What is Amniotic Band Syndrome?

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  • เผยแพร่เมื่อ 7 ก.ย. 2024
  • Description of Amniotic Band Syndrome. Presented by Michael Harrison MD, Director Emeritus of the UCSF Fetal Treatment Center

ความคิดเห็น • 61

  • @TheMrshall2010
    @TheMrshall2010 6 ปีที่แล้ว +17

    My son is seven and has foot deformities due to amniotic bands he is not embarrassed at all and says it makes him special bless all you youngsters for sharing your stories

  • @amazedfool
    @amazedfool 13 ปีที่แล้ว +12

    I was born with ABS too. I'm missing my left pinky, and most of my fingertips, my right foot is way smaller than my left, and my left was a club foot. I've never met anyone else with ABS, so it's really cool to know you guys exist.

  • @K._Oss
    @K._Oss 13 ปีที่แล้ว +8

    I'm 16, a drummer, and I got ABS; I refer to it as "Stumps for Fingers Disease". My musical endeavors have helped me deal with this bullshit for years.

  • @TheNeeyang
    @TheNeeyang 5 ปีที่แล้ว +7

    Today I found out my son has this, he is missing his whole left hand at our ultrasound. I’ve been crying all day. I know that my little one is going to need a lot of love everything will be okay.

    • @mrs.cloveskitchen2016
      @mrs.cloveskitchen2016 5 ปีที่แล้ว +3

      Nkha92 Hi! I know how you feel. ❤️ Im 27 weeks pregnant and also found out that our little girl is missing his left forearm. It was really hard at first But I know that with our families and friend they will be love. We need to be strong for them. Good thing in this day and age theres a lot of high technology. Hugs!!

    • @TheNeeyang
      @TheNeeyang 5 ปีที่แล้ว +2

      Mrs. Clove's Kitchen omg yes!! I’m only 19 weeks so I guess they caught it pretty early. We’re going to do an amnio and see if there’s any more info we need to know regarding our baby. But it’s been tough & our family knows it’s going to be a life changing journey. Thank you for replying it really warms my heart that I’m not the only one.

    • @mrs.cloveskitchen2016
      @mrs.cloveskitchen2016 5 ปีที่แล้ว +2

      Nkha92 I found this group called Lucky fin project in Facebook or instagram. So many inspirational stories. We are not alone 💕💕hugs!!!

    • @mrs.cloveskitchen2016
      @mrs.cloveskitchen2016 5 ปีที่แล้ว +3

      Nkha92 And also please always be strong, In the past days I experienced some down time and so many negative thoughts entered my mind and I realized its not healthy to my baby.
      Always see the bright side. Our babies will be awesome. They may be different but they will be differently capable and they can live on their own.

    • @kaseyjean
      @kaseyjean 5 ปีที่แล้ว +5

      I saw your comment and instantly wanted to reach out. My name is Kasey, I was born with amniotic band syndrome 28 years ago - and I am missing parts of both hands and feet. I have grown up surrounded by love and optimism / confidence and was taught to do everything the other kids could do. I became a varsity athlete and even competed in college. I started a business at 18 years old, now run a large company with multiple employees, met the love of my life who also works for my company now full-time... all because of my family constantly believing in me and setting me up for success. I had some family members treat me like glass, but with ABS you can still do absolutely anything you put your mind to

  • @jem42007
    @jem42007 12 ปีที่แล้ว +2

    I am 29 years old and I too was born with ABS and am glad to know there are others who exist with the same condition. I have my two middle fingers webbed together left hand, my index finger half sized, my left leg almost severed (the docs saved it), my left toes webbed together and my right foot has all of two and a half toes. I am blessed to have only cosmetic attributes as a result of ABS. God bless you all who educate those who dare to ask!

    • @karenb2873
      @karenb2873 4 ปีที่แล้ว

      OMG...........My babygirl was born the same way..........she was born at 24 weeks and died shortly after..........they sent me home with no explanation.i figured what it was from the internet.............that was 21 years ago..........God bless you and yours..............

  • @ledzepchick99
    @ledzepchick99 13 ปีที่แล้ว +2

    I'm 17 years old and I was born with ABS. My left foot is half the size as the other one. It's nice to finally have it explained and to know that I'm not alone.

  • @Faru-fari77
    @Faru-fari77 2 ปีที่แล้ว

    How beautiful the doctor is 🥺💞💞

  • @brightcolours234
    @brightcolours234 13 ปีที่แล้ว +1

    im 16, and my mom was told when i was born this is what happened to me, but ive never really had it explained to me, this helped :)

  • @jamesencinas50
    @jamesencinas50 11 ปีที่แล้ว +1

    I am as well victim to ABS I am 24 years old now. I was born about a month premature . Due date was January 28 and was born on December 25 1988. In my case I have bands wrapped around both of my hands preventing six fingers to develop including a thumb, which later I had a toe thumb transplant, which they took my second two from right leg to right hand. I also had them wrapped around my left leg three bands that is. This resulted to a club foot, and require a prosthesis.

