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Twitching with Joy 01/17/2009
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I wrote a post below about diet and TS. For two years I was a diet nazi. Nothing that he was even slightly allergic to was allowed. Maybe once a year on a birthday.

I have since lifted the diet ban. We eat only "approved" foods on a daily basis, but if there's a birthday party or it's a special holiday (Halloween, Christmas, Thanksgiving) we eat a bit of the forbidden foods such as pizza or cake and icecream.

If I was at all wishy washy about my decision to do this, all I had to do was view this photo taken last night at Stink's very small six year old birthday gathering at our home. Similar to the expression he had at his cousin's bowling party last week, my heart melts with joy when I see his exhuberance.

And the irony of my minor food transgressions? No visible tics as a result. Sometimes happiness overrides anxiety over not getting to eat what everyone else does. More on this at a future post.

Also, please see this post below which answers the question about having a child with a person who you suspect has TS. It's my opinion only, of course, and would love to hear yours.


More of my writing can be found daily at BabyCenter and Good Housekeeping.


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    TICKED OFF: TOURETTES TALK

    "When You Can't Fix the Tics, Fix Yourself"

    Consider this is your 12-Step Tourettes Support Group where we will encourage each other to:

    1. Accept the tics we cannot change

    2. Change the tics we can

    3. And have the wisdom to know the difference.

    ABOUT ME
    My son, Stink, was diagnosed with mild Tourettes when he was 4. I was terrifed he would curse, shriek, scream and hump busses.

    Quite the opposite, he is highly creative, social and thriving.

    I keep his tics at a minimum through a gluten free/caesin free diet.

    While I haven't eliminated his tics altogether, I'm eliminating fear through a good dose of humor and acceptance.

    I hope you'll join me so we can support each other on this crazy journey. Welcome to Ticked Off.

    Picture
    I write weekly for the New Jersey Center for Tourette Syndrome blog. Come visit me, and other awesome parents, for some daily support!

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