Wednesday, August 7, 2013

Coronal Craniosynostosis Info



Bird's eye view of Alice's skull before her surgery.
You can see the right side has grown outward like it's supposed to
and the left side that is fused is unable to grow outward.

Helmet therapy is coming along. Alice has been such a good baby through all of this. She really has such a wonderful disposition about her. She had another helmet adjustment this week. Hanger is who we go to for the helmet. Daniel is wonderful...he really takes his time and makes sure the helmet is fitted correctly and that she is comfortable. He took measurements of her head yesterday and the left side of her head has grown outward 5mm since her first measurement before the surgery. So that's good news, it's moving outward like it's supposed to be and the right side of her head has pressure on it from the helmet to keep that side held back so the head can shape correctly. She will need a new helmet approximately every 3 months. She has helmet adjustments every 2 weeks...for up to 12-18 months.



Alice's first bite of baby food...she's not a fan!
Like her facebook logo? :)


Here are a couple links to short videos about about endoscopic treatment of Coronal Craniosynostosis and helmet therapy. Most doctors only do this endoscopic procedure up to 3 months of age. When we found out about Alice's diagnosis we were told we were outside of that window...but there are a few doctors out there that will push that window up to 5-6 months, which Alice barely fell into. We had to put alot of work into getting it approved but thankfully it worked out. Not everyone will benefit from the endoscopic procedure but thank goodness they were willing to give it a shot with Alice and we are hopeful! We are praying that she can avoid another surgery. So please keep those prayers coming!

https://www.youtube.com/watch?v=iR4ZReczojo

https://www.youtube.com/watch?v=N001zAeFOHk
































1 comment:

  1. Hi! My name is Marla. My son is 4 months old and having a ct scan tomorrow to confirm coronal craniosynostosis. I am very interested in seeking endoscopic surgery for him and would love to know the surgeons you found who were willing to perform this procedure after the 3 month window. I couldn't find the link you mentioned. If you have time, I would love to hear from you at peejinkers@conwaycorp.net. Alice is precious! My son looks a lot like her before pictures. Thank you for all the information you have provided on your blog and fb page.

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