This isn't my blog, it's Zack's. Zack arrived here seven weeks early, he had no heartbeat and wasn't breathing. He suffered catastrophic damage to his brain, he has cerebral palsy, problems with his hearing, vision and feeding. Our lives are both challenging and extraordinary. He is a gift. I hope that for whatever reason you find yourself reading this blog it can go some way to help those in the same situation and some way to remove the cloak that covers parenting a child with disabilities.
Monday, 7 February 2011
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It has been a full year, 12 months, 365 days since Zack passed. The 3rd April was a tough day. The weather was glorious, the sun shined an...
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Sometimes I don't know what Zack has to complain about, I mean he has had a lovely week so far. Okay it didn't start off too well, ...
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Oh there have been many sleepless nights in this house. And it is not because of the youngest member of our family, nope, it's all down ...
3 comments:
That is AWESOME. Also, Zack is ridiculously cute.
Learning stuff like that so young is a fantastic sign for getting the hang of more complex communication techniques, incidentally.
Thanks for the video!
Thanks for the comment Becca, glad you like the video.
Hooray for Zac - that's amazing. And Happy Birthday!
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