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I have been on this website since Oct. and have been scared to talk to anyone !

I was diagnosed with BC in Oct. 2003, my mother and 1st cousin died from it

around ther early sixtys, I got it at 46 (my birthday actually) It started with

a routine mammo. second set mammo. and then biopsy. I went in for a lumpectomy,

and the doctor said there was so much in there if they took any more out I

would have no breast, so I went back in and had a masectomy. My doctor was so

amazed that I was so full of cancer and it had not spread. He even used me in

one of his lectures. I've never needed chemo or any type of meds. They didn't

even have to take my lymph. My mother was not that lucky, and I realize that so

many other women aren't either. Thats why I have been scared to talk to anyone,

because I haven't gone through even a quarter of what most women have through.

I don't even feel worthy to be here. I love and admire all you women who have

fought this fight, and for anyone who

is newly diagnosed, try not to be scared it's not always bad news. The only

thing I've had to worry about is how to get my reconstructive surgery finished.

I'm half done, but that's nothing!!! Not considerd what other women have gone

through. I salute you!!! Love You All !!!!

DING

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Hi Ding,

welcome to the group that no one voluntarily joins :-)

I'm glad you're doing well. Did you have genetic testing since you have

relatives with bc?

-

Ding Mancuso wrote on 12/22/2006, 5:04 AM:

> I have been on this website since Oct. and have been scared to talk to

> anyone ! I was diagnosed with BC in Oct. 2003, my mother and 1st

> cousin died from it around ther early sixtys, I got it at 46 (my

> birthday actually) It started with a routine mammo. second set mammo.

> and then biopsy. I went in for a lumpectomy, and the doctor said

> there was so much in there if they took any more out I would have no

> breast, so I went back in and had a masectomy. My doctor was so

> amazed that I was so full of cancer and it had not spread. He even

> used me in one of his lectures. I've never needed chemo or any type of

> meds. They didn't even have to take my lymph. My mother was not that

> lucky, and I realize that so many other women aren't either. Thats

> why I have been scared to talk to anyone, because I haven't gone

> through even a quarter of what most women have through. I don't even

> feel worthy to be here. I love and admire all you women who have

> fought this fight, and for anyone who

> is newly diagnosed, try not to be scared it's not always bad news. The

> only thing I've had to worry about is how to get my reconstructive

> surgery finished. I'm half done, but that's nothing!!! Not considerd

> what other women have gone through. I salute you!!! Love You All !!!!

>

>

> DING

>

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Welcome to the group. Did he say why they didn't take any lymph nodes and why no

chemo or anything? Normally unless your breast cancer is DCIS you always have

either chemo and radiation, or just chemo or just radiation.

Hugs

nne

Breast Cancer Patients Soul Mates for Life

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

BreastCancerStories.com

http://www.breastcancerstories.com/content/view/433/161/

Angel Feather Loomer

www.angelfeatherloomer.blogspot.com

Check out my other ornaments at

www.geocities.com/chucky5741/bcornament.html

Lots of info and gifts at:

www.cancerclub.com

NOT SURE !

I have been on this website since Oct. and have been scared to talk to anyone

! I was diagnosed with BC in Oct. 2003, my mother and 1st cousin died from it

around ther early sixtys, I got it at 46 (my birthday actually) It started with

a routine mammo. second set mammo. and then biopsy. I went in for a lumpectomy,

and the doctor said there was so much in there if they took any more out I would

have no breast, so I went back in and had a masectomy. My doctor was so amazed

that I was so full of cancer and it had not spread. He even used me in one of

his lectures. I've never needed chemo or any type of meds. They didn't even have

to take my lymph. My mother was not that lucky, and I realize that so many other

women aren't either. Thats why I have been scared to talk to anyone, because I

haven't gone through even a quarter of what most women have through. I don't

even feel worthy to be here. I love and admire all you women who have fought

this fight, and for anyone who

is newly diagnosed, try not to be scared it's not always bad news. The only

thing I've had to worry about is how to get my reconstructive surgery finished.

I'm half done, but that's nothing!!! Not considerd what other women have gone

through. I salute you!!! Love You All !!!!

DING

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Hi Ding, I know exactly how you feel. I had a bilateral mastectomy for ILC this

year and had 2 nodes removed (sentinal nodes) that were clear so I didn't have

chemo or radiation either. It does make you feel like your experience is

nothing compared to what you read here. There are some very courageous and

inspiring women here. But as one of the ladies at the cancer library told me

that no matter what my personal experience was I was still a survivor and not to

belittle myself by thinking otherwise. So you remember that too, we are all

survivors!

NOT SURE !

I have been on this website since Oct. and have been scared to talk to anyone !

