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Re: Future worries

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Hi Deborah,

I'm sure that all of this is still so new for you. This is a wonderful,

supportive network of friends. I wish you the best in this " new territory. " It

sounds like you've gone through the most difficult phases of treatment already.

At least in my own case, radiation was far " easier " than chemo. If you ever

feel like just talking or venting, feel free to write, either on list or off.

Jill

carpediemdaisy@...

Re: Future worries

I just joined this site yesterday, but it definitely looks like you have alot

of friends here!

Hang in there. This is the most crazy time (the first month or so after

surgery). Things will clear up and treatments assigned. Remember you have lots

of friends here who can appreciate what you're going through.

" D. A. Marrs " wrote:

Hi, I just completed chemo and had a double mastectomy on 9-7-06. Will

start radiation tommorow. (Stage 111bc)I am 52 years old and really

interested in visiting with anyone with my similar statistics or anyone

that might just like to talk. This disease has been devasting to me and

I sometimes find it hard to talk with family and friends that have no

idea what races through your mind a million times a day.

Happy thoughts!

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Hi Deborah and welcome to the group. Congrats on completing your

chemo. Future worries..........I think that we all can say that we

have them, that's the scary part of this diagnosis. You're in

remission until you're not. We all get petrified at times and for me,

it's the support of friends and family that keep me going on a day to

day basis. Some day's I " go " easier than others, and some day's are

just endless worries and many tears. All we can do is share our

experiences, hoping to gain comfort and knowledge and this group is

wonderful on both of those fronts. Welcome again - and I look forward

to hearing from you.

Ellen

>

> Hi, I just completed chemo and had a double mastectomy on 9-7-06.

Will

> start radiation tommorow. (Stage 111bc)I am 52 years old and really

> interested in visiting with anyone with my similar statistics or

anyone

> that might just like to talk. This disease has been devasting to me

and

> I sometimes find it hard to talk with family and friends that have

no

> idea what races through your mind a million times a day.

> Happy thoughts!

>

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