My name is Kathryn Caron and I am the mother of a 23 year old young lady named Brooke. Brooke was diagnosed with TS at the age of 10. Living in Maine and having a daughter diagnosed with TS has had its share of obstacles. Being a pretty rural state, we struggled to find any support, anywhere. As parents, we tried reaching out to other TS programs, however we were really aiming to find one close to home. The closest organization was located in New Jersey. I reached out to Laura (founder and president of TSF) who immediately (along with her staff) welcomed our family with open arms! Since 2011 or so, we have been building our relationship with the TSF! They have helped us gain awareness in Maine where we now have February recognized as Turner syndrome Awareness Month and now, my daughter Brooke and I are co-hosting a podcast called "Butterfly Pod-Talking Turner syndrome" where we are sharing stories of so many beautiful TS ladies both in Maine and now, stretching into New Hampshire! The TSF has been a HUGE support! We are beyond grateful to call them "Family"!
The people whom I’ve met over the past 10 years are united in raising awareness of Turner Syndrome. They are dedicated to creating a better understanding of the disorder and saving lives. Women, and families such as mine, benefit knowing that there are advocates dedicated to impacting lives. It’s a duty and honor to support this cause.
Always happy to support TSF!
TSF creates multi-faceted programs that fill the needs of women and girls with TS. Anything you need is available on the TSF website free of charge.
I volunteer as a Facebook page moderator for TSF and I love it! It’s such a great way to share and create awareness about Turner Syndrome and the community is amazing!
When my daughter, Julie, was born with Turner Syndrome we had never heard of it before. We found that most of the doctors we took Julie to see had never seen a Turner Syndrome patient before and so they could not answer a lot of our questions about Turner Syndrome. That is where the Turner Syndrome Foundation has come into being a major asset to our family in answering medical, behavioral, intellectual and social questions. Without this organization families would be left in the dark and not understand that certain medical issues and behavioral issue are due to the missing X chromosome. For my family it was good to learn that we were not alone in our search for answers, and that TSF was able to tell us the connection to the missing X chromosome and to provide names of doctors who could help us find answers. TSF is a vital tool in helping us to understand and navigate through the TS issues.
I have been involved with TSF and been a donor for several years. It is amazing what we can do with great volunteers and hard earned funding. The ED has great ideas to help women and families dealing with TS. Unfortunately, we have to choose which ones we can fund! I wish TSF could attract the type of funding and attention that the big charities get. Imagine the things we could do =)
I became involved with Turner Syndrome Foundation when I was involved with many young ladies in a pediatric endocrinology clinic. I was so impressed, as a nurse, that TSF offers education, at no charge, for patients, parents, educators, and health care providers. There is so much information available on the web site to support the families of these ladies, young or aging.
There is also support regarding ways to maneuver the health insurance challenges. Questions about the actual genetic syndrome can be answered by medical providers, social workers, and those who have or are experiencing TS. There are opportunities to participate in research and to see what the latest findings are in sub specialities that treat the various aspects of TS. There are always ideas to address in the future being formulated.
The early diagnosis of TS was the initial goal when TS was founded. Now the information available covers the life span of the individual as well as so much support for ladies and their families.
This organization provides education and support for health care providers, educators, parents and patients with Turner Syndrome. The education is updated and available to all online. TSF does not charge dues to participants. Answers to questions can be obtained from healthcare professionals. This organization has done so much for this clientele over the years and has recently added the opportunity to participate in a data base which would help improve care and early diagnosis.
i Must admit out of any other educational sights on TS the foundation I find it personally the best Theirs always a person on the other end trying too help youin anyway they can ,and it’s very much appreciated. I’d definitely recommend the foundation if you need any form of help. Thank you all the way from Bonnie Scotland
My daughter has Turner's Syndrome. She was diagnosed at 18. She had all the health conditions associated with Turner's as well as both physical/anatomical characteristics, and delayed learning disabilities . She continues to maintain her health.
My name is Sarah. I was diagnosed before birth with Turner Syndrome, and have always strived to not only be the best advocate for myself, but also for other girls, and women affected by TS. A couple years ago I was looking to get more involved with the TS community, and I couldn't be happier or more grateful that I came across the Turner Syndrome Foundation. From the start I have felt apart of such a loving, caring community, I am in awe of all the hard work everyone involved with the foundation contributes in terms of advocacy, raising awareness, research initiatives, and making sure that every girl and woman affected by TS has the best quality of life possible. I have had the opportunity to organize a couple fundraising campaigns, participated in the NJ marathon a couple years ago as a member of team TSF, and most recently attended the retreat weekend the foundation recently hosted. I am looking forward to experiencing my first workshop. The foundation does so much to improve the lives of every girl, and woman affected by TS and I couldn't be more honored to be a small part of it all. I am looking forward to getting even more involved in the near future.
