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Hi Debra,

Thats what I had when I had my chemo in 1990. I got the Fluorouracil and

Methotrexate in an IV push the first two Tues. of the month, then the third

week I took Cytoxan pills and the fourth week I rested and then started over

for the 6 months. I was receptor neg. so couldn's do the Tamoxifen but I am

doing fine so far. I had no problems at all. I little bit of nausea but the

antinausea pills took care of that. I didn't loose all of my hair it just

thinned. I will keep you in my prayers.

Hugs

nne

Breast Cancer Patients Soul Mates for Life

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Has anyone taken

> the following combination re: chemp therapy....Fluorouracil,

> Methotrexate and Cytoxan????

> My oncologist has suggested chemo but has admitted that I am a

> borderline case and radiation and change from tamoxifrn to arimex

> would be enough. The only reason she is leaning slightly more

> towards chemo is that the hormone levels of this tumor were lower

> than the first bout I had three years ago.. thanks for any info...I

> have a decision to make and respect your opinions....much love, deb

>

>

>

>

>

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Guest guest

Thanks nne....the only reason she is suggesting the chemo is

that first time hormone levels were 90%/70%...this time the numbers

are much lower...40%/30%...She also said my hair would thin but not

all fall out...Thanks for your imput...lots of thinking to do and you

have helped....love, deb

> Hi Debra,

> Thats what I had when I had my chemo in 1990. I got the

Fluorouracil and

> Methotrexate in an IV push the first two Tues. of the month, then

the third

> week I took Cytoxan pills and the fourth week I rested and then

started over

> for the 6 months. I was receptor neg. so couldn's do the Tamoxifen

but I am

> doing fine so far. I had no problems at all. I little bit of nausea

but the

> antinausea pills took care of that. I didn't loose all of my hair

it just

> thinned. I will keep you 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

> Has anyone taken

>

>

> > the following combination re: chemp therapy....Fluorouracil,

> > Methotrexate and Cytoxan????

> > My oncologist has suggested chemo but has admitted that I am a

> > borderline case and radiation and change from tamoxifrn to arimex

> > would be enough. The only reason she is leaning slightly more

> > towards chemo is that the hormone levels of this tumor were lower

> > than the first bout I had three years ago.. thanks for any

info...I

> > have a decision to make and respect your opinions....much love,

deb

> >

> >

> >

> >

> >

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Guest guest

Thanks nne....the only reason she is suggesting the chemo is

that first time hormone levels were 90%/70%...this time the numbers

are much lower...40%/30%...She also said my hair would thin but not

all fall out...Thanks for your imput...lots of thinking to do and you

have helped....love, deb

> Hi Debra,

> Thats what I had when I had my chemo in 1990. I got the

Fluorouracil and

> Methotrexate in an IV push the first two Tues. of the month, then

the third

> week I took Cytoxan pills and the fourth week I rested and then

started over

> for the 6 months. I was receptor neg. so couldn's do the Tamoxifen

but I am

> doing fine so far. I had no problems at all. I little bit of nausea

but the

> antinausea pills took care of that. I didn't loose all of my hair

it just

> thinned. I will keep you 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

> Has anyone taken

>

>

> > the following combination re: chemp therapy....Fluorouracil,

> > Methotrexate and Cytoxan????

> > My oncologist has suggested chemo but has admitted that I am a

> > borderline case and radiation and change from tamoxifrn to arimex

> > would be enough. The only reason she is leaning slightly more

> > towards chemo is that the hormone levels of this tumor were lower

> > than the first bout I had three years ago.. thanks for any

info...I

> > have a decision to make and respect your opinions....much love,

deb

> >

> >

> >

> >

> >

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Guest guest

--

Hi Debra, I also had CMF, 9 courses, concurrent with radiation. If

you have any questions just let me know!

Hugs, Elaine

- In breastcancer2 , " Debra " <dacl1217@a...> wrote:

> the following combination re: chemp therapy....Fluorouracil,

> Methotrexate and Cytoxan????

> My oncologist has suggested chemo but has admitted that I am a

> borderline case and radiation and change from tamoxifrn to arimex

> would be enough. The only reason she is leaning slightly more

> towards chemo is that the hormone levels of this tumor were lower

> than the first bout I had three years ago.. thanks for any

info...I

> have a decision to make and respect your opinions....much love, deb

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Guest guest

Hello Amber,

My bc was infiltrating ductal, stage 1, no nodes involved. It was

moderately aggressive and highly HR+. My surgeon and my med onc both

said I had to have chemo because I was under 50 years old and still

having periods. My rads onc thought it was a good idea, but not

absolutely necessary. I went with the chemo as I wanted any edge I

could get.

Because I had no positive nodes, I was able to have CMF, otherwise I

would have had CAF.

My med onc calls CMF " chemo light " . In October it will be 7 years

since my last treatment, and I am still cancer free.

Hugs,

Elaine

> Hi Elaine:

>

> <<I also had CMF, 9 courses, concurrent with radiation. If you

have any

> questions just let me know!>>

>

> ==>Was yours a slow growing or low grade cancer? I'd rather have

CMF than

> AC+T myself. How badly did your hair thin on the CMF?

>

> ~Amber

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