Did you see a pediatric cardiologist? If you find out early, do not force your children to eat and gain weight I was forced to take weight on pills because some quack said I didn’t weigh enough. Submit a new question, I underwent an IVF cycle and got pregnant but miscarried at 9 weeks. New Reply Follow New Topic. Turner syndrome occurs when part or all of one of your X chromosomes is missing. People with the same disease may not have Your email address will not be published. The doctor set her up with a endocrinologist at the university in our state. Facts about causes, diagnosis and treatments You may want to review these resources with a medical professional. R We just found out that my daughter is carrying a ts child. It may be 10 or 20 years before you get your answers as to why. She graduated from the University of Georgia with a marketing dergree. I’m so desperate for help. I feel God still has me here for some reason. https://www.facebook.com/pages/Head-Soccer-Cheats-And-Hack/1401095683509651, THANKS. She started teasing me about the poor breast development, too. I do not have children but my many nieces and nephews. These chromosomes contain the genes and DNA responsible for building the body. Continue the good work! My daughter is having problems learning in class. She is alomst 31 now and a very deep loving person. many lead sucessful, happy and productive lives. My Baby Has Turner Syndrome Congratulations! These difficulties often lead to problems in everyday functions although most adults with Turner’s Syndrome may lead productive lives. If, based on signs and symptoms, the doctor suspects that your child has Turner syndrome, a lab test will typically be done to analyze your child's chromosomes. I am now on ozempic and am losing weight. Usually females with this condition reach fifty years of age but if complications that can be associated with this syndrome are not detected they can die at an early age. The patient can usually have a normal life if treatments are carefully monitored. She also had a saggital craniectomy at age three months, I am a registered nurse who worked for about 27 years. I have been described by family and friends as the kindness, generous ,. She loves math too! So when I was 3 weeks old and finally weighed 5 pounds they let me go home, But then told my parents not to geet attached to me because I would be here by my second b-day, Well I passed that b-day thanks be to GOD and my eighth b-day they said I wouldn’t see either. Our daughter was diagnosed at 5 years old. She’s working on a Master’s degree now, and there’s a 40 year old man teasing and harrassing her because she raises her hand to answer questions. Not every woman or a child with TS is the same . Untuk io can be an thrilling approach based mostly *multiplayer game available on House I have had had several serious heart problems but not until I was in my late 30’s. Once these were fixed she got pregnant immediately after the next two frozen embryo transfers. Genetics Education Materials for School Success (GEMSS), Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Human Genome Research Institute's. Fear not. Read more about treating Turner syndrome . The thought of losing a pregnancy weighs heavy.… (My mom always says Patience is a Virtue) My husband and I would love to try in vitro or adopt but can’t afford it. Turner syndrome can potentially significantly affect quality of life. Turner Syndrome – Life expectancy Women living with Turner syndrome live up to fifty years. We stopped seeing each other as often because his family moved into town. Enlargement of the distal femoral epiphysis, a low or indistinct hairline in the back of the head, swelling (lymphedema) of the hands and feet. When this is not given, females only reach an average height of less than five feet. My mother was most certainly saddened by the news but set about encouraging resilience in her youngest daughter. Some may elicit very early signs of impaired growth and physical defects. my world felt like it was turning upside down until i saw this post! I was lucky that the teasing was minimal. I’m a 40 yr old TS lady and even with growth hormones only reached 149 cm. We weren’t serious then but I took her to an IVF centre as I felt for her and believed this new treatment option could help her. It improves breast development, pubic hair growth; and increases the width of the pelvis and the development of other secondary sex characteristics. If you have any worries or questions, please email me. During conception, the sex chromosomes are not transferred properly leading to the condition. WHO HAD TS DONT MAKE YOURSELF SAD EVERYTHING WILL BE OK. EVERYTHING IS POSSIBLE IN LIFE. You know therefore significantly when it comes to this matter, produced me individually believe it from a lot of numerous angles. It would be nice to talk with another to help me understand. Angel inside of me has turners syndrome I’m