Craniosynostosis | Fitz’s Story

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  • Опубликовано: 25 мар 2019
  • When Fitz was born, it was obvious that his skull was misshapen. By 5 weeks old, Fitz had been diagnosed with craniosynostosis, and his parents met with pediatric neurosurgeon Eric Jackson. Watch to learn about the minimally invasive surgery performed by Jackson, which combined with a helmet is helping Fitz’s skull grow in a normal shape.
    To learn more, visit hopkinsmedicine.org/pedsneurosurgery.
    Learn more about Eric Jackson at hopkinsmedicine.org/Eric-Jackson.
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Комментарии • 65

  • @zdenawilson7277
    @zdenawilson7277 2 месяца назад +1

    Such a gorgeous child ❤

  • @janellevillanueva6203
    @janellevillanueva6203 4 года назад +4

    Your story makes me emotional!! Bless you and your family i hope your baby grows big and strong. My son might either have plagiocephaly or craniosynostosis I'm praying whatever he has that he will be okay and grow to be a strong boy he'll be 7 months on the 10th of this month! 💕❤

    • @misatoholic
      @misatoholic 3 года назад

      janelle Villanueva
      I had that

  • @crujones4046
    @crujones4046 4 года назад +21

    My son was born with sagittal Craniosynostosis. It was rough at first especially not knowing what we were in for. He’s three now and doing great. Just remember parents this is fixable and it gets better.

    • @floragjinovci3759
      @floragjinovci3759 4 года назад

      Did he had fluids (liquid) in his head after surgery? Im worried for my nephew because he had the same surgery and they noticed liquids in his head!

    • @crujones4046
      @crujones4046 4 года назад +1

      Flora Gj- no I never noticed anything like that. My son had the endoscopic surgery. And we were constantly in and out of the hospital getting him checked. If there is something wrong I’m sure they’ll catch it. Don’t worry 😉 Have a good day.

    • @floragjinovci3759
      @floragjinovci3759 4 года назад +2

      @@crujones4046 Thank you for your response! I'm calm right now because the doctors said that's normal and that he is doing very well 😊.

    • @crujones4046
      @crujones4046 4 года назад +4

      Flora Gj- no prob. I was a mess when we got the diagnosis. Till I started doing some research “googling and RUclips” I realized this was fixable and he was going to live a normal healthy life. And I hope I can make at least one family going through this feel at ease.

    • @Adi-wx2xn
      @Adi-wx2xn 4 года назад

      @@crujones4046 Hey, I was born with sagittal Craniosyntosis but I didn't get a surgery when I was a child and now I am a teenager. What are the others symptoms that I could have? The doctor said that I don't got nothing and it's just my skull but now it's very long and narrow. Please respond and sorry for my bad grammar.

  • @jennakrehbiel3562
    @jennakrehbiel3562 2 года назад +5

    My Theodore is 3 months old and we are gearing up for surgery in a few weeks. I've been really emotional about it. This was really helpful

    • @jennakrehbiel3562
      @jennakrehbiel3562 2 года назад

      @Judy they pushed us back to April 6th😔 he will be days shy of 6 months old. Very frustrating. I hope you get everything over with asap and can be on the other side of surgery soon!

    • @serpany2044
      @serpany2044 Год назад +1

      I was born with it I’m 14 now and perfectly healthy, although I have a massive head scar. How is ur baby doing now?

    • @jennakrehbiel3562
      @jennakrehbiel3562 Год назад

      @@serpany2044 he is doing very well! He is a happy and healthy 8 month old baby!

    • @emily_ane1194
      @emily_ane1194 Год назад

      @@jennakrehbiel3562hi there. I also have a 3 month old and we just found out that his soft spot is closed. I’m so nervous. How’s your son doing after the surgery? How was the process?

  • @2degucitas
    @2degucitas 3 года назад +1

    I love these helmets. They push and mold the head while it's new and soft.

  • @shadrach6299
    @shadrach6299 3 года назад +2

    What a cute baby!

  • @mcbrolax1771
    @mcbrolax1771 5 лет назад +4

    An amazing Story, though allergy season is coming way too early for me.

    • @misatoholic
      @misatoholic 4 года назад +1

      I have it to well i had

  • @swatiutkur
    @swatiutkur 3 года назад

    This made me emotional! How’s he doing now? Is it treatable

    • @mackmadrid
      @mackmadrid 11 месяцев назад

      It is, the surgery has a 99 percent success rate

  • @serpany2044
    @serpany2044 Год назад +1

    I was born without a soft spot I have had a huge scar going across my head my whole life becides that I’m 14 now with no other health issues for parents with children with this issue I hope you’re children live through it i was 6 months old when I went into my surgery and live a normal life today the scar on my head all though I hate having one makes me who I am today

    • @westonadams7135
      @westonadams7135 Год назад

      Mine is right down the middle 5 or so inches long.. If parting your hair in the middle was still a hair style, I'd have the perfect part! It is going to suck when I start balding and have to shave my head. Mine was done in the late 80s so my head isn't in the greatest shape..

    • @mackmadrid
      @mackmadrid 11 месяцев назад

      Me too, I’m 12 nd I got this big scar on my head I cover it w my fluffy hair lowk scared for when I start balding nd I got the scar

  • @adamhynes296
    @adamhynes296 2 года назад +4

    I had a bad case of this when I was little. The surgery took 10 hours! I'm fine now though

  • @mackmadrid
    @mackmadrid 11 месяцев назад

    Yooo I had this too I got surgery and now I have a big scar going across my whole head from the surgery

  • @deb310red
    @deb310red 4 года назад +3

    What happens to people who were not diagnosed and treated in childhood?

