Living with Turners Syndrome
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- เผยแพร่เมื่อ 9 พ.ค. 2022
- Diagnosed with Turner syndrome from an early age, Charlotte has always been aware of her condition and is managing it well, thanks to her supportive family. See what life is like for them as a family, when one member is living with a growth disorder. Despite being a young age, Charlotte knows exactly what she wants to be when she grows up and there’s nothing that can stop her. You can watch her inspiring story here and visit www.morethanheight.com to learn more about growth disorders.
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Thanks for sharing your story, Charlotte! I'm 28 and have mosaic Turners. I'm American, but living and teaching English in France, so I'm very independent and loved what you said about not letting anything stop you from living your life.
Hey Charlotte! I am 26 and I was also diagnosed with Mosaic Turner Syndrome when I was 9 years old. Wish you all the best :)
Good luck Charlotte from a 15yr old girl with TS❤❤❤
Charlotte I wish you the best reaching your dream of being a teacher! I’m a 48 year old TS sister who is also a science teacher!
I’ll be 48 in august
I'm happy you made to 48. I don't think I will... Turner sucks, big time. I'm 24, and I have been depressed ever since the age of 10 (I was diagnosed at 5, but at that age I didn't have the mental capacity to understand what's going on). Hate myself everyday. Hate the shortness. Hate being neither male, nor really properly female. Hate the thyroid condition. Hate the psoriasis. Hate the swollen legs. Hate having to fucking estrogen...
@@user-cv8ui5ir2d Don't give up , talk to someone , I know it's hard I have TS too , Went through two bad bouts of depression as a teenager , Get support from family , friends and your medical team, You are a woman, Just one who happens to have a medical condition, Keep going and be as healthy and happy as possible.Good luck for your future x.
@@user-cv8ui5ir2d❤
I also have turners syndrome too and would love to share my story with yo all!,.. So I also had a lot of growing problems, ear infection, etc,.. but when I was about 6, I had stopped growing completely and thats how my parents knew something was wrong,. so they had a karyotype done on me (my parents are both physicians), and thats how I found out I had it,. I then got growth hormones to help,.. I also have had a moderate hearing loss since age 7,8,., learning disabilities, etc,.. But now I am 22, almost 23 in month, and I just finished my 3rd year of university with almost a 4.0 GPA! (last semester got 3.9, but still waiting to see how I did this semester but I think it all went ver well) getting a BA in music, since I sing and play piano, and then plan to be an audiologist,. exactly what I ever wanted,..
Thank you for sharing your story, Charlotte! I’m 23 also with classic TS and am a 6th grade teacher :)
Can yo do s**xx
Is it true that classic turner syndrome has many more features and complications than mosaic? Got a dx of our little one having classic
I would say, yes. Because, with the mosaic variation, only certain cells in the body are missing the second sex chromosome. With the classic one, all cell have only one chromosome in them. @@ldee4127
Hi Charlotte, My name is Abby and I am 25 year old who lives with Mosaic Turner syndrome (diagnosed at 10). I am a speech language pathologist at a middle school. Remember you can do anything you put your mind too- your dreams are achievable.
That’s actually a great way to look at life, an opportunity doesn’t define who you are and what you can accomplish. ❤️
I have a classic form of Turners,too. I am 43 years old, born and raised in Ukraine.
In Ukraine I worked as a nurse for 13 years, than 5 years ago I moved to Austria.
I've been happily married for 17 years.
I would be happy to get to know somebody who has Turner Syndrome,I've never met someone like me :)
Hi! So happy to read your success story. I am having a baby with Classic TS. So it’s nice to hear good outcomes
I also live with Turner Syndrome!
You go girl!!
i love u guys, I lost my baby girl and she was diagnosed but sadly passed away, i wish i could hug her
@@johnnysslut Im so so so so sorry. I have Turners and i almost passed.
@Just _ sophia what is truner syndrome??can human died with this disease😢
@@The_Great_Humanit's not a disease. I suppose you know that human females have XX chromosomes while the males have XY. If the chromosomes don't separate properly during segregation (during cell division) it leads to gain/loss of a set of chromosomes. In the case of Turner's syndrome,one X chromosome is lost from the cell. Therefore,it is usually said that the females with this syndrome are not 'feminine'. They are also sterile (can't reproduce)
@@The_Great_HumanIt is a chromosomal disorder in which the female has X0 chromosome instead of XX which makes them sterile.They also lack some of the female secondary sexual characters.
Thank you for sharing
Thank you Charlotte! Remembering your story helped me to understand Turner Syndrome for a test that I am taking. See how you teach? You can do it!
Menschen mit Übergewicht oder Adipositas* haben im Vergleich zu Menschen mit gesundem Gewicht ein erhöhtes Risiko für viele schwere Krankheiten und Gesundheitsprobleme.
