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Thread: Cranio kids and ear infections

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    Mama Musica Mama Musica's Avatar
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    Default Cranio kids and ear infections

    Max has chronic ear infections. We took him in yesterday, and he has a double ear infection. It's his second ear infection in a month, and his sixth or seventh in the past year. Pediatrician says it's time for tubes, and I agree and am grateful! I was able to get an ENT scheduled to put the tubes in when they do his second surgery in March, so that's convenient as well.

    What boggled my mind though is that she told me that kids with craniofacial issues often have chronic ear infections, so much that the ENT's usually recommend putting tubes in prophylactically. Sure wish they would have told me that six ear infections ago.

    So what about everyone else? Do your kiddos get lots of ear infections? Did they need tubes?

    Its funny, because I'm mostly just relieved about him getting them. Earlier in my parenting career, I would have freaked out at the idea of surgery, but now, it seems so minor in the face of his second CVR in one year...
    Stacy
    Mom to Abby (9), Ashlynn (7) and Max (11/13/08) and Ian (11/23/10)
    Max's CVR/FOA for Metopic Synostosis May 1st, 2009.
    CVR/FOA #2 March 30, 2010 at Primary Children's in SLC, UT with Dr Morales and Dr Brockmeyer.

    Blogging about it (and anything else I want to talk about) here: http://www.sanityforstacy.blogspot.com

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    Registered User Janet Test Rep Janet Test Rep Janet Test Rep Janet Test Rep Janet Test Rep Janet Test Rep Janet's Avatar
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    Fiona is just over 3 and never has had one, my non cranio kids is almost 11 and never has had one either.....I know how lucky we are.
    Mom to Noah (no cranio)
    Fiona (Metopic):
    Surgery #1 CVR/FOA 9-26-07 (age 10 months) Sick kids in Toronto with Dr. Phillips (PS) Dr Kulkarni (NS)
    Surgery #2 Cyst removed over left eye 9/08 Dr. Phillips (PS)
    Surgery #3 Cranioplasty 10-18-11 (almost 5 years old) for soft spots filled in with titanium plates/peek implant from bone resorption and scar revision. Dr. Phillips


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    Administrator *Jessica* is on a distinguished road *Jessica*'s Avatar
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    Jeffrey ALWAYS had an ear infection! Not one since the tubes got put in in Nov!! I only wish we had done tubes sooner! As for the ease of the surgery, I didn't even have time to sit down and get comfortable before it was time to pick him up in recovery! Quick, easy, and over!
    Jessica
    Jeffrey James
    Metopic, Surgery June 2009, Vanderbilt

  4. #4
    Nezzy will become famous soon enough Nezzy's Avatar
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    I don't know...I think so many kids have this problem that I'm not sure it would be cranio related. But who knows.
    Heather
    Nicholas - born 3/4/09. Sagittal Synostosis. Posterior CVR 9/15/09 with Dr. Fearon and Dr. Sacco - Medical City Dallas.
    http://www.caringbridge.org/visit/NicholasNezich
    http://www.onetruemedia.com/shared?p...3242&skin_id=0

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    Moderator Shar will become famous soon enough Shar's Avatar
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    I'm with Heather. My oldest had many, many ear infections. My other kids, not so much -maybe two each? The only difference is that my oldest was in daycare and I've been home with my other kids.

    H does have this thing she was born with where her right ear canal looks narrower and she has a "pit" scar in front of her ear, on her high cheek (just under her cheek bone) that she was born with. All doctors we've asked about it can only give a guess as to what the scar is. Nothing they've said really fit when I googled it. Maybe related to the ear structure? IDK, but her hearing has always seemed fine and her development is advanced.
    Shar
    Mom to H (11/2007 ~ born with a Metopic Ridge, no surgery needed)

  6. #6
    Momof2Boys is just starting out Momof2Boys's Avatar
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    Justin (cranio kid) has had several ear infections but not enough to have tubes placed. He is actually getting his tonsil and adenoids removed next month for sleep apnea. He does get very congested alot and has alot of allergies. My other son (noncranio) would get ear infection one right after another. At 2 1/2 we were finally sent to an ENT and he had Ear tubes, Tonsils and Adenoids removed. I was so glad for the ear tubes since at 2 1/2, he did not talk. Afterwards, the words just started coming one after another.
    Glad you are having them put in.
    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