    • @blouise16
      @blouise16 4 года назад

      deb310red depending on severity, some can grow out of it and some can get swelling on their brain. Since the sutures are closed early it’s pretty easy to tell, unfortunately the more visible on the outside, the more severe it is typically

    • @PlayerofNoobishness
      @PlayerofNoobishness 4 года назад +5

      It could cause blindness or developmental issues. Otherwise, the skull just looks odd and I'm sure kids make fun and/or stare.

    • @ratedr7845
      @ratedr7845 3 года назад

      @Basse nope, your head is hardened

    • @sofiaharper6349
      @sofiaharper6349 2 года назад +2

      @@PlayerofNoobishness This finally makes so much sense.. I always wondered why I got bullied so bad. It finally makes sense why I look so different than others..

    • @keke9670
      @keke9670 6 месяцев назад +1

      ​@@blouise16mine is severe and as far as I can tell my intellect and abilities weren't affected. Before I learned about the condition, I was well-adjusted, got above average grades, had normal friends, and excelled at track & field. I'm also gifted at art and see life from a creative perspective. My biggest handicap has been the emotional distress I developed after learning about the condition. I began recognizing how I'm different and observed the ways people have treated me differently throughout my life. This caused me to isolate myself from my friends and make poor decisions. It's horrible and I wish no child ever experienced this. Sadly our stories are always similar.

  • @rewa9236
    @rewa9236 2 года назад

    My 30w fetus diagnosed dolicephelic head I am so worried about his mental health . Is there any chances of mental abnormalities.please reply

    • @JohnsHopkinsMedicine
      @JohnsHopkinsMedicine  2 года назад

      Hi, thank you for reaching out to us. Unfortunately, because each person’s medical situation is different, we are unable to provide treatment recommendations or second opinions via this form of communication.
      If you would like to request an appointment at one of our hospitals, please call 888-872-1408. Our specially trained medical concierges can arrange consultations or treatment plans with the most appropriate specialists. Johns Hopkins USA can also provide language interpretation, financial counseling, assistance with travel arrangements and anything else to help make Johns Hopkins feel as close to home as possible.

  • @misatoholic
    @misatoholic 4 года назад +6

    YAY! I HAVE THAT TO BTW!

  • @mangopie3542
    @mangopie3542 2 месяца назад

    Can neurosurgeons do research like this along side their career and how much time could they spend on their research and does the research neurosurgeons do have to be neurological based or could they be for example gene editing and cancer and epidermis molysis bullosa

    • @philhobrla8489
      @philhobrla8489 17 дней назад

      There are variable levels of - and funding for - research, with “physician-scientists” (MD/PhD) being what I think you are referring to.

    • @mangopie3542
      @mangopie3542 17 дней назад

      @@philhobrla8489 yes you answered my question, thank you

  • @radhakrishna.daasi...
    @radhakrishna.daasi... 5 лет назад +1

    Meri beti ki v surgery hui h nd mujhe uske liye cranial helmet chahiye jo india m available ni h

    • @tasavvurhusain7366
      @tasavvurhusain7366 5 лет назад +1

      Kaha se surgery karayi hai aapne. Please bata de.
      Kya me aapse Baat kar sakta hu. Muje bhi surgery karani hai baby ki. Mera no. 09717712456 hai. Pls help.

    • @sarahsiddiqui4317
      @sarahsiddiqui4317 5 лет назад

      Krishna Soni aap ne surgery Kahan se krwayi hai please batain

    • @tarun3138
      @tarun3138 2 года назад

      @@tasavvurhusain7366ty sir

  • @ivaniaflores6630
    @ivaniaflores6630 2 года назад

    Interesante

  • @nelsonleon6874
    @nelsonleon6874 Год назад

    So fking sad my parents didn't do this to me know I'm 32 and my is back back is too long and everyone looking a me ... and I can't fix my head know. So parents take actions don't wait.

  • @pennym6576
    @pennym6576 5 лет назад +1

    ❤️❤️

  • @opod892
    @opod892 2 года назад

    I have carnosytosis but my parents and doctors in my country didn't know this disease and I am still 18+ what I should do?????

    • @david1399
      @david1399 2 года назад +1

      Same bro i think i have it. I wana talk to u as I never met another pers with it. Can u message me back

    • @opod892
      @opod892 2 года назад

      Yah bro

    • @antonioblagaj4285
      @antonioblagaj4285 Год назад

      @@opod892 I have a 2-month-old son, he was diagnosed with sagittal craniostenosis, the doctor says that if the head circumference grows normally, there is no need for surgery, but my son's head has an elongated appearance, I wonder if we can hear each other somewhere, like Facebook or Instagram to share experiences?

    • @opod892
      @opod892 Год назад

      @@antonioblagaj4285 yes ofcourse

  • @philmstud2k
    @philmstud2k 4 года назад

    No hope for a solution for adults who have this now who never had it corrected, huh?

    • @2degucitas
      @2degucitas 3 года назад +1

      I don't see why not. The surgery would be in several stages.

    • @Stormmud
      @Stormmud 3 года назад

      Man don’t let them open your head and cut your skull. This isn’t normal. The moment they open things up your gonna have an array of more problems.

  • @scottcarey5573
    @scottcarey5573 5 лет назад +5

    No seriously... it's just allergies. My eyes always get watery in the spring. :)

    • @misatoholic
      @misatoholic 4 года назад

      just because you think it's busy season does it mean if your pregnant your child will have this know it's a gene or sometimes I can be aging but sometimes it's not it's really unknown and I have it too so I mean I had it I had surgery obviously

  • @isma9711
    @isma9711 4 года назад

    😍😍😢

  • @chipirox
    @chipirox 3 года назад

    dream be like

  • @papagrande7448
    @papagrande7448 4 года назад

    Tryna see what that weird baby woman on tik tok has.