  • @Branflakes1503
    @Branflakes1503 5 ปีที่แล้ว +2

    I consider my self lucky I was born with ABS all my fingers on my left hand were webbed together and some were on my right hand I have no thumbs on ether hand . After years of surgery I have all my fingers separated and only have slight deformations. Also I have no does on ether foot. I'm glad to know I'm not alone and wish everyone the best

    • @33eternal73
      @33eternal73 2 ปีที่แล้ว +1

      OMG! Go the same condition on hands&feet. Missing toes causes walking hard. Can you jump and run well? So glad to know there are others like this around the world!! I hope we can connect :D 😊

    • @33eternal73
      @33eternal73 2 ปีที่แล้ว

      I’m wondering did you get surgeries? 😁

  • @Ownlyanangel
    @Ownlyanangel 12 ปีที่แล้ว

    Yes I am a freak, and I love it. Thank you for your compliment. From you, it means the world.

  • @luckybubba9able
    @luckybubba9able 10 ปีที่แล้ว +1

    thank you for that you are amazing

  • @MemestiffGaming
    @MemestiffGaming 5 ปีที่แล้ว +1

    Learning about this thanks to Shaquem Griffin

  • @WENEEDBACKUPNOW
    @WENEEDBACKUPNOW 13 ปีที่แล้ว +1

    @Bluefirefoley im 24 and also have ABS and im missing fingers on my right hand and i have to have the bands removed on my left foot and ankle because i cant take the pain anymore. i just wanted u to know that u are not alone friend.....

    • @rosskstar
      @rosskstar 4 ปีที่แล้ว

      So the band becomes part of your body but like a scar i spose...?

  • @irenedavo3768
    @irenedavo3768 ปีที่แล้ว

    Watching October 2022

  • @evilherojoseph
    @evilherojoseph 12 ปีที่แล้ว

    Me too ! Well not exactly the same but kind of .

  • @tiffanymarkins8903
    @tiffanymarkins8903 ปีที่แล้ว

    My daughter was born with amniotic band syndrome she has no left feet

  • @riahsaurXD
    @riahsaurXD 13 ปีที่แล้ว

    @WENEEDBACKUPNOW I'm missing fingers on my right hand too. #FingerMissingBuddies.*( Jk, that just sounds awful. )* Two of my toes are webbed together, and the bone in my left hand for my thumb never grew in. I also had a clubbed foot when I was born...

  • @janayadams9331
    @janayadams9331 2 ปีที่แล้ว +1

    I’m 28 & have ABS

    • @33eternal73
      @33eternal73 2 ปีที่แล้ว

      Same condition here! Did you get surgeries for it? How's it now.😀😊

  • @keerthanakarthik8547
    @keerthanakarthik8547 7 ปีที่แล้ว

    My baby have a ambiotic band syndrome in 4th month pregnancy we will find and abort but I feel alone without my child my only question is ,is it possible to come back to my 2nd child is there any treatment to avoid this i felt so sad my age is 23 and my husband age is 35 is it any problem

    • @Enrique-sy3nc
      @Enrique-sy3nc 6 ปีที่แล้ว

      I'm sorry for your loss. It is unlikely to occur in future pregnancies. Most cases occur sporadically. Here you can read more on the subject rarediseases.org/rare-diseases/amniotic-band-syndrome/
      Here's another web page: rarediseases.info.nih.gov/diseases/429/amniotic-band-syndrome

    • @princesanjay7805
      @princesanjay7805 4 ปีที่แล้ว

      sir now im 24 week pregnet In scan found 2 amniotic band Its effect my baby I pregnet after a very long time marrige 17 years pleas tel me sir its really affect on baby

    • @keerthanakarthik8547
      @keerthanakarthik8547 4 ปีที่แล้ว

      Madam what is the current baby situation pls tell me fast because it affect ur baby am already face this situation u take nt scan and what doctor says ?? What is the situation now

    • @princesanjay7805
      @princesanjay7805 4 ปีที่แล้ว

      @@keerthanakarthik8547 hai now I'm in 24 weeks pregnet Yasturday did my Anomaly scan Softer said I have Two Amniotic bands And said if baby stuck in this band put hand leg it's will Cut so told me Do agin scan in Coming my 30 weeks and 33 weeks So I'm tens lot Pleas tel me If you have any knowledge about this situation

    • @keerthanakarthik8547
      @keerthanakarthik8547 4 ปีที่แล้ว

      @@princesanjay7805 sister doctor said any word amiotic band syndrome ?? My baby have a syndrome so oly it affect hand and leg . i find it in my 15 th week so we abort same prob for my baby one leg and one hand had a amiotic band but u r in 24 week doc y dont find before it. Sister baby ku blood circulation erukathu that band place so u please do any action otherwise baby life long problem survive . this is my baby sitiation so i dont know whether it is affect u baby or not .baby have any problem from band doctor said anything to u ?? Am from tamilnadu trichy when u free please reply me or i will give my number

  • @OttersMum
    @OttersMum 3 ปีที่แล้ว

    So this shouldn't be hereditary?

    • @33eternal73
      @33eternal73 2 ปีที่แล้ว

      I heard people got it from her grandmother. Do you have ABS too?

  • @keerthanakarthik8547
    @keerthanakarthik8547 7 ปีที่แล้ว

    Pls reply me any body