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Turner Syndrome Foundation
Turner Syndrome Foundation

Advocacy Awareness Education Research

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Turner Syndrome Foundation
Turner Syndrome Foundation

Advocacy Awareness Education Research

  • HOME
    • PATIENT WELCOME
    • PATIENT REGISTRY
    • WHO WE ARE
    • OUR VISION
    • OUR MISSION
    • BLOG
    • NEWSLETTER
    • CONTACT US
  • About TS
    • WHAT IS TURNER SYNDROME?
    • TREATMENT
    • LEARNING & EDUCATION
    • LIFE STAGES
    • RESEARCH
    • RESOURCES
    • WEBINARS
  • Get Involved
    • VOLUNTEER
    • GET INVOLVED with TSF
    • ADVOCATE For Turner Syndrome
    • Ways to Take Action
    • Online Fundraising
    • Individual Volunteer
  • Support Us
    • Ways to Give
    • 1938 Collective Monthly Giving
    • Partnerships
  • Events
    • Upcoming Events
    • Fundraising Events
    • Plan an Event
  • PROVIDERS
  • HOME
    • PATIENT WELCOME
    • PATIENT REGISTRY
    • WHO WE ARE
    • OUR VISION
    • OUR MISSION
    • BLOG
    • NEWSLETTER
    • CONTACT US
  • About TS
    • WHAT IS TURNER SYNDROME?
    • TREATMENT
    • LEARNING & EDUCATION
    • LIFE STAGES
    • RESEARCH
    • RESOURCES
    • WEBINARS
  • Get Involved
    • VOLUNTEER
    • GET INVOLVED with TSF
    • ADVOCATE For Turner Syndrome
    • Ways to Take Action
    • Online Fundraising
    • Individual Volunteer
  • Support Us
    • Ways to Give
    • 1938 Collective Monthly Giving
    • Partnerships
  • Events
    • Upcoming Events
    • Fundraising Events
    • Plan an Event
  • PROVIDERS

  • HOME
    • PATIENT WELCOME
    • PATIENT REGISTRY
    • WHO WE ARE
    • OUR VISION
    • OUR MISSION
    • BLOG
    • NEWSLETTER
    • CONTACT US
  • About TS
    • WHAT IS TURNER SYNDROME?
    • TREATMENT
    • LEARNING & EDUCATION
    • LIFE STAGES
    • RESEARCH
    • RESOURCES
    • WEBINARS
  • Get Involved
    • VOLUNTEER
    • GET INVOLVED with TSF
    • ADVOCATE For Turner Syndrome
    • Ways to Take Action
    • Online Fundraising
    • Individual Volunteer
  • Support Us
    • Ways to Give
    • 1938 Collective Monthly Giving
    • Partnerships
  • Events
    • Upcoming Events
    • Fundraising Events
    • Plan an Event
  • PROVIDERS
TS family
Nov 11 2019

Three Women Connected by TS

1 Comment | Personal Stories | November 11, 2019

Subscribe to our blog Laura Fasciano, Dawn Petr, and Lori Kobular, are friends, mothers, volunteers, and TSF Board Members. But they weren’t always united over the common goal of making a difference for all women and girls affected by TS. Turner Syndrome, a condition often seen as rare and random, influenced on each of their lives in a major […]

Three Women Connected by TS Read More

Nov 29 2018

From Heartbroken to Hopeful

Leave a Comment | Personal Stories | November 29, 2018 | TS Stories

Subscribe to our blog Kourtney’s Story “My pregnancy with Natalie was my third pregnancy. After two fetal loses, the doctors were watching me closely and considered me high risk. We were terrified to get our hopes up that this pregnancy would be successful. At 10 weeks we had an ultrasound and they found a cystic

From Heartbroken to Hopeful Read More

Jul 11 2017

Meant to Live

13 Comments | Personal Stories | July 11, 2017 | TS Stories

Subscribe to our blog Ivy was diagnosed with Turner Syndrome at 16 weeks in utero. The doctors gave us no hope that she would live. But 20 weeks later, our little girl beat the 1% odds and came screaming into this world and she’s been a fighter ever since. After open heart surgery and 5

Meant to Live Read More

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  • P. O. Box 726, Holmdel, NJ 07733:
  • 1 Bethany Rd, Bldg 1, Ste 5, Hazlet, NJ 07730
  • 800-594-4585
  • info@tsfusa.org
  • M-F, 9am-5pm EST
  • SMS Chat #732-782-5575

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Upcoming Events

Jan 14
January 14 - March 31

Study – Health in Women with Turner Syndrome

Free
Online
Mar 27
8:00 pm - 10:00 pm EST

Star Sisters Monthly Meet Up Event

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