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DONNA I NOTICED THE LAST FEW DAYS THERE WASNT MUCH MAIL GOING THROUGH .... I FIGURED EVERYONE WAS JUST TO BUSY TO WRITE ,,,

ROMIE

Hi Friends,

My daughter has been using the puter again finishing up a research paper for college and then today when I finally have opportunity to catch up on my emails, I see I haven't gotten any. I think our internet and email was on the blink once again.

I felt so sorry for my daughter last night. She had worked for days on a 5 page research paper due today. At midnight last night our puter froze up and she was trying to help it along and lost 3 out of 4 pages she had completed. She was crying so hard over this. Her brother came in and saved the day. He knew we had auto save on the puter and was able to retreive most of what she lost. She would have had to start over if he hadn't found it. I have never even heard of the auto save setting.

My neurologist went over my MRI results with me. I do have 2 bulging discs, but so far they are not pressing on nerves, so I will just need pain meds and physical therapy for now. I am very very thankful for that. I have had 3 major surgeries since March and I have had enough. I am not sure I would do a back surgery anyway. I did tell him how his nurse scared me so bad and he took the heat for that. He didn't feel like I needed to hear bulging discs over the phone. Go figure!!

Thank you all for the lovely Christmas cards. , I got yours today, and wondered if I was going to open it and find a snowball (I was hoping)!!!

I hope I haven't missed too much news. I have gone to the LUPIES board but it is not as easy to catch up on news there.

Hope you are all having a pain free night.

Love, Donna

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  • 4 months later...
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--welcome sandy my name is cheryl i'm a 8 yr bc free and wanted to

say girl we all are here for you we been through it or going through

it and sweetie if you scared and just nbed somebody to lean oon we

are here girl we are one big family in breast cancer and each know

you pain and we woill let you have the whole board and let you talk

but we will pray with you we will cryu with you we will laugh with

you but whatever you do dont ever give up that positve attitude keep

that positve attitude donr think you going to die just stay with

hope and chemo helping that is a good sign and it could put it to

stop, just keep hope girl dont ever stop your hope i will put you in

my prayer group my name is cheryl and there is z bunch of great

ladies here so just write you want they all will help you through it

and dont give up girl we are all there for you and welcome to this

group you in the best on the web in my book

cheryl

> Hi everyone,

>

> I just joined the group today and want to introduce myself. My

name is Sandi. I was diagnosed with breast cancer on January 15th

of this year. I thought that the surgeon standing over me that day

telling me that he was sorry but it is what we suspected was the

worse day of my life but it got worse when he told me that the lymph

nodes were infected and yes it did spread. Both to my skull and to

my spine. They said that I am not curable but I am treatable. The

good part is that the chemo is working. The tumors are shrinking.

At least the ones in my breast because those are the only ones that

my Oncologist was able to measure with her fingers. But next week I

am taking new scans and we will have a better picture. The bad part

is that although the chemo is saving my life, it isn't easy dealing

with the side effects. It is worth it of course and I will get

through it but I guess I need a bit of support from people that have

or are walking in my shoes.

>

> Sandi

>

>

>

>

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Sandi,

Welcome. I'm so sorry your initial diagnosis was so scary. Although this is

a wonderful group of women, most of the women here are not yet stage IV.

So, while you're more than welcome and we will do our best to help you, you

might find more helpful advice at a Stage IV spinoff group. To sign up, go to:

http://groups.yahoo.com/group/stageivbreastcancer/

Do whatever you did to join here.

Meanwhile, there are some women here whose cancer has metasticized, and

cancer is cancer. We all live with that fear and none of us know how long

we'll live for. The only thing we know for sure is we will die, from cancer

or something else.

That's great that the tumors in your breast are shrinking. The others most

likely are, too; you just need the tests to confirm. Not everyone on this

list has been through chemo but a lot of us have and yes, it sucks. I

didn't vomit, but I was very weak and ended up hospitalized twice. There's

no way around it. You just have to find a way to live with it that's got

enough quality of life to make it worthwhile. All sorts of different things

help. This email group, an in-person support group, reading books by

survivors, reading plain old escapist fun books, taking whatever support

you can from your family and/or friends, and time. Time is the best. Things

that seem totally impossible now can and do become part of everyday life,

eventually.

Many women live with Stage IV cancer for way longer than their doctors ever

thought possible. I wish you the very best, and hope that we can help you

through the really tough parts.

