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Hi everyone!

I just joined today and wanted to introduce myself. My name is Val, and

my breast cancer was found in Nov 2006. I had my regular mammo and they

found calcifications that they biopsied a week later. I had a 5.5 mm

tumor, infiltrating ductal, estrgen and progestron negative, HER2/neu

amplified. Lymph nodes were clear. They tell me becasue of the HER2 and

the fact that there have been close family members who have had breast

cancer (including and uncle) that the chemo and Herceptin are

recommended. We, (DH and I)decided to go with it. He wants to keep me

awhile longer if he can :-) I have been to the hospital twice this week

for PET/CT scan and MUGA scans, I get a port put in the 3rd and chemo

starts the 10th. I have been told I WILL lose my hair. I never thiught

this would bother me but I am finding that yeah..maybe I DO want a wig!

My hair stylist/friend said she would help me however she can. We are

going to try and make it as fun as we can, new hair color, but similar

style, funky hats, etc. I am just trying to figure out best time to get

it and how long I may need it?? I know everyone is different. I'll read

some more posts and see what advice I can gather...I basically wanted

to say hello!!

Val

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Hi Val and welcome to the group. I was diagnosed in May 1990 with infiltrating

ductal carcinoma the tumor was 2.5 cm I was Stage II.. I had one bad node out of

23. I had 6 mo of chemo (12 treatments) no radiation or reconstruction. I will

keep you in my prayers. Sounds like you have a good outlook.

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

Newbie here too!

Hi everyone!

I just joined today and wanted to introduce myself. My name is Val, and

my breast cancer was found in Nov 2006. I had my regular mammo and they

found calcifications that they biopsied a week later. I had a 5.5 mm

tumor, infiltrating ductal, estrgen and progestron negative, HER2/neu

amplified. Lymph nodes were clear. They tell me becasue of the HER2 and

the fact that there have been close family members who have had breast

cancer (including and uncle) that the chemo and Herceptin are

recommended. We, (DH and I)decided to go with it. He wants to keep me

awhile longer if he can :-) I have been to the hospital twice this week

for PET/CT scan and MUGA scans, I get a port put in the 3rd and chemo

starts the 10th. I have been told I WILL lose my hair. I never thiught

this would bother me but I am finding that yeah..maybe I DO want a wig!

My hair stylist/friend said she would help me however she can. We are

going to try and make it as fun as we can, new hair color, but similar

style, funky hats, etc. I am just trying to figure out best time to get

it and how long I may need it?? I know everyone is different. I'll read

some more posts and see what advice I can gather...I basically wanted

to say hello!!

Val

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Hi Val,

Another her2 sister! I'm curious what chemo your doctor is recommending.

There were some recent articles about certain treatments shown to be

very effective for er/pr- her2+ women that did not include adriamycin.

Here it is:

Taxotere®-based Regimens with Herceptin® in Women with Early-stage

HER2-Positive Breast Cancer Demonstrate the Highest Reduction in the

Risk of Death to Date and Provide a Treatment Option Without Anthracyclines

Results of Second Planned Interim Analysis of Phase III Study: BCIRG 006

SAN ANTONIO, Dec. 14 /PRNewswire-FirstCall/ -- The Cancer International

Research Group (CIRG) and sanofi-aventis today announced the results from

the second interim efficacy and safety analysis from the BCIRG 006 Phase

III breast cancer study, which confirms, at a 3-year median follow-up, that

Herceptin® combined with Taxotere®-based regimens significantly

improved disease-free survival for women with early HER2-positive breast

cancer.

The BCIRG 006 study randomized patients to receive the control arm AC-T

[4 cycles of doxorubicin (A) and cyclophosphamide © followed by 4 cycles

of Taxotere® (T)], or either of two experimental Herceptin®-(H) and

Taxotere®- based therapies: AC-TH (adds 1 year of Herceptin® treatment

to the AC-T regimen with Herceptin® starting concurrently with

Taxotere®), or TCH (6 cycles of Taxotere® and carboplatin © with 1

year of Herceptin® starting at the first cycle). Patients were

prospectively stratified according to their nodal status and hormone

receptor status.

The primary endpoint was disease-free survival (DFS). Secondary

endpoints included overall survival (OS), safety, including cardiotoxicity,

and pathologic and molecular markers. The safety analysis was performed

by an Independent Data Monitoring Committee.

