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I Have To Do Something...

This post was written retrospectively...

March 19

When James was a baby, he was late to walk.  He was out-toed and flat footed, and hyper flexible.  We saw an amazing physiotherapist at the IWK named Kyleigh.  We saw her a few times a year when he was a toddler, and she has kept him on as a patient, seeing him just once a year.  We see her in the Ortho clinic at the IWK.  

I had been doing some reading online about kids with Perthes, and every case I read about involved the kids seeing both ortho Drs and physio. This reminded me of Kyleigh. So I googled her name and IWK, and found her email address.  I wrote to her, just reminding her of who we are, and then letter her know of James' diagnosis.  I asked if we could push up our annual appointment, or let me know how to make an appointment with her.  She wrote me back the next morning (amazing!) and scheduled us for an appointment for March 28 (next week!).  She also let me know she has worked with Perthes kids before, and can answer any questions we may have.  I'm very anxious for this appointment. 

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