Upgrading Again

It is that time again. It's been a little over 5 years since her last upgrade and although we were hoping to make it through fall before we began the lengthy process of an upgrade, one of her processors quit. For good kinda quit, like the clinic said she needs a new one. The other one still works part time which is probably worse than not working at all so she is getting by with her backups (Freedoms) which are obsolete. So you see we are kinda in a pickle.

We sent in the order forms last week and the ball is rolling but I don't look for her to be in them before school starts back in August. When we get an idea that they are shipping out we will go ahead and make an appointment with the clinic so she can be delayed no more. Just in time for volleyball season!

She is super excited to get new N7s and can't wait for them to work directly with her iPhone. She loves music so the Bluetooth capabilities are calling her name. The struggle will be worth it in the end.

Sports and Cochlear Implants

Though there are many options these days for kids who hear with cochlear implants AND also play sports, I'm going to show you what works for us. The trick is to know your options, and find what works for you and your child!

My daughter is our athlete. She is going on 14 (I know!!) and has had her implants for almost twelve years now. She became an athlete in 7th grade when she made the volleyball team. Her height is perfect for such a sport and after the season was over, she tried out and made the softball team. She is learning but doing well in both sports. Her teammates and coaches couldn't be more supportive and the encouragement has certainly boosted her assurance, and confidence.

I have (out of necessity) learned to do braids. One thing at the end of the season we learned is that double braids help hold the processors on. She has long hair and the braids on each side running behind the ears are great. I wish I could braid tighter than what I do but hey, practice will help that! She bought some skinny headbands that she says help also. At first she was simply pulling her hair back in a pony tail and using double sided fabric tape directly on her processors and that worked for a while but these other options were better due to sweat causing the tape to lose its stick. This basically got us through the majority of both seasons. We now know what to do for next year as she enters 8th grade playing both sports again.

If your child wants to play sports, go for it! Let the coaches know you are experimenting with head gear options and they may even have great advice!

Deaf Child Behind The Wheel

Radio off, windows up, minimal talking and we are off. I guess I am as nervous as any other parent giving full control of a massive deadly weapon to their 15 year old child.

Truthfully, I thought the fact that he is hearing impaired would multiply that fear ten fold but so far, that isn't really a factor. He does a great job. We have had him drive at various times, even at night and in heavy rain. Next on our list is completely deaf...just down the road and back. He has to learn what it feels like so if batteries die, he don't panic and wreck trying attain his sound back. He needs remain calm, remain in control and get to where his going safely.

I think our biggest concern is (as he gets older), if he were to get pulled over, would he be able to safely communicate to an officer at a distance that he is hearing impaired. We are hoping to find something tag or window related that would state or warn of this immediately. We also have this concern (and in his billfold) that if unresponsive due to a wreck or whatever that he can't have MRIs due to the magnets in his head without first removing them.

So far, just having a permit isn't that bad. As 16 approaches, my anxiety heightens when I realize he will not want me to ride with him anymore. 😭

I Want You to Hear

Sensorineural. Conductive. Audiogram. Milestones. What are all these new vocabulary words being thrown at me and my new baby? This became our reality years ago when my first child failed his newborn hearing screening. His tiny little ears were soon adorned with rather large super-powered hearing aids. The best of the best on the market and even those floppy devices couldn’t bring enough sound to those tiny ears, to hear my voice.

Having no history of hearing loss on either side of the family, we didn’t even know what questions to ask at that point. Months passed by, then years. We introduced him to his new little sister with what little signs and gestures we had developed as our communication methods. We were introduced into the Cochlear family by our doctor as our next step toward living in a hearing world full of possible speech, language, music, and voices.

While little sister was developing her babble, her various toddler words, we were shocked to find out she too had hearing loss. She soon progressed to severe levels as we prepared to our son to undergo his first cochlear implant surgery. Our hopes were high and expectations low as our now almost four year old would either soon begin to hear the world that had been so quiet, or he would remain in silence.

Not only would he receive the gift of hearing, but his sister would soon follow in his footsteps. We had therapy as a family to learn how to learn how to hear and how to develop appropriate speech and language. It was hard work for everyone on our team but both children are in public school, playing sports, playing instruments, enjoying their friends’ laughter and not enjoying their mother’s singing.

Now Cochlear introduces their new website as a resource for parents finding themselves facing a similar situation as we did years ago. A place to answer the daunting questions that linger can be accessed from almost anywhere. Find out more about the advanced implantable hearing solutions by Cochlear by visiting   www.Iwantyoutohear.com

This is a sponsored post from Cochlear written only by me. My opinions are my own.