Plateau

I think we have hit a plateau. It was going to happen, things just can't keep going at break neck speed. It just isn't possible.

Isobel is continuing to progress with her AVT but the rate is slowing down. We are getting some more refined sounds, spontaneous talking and the following of instructions.It has however, got somewhat harder for Isobel now, and she is feeling the difficulties.

I can't let her see my mouth anymore when we do our little sessions together and so she can't rely on lip-reading. She is finding this most challenging and frustrating. She often pulls at my hands or whatever I am using to hide my lips. It is a coping strategy that she has been using for a long time and so it is difficult for her to break the habit of looking and to use her ears instead.

It is so difficult at times for me, I am her Mum and her teacher. The teacher inside knows that this is conditioning and we will get through it and have her use her ears. The Mum however just sees her little girl sad and angry and I feel quite guilty because I am causing it. It is a necessity though, and we must ride this storm. 

We shall keep going and hopefully, we shall get through this difficult patch and come out the other end stronger and hopefully a little bit wiser.

It wouldn’t be fun if it was too easy… right?

Push it down the stairs...

Did you ever have a slinky? I'm talking about the rainbow coloured kind, not the one that forms the body of a dog (Toy Story).

Well I happened to find one in the supermarket here and added it into the rewards that Isobel gets when she completes a task or imitates a word correctly. They are just a selection of cheap, fun toys/things that she sees as a real treat when she does well.

By far and away the slinky is her favourite. That is after she had seen how it works. The first hurdle of course was living in an apartment we have no stairs, so we had to venture out into the corridor the find the perfect platform for the slinky.

Now the reason for my long winded introduction. We have had Isobel's first 5 word phrase. 'Push it down the stairs.' It started with 'push it..., push it...' every time she tipped it off the edge of the step. Now we get some version of the whole phrase with each step the slinky is pushed down.

Slinky! Everyones favourite toy.

Chatterbox

Where has the time gone? We have had such a busy time lately!

We had Isobel's AV Therapist out to visit us here in Korea and what a week we had. Intensive! She went to school with Isobel each day and provided well received tips and advice on how to help Isobel. We had afternoon sessions that lasted around 90 minutes each day and all the bits in between in which to squeeze opportunities to model, imitate and just talk, talk, talk.

It was tiring, but so well worth it. Isobel has turned into quite a little chatterbox, she hasn't stopped talking and singing since Cheryl left. We are getting more and more words out of her and longer phrases and sentences. We are just so excited by all of this.

She is continuing to do better in school, joining in on some of the class songs and 'reading' to her classmates. This involves her grabbing a random friend and sitting them on the carpet. She then chooses a book, sits on a chair and reads to them. This is story time type reading, holding out the book and pointing at the words and pictures. This continues until the friend wishes to 'escape' and play something else. At this point they are told to 'sit down', 'stop' and 'listen'!

We have really been working on her being able to say her friends names nice and clearly so she can find a non-physical way of getting their attention. By all accounts, this seems to be working and with some interpretation from her teacher, she is sharing and playing with her friends quite nicely.

Watching her play with her little sister for a brief moment this evening was lovely. They were building a tower and Isobel was able to clearly explain to Estella that the strip she wanted to attach was in fact too big because it had 4 sections. What she really needed was a 2 sectioned piece:


Isobel:  No Estella, too big
            See, four
Estella: Four
Isobel:  This one, two
Estella: Two, OK

And the tower was built! Isobel is getting quite good at helping her little sister out.

Wonderful Technology

I was looking through posts on the Facebook group Parents of Children with Hearing Loss and somebody had posted this video. It is a wonderful video about nine different children who had cochlear implants fitted. They were all different ages when they were implanted, and had varying degrees of pre-implant hearing experience. Subsequently, they are at a different stage of their hearing life with implant use.

Even though Isobel doesn't need the implant right now, we never know what the future may hold for her. Several of these children started out with hearing aids and then needed cochlear implants when the aids couldn't help them any more.

It brought tears to my eyes to watch in amazement how articulate these children are. It was truly difficult to believe that some of them had any hearing difficulty what so ever, especially the young boy explaining all about hockey.



I am so glad that as we go through this journey with Isobel, that we are going through it now. With all the technological advancements being made in this field the future can only be bright for Isobel. She is lucky to be a 21st Century child with these solutions for her problem, what would it have been like for her 50 years ago or 100?

More importantly, I wonder what it is going to be like for her in the future...

It's All Good

We took Isobel for a hearing test today, she did fantastically at well performing the task again. Now she knows what to do there really is no stopping her. Of course the promise of an ice-cream is very good at focusing the mind on the task in hand.

The doctor was pleased with her results and said that she is hearing at around 40db with her hearing aids in. For those of you that have been following the blog, you will know that this is well within the speech banana, and so this is very promising for her speech progress. She is even able to hear some of the higher frequency 20db sounds if the volume is increased slightly when saying them so progress is indeed happening. Because of this progression, we have 6 more months with the hearing aids and no cochlear implant surgery. If she continues to progress in this fashion, we may be in the situation where she won’t ever need to have the implant, the hearing aids alone will do the trick and in 18 months, Isobel with have caught up with her peers in terms of Auditory-Verbal ability. As you can imagine, this news is thrilling for us.

Also, Isobel’s AV therapist is coming out to Korea next week to give Isobel, and us, some intensive therapy. She will be coming in to observe her at school and working with us as a family. We are very much looking forward to this time to really learn more about helping Isobel move forward.

Corben Family

Finally, we have had a break through with the medical Insurance who have agreed to make a one-time exception and cover expenses related to Isobel’s hearing aids, tests and medical bills. This coupled with a generous donation by the community we work with puts us in good shape for the next few years working through the financial side of this adventure.

Things are continuing to look up for us!