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In a message dated 12/14/1999 8:31:40 PM Eastern Standard Time,

slowens@... writes:

<< Now I am ready for bed and I don't think I will even snap at my

husband. Thank you everyone.

Elena,

Yet another benefit from tae-bo that no one would have ever expected!!!

>>

actually, my husband has mentioned that I am alot calmer than I used ot be

Barb

who still snaps but not as often nor as loudly

AKA:POMBarb, Mad-Dame Yenta, Tae-Bo Barb

" Cats and Teens will do what they want and

Dogs and Parents just better get used to it "

<A HREF= " http://hometown.aol.com/horsemom2/myhomepage/index.html " >Barb's

Places on the web</A>

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  • 9 years later...

HI ,

If you are looking into Shriners at Erie I have contact information. You would just need to call the Care Coordinator (she is wonderful) and she will set it all up for you. She walked us through everything. She was helpful and kind. Email me if you want and I will give you her contact information if you do not already have it.

Remember that you are not alone! Hang in there.

Jill

Subject: ThanksTo: infantile_scoliosis Date: Wednesday, February 4, 2009, 1:41 PM

Thanks to everyone for the well wishes, information and support. Many have emailed me privately and I cannot express how valuable this information is to us. While I'm still feeling extremely overwhelmed, at least I have a handle on the right questions I need to ask and the right testing I need to ensure is complete.As I've mentioned before, we have one second opinion appointment scheduled with Duke and I've submitted my application to the local Shriners Temple in our area. The lady I spoke with admitted she was new but that she would find out what to do with our form and get back with me. So far - nothing. Can anyone explain the process to me? I downloaded the form from the hospital's website and included sponsor information. What happens next? How do I make sure it gets sent to the right hospital? The more I research, the more I believe that we might be better off at one of the hospitals in

Pennsylvania. Anyone have any suggestions?I appreciate everything you guys have done for us so far. I no longer feel like we are the only parents on the planet facing these decisions.With love, (mommy to ^Hope Marie^ 06/04/05 and Elijah, congenital scoliosis/kyphosis)

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