In terms of a reduction in the risk of death, 41% (p < 0.0041) and

34% (p < 0.017) of patients in the AC-TH and TCH arms, respectively when

compared with the non-Herceptin-containing control arm. The relative

reduction in the risk of relapse was 39% (p < 0.001) and 33% (p =

0.0003) for AC-TH and TCH respectively vs. control. This interim

analysis showed that 92% and 91% of patients were alive at 4 years in

the Herceptin/Taxotere-containing arms (AC- TH and TCH) respectively

compared to 86% in the AC-T arm. Of note, TCH (combination of

Taxotere®/carboplatin/Herceptin®), the regimen without

anthracycline, demonstrated similarly significant improvement in disease

free and overall survival as the AC-TH arm. However, the TCH arm yielded

a five- fold decrease in significant cardiotoxicity when compared to the

anthracycline/Herceptin®-containing arm.

These data were presented at the 29th annual San Breast

Cancer Symposium (SABCS) in San , TX - USA.

" This trial demonstrates an optimal therapeutic index for these

patients with the use of TCH (which did not include doxorubicin), thus

avoiding the significant cardiac damage related to the sequential use of

anthracyclines and Herceptin®, " said Dennis Slamon, PhD, MD, Co-Chair

of the BCIRG 006 study and Director of Clinical and Translational

Research at

UCLA's Jonsson Comprehensive Cancer Center. " In this interim analysis, 6

cycles of chemotherapy in the TCH regimen provided similar benefit as

AC-TH (8 cycles of chemotherapy in total) without increasing

cardiotoxicity. In addition, no secondary leukemias have been observed

so far in the TCH arm compared to four leukemia events in the

anthracycline-containing arms,

although further long term hematologic adverse event follow up will

continue. These data should help influence daily practice with TCH being

considered an option for women with early stage HER2 positive breast

cancer, irrespective of nodal status. "

The cardiac toxicity of the 2 experimental arms significantly

favored the TCH regimen. No cardiac deaths were observed in either arm.

There were 20 congestive heart failure events in AC-TH versus four in

the TCH arm.

Moreover, there were 50% fewer asymptomatic declines in cardiac function

in the TCH arm as compared to AC-TH. Also, in terms of other toxicities,

the TCH arm appeared to be superior to AC-TH with regards to the main

toxicities in particular sensory neuropathy (36.1% vs 49.7%), nail

changes (28.7% vs 43.6%), and myalgia (38.6% vs 55.5%). However, more

grade 3 and 4 thrombocytopenia (5.4% vs 1.2%) and anemia (5.8% vs 3.1%),

were observed in the TCH arm compared to the AC-TH arm.

About the BCIRG 006 Study

The BCIRG 006 study was designed to maximize efficacy while minimizing

toxicity in adjuvant Herceptin®-based therapies. Between April 2001 and

March 2004, the study enrolled 3, 222 women with early stage HER2-positive

breast cancer, with positive axillary lymph nodes (LN) as well as those

without LN involvement.

In this second interim analysis, at a 3-year median follow-up, AC-TH

and TCH significantly improved DFS and OS as compared to the control arm.

The relative reduction in the risk of relapse was 39% (p < 0.001) and 33%

(p = 0.0003) respectively, for AC-TH and TCH vs control. The relative

reduction in the risk of death was 41% (p < 0.0041) and 34% (p < 0.017)

respectively, for AC-TH and TCH vs control.

In addition, the absolute DFS benefit at 4 years is similar for the two

Herceptin®-containing arms (6% and 5% for AC-TH and TCH, respectively).

Notably, the same level of DFS and OS benefit was also obtained for the 29%

of node negative patients enrolled in the study.

In terms of safety, there was a significant difference in the major

toxicity that has been consistently seen with Herceptin®-based therapies

i.e. cardiac toxicity. Common to all of the Herceptin® adjuvant trials

was the evaluation of congestive heart failure and cardiac-related deaths.

As mentioned above, the cardiac toxicity of the 2 experimental arms

significantly favored the TCH regimen. Further, in terms of other

toxicities, the TCH regimen appeared to also be superior to the AC-TH arm.