Jill

At 10:21 PM 4/30/2003 -0400, you wrote:

>Hi everyone,

>

>I just joined the group today and want to introduce myself. My name is

>Sandi. I was diagnosed with breast cancer on January 15th of this

>year. I thought that the surgeon standing over me that day telling me

>that he was sorry but it is what we suspected was the worse day of my life

>but it got worse when he told me that the lymph nodes were infected and

>yes it did spread. Both to my skull and to my spine. They said that I am

>not curable but I am treatable. The good part is that the chemo is

>working. The tumors are shrinking. At least the ones in my breast

>because those are the only ones that my Oncologist was able to measure

>with her fingers. But next week I am taking new scans and we will have a

>better picture. The bad part is that although the chemo is saving my

>life, it isn't easy dealing with the side effects. It is worth it of

>course and I will get through it but I guess I need a bit of support from

>people that have or are walking in my shoes.

>

>Sandi

>

>

>

>

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  • 4 weeks later...
Guest guest

Eva,

I will keep your Dad in my prayers.

Hugs

nne

Breast Cancer Patients Soul Mates for Life

http://www.geocities.com/chucky5741/breastcancerpatients.html

Check out my breast cancer ornaments at:

http://www.geocities.com/chucky5741/bcornament.html

also check out my other ornaments and lots of nice gifts at:

http://www.cancerclub.com

Hi Everyone

Hi,I just want to ask you all for a prayer for my dad.He had a heart

attack tonight plus he has phnmonia.It was real touch and go there

for a while but the dr. got him stabalized and when I left the

hospital he was looking alot better.Will update you all when I know

more tomorrow.

Thank you all Eva

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He's on my prayer list ....keep us posted. doris

> Hi,I just want to ask you all for a prayer for my dad.He had a heart

> attack tonight plus he has phnmonia.It was real touch and go there

> for a while but the dr. got him stabalized and when I left the

> hospital he was looking alot better.Will update you all when I know

> more tomorrow.

> Thank you all Eva

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  • 1 month later...
Guest guest

Jeana, you are soooooooooo evil...just you wait until you get here for

the race and hear me when I go onstage. I might embarass you and ask

you to come up and say a few words. HA! Remember my husband is the

race chair so he will let me do it!

> Oh I think Doris will have some suggestion for you lol. How exciting

to be

> chosen I know you will do a good job, maybe you will remember where

you are

> from. lol Doris didnt hehe

> Hi everyone

>

>

> > Hope everyone is doing okay.I thought I would check in, I haven't

> > posted in a while, although I do read the posts every single day. I

> > thought I would share some exciting news with you. I have been

> > chosen by our local health district to be in a series of media ads,

> > promoting breast cancer awareness. The health district was the

> > receipient of a grant from the Komen Foundation, and it is being

> > used for his campaign. A group of women from various walks of life

> > and ethnic backgrounds, bc survivors all, will be interviewed by the

> > local newspaper, and also do a 60 second radio spot, about the

> > importance of " breaking the silence " . One survivor will be

> > featured each week, and in October, a large group interview with

> > photos and stories, will be in the paper. I am so excited, and so

> > honored to represent bc survivors. I was asked to think about what

> > was the most important thing to me.....it is a hard choice. Early

> > detection? Mammograms, BSE,positive outlook? Any suggestions?

> > Anyway I will keep you posted on how this goes along.

> > Hugs and Loves to all

> > Elaine

> >

> >

> >

> >

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Hi Sue,

I have had several bone scan since my diagnosis in 1990. To me the worst part is

the time you have to wait between the injection and actual scan. You are in my

prayers.

Hugs

nne

Breast Cancer Patients Soul Mates for Life

http://www.geocities.com/chucky5741/breastcancerpatients.html

Check out my breast cancer ornaments at:

http://www.geocities.com/chucky5741/bcornament.html

also check out my other ornaments and lots of nice gifts at:

http://www.cancerclub.com

Hi Everyone

Hope everyone is doing well today. I go for my first bone scan this

morning. A little nervous but everyone keeps telling me its just

routine. I hope everyone has a great day.

Sue

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Guest guest

If I were you, I'd use the time to say you were thankful you had the kind

of breasts that respond well to mammograms and make early detection

possible. Many women, like myself, have dense cystic breasts, so that

tumors don't show up in mammograms or even self-exams. When I was diagnosed

with Stage III bc, my mammogram was clean! It was ultrasound that showed

something was wrong, and a biopsy that showed that the cancer had already

travelled through every possible conduit and said I very likely had cancer

in my veins and lymph nodes, which turned out to be true. I'd say something

like " I'm so grateful I was born with the kind of breasts that respond well

to mammograms. If you're a woman and you have dense or cystic breasts, ask

your doctor about ultrasounds, especially if you have a family history of

breast cancer. If you don't know what dense or cystic breasts are, make an

ob/gyn appointment and find out. "

Of course that's just me, but there are many women in my position, and now

it turns out that hormone replacement drugs can cause dense breast tissue

and make it impossible for mammograms to find early detection, so it would

be a way of using your time to help others. However, other women's

suggestions are good, too, and ultimately, it's your choice. Whatever you

feel most grateful for is what you should say. If you're not sure, sit down

alone, in a quiet space, and allow the thoughts to come to you. I'm sure

you'll find what's right for you.

