"When one door of happiness closes, another opens;
but often we look so long at the closed door that we do not see the one which has opened for us."
Helen Keller

Friday, September 9, 2011

Brycen & the Dentist

Brycen had his dental procedure completed this morning.  He did awesome and we have noticed no side effects from the anesthesia to this point.  Unfortunately, the tooth could not be saved (it was a baby tooth in the back of his mouth), but we did find out that the dentist is almost positive there was a developmental defect in the tooth where the enamel did not form properly so it really couldn't be prevented. 

Brycen getting sleepy after the oral meds.
Brycen's tooth that was removed...the top
had a huge hole with the nerve showing.
We're not sure how much Brycen understood of our visit to the hospital, though we do know the oral sleepy meds they gave him shortly after we arrived has an amnesia effect which prevents him from remembering the need to hold him down for it or anything else.  Once he was in the "operating" room, he was given a small amount of gas in front of his face to put him to sleep further.  Then they were able to administer the rest of the anesthesia through an IV in his foot.  He came out of the anesthesia great...and was even a big boy to sit on the bed to be wheeled back to us in the private room.  He did start to cry for a few minutes, but calmed down within 10-15 minutes and was ready to watch YouTube train videos while we waited to be discharged.



Being wheeled back to us after recovery.

Watching YouTube train videos while waiting for discharge.
Due to it being his back tooth that was removed, he needed a spacer inserted to prevent his 6yr molars from coming in crooked.  Unfortunately, the spacer is something that might bother him and could possibly pry away from his gums if he wanted to.  If he does that, we are to return to the dentist to have her check on it, as well as the next sets of molars will be watched.  If they do come in crooked, he may need a future procedure to have those removed as well to prevent further problems.  Otherwise, we are in the clear until his next appt in March.

As of right now, I understand that he still needs to be watched over the next several days as he may have some hidden side effects to the anesthesia such as regression.  We are not seeing anything right now, but since Autism is a neurological disorder, anesthesia can interact with the brain in other ways that it doesn't for the "normal" child.  Thank you to everybody who gave advice over the last few days as we prepared for Brycen's first time with general anesthesia!  I appreciate all the knowledge and support during a very nervous time!

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Autism and Our Family

"Autism"----It's one word that can change the life of a child and family in so many ways. Autism Spectrum Disorders are being diagnosed at a rate of 1 in 68 children currently. If you do not already know someone that has been diagnosed, the statistics say it won't be long before you do.

Our son developed typically until around the time he turned 2 years old. We heard words...we saw him play with other kids...we watched as he played with his toys appropriately...we made eye contact with him...overall we understood his wants and needs. In a matter of a few months, that was all taken away from him. He began lining up toys, lost all of his words and signs except for one word "ball", ignored other kids, could not sleep through the night, lost eye contact and the ability to follow directions, and he had no way of letting us know what he wanted or how he felt. It was heartbreaking to see something happening to our child that we couldn't stop!

Brycen began receiving home therapy 1-2 times per month for about 6 months before we realized it wasn't just developmental delays. We knew it was Autism...we just didn't want to say it outloud to anyone. He was officially diagnosed with Autism (classic form and regressive), as well as Mental Retardation in August 2009 by the University of Iowa Hospitals and Clinics.

We continue to learn as we make our way through this journey with Brycen and we will continue to share this journey with you on this blog! The blog has been a great therapy for us to be able to vent our frustrations and struggles with accepting that we have a child with special needs, while sharing how blessed we are to have a child teach us what life truly means. It has also been a great way to inform others of his progress and changes over the last couple of years.

Thank you for your support of Brycen and our family! We hope you are able to learn something through this blog no matter if you are a parent of a child with special needs or a neurotypical child, a teacher or therapist, a family member, or just someone that is interested in the journey that a family goes on as they learn their child is battling a life-long disorder.