The BCIRG investigators and leadership wish to express their deep

appreciation to the women who willingly participated in this randomized

controlled trial and their commitment to improving outcomes for all women

challenged with breast cancer. Slamon noted that, " They are our colleagues

in this study rather than the research subjects. "

The study was sponsored by sanofi-aventis, had financial support from

Genentech, and was conducted by CIRG.

Indications and Usage

Breast Cancer

Taxotere® is indicated for the treatment of patients with locally

advanced or metastatic breast cancer after failure of prior chemotherapy.

Taxotere® in combination with doxorubicin and cyclophosphamide is

indicated for the adjuvant treatment of patients with operable

node-positive breast cancer.

About TAXOTERE®

Important safety information

WARNING: Taxotere® treatment can cause serious, physically limiting,

and potentially life-threatening side effects, such as infection, low

blood-cell counts, allergic reaction and retention of excess fluid (edema).

Taxotere® should not be given to patients with low white-blood-cell

counts, abnormal liver function, or a history of allergic reactions to

Taxotere® or any of the ingredients in Taxotere®.

Before each Taxotere® treatment, all patients treated with

Taxotere® must receive another medicine called dexamethasone. This drug

can help reduce the risk of fluid retention (edema) and allergic reactions.

Taxotere® should be administered only under the supervision of a

qualified physician experienced in the use of anticancer treatments.

Appropriate management of complications is possible only when adequate

diagnostic and treatment facilities are readily available.

Treatment-related acute myeloid leukemia (AML) has occurred in patients

given anthracyclines and/or cyclophosphamide, including use with

Taxotere® in adjuvant therapy for breast cancer. The most common severe

side effects are low white-blood-cell count, anemia, fatigue, diarrhea, and

mouth and throat irritation. Low white-blood-cell count can lead to

life-threatening infections. The earliest sign of infection may be fever,

so tell your doctor right away if you have a fever. Other common side

effects from Taxotere® include nausea, vomiting, hair loss, rash,

infusion-site reactions, odd sensations (such as numbness, tingling, or

burning) or weakness in the hands and feet, nail changes, muscle and/or

bone pain, or excessive tearing.

Because of the potential risk of fetal harm, pregnant women should not

receive Taxotere®. Women of childbearing potential should avoid becoming

pregnant during treatment with Taxotere®.

Before receiving Taxotere®, tell your doctor if

* You have any allergies

* You are taking any other medicines -- including nonprescription

(over-the-counter) drugs, vitamins, and dietary or herbal supplements

When taking Taxotere®, contact your doctor if

* You have symptoms of an allergic reaction (warm sensation,

tightness in

your chest, itching/hives, or shortness of breath)

* You experience any other side effects

For full prescribing information, including boxed WARNING, call

or visit

http://www.fda.gov/cder/foi/label/2006/020449s039lbl.pdf.

About CIRG:

BCIRG is the breast cancer division of the Cancer International

Research Group (CIRG). CIRG has performed a number of new and innovative

clinical trials with new cancer therapies. Active participation by its

global network of dedicated cancer research leaders and investigators has

made CIRG the success it is today. The organization is dedicated to

bringing rational and innovative therapeutic concepts into the clinical

trial setting through translational approaches based on the underlying

biology of the disease. To further this objective, CIRG recently merged

with Translational Oncology Research International (TORI). TORI is a

smaller clinical trials group directly linked to several basic research

laboratories in which new therapeutic molecules are evaluated.

CIRG has offices located in Paris (France) and Edmonton Alberta

(Canada). For information about CIRG, please visit our website:

http://www.cirg.org.

Valma wrote on 12/28/2006, 4:47 PM:

> Hi everyone!

> I just joined today and wanted to introduce myself. My name is Val, and

> my breast cancer was found in Nov 2006. I had my regular mammo and they

> found calcifications that they biopsied a week later. I had a 5.5 mm

> tumor, infiltrating ductal, estrgen and progestron negative, HER2/neu

> amplified. Lymph nodes were clear. They tell me becasue of the HER2 and

> the fact that there have been close family members who have had breast

> cancer (including and uncle) that the chemo and Herceptin are

> recommended. We, (DH and I)decided to go with it. He wants to keep me

> awhile longer if he can :-) I have been to the hospital twice this week

> for PET/CT scan and MUGA scans, I get a port put in the 3rd and chemo

> starts the 10th. I have been told I WILL lose my hair. I never thiught

> this would bother me but I am finding that yeah..maybe I DO want a wig!

