It has been tough for Matt – he has really been feeling unwell. He has been so droopy and clinging. I can’t explain to him what is happening to him, so on one level I have felt frustrated. But on the other hand, since I cannot rely on words for explaining, I have discovered a very precious way of communicating comfort and reassurance to him – through song. My song. Now I am not a great singer by any stretch of the imagination, yet my simple tunes, though sung in a slightly off key manner, seem to really touch him. On Monday night he woke up with such a high temp that he was shivering so violently that he could hardly move his limbs. Whilst we were waiting for his temperature to come down, I cuddled him on my lap with his head against my chest. I could tell that he was tense and confused about what was happening to him. I started singing and immediately he calmed him and snuggled in closer. He knew that he was safe. I know he felt my love and care for him through my song. Music has many values, but over the past few days I have seen its visible effects on Matt’s body. I have been struck by what an amazing gift music is to us as humans.
Our son Matt has brought such joy to us and through him we have learnt so many things about ourselves and life. He has a rare genetic syndrome called Rubinstein-Taybi Syndrome. This blog is where we process the things we have learnt, where we share our challenges and pains, and where we celebrate small victories.
Wednesday, August 26, 2009
My song
It has been tough for Matt – he has really been feeling unwell. He has been so droopy and clinging. I can’t explain to him what is happening to him, so on one level I have felt frustrated. But on the other hand, since I cannot rely on words for explaining, I have discovered a very precious way of communicating comfort and reassurance to him – through song. My song. Now I am not a great singer by any stretch of the imagination, yet my simple tunes, though sung in a slightly off key manner, seem to really touch him. On Monday night he woke up with such a high temp that he was shivering so violently that he could hardly move his limbs. Whilst we were waiting for his temperature to come down, I cuddled him on my lap with his head against my chest. I could tell that he was tense and confused about what was happening to him. I started singing and immediately he calmed him and snuggled in closer. He knew that he was safe. I know he felt my love and care for him through my song. Music has many values, but over the past few days I have seen its visible effects on Matt’s body. I have been struck by what an amazing gift music is to us as humans.
Thursday, August 13, 2009
A Matt look-alike
Last week Matt and I met a tiny little baby called Samuel. He has a full head of hair – dark black. He has a big red birth mark on his forehead. He has the cutest face. He has thumbs that are elegantly angled outward. He looks like a new born Matt, only smaller. He looks like he could be Matt’s younger brother. In some ways he is.
Yes I finally met another child with Rubinstein Taybi Syndrome. This was a day I have been longing for and dreaming about for a long while.
Last week Thursday Samuel came to visit us with his mom and dad. I had been in telephonic contact with them for a few weeks and finally things worked out for us to meet. I know that Sam’s parents are still trying to find their way in "Holland" and so they were probably not so excited about meeting me as I was to meet them. But for me it was so precious – knowing that we are not alone anymore. Being in physical contact with someone on the same journey – words can’t describe that feeling of camaraderie. I know our friendship will grow from here.
Pray for little Sam, who was born prematurely, and is facing a number of health challenges. I was so overwhelmed and so overjoyed at meeting them that I forgot to take photos. Hopefully we will be able to visit them soon and I can get some pics – so watch this space.
Wednesday, August 5, 2009
I will still hope
Saturday, August 1, 2009
Hair
Wednesday, July 22, 2009
Sunday, July 19, 2009
Blossoms
He uses both PECS and Signing to communicate. He usually uses signing to express a need for food or drink or some action that he requires, like jump or spin. He is also uses signs to name farm animals. He uses PECS to request items that he desires. Most of his toys are stored in plastic boxes with pictures of them on the boxes. He removes the picture of the toy that he wants and brings it to me when he wants to play with it.
We also have a place in the kitchen where pictures of various food items are on display. Like most kids he is only really interested in the chips and biscuit pictures.
It’s been brilliant to see Matt express his likes and dislikes – for example his passion for seeing his mom and dad show affection. Whenever Lloyd comes home, Matt comes running to me and shows me the sign for “kiss” over and over until I ask him who I must kiss - he replies by signing "dad". When I kiss Lloyd, Matt visibly melts with delight. Only then will he give his dad a kiss.
I am thrilled that we have these two methods of communication. I often imagine what Matt’s world would be like if he didn’t have these two avenues of expressing himself.
There are some limitations though. Matt’s vocab is limited to what I can teach him, and I only know so many signs. Unlike other kids who hear everyone talking all the time, and can pick up any word that might seem interesting to them – Matt can only learn signs that I teach him. He might want to tell me about the singing octopus toy that we have; or point out to me the bright green frog at the aquarium but he doesn’t have the signs for those. I have noticed how kids often come up with the cutest or weirdest thoughts on matters that you did not expect them to have an opinion. Matt can only comment on the things for which we have given him the signs. It saddens me to think that he might like the rainbow that Barney sings about, or be drawn to the stingray puzzle piece and I won’t know that. I love hearing my friends share about how their little one said “the funniest thing other day”, but I do feel bleak that Matt doesn’t have that full freedom of expression because I can’t give him signs for every word.
My ongoing prayer is that God will equip us to help Matt to one day be able to express himself without limits. I am not sure what that will look like. I know that full communication is not necessarily reliant on speech, but I do still pray that Matt will speak one day. In the mean time I am determined to equip myself and those around me with as many resources to help Matt communicate to the full.
Our Speech Therapist saw Matt this week and feels that he is ready to move onto the 4th Phase of PECS. He is now able to discriminate well between pictures, and is able to correctly choose the picture to express his preference. I am still to find out all about phase 4, but I think it entails storing all the pictures in a folder and using that as a base from which Matt can remove the photo of the item he requires. I have already developed such a folder for my own storage purposes, but now Matt gets to use it too. So watch this space.
Saturday, June 27, 2009
Saturday, June 20, 2009
What Matt learnt in KZN...
Discovery #1 - Farm animals are FUN!
These were the friendliest (and non-biting) goats we have encountered. They loved eating mealies (corn) from people's hands! Once Matt got used to it he found it quite entertaining. The mealies were given to us in recycled tins and Matt had to stick his hand right in to get them - great sensory experience for him.
Discovery #4 - Shapes are FUN
Discovery # 5: We can sign what we see in books
It would seem that our little Matt not only enjoyed his time away but learnt lots of cool stuff too. Visit our blog tomorrow for installment #3 of our trip - we show you a profitable way to spend your waiting time at the airport.
Friday, June 19, 2009
Our KZN Holiday part 1
We spent the rest of the week staying with friends and family. It was so good to connect with friends who we haven't seen in too long.
Breakfast time and Matt found the ancient coffee grinder (that still grinds excellent coffee) to be of great interest!
Matt even joined the Tooke boys rugby game!
Watch this space for more on what Matt discovered in KZN. (For some reason it is taking ages to upload photos this evening - so I will post more tomorrow, if I keep trying now its gonna drive me mad! )