  7. #7
    angeleka is just starting out angeleka's Avatar
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    Andrew had a couple of ear infections before surgery. He had several in the first few months post op, but has not had one in a very long time. Before surgery, in his preop assessment, the PS mentioned that he had very large ear canals and should not have too many issues with ear infections. I think the bunch Andrew had after surgery were just to prove that doc wrong. :)
    So far we have been pretty lucky. We were on the path to tubes, but all has been well long enough that they are not an issue any more... or at least for right now. I think every kid in DH's family has ear tubes, so I kind of expect some issues later on in his life anyway.... not sure if that is technically genetic, but there are a lot of coincidences in his family if it isn't.

    Angi


    http://www.carepages.com/carepages/loveforandrew


    http://www.onetruemedia.com/shared?p...edium=text_url


    http://www.craniokids.org/support/showthread.php?t=4637

    Andrew - born 8/11/07 (Metopic, CVR surgery completed on 6/18/08 at U of M)

    Cheyenne Rose - born 4/18/10 with a patent urachus. Surgery at William Beaumont Hospital in Royal Oak, MI on 4/19/10.


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    Holly is just starting out Holly's Avatar
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    I took Tyler to the ENT to get his tonseils looked at and the ENT wants to take out his tonsies, adnoids and maybe put tubes in his ears. Tyler only has a few ear infections a year. But when we went to the appt. one ear had alot of fluid and the other had alot of wax. If it has cleared up before surgery he wont do tubes. I can see were an adnormal head shape could cuz the ears to not function properly.
    Holly~ wife to Trevor mommy to Tyler and Jakob
    Tyler born 5~23~05 surgery for sagittal cranio 11~17~05
    Jakob born 3~15~07 surgery for sagittal w/slight metopic 9~27~07. Also Jakobs aortic valve on his heart is bicuspid.
    Emmaleigh born 8-13-11

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    cheryl2 is on a distinguished road cheryl2's Avatar
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    Clara only had one ear infection, but she had chronic fluid in her ears. She ended up with tubes since she is already deaf in one ear. So with fluid filling up her only good ear, it was impacting her hearing and speech development. For the past couple years, she's been good.
    Cheryl (mom to Clara, born 11/5/02)
    profound unilateral hearing loss
    Saethre-Chotzen syndrome
    Right coronal cranio-CVR/FOA 9/15/03; cranioplasty 4/5/05
    ear tubes-6/30/04, 5/9/06
    ptosis surgery-7/1/05, 8/13/10
    strabismus surgery-10/11/05, 5/9/06

  10. #10
    Moderator craniomommynbaby is on a distinguished road craniomommynbaby's Avatar
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    Yes, chronic ear infections can be a result of cranio. At least for coronal cases, the eustachian tubes may not be angled properly for fluid to drain, leading to excess fluid sitting behind the ear drum and even ear infections. I had very bad ones in my right ear as a child, which is my affected side. If I am not careful about draining and cleaning my ears after swimming and such, then I can still get infections now. As a result of all the infections and no tubes, I have a scarred ear drum, some hearing loss, and a severe penicillin allergy.
    In Simon's case, the ENT said that it is common for them to just keep the tubes in cranio kids at least for the first few years of life because of the issue with the eustachian tube. Simon's third set of tubes was the t-tubes, so we won't have to think about doing those again for a few years.
    Cindy
    *Skull bone removal surgery in summer of '77 for right unicoronal*
    Mommy to Simon
    *CVR w/ FOA surgery on June 29, 2005 for bicoronal*
    *CVR with bone graft and bone paste surgery on July 15, 2009 for bicoronal and defects*
    *Bone grafts and titanium plates on June 27, 2012 for defects*
    Soul Mate to Chris
    See our cranio journey at
    www.thescofieldfamily.com/craniosynostosis.html AND http://craniomommynbaby.blogspot.com

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