> My hair stylist/friend said she would help me however she can. We are

> going to try and make it as fun as we can, new hair color, but similar

> style, funky hats, etc. I am just trying to figure out best time to get

> it and how long I may need it?? I know everyone is different. I'll read

> some more posts and see what advice I can gather...I basically wanted

> to say hello!!

> Val

>

>

>

>

>

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--Thanks for the info! I, in fact will be put on Taxotere and Cyclo

(as the nurses were calling it) Along with the Herceptin. My older

sister (who is a 13 year survivior and a Home Hospice Nurse) says these

are commonly used. Little Sis has to make sure she takes her pathology

report when she visits her this weekend LOL! Sometimes having a sister

like this is good but sometimes it isn't. :-) She probably knows TOO

much about the condition! Ahh, but she means well! I am looking forward

to being in this group, looks like I will get lot's of good advice and

support.

Val

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my diagnosis came prior to the san antonio conference - I'm early

stage, her2+, no node involvement, and had A/C (which I tolerated

remarkably well) followed by taxotere (which kicked my ass) and

herceptin. I finished taxotere in the middle of november (but am

still experiencing the effects - just lost a nail :( and one is

about to fall off...)and am on herceptin till next summer...

peace

marisa

>

> Hi Val,

>

> Another her2 sister! I'm curious what chemo your doctor is

recommending.

> There were some recent articles about certain treatments shown to

be

> very effective for er/pr- her2+ women that did not include

adriamycin.

>

> Here it is:

>

> Taxotere®-based Regimens with Herceptin® in Women with Early-

stage

> HER2-Positive Breast Cancer Demonstrate the Highest Reduction in

the

> Risk of Death to Date and Provide a Treatment Option Without

Anthracyclines

>

> Results of Second Planned Interim Analysis of Phase III Study:

BCIRG 006

>

> SAN ANTONIO, Dec. 14 /PRNewswire-FirstCall/ -- The Cancer

International

> Research Group (CIRG) and sanofi-aventis today announced the

results from

> the second interim efficacy and safety analysis from the BCIRG 006

Phase

> III breast cancer study, which confirms, at a 3-year median follow-

up, that

> Herceptin® combined with Taxotere®-based regimens significantly

> improved disease-free survival for women with early HER2-positive

breast

> cancer.

>

> The BCIRG 006 study randomized patients to receive the

control arm AC-T

> [4 cycles of doxorubicin (A) and cyclophosphamide © followed by

4 cycles

> of Taxotere® (T)], or either of two experimental Herceptin®-

(H) and

> Taxotere®- based therapies: AC-TH (adds 1 year of Herceptin®

treatment

> to the AC-T regimen with Herceptin® starting concurrently with

> Taxotere®), or TCH (6 cycles of Taxotere® and carboplatin ©

with 1

> year of Herceptin® starting at the first cycle). Patients were

> prospectively stratified according to their nodal status and

hormone

> receptor status.

>

> The primary endpoint was disease-free survival (DFS).

Secondary

> endpoints included overall survival (OS), safety, including

cardiotoxicity,

> and pathologic and molecular markers. The safety analysis was

performed

> by an Independent Data Monitoring Committee.

>

> In terms of a reduction in the risk of death, 41% (p <

0.0041) and

> 34% (p < 0.017) of patients in the AC-TH and TCH arms,

respectively when

> compared with the non-Herceptin-containing control arm. The

relative

> reduction in the risk of relapse was 39% (p < 0.001) and 33% (p =

> 0.0003) for AC-TH and TCH respectively vs. control. This interim

> analysis showed that 92% and 91% of patients were alive at 4 years

in

> the Herceptin/Taxotere-containing arms (AC- TH and TCH)

respectively

> compared to 86% in the AC-T arm. Of note, TCH (combination of

> Taxotere®/carboplatin/Herceptin®), the regimen without

> anthracycline, demonstrated similarly significant improvement in

disease

> free and overall survival as the AC-TH arm. However, the TCH arm

yielded

> a five- fold decrease in significant cardiotoxicity when compared

to the

> anthracycline/Herceptin®-containing arm.

>

> These data were presented at the 29th annual San

Breast

> Cancer Symposium (SABCS) in San , TX - USA.