I was diagnosed with BC in Oct. 2003, my mother and 1st cousin died from it

around ther early sixtys, I got it at 46 (my birthday actually) It started with

a routine mammo. second set mammo. and then biopsy. I went in for a lumpectomy,

and the doctor said there was so much in there if they took any more out I would

have no breast, so I went back in and had a masectomy. My doctor was so amazed

that I was so full of cancer and it had not spread. He even used me in one of

his lectures. I've never needed chemo or any type of meds. They didn't even have

to take my lymph. My mother was not that lucky, and I realize that so many other

women aren't either. Thats why I have been scared to talk to anyone, because I

haven't gone through even a quarter of what most women have through. I don't

even feel worthy to be here. I love and admire all you women who have fought

this fight, and for anyone who

is newly diagnosed, try not to be scared it's not always bad news. The only

thing I've had to worry about is how to get my reconstructive surgery finished.

I'm half done, but that's nothing!!! Not considerd what other women have gone

through. I salute you!!! Love You All !!!!

DING

____________ _________ _________ _________ _________ __

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What a survivor you are! I admire the strength that you have. I

just recently had a mastectomy-December 11, 2006-after a diagnosis of

invasive duct carcinoma. My tumor was caught early through a

mammogram and ultrasound. I am looking at reconstruction. I see my

oncologist on Jan.3 to see what options are for treatment. Also

reconstruction surgeon on January 31, second opinion.

I wish you well and will keep you in my prayers.

Happy Holidays to you and your family.

Jan K

>

> I have been on this website since Oct. and have been scared to talk

to anyone ! I was diagnosed with BC in Oct. 2003, my mother and 1st

cousin died from it around ther early sixtys, I got it at 46 (my

birthday actually) It started with a routine mammo. second set

mammo. and then biopsy. I went in for a lumpectomy, and the doctor

said there was so much in there if they took any more out I would

have no breast, so I went back in and had a masectomy. My doctor was

so amazed that I was so full of cancer and it had not spread. He even

used me in one of his lectures. I've never needed chemo or any type

of meds. They didn't even have to take my lymph. My mother was not

that lucky, and I realize that so many other women aren't either.

Thats why I have been scared to talk to anyone, because I haven't

gone through even a quarter of what most women have through. I don't

even feel worthy to be here. I love and admire all you women who have

fought this fight, and for anyone who

> is newly diagnosed, try not to be scared it's not always bad news.

The only thing I've had to worry about is how to get my

reconstructive surgery finished. I'm half done, but that's

nothing!!! Not considerd what other women have gone through. I

salute you!!! Love You All !!!!

>

>

> DING

>

> __________________________________________________

>

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nne: I don't mean to be stupid but I don't always know what the

abbreviations mean on this web site. What is DCIS?

Thanks.

Jan

& nne Svihlik moochie1@...> wrote:

Welcome to the group. Did he say why they didn't take any lymph nodes

and why no chemo or anything? Normally unless your breast cancer is DCIS you

always have either chemo and radiation, or just chemo or just radiation.

Hugs

nne

Breast Cancer Patients Soul Mates for Life

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

BreastCancerStories.com

http://www.breastcancerstories.com/content/view/433/161/

Angel Feather Loomer

www.angelfeatherloomer.blogspot.com

Check out my other ornaments at

www.geocities.com/chucky5741/bcornament.html

Lots of info and gifts at:

www.cancerclub.com

NOT SURE !

I have been on this website since Oct. and have been scared to talk to anyone !

I was diagnosed with BC in Oct. 2003, my mother and 1st cousin died from it

around ther early sixtys, I got it at 46 (my birthday actually) It started with

a routine mammo. second set mammo. and then biopsy. I went in for a lumpectomy,

and the doctor said there was so much in there if they took any more out I would

have no breast, so I went back in and had a masectomy. My doctor was so amazed

that I was so full of cancer and it had not spread. He even used me in one of

his lectures. I've never needed chemo or any type of meds. They didn't even have

to take my lymph. My mother was not that lucky, and I realize that so many other

women aren't either. Thats why I have been scared to talk to anyone, because I

haven't gone through even a quarter of what most women have through. I don't

even feel worthy to be here. I love and admire all you women who have fought

this fight, and for anyone who

is newly diagnosed, try not to be scared it's not always bad news. The only

thing I've had to worry about is how to get my reconstructive surgery finished.

I'm half done, but that's nothing!!! Not considerd what other women have gone

through. I salute you!!! Love You All !!!!

DING

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DCIS = Ductal Carcinoma In Situ (Stage 0).

-

Jan Koelsch wrote on 12/22/2006, 10:59 PM:

> nne: I don't mean to be stupid but I don't always know what the

> abbreviations mean on this web site. What is DCIS?

>

> Thanks.

> Jan

>

> & nne Svihlik moochie1@...> wrote:

> Welcome to the group. Did he say why they didn't take any

> lymph nodes and why no chemo or anything? Normally unless your breast

> cancer is DCIS you always have either chemo and radiation, or just

> chemo or just radiation.

> Hugs

> nne

> Breast Cancer Patients Soul Mates for Life

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

> BreastCancerStories.com

> http://www.breastcancerstories.com/content/view/433/161/

> Angel Feather Loomer

> www.angelfeatherloomer.blogspot.com

> Check out my other ornaments at

> www.geocities.com/chucky5741/bcornament.html

> Lots of info and gifts at:

> www.cancerclub.com

> NOT SURE !