scared to death.but abortion is not a option I love my baby no matter what I just want it to be happy an healthy in her journey. Funnier even when she spoke! It is difficult to make predictions about how the disease will progress for an individual. My four year granddaughter has Turner syndrome and she has most of the symptoms. Obstructive lesions in the left side of the heart are commonly seen which significantly reduce the blood flow in the heart. Thankfully I have an amazing family unit and friends. It is approved by the Food and Drug Administration for the management of Turner’s Syndrome. She never let up about it. 7. The most common karyotype of individuals with Turner’s Syndrome is 45XO or a non disjunction of the chromosomes. Best, Mary B. I am 26 and I have Turner Syndrome. Then finally when I hit my teenage years I was only going every three months. My sister turned 52 this past September, she was a year younger than me. My Mum always made sure she never treated my sister differently and she used numerous flash cards to teach us everything she could. I have lived such an amazing life with my husband, we’ve done everything we want to do and continue to do more. She plans to go to college and have a career. Not being able to have children isn’t as hard for me to cope with, If people in your family REALLY love you, they wouldn’t treat you that way, and if A guy really loves you, he wouldn’t leave you like that because of not being able to have children. My little brother was born just a year and a half after her without any genetic anomolies. But worries all the time. Females with this Syndrome can reach as old as 50 years of age. Diagnosed last year with turners.. She in COLLEGE. She is 13 weeks and has not had any signs on ultrasounds, however the cvs test came back with the list chromosome. I started on estrogen and progesterone at 14. I am sat in a local library in Berkshire having read the majority of the above letters; I feel very upset reading about all your experiences. That’s LIFE …. I have a pacemaker. .it’s all good, I have both. Hang in there girls! Since the condition is associated with chromosomal aberrations, there is no current cure to completely eradicate the condition. Just keep Faith & Trust in God! Not all Ts kids are the same just as no 2 people are the same. Up until then I had displayed no symptoms in regard to Turner’s Syndrome, however, when I was 15 @ had not started menstruating my mother became concerned @ took me a Doctor who then referred me to an endocrinologist: The irony of it is that my mother’s maiden name is turner: I am a registered nurse & have done a lot of travelling: I also have some wonderful friends & family: In fact my mother initially blamed herself because at the time she was pregnant with me she took a morning sickness drug which a few years later was taken off the market as it was deemed the cause of some birth defects: I have not had any children but I do have my nieces & nephews& great niece & nephew who I love dearly: I would love to hear from any other Turner’s Syndrome people out there& share their stories: Thank you for your positive post. Try our interactive tool for help finding information, services, experts, financial aid, and more! Just when you think she’s turned a corner, something happens. If you do not want your question posted, please let us know. Has anyone else had this issue and if yes, have you had any successful treatments for it? 5. Life expectancy is slightly shorter than average but … I’m 19 years old living with turners syndrome. Everyone loves her and she lives a completely normal life. Thank You, Will need your support when learning with math, let the math teacher know so he or she can provide extra time for tutoring since it will be harder to memorize. Believe it or not, even doctors were making wise-ass cracks at me. I would feel your pain!!! I never seen myself as different . We divorced in l989. It can help clear up some of the misconceptions about TS. I did try to do the hormone replacement but stopped it. My daughter is 18. A registry supports research by collecting of information about patients that share something in common, such as being diagnosed with Turner syndrome. Hormones replacement therapy can help. My daughter also has a mental stress problem so a little beauty therapy helps now and then. That hasn’t stopped her from charging forward. Turner's syndrome, also known as gonadal dysgenesis or Turner's mosaicism, is a genetic condition that is without a cure. This article is wrong and will promote fear in women with TS . Super smart, A student, but worked extremely hard to get those A’s which are so important to her. For girls and women who are treated promptly and follow their treatment plans, they can have a normal or near-normal life expectancy. I feel a little beauty therapy made my daughter (who has TS) and I feel much better in about two seconds. Girls and women with