> " This trial demonstrates an optimal therapeutic index for

these

> patients with the use of TCH (which did not include doxorubicin),

thus

> avoiding the significant cardiac damage related to the sequential

use of

> anthracyclines and Herceptin®, " said Dennis Slamon, PhD, MD, Co-

Chair

> of the BCIRG 006 study and Director of Clinical and Translational

> Research at

> UCLA's Jonsson Comprehensive Cancer Center. " In this interim

analysis, 6

> cycles of chemotherapy in the TCH regimen provided similar benefit

as

> AC-TH (8 cycles of chemotherapy in total) without increasing

> cardiotoxicity. In addition, no secondary leukemias have been

observed

> so far in the TCH arm compared to four leukemia events in the

> anthracycline-containing arms,

> although further long term hematologic adverse event follow up will

> continue. These data should help influence daily practice with TCH

being

> considered an option for women with early stage HER2 positive

breast

> cancer, irrespective of nodal status. "

>

> The cardiac toxicity of the 2 experimental arms significantly

> favored the TCH regimen. No cardiac deaths were observed in either

arm.

> There were 20 congestive heart failure events in AC-TH versus four

in

> the TCH arm.

> Moreover, there were 50% fewer asymptomatic declines in cardiac

function

> in the TCH arm as compared to AC-TH. Also, in terms of other

toxicities,

> the TCH arm appeared to be superior to AC-TH with regards to the

main

> toxicities in particular sensory neuropathy (36.1% vs 49.7%), nail

> changes (28.7% vs 43.6%), and myalgia (38.6% vs 55.5%). However,

more

> grade 3 and 4 thrombocytopenia (5.4% vs 1.2%) and anemia (5.8% vs

3.1%),

> were observed in the TCH arm compared to the AC-TH arm.

> About the BCIRG 006 Study

> The BCIRG 006 study was designed to maximize efficacy while

minimizing

> toxicity in adjuvant Herceptin®-based therapies. Between April

2001 and

> March 2004, the study enrolled 3, 222 women with early stage HER2-

positive

> breast cancer, with positive axillary lymph nodes (LN) as well as

those

> without LN involvement.

> In this second interim analysis, at a 3-year median follow-

up, AC-TH

> and TCH significantly improved DFS and OS as compared to the

control arm.

> The relative reduction in the risk of relapse was 39% (p < 0.001)

and 33%

> (p = 0.0003) respectively, for AC-TH and TCH vs control. The

relative

> reduction in the risk of death was 41% (p < 0.0041) and 34% (p <

0.017)

> respectively, for AC-TH and TCH vs control.

> In addition, the absolute DFS benefit at 4 years is similar

for the two

> Herceptin®-containing arms (6% and 5% for AC-TH and TCH,

respectively).

> Notably, the same level of DFS and OS benefit was also obtained

for the 29%

> of node negative patients enrolled in the study.

> In terms of safety, there was a significant difference in the

major

> toxicity that has been consistently seen with Herceptin®-based

therapies

> i.e. cardiac toxicity. Common to all of the Herceptin® adjuvant

trials

> was the evaluation of congestive heart failure and cardiac-related

deaths.

> As mentioned above, the cardiac toxicity of the 2 experimental arms

> significantly favored the TCH regimen. Further, in terms of other

> toxicities, the TCH regimen appeared to also be superior to the AC-

TH arm.

> The BCIRG investigators and leadership wish to express their

deep

> appreciation to the women who willingly participated in this

randomized

> controlled trial and their commitment to improving outcomes for

all women

> challenged with breast cancer. Slamon noted that, " They are our

colleagues

> in this study rather than the research subjects. "

> The study was sponsored by sanofi-aventis, had financial

support from

> Genentech, and was conducted by CIRG.

>

> Indications and Usage

> Breast Cancer

> Taxotere® is indicated for the treatment of patients with

locally

> advanced or metastatic breast cancer after failure of prior

chemotherapy.

> Taxotere® in combination with doxorubicin and

cyclophosphamide is

> indicated for the adjuvant treatment of patients with operable

> node-positive breast cancer.

>

>

> About TAXOTERE®

> Important safety information

> WARNING: Taxotere® treatment can cause serious, physically

limiting,

> and potentially life-threatening side effects, such as infection,

low

> blood-cell counts, allergic reaction and retention of excess fluid

(edema).

> Taxotere® should not be given to patients with low white-

blood-cell

> counts, abnormal liver function, or a history of allergic

reactions to

> Taxotere® or any of the ingredients in Taxotere®.

