Springfield toddler continues on road to recovery after major skull surgery

Springfield toddler continues on road to recovery after major skull surgery

Reported by: Chris McKee
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Updated: 11/15/2011 7:46 am

SPRINGFIELD, Ore. (KMTR) -- A Springfield baby born with a rare medical condition is now on the road to recovery after a major surgery for a rare birth defect called “craniosynostosis.”

Back in July 2011, NewsSource 16 introduced you to a 7 month old baby named Gabriella Todd. At two months old Gabriella was diagnosed with craniosynostosis, a premature fusion of the bones making up the skull.

(Read NewsSource 16's original story at the following link: http://www.kmtr.com/news/local/story/Springfield-parents-warn-others-about-babys/-WOxZxGhYkeSbiDOjVe_IA.cspx.)

Now 11 months old, Gabriella is talking, walking, and by all accounts, she's thriving. All of this just three weeks after a traumatic operation on Halloween weekend, where doctors reshaped her head in order to reset her skull and keep her from any harm as she continues to grow.

With a big smile, it's hard to tell that just three weeks ago Gabriella Todd was in the hospital.

“Not knowing what the outcome will be or how she'll handle it,” says Eric Todd, Gabriella's dad.

“It's been pretty overwhelming, you don't have a lot of other people you can draw from,” says Theresa Todd, Gabriella's mom.

At just two months in to Gabriella's life, Eric and Theresa noticed a problem with Gabriella's face.

With a flat spot on her face, the Todd's took Gabriella in for an x-ray and confirmed their suspicions.

“Those sutures.. Don't fuse together until you're between 20 to 30 years old,” says Theresa, pointing to an x-ray of Gabriella's skull.

Through the x-ray, doctors found that a few of the bone plates in Gabriella's skull had fused together before she was born. The condition, craniosynostosis, effects about 1 in every 2,000 babies.

Without treatment, the condition can lead to sight and hearing loss among other serious developmental issues.

“Early morning of the 27th, is when we had to take her in,” says Eric.

On October 27th, 2011, Gabriella was given over to the care of doctors in Seattle where they put her under the knife. Doctors broken several of the bones in Gabriella's skull.

After about 4 hours, seeing her for the first time, the Todd's had a mixture of emotions.

“We were kind of devastated because you see her struggling, you know what she's just been through,” says Theresa.

“On top of that was relief, because it's over,” says Theresa.

Just moments out of the operating room, the scars were clear. Gabriella's incision spans from ear to ear across the top of her head.

But progress was also apparent.

“Now it's rounded out and shaped like the other side. The eye doesn't have the surprised look at it always did before and most important thing is that they broke that fusion, to allow her brain to go,” says Theresa.

Through the pain, the nerves, the traveling, and the swelling of Gabriella's entire face, the Todd's have endured through Gabriella's surgery.

Looking at the pictures, just hours after the surgery, Gabriella's face began to swell so much her nose was barely visible. Her eyes also swelled shut.

“She's waking up and she can't see and she's panicking, but she handled it very very well,” says Theresa.

Today, the Todd's continuing working through one of the biggest challenges in their lives. In the meantime, they hope other parents learn from their story.

“You need to go with your gut and if you see something unusual about their head shape, you need to follow up with it and... Just because you get the answer you know, 'they're OK,' it's not necessarily the answer you should go with, you know, just make sure.” says Theresa.

Financially, the Todd's say insurance is covering medical costs, but travel costs have been a huge burden.

Gabriella will go back to the doctor next week for a follow up. Doctors say she still has some swelling in her face. Doctors will see Gabriella again at 3 months and one year to make sure things are healing properly.

6 Comment(s)
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The views expressed here do not necessarily represent those of NewsSource 16

springfieldmom - 11/16/2011 8:52 AM
1 Vote
I am very sorry spriggee that your family also has to travel this very difficult journey. I am not sure how you have tried to contact us I as I haven’t received any messages or I defiantly would have responded. I agree that is helpful to have the support of other families that have been through it, as cougar68 pointed out I have actually been in contact with many other cranio families along the way. I actually mentioned this in the interview as well as some of the wonderful support groups and charities that are involved in bringing awareness to Craniosynostosis but it did not make it to the broadcast. As for inaccurate information, one of the frustrating things about the media is that there is a lot that is edited out or taken out of context. I am not sure if you noticed but all of the quotes in the story are incomplete sentences, with part of the statements left out. For example “those sutures…don’t fuse until your 20 or 30 years old” was in reference to “some of the sutures” not ALL of the sutures. I could go on but I imagine you get the point. And while that may be the case, I still would like to thank KMTR for the effort they made to help bring awareness to such an important cause. I would defiantly like to clarify though that we did not reach out to the media for any kind of support. Our goal for reaching out is purely to help spread awareness about a medical condition that many people have never heard of and that has a major impact on the lives of not only the affected child but also on the entire family.

Cougar68 - 11/15/2011 10:38 PM
1 Vote
All I can say is that I know this family personally. I know for a fact that they have done extensive research on Cranio and that you have to keep in mind that there is a lot that gets cut out of the news stories. I can also say that they have found some great support groups on the internet and met some other wonderful Cranio parents. One of which even sat through the surgery with them. I know that this family is more then willing to talk and support others. I am not sure who this Spriggee person is but I can asure you that they would have never not responded to anyone. I am not sure how you are trying to get in contact with the family but to make is sound like they are trying to do this for the media attention is not fair.

Zebra - 11/15/2011 11:00 AM
0 Votes
Financial help is available for people who must travel for medical care. Several organizations provide free airfare, and others offer small cash grants to offset costs. An online search will reveal the details. It is very helpful to connect with other people who are experiencing similar medical crises, especially if the medical condition is rare, poorly understood; if it requires intensive or prolonged treatment; or if it requires alterations in approaches to education, sports, daily activities, etc. I urge this family to use the internet to make lifelong connections through support groups, mentors, researchers, etc. As their daughter grows, she may develop other health-related concerns that can accompany pediatric craniosynostosis, and having friends with the same condition(s)can make the journey a lot easier. Best of luck!

spriggee - 11/14/2011 11:54 PM
0 Votes
I do hope she has a fantastic recovery, I don't like the misinformation in the process...

spriggee - 11/14/2011 11:53 PM
0 Votes
AND the 'facts' ARE NOT CORRECT!!!!!!!!

spriggee - 11/14/2011 11:45 PM
1 Vote
Our daughter has gone through TWO Craniosynostosis repairs of her right-coronal suture... I've reached out(now, TWICE) to this family without responses... wonder why they reach out to the PUBLIC but don't respond to those who have been through what they're reaching out to the MEDIA for... hmph.
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