Re: Where's the support for Cindy C?

[Guest guest]

Well, thank you , I'm in Michigan just a bit south of Detroit. Any Drs

names are appreciated. My insurance and I are about to battle again.

Lots of people can't have MRI's, I don't think that will have any baring on

getting into the study. It is just one of many tests.

I'm sorry your parents don't get it. I just don't understand that as a mom, but

I know your not alone. There are many young people here that don't get the

understanding of their parents. Well, not just the young, I hear it all the

time. So sorry hun. just keep fighting for your self. We're here for you.

Cindylowho

Re: Where's the support for Cindy C?

> Thanks Patti, all this new info has been a bit over whelming. When I feel

like this I tend to sit on the PC to unwind. So I have been here all day. I

think I'm wearing this chair out. It just doesn't seem padded any more.

HMMM.

>

> Thanks , I know your new. I don't expect everyone to answer. I'm just

scared, and venting. I know everybody is going through their own stuff.

>

> Many of you have contacted me at home. Thank you. I'm just kind of

spinning right now with all this new info. What to do next, where to go,

what do I do first, How do I find the right Docs that my insurance will

cover? It will take me a few days to digest all this and I will be ready to

fight again. I've done it before, I'll do it now. I won't let him down.

>

> Thanks all for your thoughts and prayers. I am scared, but I will find the

answers. First thing has to be to deal with his heart. But I'll look for a

neuo Doc right away too. This nerve damage has to stop, before he moves

wrong,and all is lost. He and I both need a day or to to digest all this.

I'll contact his primary tomorrow to get this all started.

>

> Thank you, my family of choice. I know you are all there for me.

> Cindylouwho

>

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