Our Journey

I am Alex, the father of a beautiful baby daughter with Sandhoff Disease, a rare form of Lysosomal storage disease, similar to the Leukodystrophy in Lorenzo's Oil (the movie). Artemissia was the only known case in Australia. At 6 months old the first signs of this aggressive disease began to emerge. We went to the doctors thinking it was a reaction to immunisation but no-one knew. We waited to see a neurologist but the disease was advancing. One day before her 1st birthday she went floppy. Our nightmare had begun, and even though Artemissia passed away more than 2 years later on the 13th of December 2010, the nightmare continues today. A family no more. Here you see a father's journal, emotions and thoughts. barely a glimpse of the reality, but enough.

Tuesday, June 14, 2011

At last, sun shine.

The sun shone on us today out at Eviron, Artemissia's resting place. I couldn't resist taking a short video to show how you beautiful and peaceful it really is. It's hard but you come to terms with it, realise it, and accept it. The hardest journey for any person. Words don't cut it!

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