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Re: Patty & Isabella

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Im sorry Patty. Its good that Isabella is a patient in Rochester as they

are super experienced and will help you when the surgery bridge must be

crossed. Until then, buying more growth time w/ properly applied serial

edf is the Gold Standard. Even for kids that may have missed their window

to be completely cured. Hang in and rely on us when u need too. Many

families on CAST have missed the window and will be here to support you.

Sincerely,

HRH

> Sorry, I have yet been out of the loop again but since our casting last

> week, I have been putting in some long hours at work. I haven't been too

> eager to post either since we didn't hear what we wanted to at this last

> casting. Unfortunately, our doc thinks Isabella isn't going to correct on

> her own and so he said at some point, we will have to do surgery. I was

> very upset but stayed strong for Isabella. Since we seem to be going

> nowhere, we opted for a waterproof cast (only approved since we haven't

> had improvement) for the summer and then we will most likely go back to

> the plaster in August. While there, the doc x-rayed her arm and said it is

> healing nicely so he put her in a short arm waterproof cast. It's just

> been a horrible past 2 months for her with this news, breaking her arm,

> and to top it off, she fell Thursday night and split her head open at her

> eyebrow and had to get stitches so yet again, no water!!!!!!!!!

> Patty, mom of Isabella, 2 years old, in 6th scoli cast (Rochester) & now

> an arm cast & mom to & Evan

>

>

>

>

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