Jill

p.s.Congrats! Sounds like fun. :)

>button50_1 wrote:

>Hope everyone is doing okay.I thought I would check in, I haven't

>posted in a while, although I do read the posts every single day. I

>thought I would share some exciting news with you. I have been

>chosen by our local health district to be in a series of media ads,

>promoting breast cancer awareness. The health district was the

>receipient of a grant from the Komen Foundation, and it is being

>used for his campaign. A group of women from various walks of life

>and ethnic backgrounds, bc survivors all, will be interviewed by the

>local newspaper, and also do a 60 second radio spot, about the

>importance of " breaking the silence " . One survivor will be

>featured each week, and in October, a large group interview with

>photos and stories, will be in the paper. I am so excited, and so

>honored to represent bc survivors. I was asked to think about what

>was the most important thing to me.....it is a hard choice. Early

>detection? Mammograms, BSE,positive outlook? Any suggestions?

>Anyway I will keep you posted on how this goes along.

>Hugs and Loves to all

>Elaine

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Guest guest

Best of luck, Sue. It *is* routine, but that doesn't make it not scary. For

the first time this year, I was terrified waiting for the results of my Pap

Smear. I think it's normal for us, now that we've had our " safety bubble "

popped, to become very anxious about every little test. It's just another

side effect of breast cancer... I hope it will wear off with time.

Jill

At 10:35 AM 7/11/2003 +0000, you wrote:

>Hope everyone is doing well today. I go for my first bone scan this

>morning. A little nervous but everyone keeps telling me its just

>routine. I hope everyone has a great day.

>Sue

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Cool. I'm so glad for you, Georgia, AND of course glad that it came out

ok!!! My HMO doesn't use that test. But I've been told many times I need to

work on patience and faith, so maybe it's not a bad thing that I have to

wait for test results. I'm having some more tests soon; one (colonoscopy)

I'll find out right away and I interviewed the doctor first to make sure

he'd tell me straight out if something looked like it could be cancer. The

other is just a bone density test for osteoporosis. Not that osteo... isn't

a serious medical problem. But I'm less scared of that than cancer. I don't

think you die directly from osteo, though I'm sure it's very painful and

scary to have.

Jill

At 10:24 PM 7/12/2003 -0700, you wrote:

>When I went for my pap this year they offered me a new test that tells you

>the results before you leave the office. It is called pap sure, and it

>uses a disposable light the see any color changes in the uterus....It was

>good to leave the office with an " everything looks ok, while waiting for

>the regular test results....georgia

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Forty dollars!!! That's almost the price of taking my daughter and a friend

to the movies. It's certainly worth it, in my opinion. But here in Boston

it would probably be more like $140 if not $1400. The standard of living is

very high, here.

So what were your bone density test results?

There's probably no need for you to have a colonoscopy. The only reason I'm

getting one is that my mother died of bc and her father died of colon

cancer. It's not standard procedure.

Best of luck on the estrogen test.

I keep forgetting if it was you and I or Gloria and I who were radiation

twins. It seems like we're Arimidex twins now. :) I still remember your

classic " Georgia peach fuzz. " Are you wearing your hair now that school is

out? It's probably much longer than one and a half inches. Can you tell me

how long it is so I can feel sorry for myself? :) I hope I was right and it

is you who gets to shed the wig and wear her " new do. "

Jill

At 07:18 PM 7/13/2003 -0700, you wrote:

>My insurance did not pay for the papsure either. The office said it is so

>new insurances are not paying for it. It cost me $40.00 up front, but

>since it was two weeks before getting my other results, it was well worth

>the money.....I'm not ready for the colonoscopy yet...all in due time. I

>picked up the results from my bone density test, and hope to have the

>results from the estrogen test soon......2 bench marks I plan to keep an

>eye on......georgia

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Oh, Lucilla. I wish I had them. I'm sorry for your colon cancer scare. I

know things are really rough for you now. All I can do is wish you peace

and love and grace. Those are magic words in a way, but not in the way we'd

like them to be...

Jill

I am scare now to do another one, this breast cancer thing is sure heavy.

Tell me the magic words...

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