My name is Natalie my husband Ben is a SAHD and I work 4 days a week at the moment for state government in a great workplace which has made returning to work after both children easier to settle into.
Our children are our world and have been very lucky to have our own pigeon pair, nothing has ever been so special and so inspiring, they make me realise I am still learning and teach me how to appreciate everything in the world again, they see things we sometimes forget are there, I love them to pieces.
I also have a Movement Disorder called Cervical Dystonia &/or paroxysmal kineosogenic choreoathetosis where I twist like a person with cerebral palsy (My aunty has severe cerebral palsy from birth trauma) it appears to be genetic. I had episodes fully aware but twisting and flaling limbs, slurred speech each time I get up, though ok on medication. It is not epilepsy but very very simialar and uses simialr medications to control. Anyone with similar condition I would love to get to know.
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Australia 
Member » VenusMercury
22:18
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