> Before each Taxotere® treatment, all patients treated with

> Taxotere® must receive another medicine called dexamethasone.

This drug

> can help reduce the risk of fluid retention (edema) and allergic

reactions.

> Taxotere® should be administered only under the supervision

of a

> qualified physician experienced in the use of anticancer

treatments.

> Appropriate management of complications is possible only when

adequate

> diagnostic and treatment facilities are readily available.

> Treatment-related acute myeloid leukemia (AML) has occurred

in patients

> given anthracyclines and/or cyclophosphamide, including use with

> Taxotere® in adjuvant therapy for breast cancer. The most common

severe

> side effects are low white-blood-cell count, anemia, fatigue,

diarrhea, and

> mouth and throat irritation. Low white-blood-cell count can lead to

> life-threatening infections. The earliest sign of infection may be

fever,

> so tell your doctor right away if you have a fever. Other common

side

> effects from Taxotere® include nausea, vomiting, hair loss, rash,

> infusion-site reactions, odd sensations (such as numbness,

tingling, or

> burning) or weakness in the hands and feet, nail changes, muscle

and/or

> bone pain, or excessive tearing.

> Because of the potential risk of fetal harm, pregnant women

should not

> receive Taxotere®. Women of childbearing potential should avoid

becoming

> pregnant during treatment with Taxotere®.

> Before receiving Taxotere®, tell your doctor if

>

> * You have any allergies

>

> * You are taking any other medicines -- including

nonprescription

> (over-the-counter) drugs, vitamins, and dietary or herbal

supplements

>

> When taking Taxotere®, contact your doctor if

>

> * You have symptoms of an allergic reaction (warm sensation,

> tightness in

> your chest, itching/hives, or shortness of breath)

>

> * You experience any other side effects

> For full prescribing information, including boxed WARNING,

call

> or visit

> http://www.fda.gov/cder/foi/label/2006/020449s039lbl.pdf.

> About CIRG:

> BCIRG is the breast cancer division of the Cancer

International

> Research Group (CIRG). CIRG has performed a number of new and

innovative

> clinical trials with new cancer therapies. Active participation by

its

> global network of dedicated cancer research leaders and

investigators has

> made CIRG the success it is today. The organization is dedicated to

> bringing rational and innovative therapeutic concepts into the

clinical

> trial setting through translational approaches based on the

underlying

> biology of the disease. To further this objective, CIRG recently

merged

> with Translational Oncology Research International (TORI). TORI is

a

> smaller clinical trials group directly linked to several basic

research

> laboratories in which new therapeutic molecules are evaluated.

> CIRG has offices located in Paris (France) and Edmonton

Alberta

> (Canada). For information about CIRG, please visit our website:

> http://www.cirg.org.

>

>

>

>

> Valma wrote on 12/28/2006, 4:47 PM:

>

> > Hi everyone!

> > I just joined today and wanted to introduce myself. My name is

Val, and

> > my breast cancer was found in Nov 2006. I had my regular mammo

and they

> > found calcifications that they biopsied a week later. I had a

5.5 mm

> > tumor, infiltrating ductal, estrgen and progestron negative,

HER2/neu

> > amplified. Lymph nodes were clear. They tell me becasue of the

HER2 and

> > the fact that there have been close family members who have had

breast

> > cancer (including and uncle) that the chemo and Herceptin are

> > recommended. We, (DH and I)decided to go with it. He wants to

keep me

> > awhile longer if he can :-) I have been to the hospital twice

this week

> > for PET/CT scan and MUGA scans, I get a port put in the 3rd and

chemo

> > starts the 10th. I have been told I WILL lose my hair. I never

thiught

> > this would bother me but I am finding that yeah..maybe I DO

want a wig!

> > My hair stylist/friend said she would help me however she can.

We are

> > going to try and make it as fun as we can, new hair color, but

similar

> > style, funky hats, etc. I am just trying to figure out best

time to get

> > it and how long I may need it?? I know everyone is different.

I'll read

> > some more posts and see what advice I can gather...I basically

wanted

> > to say hello!!

> > Val

> >

> >

> >

> >

> >

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Hi Val,

I'm glad you're doing TCH, which studies have shown is the most

effective treatment for er/pr- her2+ women. You must be from Canada

because I think that treatment is widely used there, unlike the US.