Turner syndrome need ongoing medical care from a variety of specialists. Hello. Other than medication regimes, I feel like the average woman. She has many good friends and teaches special education, touching the lives of many with her loving ways. Meet some adult ladies with Turner’s Syndrome. Until now, no two females with Turner’s syndrome have shared the same set of symptoms. It is good to hear that she can have a normal life and achieve whatever goals she might have. She’s never had a date. I know she is on a regime of some kind of medication for TS. I was not diagnosed until age 22 or 23. And you can look our website about proxy list http://proxylistdaily4you.blogspot.com/. Your granddaughter and my sweet girl sound so much alike when she was that age. I send my thoughts and love to you and your family.xx. Most of the early deaths are due to heart and kidney problems. I also tell my children everyone has something, either it is on the inside or the outside but everyone has something. My daughter was diagnosed at age 11 and she is 23 now. This seems to help all my children especially when they feel they are the only one dealing with something whether it is TS, ADHD, Diabetes, etc. Up until recently, women with Turner’s syndrome did not have access to focused health care, and thus quality of life was reduced in a significant number of women. She had been married for 13 years to a great guy. I am what they call a Mosaic; some of my cells are normal, some are not. My daughter is checked every 5 years. Hi My name is Julie, I am 57 years old & was diagnosed with Turner’s Syndrome when I was 15 years old. Ive plenty of friends . And accept you for who you are, and for you health, leave it to the Doctors, just go to your appointments, enjoy your life and find support groups around your area if you have questions talk about it. You r blessed! After a few years of dating we married and entered a donor egg IVF program. There are also lifelong medical problems they must also manage. And to hear you don’t need to be on hormone therapy for life, cause this will be the first year not taking the hormone therapy. She reached a Height of 5’4″ started hormone therapy at age 12 or 13. I am 57 years old and have mosaic Turner syndrome. I have lived with TS but have tried not to let it define me in fact I have only ever discussed the fact I have TS with my immediate family. Sex hormones are usually given to improve sexual development. what is the life expectancy for turner syndrome . This is one of the main reasons why licensed healthcare professionals are advised to focus on searching for and examining these malformations as … Thanks. Learn about Turner syndrome, an abnormality in the X chromosome of females that leaves them infertile. Her only symptom is short stature. They can direct you to research, resources, and services. If you find someone to love and who loves you TS won’t stand in the way of a good sex and a life together. Females with Turner’s Syndrome usually reach 50 years of age. 1986; 40:97–102. This table lists symptoms that people with this disease may have. (HPO). I am a 45 year old ts woman . When Turner’s Syndrome is detected before delivery, parents undergo genetic counseling to help them cope with the condition. She doesn’t seem to make a lot of friends, which bothers me more than it does her. I have been married to a wonderful man for twelve years. I had no idea of symptoms to look for or what it was. I did struggle somewhat in math , but I compensated and spent extra time mastering concepts. I am glad I am reading this site, it is helpful and supportive for women with TS. If you are not confident in yourself it is reflected in how you come across in your relationships. These resources can help families navigate various aspects of living with a rare disease. She was diagnosed before birth. She struggled with social skills. I took many difficult math courses and succeeded. Life expectancy in Turner Syndrome patients Women who have Turner Syndrome have a relatively lesser life expectancy compared to other healthier women. My best friend of 40 years has TS and she is the most wonderful, beautiful person I know. The most common congenital heart anomalies include post-ductal coarctation of the aorta, bicuspid aortic valve, partial anomalous venous drainage, aortic valve stenosis, aortic dissection, dilatation and rupture and hypoplastic left heart syndrome. I count my blessings everyday that I am so healthy. Other complications include obesity, high blood pressure, cataracts and arthritis. Diagnosed at birth.. for your site to say I only have 10 more years left is stupid and disgraceful.. Read and get your facts straight…girls younger than me read this. For me, I think it is the infertility that is an issue. The condition may also be seen during ultrasounds where an abnormality in the kidneys and heart is detected. 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