Sunday, February 24, 2013

Swimming with Cochlear


We were invited, along with a few other families, to try out the waterproof swim gear coming out soon from Cochlear. You really can't see the bags from this photo because Gman needed a swim cap to hold them on his little malformed ears but other kids were able to wear them with a small band holding them in place. Are they completely ready for the market, not exactly but with just a few small touch ups I think they'll be a huge hit.

Did they work? YES! They did the job. His implants did not get wet and for the first time, he could swim, and go under water, and still hear wearing his processors the whole time with only a slight compromise in sound quality. The echo from the swimming area was a challenge anyway but if I took him down to the other end of the pool, covered my mouth so he couldn't speech read, ask him questions....HE COULD ANSWER THEM!!

He had to be very gentle before he put the swim cap on ducking under the water very easily or the coils (magnets) wouldn't hold. He tried the headband the other kids were wearing and it still wasn't enough but a swim cap held everything on great! The best part? He loved it. He smiled and said he liked being able to hear while he was in the pool. I watched him splash and make noises with some of the swim toys just to hear them. That was pretty awesome!

The only negatives I could see: I would prefer a brighter color (not clear) because we go to lakes a lot, should one come off, I'd like to see where it is. Also, the bottom of the product needs to be less "stiff". It rubbed into his neck and was uncomfortable. It didn't appear to be a problem with everyone depending on the child but more than one person had this issue. I like the fact that they will be affordable but we would probably use like 10 a day during summer with both kids and both ears so it would be nice if you didn't have to rip the bag open to get the processors back out and reuse them all day and just throw them away at the end of the day.

My friend Lisa was there also and she did her best to "drill" Cochlear for inside information on the N6's or the next processors due out in Fall from Cochlear. We are holding off to upgrade Brooklyn until the new ones come out so we are hoping they are as awesome as they plan. Sounded to us like they will be better for the kids in classrooms and possibly come with a lapel mic for teachers to use in place of FM systems since the new chip would make things easier for the kids changing environments. We shall see and our hopes are high.

Tuesday, February 12, 2013

Not so Good

Well, we thought we were doing great.....however, after MAPping both children today, we popped them into the booth and obviously from the chart, they hear great with their cochlear implants...
(You need them to hear within or above the speech banana if at all possible which both of my kids do, thankfully)


...the bad news? They don't hear great in noise. In fact, you can see from the numbers over to the side, that they both drop to less than 1/2 of clear understood speech. Brook uses an FM in class and she does really well with it, however, little man has abandoned this as of fifth (really fourth) grade. So, he's trying a noise program right now (which he doesn't love) but he'll either adjust, use the FM again for class, or settle. I'm hoping the new program will help him out. I can't imagine only getting 46% of the information all day long.

On a lighter note, this is the difference in words they create outside the booth door while waiting on each other........

She innocently works away at Bat, Sunroof, and many other common words, while he is completely amused by his words Spaz, and turds...(boys)


Brooklyn is good for another year while Gman will go back in a month, see how the new program is working and we'll put him in the booth with this program and see if he can up his numbers any. Brooklyn doesn't seem to be that bothered in ordinary situations and since she has an FM at school, I'm not as worried about her numbers.