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Thread: asked to speak on the local news

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    Chases mom a_jessie a_jessie's Avatar
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    Default asked to speak on the local news

    i was just recently asked by our neuro and cranio docs to join them to speak about craniosynostosis and specifically chase's journey on the local news station. i am very anxious to be a part of spreading awareness but i feel like we were just diagnosed a couple of weeks ago and may not say what a parent who has already been through the surgery would. if you have any advice or maybe something specific that you might want to be heard please let me know

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    Sophia's_mom is on a distinguished road Sophia's_mom's Avatar
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    That's great! As a newly diagnosed family you'll be able to show those raw emotions that go along with this journey. I'm sure you'll do a wonderful job.
    Tessa - mom to Sophie and Ben
    Little Miss Sophie - 12/22/08 - Sagittal - Endo surgery 4/16/09 @ St. Louis Childrens
    Baby Boy Ben - 12/14/11 - No Cranio!

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    Sawyer's_Mom Sawyer's_Mom's Avatar
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    That's is great! Spread as much awareness as you can. I'm sure you'll do wonderful and at least you will get the word out there in your community.
    Amanda



    Mom to 3 boys
    Hayden - 1/8/05 - no cranio
    Mason - 3/15/07 - no cranio
    Sawyer - 9/15/09 - diagnosed as trigonocephaly secondary to metopic craniosynostosis 2/12/10
    Surgery 7/16/10 with Dr. Fearon & Dr. Sacco at Medical City Hospital in Dallas, TX.
    Loving life on the other side!!

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    lovin' my lambdoid cutie boy! evergreenmom will become famous soon enough evergreenmom's Avatar
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    Something that bothers me so much about the cranio journey is how many of us have not had it diagnosed by our pediatricians- but by ourselves! This should not be!!

    Pediatricians and Family Docs and OB's and ER staff all need to be more aware of the signs of cranio and they need to diagnose if they see it and they need to listen to parents who are asking why their kids have a different head shape. This is a condition that often does not have symptoms, but a visual clue which is the head bulging or flattening or pointing or lengthening dependent on which suture is closed... it should be a no brainer for medical professionals to be trained in how to spot this condition!! Heck if every doc would just get on this site and look at our kids pics and read our stories they would know more than they seem to be learning in med school!!!

    I guess until the medical profession gets in gear we need to raise awareness amongst families of newborns to be watching for signs of cranio!
    Kristin, Momma of two rambunctious cuties:
    Lucy born 3/05 "failure to thrive"- negative percentile on growth chart for weight 3/06 to 3/08
    Xander born 3/08 Left Lambdoid Synostosis and Chiari Malformation- Posterior CVR Surgery 2/09 w/ Dr Fearon and Dr Sacco at Medical City Hospital Dallas, TX (fought insurance and won in network gap exception) rant rant rant....

  5. #5
    Surgery date 6.3.10 Sam's Mom Sam's Mom's Avatar
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    I was lucky that my OB recognized Sam's cranio @ delivery. I was really surprised (from this community) how many kiddos were late diagnoses.
    ~Christina~
    Mom to ~Samuel Thomas~ born 2.7.10
    Sagittal Cranio: Posterior CVR on 6.3.10 @ Children's Hospital, Omaha, NE w/ Drs. Puccioni (NS) & Miller (PS).

    WE ARE ON THE OTHER SIDE!!!

    http://www.caringbridge.org/visit/samuelthomasboje

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    Momof2Boys is just starting out Momof2Boys's Avatar
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    We were lucky to have a team of NS ready for Justin when he was born. My midwife referred me to a fetal specialist after seeing a shadow on an ultra sound.

    But from other stories, when a mommy feels something is not right about their baby's head shape and the pediatrician fail to listen to your concerns, fight for your baby. A mother should always follow her gut and find doctors who will listen.
    Jamie

    Mom of 2 wonderful boys! ;)
    Wife to hubby that survived testicular cancer 2009
    Jacob - 6 years old
    Justin - 3 years old~ Right Lambdoid synostosis/
    Surgery 10/22/07 , sleep apnea, multiple food allergies, acid reflux, low muscle tone, pectus, asthma, and chiari malformation secondary to cranio.

    Faith, Hope and Love

    Justin's Story
    www.caringbridge.org/visit/justinjones

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    BusyBee is just starting out BusyBee's Avatar
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    We diagnosed ourselves from the internet - pediatrician in Hospital said she was fine!!!!
    Jo

    Mummy to:

    Anna - Nov 2004 No Cranio

    Abby - May 2008 Right Coronal Synostosis surgery Nov 17, 2008 WE ARE ON THE OTHER SIDE

  8. #8
    Terry17 Terry17's Avatar
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    Maybe you can mention this site and reassure people that the babies generally do very well with the surgery. I agree with Evergreen - early detection helps prevent further complications and generally most babies develop normally.

  9. #9
    Chases mom a_jessie a_jessie's Avatar
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    Thanks everyone i def will mention about parents sticking with their gut feelings. I know that I questioned chases neonatologist in the hospital and his pediatrician who both assured me that it was just from intrauterine pressure.. It was not picked up until i took chase to the emergency room, luckily he was only 8 weeks

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    roetik77 roetik77's Avatar
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    Our OB and all the hospital staff had NO idea about cranio!!! We had just switched pediatricians and thankfully she diagnosed it at birth. Funny thing though, the 2 days after birth, 2 of her colleges came to the hospital and BOTH looked at Cameron and down played it to just a misshpaed head from delivery. I am SO happy our new pedi caught this!!! She even said I should not look this up online. I refrained for a few weeks and then when I finally did, I found this site and it has made a world of difference. I found Dr. Staffenberg and Dr. Goodrich on here and I have complete faith in them for Cam's surgery next month. I guess just raising awareness is KEY in your interview!! I have found that many health care professionals understand the condition but don't know a "name to it". Just last week I had a dr appt for myself and talked about Cam's cranio. The dr. never heard of it but could totally relate when I explained it to him. I say get the "craniosynostosis" NAME out ther and help to educate the medical profession.
    Last edited by roetik77; 03-20-2010 at 01:11 AM.

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