My sister is a doctor, which for the most part is pretty useful. I

didn't always understand things (or I thought I understood but didn't)

and my sister was helpful in clarifying things.

-

Valma wrote on 12/28/2006, 8:07 PM:

> --Thanks for the info! I, in fact will be put on Taxotere and Cyclo

> (as the nurses were calling it) Along with the Herceptin. My older

> sister (who is a 13 year survivior and a Home Hospice Nurse) says these

> are commonly used. Little Sis has to make sure she takes her pathology

> report when she visits her this weekend LOL! Sometimes having a sister

> like this is good but sometimes it isn't. :-) She probably knows TOO

> much about the condition! Ahh, but she means well! I am looking forward

> to being in this group, looks like I will get lot's of good advice and

> support.

> Val

>

>

>

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Hee hee..sorry , Central Ohio here! :-) It must be because the 3

worked so well together the news spread. So far today I am ok. Trying

not to think about the port being put in next week or chemo starting

the following week. I am concentrating on bettering my diet again. In

April 2006 I was diagnosed with type 2 diabetes and have lost 35

pounds. The last 2 months since the cancer diagnosis I have not

watched as close and gained back 6 pounds. I know when chemo starts

my diet will be important. I have started eating my 3 fruits a day

again and lower fat foods and lot's of veggies. Now I just need to

get my hubby to stop bringing home the chips! HA HA!

blessings!

Val

> Hi Val,

>

> I'm glad you're doing TCH, which studies have shown is the most

> effective treatment for er/pr- her2+ women. You must be from Canada

> because I think that treatment is widely used there, unlike the US.

>

> My sister is a doctor, which for the most part is pretty useful. I

> didn't always understand things (or I thought I understood but

didn't)

> and my sister was helpful in clarifying things.

>

> -

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Val, hair loss will depend on the chemo you have. Do you know what the plan is

for chemo? It will also depend on you.... we are all different in how we lose it

and how it comes back. I lost mine about a couple days after my second dosage of

A/C (dose dense - every 2 weeks) but it started returning about the second

treatment on Taxotere. Funny that I lost my eye lashes and eye brows on

Taxotere, but my head started to spout hair during that treatment.

Barb

Michigan

Newbie here too!

Hi everyone!

I just joined today and wanted to introduce myself. My name is Val, and

my breast cancer was found in Nov 2006. I had my regular mammo and they

found calcifications that they biopsied a week later. I had a 5.5 mm

tumor, infiltrating ductal, estrgen and progestron negative, HER2/neu

amplified. Lymph nodes were clear. They tell me becasue of the HER2 and

the fact that there have been close family members who have had breast

cancer (including and uncle) that the chemo and Herceptin are

recommended. We, (DH and I)decided to go with it. He wants to keep me

awhile longer if he can :-) I have been to the hospital twice this week

for PET/CT scan and MUGA scans, I get a port put in the 3rd and chemo

starts the 10th. I have been told I WILL lose my hair. I never thiught

this would bother me but I am finding that yeah..maybe I DO want a wig!

My hair stylist/friend said she would help me however she can. We are

going to try and make it as fun as we can, new hair color, but similar

style, funky hats, etc. I am just trying to figure out best time to get

it and how long I may need it?? I know everyone is different. I'll read

some more posts and see what advice I can gather...I basically wanted

to say hello!!

Val

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.... Funny that I lost my eye lashes and eye brows on Taxotere, but my

head started to spout hair during that treatment.

> Barb

> Michigan

Isn't that weird? I had the same experience - now I have about a half

inch of hair on my head - kind of swirly (not quite curly), with

patches of white...(at the temples, mostly)

also, I lost the hair inside my nose (sheesh!) I'm seeing now faint

traces of eyebrows come in, but really want my lashes to grow back..

this has been a bitch, I swear ;)

marisa

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I figured out that losing the hair inside my nose explained why my nose was

running so much and the dust irritated me so much more. Lashes will grow, don't

worry.

Barb

Re: Newbie here too!

... Funny that I lost my eye lashes and eye brows on Taxotere, but my

head started to spout hair during that treatment.

