For a while I've been trying to think of a way of updating our blog without writing a short novel. There seems to be so much to say. Then, I remembered a short slide show I'd seen online when Jenna was first diagnosed (the time when I spent every minute searching the web for answers/info).
So, after discussing it with Jenna we decided this would be the best way. Just before you watch it you have to know I LOVE boasting about Jenna. I've learnt to love, appreciate and celebrate every step she has made. From arching her eye brows at 6 months to show she's happy with my cd choice, to taking things off the conveyor belt at the supermarket (last weeks shopping trip - one of best moments of my life).
If I could summaries the past six months with what you need to know here goes: In December Jenna had major brain surgery to help stop her seizures. It didn't stopped them. BUT it did change her life. The baby with the rare malformed brain, with no head control a year ago, who'd been told would severely struggle to have any physical, communication, visual and cognitive development can crawl (in her own fashion), babble, play with her ipad, clap and mostly importantly has created for herself a new chapter in life...
...."watch me mummy (Youtube link)".
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