarding experience to help others and this good cause.
Olivia is a music industry major in her senior year. She is a spokesperson for Turner Syndrome Foundation with frequent live posts, motivational messaging and inspirations through TSF social media channels.
I enjoy volunteering my time with the Turner Syndrome Foundation. Applying myself is rewarding and keeps me in tune with current technologies. Coming here, I get the satisfaction of giving back to my communityand at the same time making new friends in a pleasant office environment.
Max Mallet is a communications professional who’s passionate about giving back to his community. With experience in the nonprofit and for-profit space, Max wants to help raise awareness about Turner Syndrome both locally and nationwide.
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