Dr. Maria G. Vogiatzi and a panel of speakers
team up at New York Presbyterian after an
informative conference on Turner Syndrome
held on March 22, 2014
PATIENT & CAREGIVER
EDUCATION - INFORMATION - SUPPORT
Coordinating specialized education conferences for patients and caregivers
The purpose of patient workshops is to provide education, information and support to patients and their caregivers by experienced and knowledgeable providers. Turner Syndrome Foundation workshops have been organized since 2009, and reach patients in communities where they live. Many families travel a great distance to increase their understanding, gain new perspectives and learn about current resources.
Please join us by registering today. If you have any technical difficulty registering online, call 1-800-594-4585 to register by telephone or email email@example.com.
Children's Hospital at Montefiore, Division of Pediatric Endocrinology
Please join us for some interesting lectures, group sessions for the girls and lunch!
Date: Friday, August 1, 2014 10:30 a.m. - 3:00 p.m.
Place: The Children’s Hospital at Montefiore
The Grand Hall, Tishman Learning Center
Gun Hill Road Entrance
Time: Arrival 10:30 a.m.
Lunch will be served from 12:00- 12:45 p.m.
Lectures will start promptly at 11 a.m.
RSVP by July 27, 2014
Advanced reservations are required by completing the reservation form.
Topics may include:
Bone Issues in Turner Syndrome, Audiologic Evaluation and Management of the Patient with Turner Syndrome
When Sugar and Spice are Not So Nice: Turner Syndrome and Type 2 Diabetes Mellitus
Menstrually Speaking: Iniatiating Puberty in Girls with Turner Syndrome,
!! Advanced Registration Required: Reservation Form
or contact Laura Fasciano (732) 847-3385 or email: firstname.lastname@example.org or
Susan Wesoly, RPA-C (718) 920-4090 or email@example.com
Please see directions, parking and entrance information provided at http://cham.org/guide/directions/
If you would like to arrange an education program in your community hospital, please contact firstname.lastname@example.org.
“Beyond learning more about what is happening inside me, I met a lot of great people. I felt immediately welcomed into the TSF community with open arms. I never felt judged, which often happens being the shortest person in a room. Furthermore, I met other girls with TS for the first time in my life. I finally didn’t feel like I was alone. I could talk candidly with them about what I am going through and what I went through as a child. I’ve never felt comfortable doing that with my friends. Sure, I’ve told a few close friends what TS is and that I have it, but I’ve never went much further. As I said, I just never felt comfortable talking about something so personal. “ Jennifer
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