I still marvel at the opportunity that I have been given to contribute my thoughts to a local magazine regarding my journey with Matt. Here is my latest article.
http://www.childmag.co.za/content/world-difference
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.
Friday, September 28, 2012
Tuesday, September 11, 2012
Our own Woody
Matt's school had a Dress Up Day today. Matt hasn't shown much interest in fantasy or dress-up. But we really got into it and here he is before school this morning, ready for the fun to begin. I thought he would have undressed (his favourite sport) as soon as the hype wore off, but at the end of the school day he was still mostly in his outfit - minus hat and scarf. His teacher said he was super excited all day.
Saturday, September 8, 2012
The trampoline
A new arrival in our home - the trampoline. It took some serious tree removal to create some space in our small garden. Matt's OT has been encouraging us for a while to get one for Matt; and it has been so worth it. It has become Matt's safe space, his joyful place, his centering place, his calming place and his just-for-fun place.
And a place of bonding for his dad and brother too. Most of the time they do jump on it, as opposed to what you see below. This was a special moment when they were all enamoured by a helicopter flying over head.
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