Lachlan was born in 2010. During our pregnancy we were given a 1:2 risk of trisomy 21 ( Down's Syndrome) or trisomy 18 ( Edward's Syndrome). We never confirmed this risk and it was only after birth we found out that Lachlan had trisomy 18. Lachlan continues to defy the odds. This is his journey
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Thursday, 13 February 2014
Things I like
Information on People first Language. A person with disabilities is foremost a person. They should always be described as a person with a condition not as the condition. For example Lachlan has trisomy18. We don't have trisomy children, we have children with a trisomy. Check out this helpful chart:
http://www.inclusionproject.org/nip_userfiles/file/People%20First%20Chart.pdf
Thursday, 6 February 2014
Playing
What I like to do and how I move
I love my hanging toys
I am lifting both my legs and bottom into the air when I lay(sometimes it is not good to be to close as I sometimes let one off in this position)
Spending more and more time on my tummy instead of just going for the roll (video about a minute long)Friday, 17 January 2014
Lachlan investigating playdough
Another mum posted a link for playdough. with a really simple recipe. Cornflour and Conditioner. We decided to make it for Lachlan. Smells great. Wish I had this recipe ages ago Link below for recipe. Love the expressions on his Face
No Flash Photos Mummy!
This is my Favourite
Monday, 13 January 2014
Pictures January 2014
Just Chilling
My size pet( new Guinea pig Cookie)
Sister pic to the one for March trisomy awareness