>

> I have been on this website since Oct. and have been scared to talk to

> anyone ! I was diagnosed with BC in Oct. 2003, my mother and 1st

> cousin died from it around ther early sixtys, I got it at 46 (my

> birthday actually) It started with a routine mammo. second set mammo.

> and then biopsy. I went in for a lumpectomy, and the doctor said there

> was so much in there if they took any more out I would have no breast,

> so I went back in and had a masectomy. My doctor was so amazed that I

> was so full of cancer and it had not spread. He even used me in one of

> his lectures. I've never needed chemo or any type of meds. They didn't

> even have to take my lymph. My mother was not that lucky, and I

> realize that so many other women aren't either. Thats why I have been

> scared to talk to anyone, because I haven't gone through even a

> quarter of what most women have through. I don't even feel worthy to

> be here. I love and admire all you women who have fought this fight,

> and for anyone who

> is newly diagnosed, try not to be scared it's not always bad news. The

> only thing I've had to worry about is how to get my reconstructive

> surgery finished. I'm half done, but that's nothing!!! Not considerd

> what other women have gone through. I salute you!!! Love You All !!!!

>

> DING

>

>

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Share on other sites

Thanks.

Jan

ajtf.tm@...> wrote:

DCIS = Ductal Carcinoma In Situ (Stage 0).

-

Jan Koelsch wrote on 12/22/2006, 10:59 PM:

> nne: I don't mean to be stupid but I don't always know what the

> abbreviations mean on this web site. What is DCIS?

>

> Thanks.

> Jan

>

> & nne Svihlik moochie1@...> wrote:

> Welcome to the group. Did he say why they didn't take any

> lymph nodes and why no chemo or anything? Normally unless your breast

> cancer is DCIS you always have either chemo and radiation, or just

> chemo or just radiation.

> Hugs

> nne

> Breast Cancer Patients Soul Mates for Life

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

> BreastCancerStories.com

> http://www.breastcancerstories.com/content/view/433/161/

> Angel Feather Loomer

> www.angelfeatherloomer.blogspot.com

> Check out my other ornaments at

> www.geocities.com/chucky5741/bcornament.html

> Lots of info and gifts at:

> www.cancerclub.com

> NOT SURE !

>

> I have been on this website since Oct. and have been scared to talk to

> anyone ! I was diagnosed with BC in Oct. 2003, my mother and 1st

> cousin died from it around ther early sixtys, I got it at 46 (my

> birthday actually) It started with a routine mammo. second set mammo.

> and then biopsy. I went in for a lumpectomy, and the doctor said there

> was so much in there if they took any more out I would have no breast,

> so I went back in and had a masectomy. My doctor was so amazed that I

> was so full of cancer and it had not spread. He even used me in one of

> his lectures. I've never needed chemo or any type of meds. They didn't

> even have to take my lymph. My mother was not that lucky, and I

> realize that so many other women aren't either. Thats why I have been

> scared to talk to anyone, because I haven't gone through even a

> quarter of what most women have through. I don't even feel worthy to

> be here. I love and admire all you women who have fought this fight,

> and for anyone who

> is newly diagnosed, try not to be scared it's not always bad news. The

> only thing I've had to worry about is how to get my reconstructive

> surgery finished. I'm half done, but that's nothing!!! Not considerd

> what other women have gone through. I salute you!!! Love You All !!!!

>

> DING

>

>

Jan Koelsch

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Jan,

There are no stupid questions. DCIS is ductal carcinoma in situ. If you are

going to get breast cancer its the best one to have. Many ladies don't even need

chemo or radiation after it. Its early stage that has not spread to neighboring

tissue. Please feel free to ask any questions you may have.

Hugs

nne

Breast Cancer Patients Soul Mates for Life

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

BreastCancerStories.com

http://www.breastcancerstories.com/content/view/433/161/

Angel Feather Loomer

www.angelfeatherloomer.blogspot.com

Check out my other ornaments at

www.geocities.com/chucky5741/bcornament.html

Lots of info and gifts at:

www.cancerclub.com

NOT SURE !

I have been on this website since Oct. and have been scared to talk to anyone

! I was diagnosed with BC in Oct. 2003, my mother and 1st cousin died from it

around ther early sixtys, I got it at 46 (my birthday actually) It started with

a routine mammo. second set mammo. and then biopsy. I went in for a lumpectomy,

and the doctor said there was so much in there if they took any more out I would

have no breast, so I went back in and had a masectomy. My doctor was so amazed

that I was so full of cancer and it had not spread. He even used me in one of

his lectures. I've never needed chemo or any type of meds. They didn't even have

to take my lymph. My mother was not that lucky, and I realize that so many other

women aren't either. Thats why I have been scared to talk to anyone, because I

haven't gone through even a quarter of what most women have through. I don't

even feel worthy to be here. I love and admire all you women who have fought

this fight, and for anyone who

is newly diagnosed, try not to be scared it's not always bad news. The only

thing I've had to worry about is how to get my reconstructive surgery finished.

I'm half done, but that's nothing!!! Not considerd what other women have gone

through. I salute you!!! Love You All !!!!

DING

__________________________________________________

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