Diese beinhalten
1. Alle Todesursachen (Mortalität).
2. Bluthochdruck (Hypertonie).
3. Hohes LDL-Cholesterin, niedriges HDL-Cholesterin oder hohe Werte von 4 Triglyceriden (Dyslipidämie).
4. Typ-2-Diabetes.
5. Koronare Herzkrankheit.
6. Schlaganfall.
7. Erkrankung der Gallenblase.
8. Osteoarthritis (ein Abbau von Knorpel und Knochen in einem Gelenk).
9. Schlafapnoe und Atemprobleme.
10. Viele Arten von Krebs.
11. Niedrige Lebensqualität.
12. Psychische Erkrankungen wie klinische Depressionen, Angstzustände und andere psychische Störungen4,5.
13. Körperschmerzen und Schwierigkeiten mit körperlichen Funktionen6.
*Übergewicht ist definiert als ein Body-Mass-Index (BMI) von 25 oder höher. Adipositas ist definiert als ein BMI von 30 oder höher.
Besuch: sites.google.com/view/germany-tea4/home
I have this neat to see others with it
You are amazing 😃
God bless you
God bless all
I've got a friend with TS who is a doctor.
My doughter with ts has always been a very angry person. She screams when she is angry and it takes many many hours up to over nine hours before she quiets herself. Nothing you do changes her. She is a stubborn personality and wants things her own way. Is angry issues usual to turnéer syndrome people? Because my doughter is very much as a child with dawn syndrome. She loves to eat and she is as I said very stubborn. She wants to decide everything herself. She does not like rules. Is this something you recognizes in the turner syndrome personality? A big problem is that she screams so loud and for such long time and she even says that she does not care about the neighburs. Not okey.
Hi, thank you for sharing your experience. I understand it must be challenging to manage your daughter's emotions. Please note that due to global privacy and legal regulations, we are not allowed to give medical advice on social media. I recommend you contact your healthcare professional for guidance and help.
Sending my best wishes to you and your daughter. 💙
Take care & all the best,
Asif
Novo Nordisk
I am stubborn too, and want to do things in my own way? Hahaha, of course.
But, I really recommend you get professional help, because you can have something more than Turner, is possible, like autism, I don't know, but if the correct treatment she can get better.
I always was different, but my mom refused to treat me like someone with down and didn't let anyone treat me like that, when she discovered the Turner syndrome she had a shock, but even then she always believed in my potential.
Best wishes for her.
I am angry. But angry at NOT being fucking normal. I look at myself in the mirror and all I see is a monster. I look feminine, but I know all well that I'm neither male, nor properly female. Suffer from a major case of Napoleonic complex. I feel emotions easily, but feel ashamed for it. I feel like I got screwed over by those deleted chromosomes. Wish I had never been born. My mom doesn't understand either. But then again - she didn't have to go through growth hormone shorts every day for years, she's not super short, she produces estrogen, she has fucking boobs, she wasn't bullied because of her shortness, she didn't grow up hating herself and the world around her...
I have mosaic TS
If anyone recognizes the temper i describe of my doughter send an answer it is so important. The syndrome seem to be so much look a like dawn syndrome. So write If the anger has been a big thing for you who has turner syndrome.
I'm 19 have ts I have multiple mental illnesses- (major depressive disorder, anxiety disorders , and adhd) anger and short temper does comes with this,I don't know y'all personally but if she has any other symptoms of that kinda stuff I'd look into it for help 💕💕💕 peace and love fr
i have turner sydrome too.
I am 17 years old .. I had my period when I was almost 12 years old and completely regular , but I am short my height is 153 cm , and my weight is 37 kg . My intelligence is very normal , and I look much younger than my age also my body showed no signs of puberty .. I do not have the rest of the symptoms. Can anyone help me to know if I have Turner syndrome ?
Hi Tatiana, thank you for reaching out. Please be aware that we are not able to give any medical advice on social media due to global privacy and legal regulations. Please see your doctor and discuss your observations there. Your doctor will be able to guide you better and make further examinations if needed.
Wishing you all the best and take care 💙
Asif, Novo Nordisk
@@novonordisk okay I will .. Thank you very much for the respond 💛
@@tatianajadid262well, the Turner diagnosis is with endocrinologist, they will avaliate you and ask for exams.
People with Turner's syndrome are sterile.They won't get periods.
❤️
I don’t know what Turner syndrome is, you didn’t explain it.
Basically, we have 45 chromosomes, not 46 like the other people.
The other people have XX for girl and XY for boys, but, in Turner's syndrome we have just one X, so, we are all girls, the classic Turner lost completely the last X.
Sorry if my English get weird, Brazilian here.
And yes, I have Turner syndrome too. The classic one as the girl in the video.
The only case (syndrome) in humans where a baby can actually survive being born with only one sex chromosome. Most Turner's fetuses get aborted or are miscarried.
@@user-cv8ui5ir2d get aborted? I wonder why, because we Don't have any deficiency that would make us "parents dependents all life." But miscarriage happen a lot in these cases.
Yeah, that's what happens. Abortion is common. I have this Turner shit. And trust, I'd rather be dead.@@fabianifigueira
@@fabianifigueira I also have classical TS. I think TS, Down Syndrome, Rett Syndrome, Cri du chat Syndrome get aborted often. I do think TS is a very serious condition. C'mon, like take our medications away - and no puberty, only brittle bones, old skin, scoliosis, and early menopause. I wish I never had TS.