I've volunteered at at least 5 TSF events, and each one is better than the last. There is a real focus on community, which is something special I think other organizations are lacking. I will continue to support TSF because I've seen firsthand the impact they have on women and girls with TS.
Great place to volunteer. Laura Fasciano, the founder, works with your schedule and interest. She truly cares about the cause. The staff and volunteers work hard to support the organization’s mission of raising awareness, providing access to resources, support and community to those affected by Turner Syndrome.
Turner Syndrome Foundation helps improve lives every day with their commitment to a increased awareness through education and research initiatives. The Turner Syndrome Research eXchange is to their credit as is the access to information and support available to professionals and consumers. There are no membership dues for patients. The objective, give everyone a chance to attain good health and educational outcomes. This is a solid charity with a large active volunteer base. TSF will continue to flourish with thoughtful leadership and innovative progress.
More than awareness to reduce the age of diagnosis, TSF provides free access to education resources & support
My daughter has Turner Syndrome and we have been part of this organization since its inception. While Olivia has challenges (and who doesn't ) Turner syndrome makes her /them even more special. I can't say enough positive things about Laura and all of the board members who work tirelessly to help educate and advocate for TS. The statistics 1/2000 females have TS and 98% abort spontaneously prove that there should be more awareness out there. Please help is advocate.
TSF offers tons of resources and support to patients and professionals completely free of charge!
I volunteered at handful of TSF events and was wow-ed by all the volunteers who came together for this cause! I'll be participating in the NJ Marathon again this year to support such a great charity!
I am a volunteer with the Turner Syndrome Foundation. I found out about Turner Syndrome through a genetics class that I am currently taking. On researching TS, I found that knowledge about this disorder is severely lacking, and wanted to help spread awareness and a sense of community. I found the Turner Syndrome Foundation and was amazed that an organization dedicated to awareness, support, and research was entirely run by one woman, Laura Fasciano. Every week I see the time, love, and work that Laura and the volunteers here put into helping individuals with Turner Syndrome. I'm very lucky to be involved in such a place and see the work that they do.
Before her birth, our granddaughter, Ava, was diagnosed with Turner Syndrome. No one in our family had ever heard of Turner Syndrome and we were not able to obtain any helpful information. In 2011, when Ava was 4, our daughter found the Turner Syndrome Foundation on line and immediately connected with someone in the organization. A few months later 16 of our family members attended the TSF Family Day at the New Jersey Marathon. We were so excited to meet other TS families and, for the first time, to be given valid and encouraging information about TS! We no longer felt that we were the "only" family going through this.
The Turner Syndrome Foundation was started by one woman, Laura Fasciano, a mom whose own daughter had TS. Not being able to find any helpful information, she set out on a mission to learn all she could about TS. Since that day, she has accomplished more than any one person could imagine. She has championed the Turner Syndrome Foundation into an amazing organization supporting families' concerns, creating a community of TSF families, and bringing awareness to pediatricians and other pediatric specialists, medical students and legislators. Laura and TSF have brought hope and help to so many families! Our family is incredibly grateful!
When I was younger, my late mother was trying to find out more about this group.She first discovered this article through the renowned "Dear Abby". I joined a local group, and met many sweet young ladies ,known as true "Sisters". I enjoy keeping contact online.
We would like to share our family Christmas tradition that is bitter sweet. Every year on December 9th we search for a special Christmas ornament to remember Hannah Grace Brooks. December 9th, 2004 she died due to a heart defect related to Turner Syndrome. Hannah Grace was due to be born in early 2005. In early October of 2004, a routine sonogram showed that fluid was building up and putting pressure on her heart. This condition was steadily increasing and making it more and more difficult for the heart to do its work as she grew. Doctors proposed a very risky surgery in which fluid could be relieved in-utero, but could also cause Hannah to lose her life. The risk was such that specialists at Harvard University were petitioned to perform it and they promptly refused to operate due to the danger. After much prayer, as her parents we decided that we would put the outcome in God's hands and not try force things ourselves. To this day, we trust that He is sovereign. The day of the final sonogram, we both knew in an instant that our lives were changed forever. No heart beat was detected. Our precious little girl was finally and completely in God's presence. As a parent, you just never expect to attend the funeral of one of your children. We named her Hannah after the story in the Bible where Hannah prayed for a child and He honored her with Samuel. Just as He did with Hannah in the Bible, God blessed our lives with this child, if only for a moment.
