Savanah's Story: ROOT! ROOT! ROOT!

Thursday, March 12, 2009

ROOT! ROOT! ROOT!

Each year AG Bell puts on a speech fair at Orem Elementary. This year Savanah and her class are to perform the song "Take me out to the ball game. . ." - it's a sports themed fair this year. So this is Savanah's video of her practicing at her Grandma's house (with a little help)! She is doing so wonderfully. I picked her up from her friend's house today and was blown away with our conversation in the truck on the way home. She told me about her entire day at school, how they were learning about weather and that it is still a little bit winter outside. She told me about rainbows and that she is going to see Tinkerbell skate in one day with Grandpa and Grandma (Disney on Ice), she told me how much she loves her friend M and that she doesn't like the big boys, only little boys like T at school. I am so proud of her. I couldn't wait for the day when we would be able to talk, like actually talk. . .her listen, me listen and we both understand each other! It is so wonderful, there is never a moment that I want her to be quiet, never a moment I just want her to stop talking. If there is one thing anyone can learn from Savanah, even if you are around her for just a moment, I think you realize how much we should all cherish our ability to hear, speak, listen, sing, listen to music, hear movies, hear nature, share our opinions, express our emotions through words, listen to life. Everyday Savanah makes me more thankful, thankful for my abilities and her disabilities. She makes me thankful that she is my daughter and I her mother and for all the things she continues to teach me each day. Thanks for talking Savanah (and most of all thanks for listening and being oh so patient with me!)

1 comment:

misha~sha-sha said...: YAY! We'll be there on Friday. I'm excited to see all of the little ones singing. It's always so much fun and such a reminder of how far we've come. A great exercise in patience, right?; March 19, 2009 at 11:39 AM

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CMV, Hearing loss and Cochlear Implants

Some of you who have read our family blog are already familiar with Savanah's story. But I decided to start an entirely different blog dedicated to Savanah's journey. Her triumphs, challenges and this wonderful adventure we are all on together. Savanah failed her newborn hearing screening when she was born. We were told that she had fluid still in her ears since she was two weeks early. I brought her back to be re-tested six weeks later, and she failed again. I was told she was deaf and I was completely devastated. We have no hearing loss in our family and so she was tested through a blood test for many different things that could have caused deafness. It took several weeks for the results to come back. I had this perfect little baby who might have something wrong with her. The test that we had to wait on was called the "TORCH" test. The letters in it stands for a few common viruses and illnesses that cause deafness and the "C" stands for cytomegalovirus. Most of us have had this virus which is in the herpes family, but when contracted during pregnancy if you have never had it before can cause deafness, blindness, seizures, brain calcifications and learning disabilities and even death. When her results came back positive with this virus, our entire summer with our brand new Savanah consisted of many different doctor appointments. Traveling to Primarys, the U, ENT's, audiologists etc. It was extrememly exhausting, particularly because there was so much unknown regarding cytomegalovirus. We learned from a neurologist at the U that she would continue to shed the virus through her urine until she was about six months old and that particuarly children who had never had the virus could become infected. We had to take many precautions to make sure that did not happen.

At the six month mark Savanah recieved a hearing aid in Sept. of 04 and after a year, we noticed she was making very little progress with her speech. I started looking into alternative answers to help her to hear. We were learning sign langage as a family but it was difficut for some members of our family to learn and Savanah really wasn't very interested in signing. I wanted people to be able to comunicate with Savanah and have relationships with her. We decided a cochlear implant would be awesome and allow her to hear like a normal individual when on. Savanah recieved the cochlear implant surgery on April 13, 2007. It was such a wonderful day, the start to something big.The surgery took about an hour and a half. She recovered beautifully. She was riding her bike later that day. The incision was rather long and very easy to take care of. She was just like any other 3 year old during the recovery until she could be activated. She was activated on May 20, 2007 and since then has been a hearing girl when it is on. I highly encourage everyone who reads this blog to research cochlear implants and learn more about them. I have added some links below. Savanah has attended school through Utah Schools for the Deaf for three years. She is now catching up to her appropriate age for language and is a thriving, healthy and happy eight-year old. We are so proud of her everyday! She is mainstreaming 100% in our neighborhood school. She is on grade-level with her third grade class and loves to learn! She is a wonderful reader and always gets PERFECT scores on her spelling.

She just recently received her second cochlear implant, she was implanted on January 9th, 2013 at the University of Utah by Dr. Shelton again. The surgery went smooth and recovered quickly. She was activated on January 20th, 2013 and has absolutely loved having a second implant. She now wears two BRAND NEW N5 processors from Cochlear.