Max Galm Journey through surgery updated version

Loading...

Sign in or sign up now!
Alert icon
Upgrade to the latest Flash Player for improved playback performance. Upgrade now or more info.
3,829
Loading...
Alert icon
Sign in or sign up now!
Alert icon

Uploaded by on Apr 11, 2008

Max Galm. This video is to help spread awareness for Craniosynostosis and Positional Plagiocephaly. Two conditions that go undiagnosed for far too long.

Link to this comment:

Share to:

Uploader Comments (designertans)

  • when you say goes undiagnosed for too long i know what you mean. I was born in 1992 and though the doctors knew what was wrong (craniosynostosis) it wasn't until i was 13 that they actually put a name to it. Also i would recommend from personal experience that if your child needs to have a surgical procedure of any kind of this nature take him or her to children's hospital of either detroit or chicago. if you dont live close to there i know it may be a ways away but trust me, its worth it

  • @military6874  thank you. I hope that you will join our Facebook Page - Craniosynostosis-Plagiocephaly Support CAPPSKIDS

  • My little Ryan was born on 11/02/07 and he was diagnosed with sagittal craniosynostosis and he had surgery on 01/25/08 and so far everything is going as planed

    You have a beautyfull child may god bless

  • Thank you! Hope your child is recovering well.

see all

All Comments (18)

Sign In or Sign Up now to post a comment!
  • this sucks i have flat head well its not that serious just the back of the head is flat its not all bent and deformed that much but it just that i wish there is something i could do and i'm 13

  • ok r u maxsmommy on cappskids? i need help my daughter had surgury on oct.2008 and she hit her head really hard and know shes acting wierd is that her or have sumthin to do with her surgry?the bumb is like by her cut/..

  • @designertans sorry i posted the reply wrong but i did

  • @designertans thank you. i will

  • Hii my names shannon galm i just relized this little guy could be related to me :( I hope he has a full recovery and best wishes for every thing :)

  • Hi AMY WE LOVE YOU and MAX adding you to my favorites!!

  • Hi Max's Mommy,

    Glad to have seen the video of it all, So thankful for the Cappskids site.

    Ava's mommy

  • I have Lambdoidal Craniosynostosis. I understand everything you have gone through. I am now 21 and I only had 2 surgeries because my insurance would not cover it and my family and I finally gave up hope of them ever covering it. My family was able to come up with the money to cover my first 2 surgeries but we can't cover the other ones that I need. When I was born and throughout my childhood my doctors never believed my mom that something was wrong with my head and face.

Loading...
Alert icon
0 / 00Unsaved Playlist Return to active list
    1. Your queue is empty. Add videos to your queue using this button:
      or sign in to load a different list.
    Loading...Loading...Saving...
    • Clear all videos from this list
    • Learn more