So we choose to give each year at this time in honor of our sweet child Hannah and in honor of all of those lives who are touched by Turner Syndrome.
Three years ago, our oldest daughter was challenged to do a community service project through her Honor Society mentor. Hadley decided to make Christmas ornaments and sell them where all proceeds were donated to the Turner Syndrome Foundation. We altered our family tradition and this is the third year we are making ornaments for Turner Syndrome research. All three of her sisters are now involved in making these ornaments each year.
Some facts about Turner Syndrome:
' It affects about 1 in 2,000 female births.
' It is also known as the XO syndrome because one of the X chromosomes never crosses over. Effects are varied, depending on the amount of genetic material missing.?
' These females are short in stature and do not develop secondary sexual characteristics resulting in infertility.
' Perhaps one of the most alarming statistics is that Turner Syndrome is attributed to 15% of all miscarriages and stillbirths.
While there may be tears in our eyes because of our loss, education and research can help those affected live better. The ornaments include a butterfly which is the symbol for Turner Syndrome and a cross to remember Jesus and the life He gave so that we have eternal life and that our separation is only temporary. This will continue to be an annual tradition. Making this donation in Hannah's memory has helped our family heal from her loss.
Review from #MyGivingStory
this is my story Help me to spread the word about Turner Syndrome
My name is Kym Hall and I was diagnosed with Turner's Syndrome at 16 YEARS old.. I was born the youngest of six with my twin brother in 1971. I showed some signs growing up of Turner Syndrome but doctors never put it together till 16 . I was always the shortest in my class had the webbed neck and hearing problems. At 16 my mom was concerned about my growth and puberty so off to the doctors we went then did a DNA test which confirmed Turner Syndrome. It was scary at first not understanding Turner Syndrome and being a teen but I learned quickly not to let it stop me. Meeting others with Turner Syndrome helped me as well. I went to college got my BA and Masters in counseling.
I am currently a retired teacher and a volunteer advocate for the Turners Foundation Syndrome in my home state of New Jersey. We were instrumental in helping getting a bill passed that makes February Turner Syndrome Awareness month in New Jersey. I phoned emailed and even t t testified infront of the nj senate . I currently volunteer by talking with others about turner syndrome for The Turner Syndrome Foundation. It is rewarding and helpful.to help others
I want every Turner Syndrome baby to have the advantages I didn't have due to my late diagnosis. I have a passion for awareness and hope to allow more girls a much earlier detection.
Look up Turner Syndrome Founation at turnersyndromefoyndation.org or on YouTube search kym turner syndrome diaries for more info on my story at: https://www.youtube.com/watch?v=rb8mgXt2PPs
Review from #MyGivingStory
A committed a organization whose mission is taken seriously. They truly care about the cause they are arduously working for. Every call, every email, every personal visit is attended to as though it is coming from a family member. They go far and beyond to provide individuals with the necessary resources that will meet their needs. I’ve been a witness of their relentless and selfless work when it comes to finding answers and developing resources that will lead to a better quality of life to the women they are serving, and for them I am very thankful. TSF you rock!
I called TSF looking for information and was so pleased with the response! I could tell TSF was genuinely happy to answer my questions. Happy to know TSF has got my back when I need them!
I've attended a handful of TSF events, and I always leave impressed! The amount of support from the community is great! And it's clear that everyone, especially children, always have a ton of fun! I'm so happy to be a part of and support this community!
I volunteered at the NJ Marathon with my daughter. It was a great experience! So many people came out to support TSF, the energy was amazing!
My daughter was diagnosed with Turner Syndrome when she was 4 years old, she is 10 now. I reached out to the Turner Syndrome Foundation because I felt lost and alone. They have been a blessing to us! We've learned so much about the syndrome. We are now supported by a great community, have tons of information and resources to help our little girl, and to help others learn too - from friends, family, teachers, to doctors!
Thank you so much for being there for us!!!
We received a personalized and grateful card after a donation we made.
My granddaughter was recently diagnosed with Turner's Syndrome. I signed up with this non-profit organization because I want to be up to date with the most current research and medical breakthrough for my precious Sydney. My son is in denial. I wish there was a support group here in the southern California area. I was so thankful for the kind information that I have been given from this wonderful organization. My granddaughter had met her specialist at Children's Hospital at Orange County. Thank you again.
Advocating for patients and families, workshops, patient outreach, research. Great Foundation. They personally care about patients.
Advocating for patients, creating activities, education, raising awareness, and research
Advocating for patients, creating workshops that are free access for education and research