It didn't really hit me until we visited the classroom where my son will now be going once a week, and I saw this sign on the building. Special Education Unit.
Now the rest of the world gets to hear what I already know - just how special my child is :-)
For those who don't know, our 3rd child was born with a hearing disability (or like I told my daughter when she asked, he hears the world differently to us)
Since birth, we have been in and out of audiologists, speech pathologists, E.N.Ts and now, he has been signed up to go to Special Education classes once a week.
For me, personally and honestly, it has never been an big issue. Some days I even wished they hadn't done the newborn hearing tests and that they hadn't made us aware that he may be different to other kids. When I speak, I know he can hear - and for me, that seemed like all he needed.
Sure, sometimes I did wonder if he was ignoring me when I asked him something, or was he just being a normal 3 year old - and I think for this reason, we have been softer on him when handing out rules or discipline. We just don't know.
At times it can be very frustrating having to go to so many appointments - especially when most appointments require quietness, meaning our youngest child can't go along (thanks mum!) so extra driving, plus having to explain to my upset son he can't go to Nanna and Puppas like his sister, because we have to go to another appointment where they will tell you to be quiet, or still, or respond when told.
Of course, I'm not complaining, as the people we are dealing with are all trying to help my son - and I am so so appreciative of all the services available to children with different hearing abilities (it's amazing!) - but it's not always easy.
I am thankful for the insight it has allowed me to glimpse into the world of crazy for those who have children who do have so many special needs and uncomfortable appointments here and there. BIG applause for you mums who do this so much more often then I have had to.
At one stage, I broke down on the phone to the lady from the hospital who was my point of contact. It was all too much and was now starting to effect his lifestyle and put added stress on us. She was very understanding and asked what areas I would like to look at specifically.
For me, my two main concerns were his speech (as I didn't want him ostracised for his hearing) and to find out if it would effect his ability to learn. She then made the appropriate appointments for us with speech pathologists and examinations to test his current learning level, rather then booking us in to see everyone for everything. Since then, the appointments have been more manageable.
I also told her that I am SO thankful we have never been told he would have to be operated on. I get teary thinking of those who would have the doctor recommend their child has to undergo a knife for their benefit. What a gut wrenching decision. Thank you Father for saving me from making such a decision.
I know God created my son this way for a reason, and whatever that reason is, I don't want to change him any more then I have to.
In fact, I would prefer it would be US that needs the changing. More education on how to teach him differently. More understanding that he may need to hear AND also see our face or mouth or body to hear directions. More love and patience to see the world through his eyes.
Isn't this what makes all 'Special' kids special? :-D
This has all really made me appreciative too of the body and so many things we take for granted. It's not just a case of sound goes in and our brain can hear it. There are so many possible areas that need to be looked at. How marvellously we are made! Who but God could create something so amazing? So precise!
At one stage, I broke down on the phone to the lady from the hospital who was my point of contact. It was all too much and was now starting to effect his lifestyle and put added stress on us. She was very understanding and asked what areas I would like to look at specifically.
For me, my two main concerns were his speech (as I didn't want him ostracised for his hearing) and to find out if it would effect his ability to learn. She then made the appropriate appointments for us with speech pathologists and examinations to test his current learning level, rather then booking us in to see everyone for everything. Since then, the appointments have been more manageable.
I also told her that I am SO thankful we have never been told he would have to be operated on. I get teary thinking of those who would have the doctor recommend their child has to undergo a knife for their benefit. What a gut wrenching decision. Thank you Father for saving me from making such a decision.
I know God created my son this way for a reason, and whatever that reason is, I don't want to change him any more then I have to.
In fact, I would prefer it would be US that needs the changing. More education on how to teach him differently. More understanding that he may need to hear AND also see our face or mouth or body to hear directions. More love and patience to see the world through his eyes.
Isn't this what makes all 'Special' kids special? :-D
This has all really made me appreciative too of the body and so many things we take for granted. It's not just a case of sound goes in and our brain can hear it. There are so many possible areas that need to be looked at. How marvellously we are made! Who but God could create something so amazing? So precise!
![]() |
Inside an ear. Apparently. Easy stuff... ha! |
...and how often those of us with no hearing problems (or other health concerns for that matter) take these things for granted. I often think of this verse when overwhelmed by all this:
"Ears to hear and eyes to see— both are gifts from the LORD." Proverbs 20:12
Have you told Him thanks today for your gifts??? :-) The blessings we often take for granted?? The colours we see and the ability to hear? He didn't have to give us those things, but did!
So, from here, we will continue to keep an eye on our special boy. Kindy is watching his development there as we may still need hearing aids or devices to help him in classroom environments.
I watched him in his first day of class, and I could see that we do need to work on a lot before he's ready for full time school next year. He surely isn't at the level his older brother and sister were at his age. I just need to stop beating myself up for that also. (Oh mother guilt, go away!!!)
This special education unit looks FANTASTIC and I'm so excited to see how he will be growing from these lovely ladies. They have already noticed a few things from the short time I was there watching, so looking forward to learning from them.
![]() |
Learning through play. Love it! |
For us, we will continue to try and use our whole body to communicate with him. Get down on his level and make sure he understands. Work on his speech homework and comprehension.
My son will often respond to those who ask him questions with an 'Uh-huh' rather then a yes or no. We are still trying to work out if this is because he is uncomfortable, because he can't hear or understand the question (so 'Uh-huh' usually covers it) or if it's just the quickest way to get them to stop talking to him and it's pure laziness. Cheeky monkey has been getting away with a lot! :-)
One thing this experience has done for me though - is made me appreciative of all of my kids and also other peoples kids as individuals too. We really don't know who out there is struggling or not. Maybe the kid who is having trouble in school also can't hear? Or has never been taught how to comprehend. Teachers have an amazing mission ahead of them...
I've really enjoyed the one-to-one time I've been able to spend with my son with his needs (be it, most of it in the car driving - but we have had some great conversations and singing together!) and I get teary thinking he is growing up too fast as well. He turns 4 next week. 4 years already! Wow!
My son will often respond to those who ask him questions with an 'Uh-huh' rather then a yes or no. We are still trying to work out if this is because he is uncomfortable, because he can't hear or understand the question (so 'Uh-huh' usually covers it) or if it's just the quickest way to get them to stop talking to him and it's pure laziness. Cheeky monkey has been getting away with a lot! :-)
One thing this experience has done for me though - is made me appreciative of all of my kids and also other peoples kids as individuals too. We really don't know who out there is struggling or not. Maybe the kid who is having trouble in school also can't hear? Or has never been taught how to comprehend. Teachers have an amazing mission ahead of them...
I've really enjoyed the one-to-one time I've been able to spend with my son with his needs (be it, most of it in the car driving - but we have had some great conversations and singing together!) and I get teary thinking he is growing up too fast as well. He turns 4 next week. 4 years already! Wow!
My little man's first of many hearing tests, Nawww.... |
Thank You God for all 4 of my special kids. Love them all! :-)
Thank YOU for listening to my heart and allowing me to pour it out for you...
xKelly