> Barb

> Michigan

Isn't that weird? I had the same experience - now I have about a half

inch of hair on my head - kind of swirly (not quite curly), with

patches of white...(at the temples, mostly)

also, I lost the hair inside my nose (sheesh!) I'm seeing now faint

traces of eyebrows come in, but really want my lashes to grow back..

this has been a bitch, I swear ;)

marisa

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>

> I figured out that losing the hair inside my nose explained why my

nose was running so much and the dust irritated me so much more.

Lashes will grow, don't worry.

> Barb

I know - just complaining ;) no, whining, actually :)

peace

marisa

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I didn't take Taxol/Taxotere, just AC then Herceptin.

The eyebrows/eyelashes are just the last thing to go from the AC. I had

been warned about this so I was prepared. In fact they can fall out

several times over the course of a couple of months, but grow back quickly.

-

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My eyelashes and eybrows did not come back. I lost them in 2001.

Peggy

>

> Hi everyone!

> I just joined today and wanted to introduce myself. My name is

Val, and

> my breast cancer was found in Nov 2006. I had my regular mammo and

they

> found calcifications that they biopsied a week later. I had a 5.5

mm

> tumor, infiltrating ductal, estrgen and progestron negative,

HER2/neu

> amplified. Lymph nodes were clear. They tell me becasue of the

HER2 and

> the fact that there have been close family members who have had

breast

> cancer (including and uncle) that the chemo and Herceptin are

> recommended. We, (DH and I)decided to go with it. He wants to keep

me

> awhile longer if he can :-) I have been to the hospital twice this

week

> for PET/CT scan and MUGA scans, I get a port put in the 3rd and

chemo

> starts the 10th. I have been told I WILL lose my hair. I never

thiught

> this would bother me but I am finding that yeah..maybe I DO want a

wig!

> My hair stylist/friend said she would help me however she can. We

are

> going to try and make it as fun as we can, new hair color, but

similar

> style, funky hats, etc. I am just trying to figure out best time

to get

> it and how long I may need it?? I know everyone is different. I'll

read

> some more posts and see what advice I can gather...I basically

wanted

> to say hello!!

> Val

>

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Hi Barb.

same thing happned to me with the runny nose so now i know whats causing it. I

lost most of my eyebrows but so far the lashes are still there - lol. the hair

also went but that's what wigs, at least for me, are for.

And of course the eyes start watering also.

I wish all of you a good New Year and WE WILL ALL GET THROUGH THIS!

Ellen

--------- Re: Newbie here too!

.... Funny that I lost my eye lashes and eye brows on Taxotere, but my

head started to spout hair during that treatment.

> Barb

> Michigan

Isn't that weird? I had the same experience - now I have about a half

inch of hair on my head - kind of swirly (not quite curly), with

patches of white...(at the temples, mostly)

also, I lost the hair inside my nose (sheesh!) I'm seeing now faint

traces of eyebrows come in, but really want my lashes to grow back..

this has been a bitch, I swear ;)

marisa

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Val:

I have a niece named Val (). I actually call her Valerenee. She is

sweet and a great support for me at this time in my life.

What a shock this all must be to you and so much to think about at a time like

this! I hope that the support that you receive here will be helpful to you.

Welcome to this great and wonderful sisterhood! We are here for you.

Jan K

Valma Valmr2@...> wrote:

Hi everyone!

I just joined today and wanted to introduce myself. My name is Val, and

my breast cancer was found in Nov 2006. I had my regular mammo and they

found calcifications that they biopsied a week later. I had a 5.5 mm

tumor, infiltrating ductal, estrgen and progestron negative, HER2/neu

amplified. Lymph nodes were clear. They tell me becasue of the HER2 and

the fact that there have been close family members who have had breast

cancer (including and uncle) that the chemo and Herceptin are

recommended. We, (DH and I)decided to go with it. He wants to keep me

awhile longer if he can :-) I have been to the hospital twice this week

for PET/CT scan and MUGA scans, I get a port put in the 3rd and chemo

starts the 10th. I have been told I WILL lose my hair. I never thiught

this would bother me but I am finding that yeah..maybe I DO want a wig!

My hair stylist/friend said she would help me however she can. We are

going to try and make it as fun as we can, new hair color, but similar

style, funky hats, etc. I am just trying to figure out best time to get

it and how long I may need it?? I know everyone is different. I'll read

some more posts and see what advice I can gather...I basically wanted

to say hello!!

Val

Jan Koelsch

__________________________________________________

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