Re: Liver Metastasis

[Guest guest]

Heath, in my short time with my breast cancer diagnosis, I've been shocked to

hear from my friends about how many people they know who have Stage IV cancer,

and the cancer is either under control or in remission. You are wisely seeking

out those stories for your wife. They are where you both need to keep your

focus, there and loving that new baby of yours. You don't want to look back 5

years from now and think of the time you spent in mental suffering when you

didn't need to. I know you will hear the positive stories, too. Hang your hat

on them, not the others.

Prayers and seeing you both at peace,

Ellie

9a. Liver Metasis (sp)

Posted by: " michigangrad96 " hpapp@... michigangrad96

Date: Sun Jan 28, 2007 12:13 pm ((PST))

Looking for postive information to share with my wife. We are nine

days in with the first chemo undergone. The cancer has spread to the

lymph nodes as well as the liver. Our baby is only 6 mo.s old, and we

need something to hang on to; everything you read about this type IV is

so negative. Please, someone share some success stories with me, so I

can relate that positivity to her. This is so hard on me, I can't

imagine what it's like on her.

Namaste,

Heath

---------------------------------

Finding fabulous fares is fun.

Let Yahoo! FareChase search your favorite travel sites to find flight and hotel

bargains.

[Guest guest]

Thank you so much for the information. It's reassuring. Good luck

to you in your fight. We will all recover.

Namaste,

Heath

>

> Heath, in my short time with my breast cancer diagnosis, I've been

shocked to hear from my friends about how many people they know who

have Stage IV cancer, and the cancer is either under control or in

remission. You are wisely seeking out those stories for your wife.

They are where you both need to keep your focus, there and loving

that new baby of yours. You don't want to look back 5 years from now

and think of the time you spent in mental suffering when you didn't

need to. I know you will hear the positive stories, too. Hang your

hat on them, not the others.

>

> Prayers and seeing you both at peace,

>

> Ellie

>

> 9a. Liver Metasis (sp)

> Posted by: " michigangrad96 " hpapp@... michigangrad96

> Date: Sun Jan 28, 2007 12:13 pm ((PST))

>

> Looking for postive information to share with my wife. We are nine

> days in with the first chemo undergone. The cancer has spread to

the

> lymph nodes as well as the liver. Our baby is only 6 mo.s old, and

we

> need something to hang on to; everything you read about this type

IV is

> so negative. Please, someone share some success stories with me,

so I

> can relate that positivity to her. This is so hard on me, I can't

> imagine what it's like on her.

> Namaste,

> Heath

>

>

>

>

> ---------------------------------

> Finding fabulous fares is fun.

> Let Yahoo! FareChase search your favorite travel sites to find

flight and hotel bargains.

>

>

[Guest guest]

Hi Heath,

Was sad to read about you and your wife. A six month old baby is such a

blessing - I wish you and your wife could enjoy this time without having to

deal with cancer.

I was diagnosed 7 years ago and staged at IIIB - with inflammatory breast

cancer. I had a 40% chance of making it for 18 months - no one said

anything about a longer period of time. Like I said, that was 7 years ago.

During these past 7 years I've kept active in a couple of bc support groups,

most especially the ibc group. I am cyber friends with women who are Stage

IV for years. Their situation is treated as a chronic disease. Many

maintain a high quality of life. There are many, many success stories.

I must have missed your intro post - and I'm wondering what type of cancer

your wife has. Could it be inflammatory breast cancer (ibc)? Please give

her a hug from a sister survivor. I am sending prayers to both of you.

Regards,

Ann

Chemo Hats: www.cjhats.com

>

> Thank you so much for the information. It's reassuring. Good luck

> to you in your fight. We will all recover.

> Namaste,

> Heath

>

>

> >

> > Heath, in my short time with my breast cancer diagnosis, I've been

> shocked to hear from my friends about how many people they know who

> have Stage IV cancer, and the cancer is either under control or in

> remission. You are wisely seeking out those stories for your wife.

> They are where you both need to keep your focus, there and loving

> that new baby of yours. You don't want to look back 5 years from now

> and think of the time you spent in mental suffering when you didn't

> need to. I know you will hear the positive stories, too. Hang your

> hat on them, not the others.

> >

> > Prayers and seeing you both at peace,

> >

> > Ellie

> >

> > 9a. Liver Metasis (sp)

> > Posted by: " michigangrad96 " hpapp@... michigangrad96

> > Date: Sun Jan 28, 2007 12:13 pm ((PST))

> >

> > Looking for postive information to share with my wife. We are nine

> > days in with the first chemo undergone. The cancer has spread to

> the

> > lymph nodes as well as the liver. Our baby is only 6 mo.s old, and

> we

> > need something to hang on to; everything you read about this type

> IV is

> > so negative. Please, someone share some success stories with me,

> so I

> > can relate that positivity to her. This is so hard on me, I can't

> > imagine what it's like on her.

> > Namaste,

> > Heath

> >

> >

> >

> >

> > ---------------------------------

> > Finding fabulous fares is fun.

> > Let Yahoo! FareChase search your favorite travel sites to find

> flight and hotel bargains.

> >

> >

[Guest guest]

Thank you for the inspiration.

heath

> > >

> > > Heath, in my short time with my breast cancer diagnosis, I've

been

> > shocked to hear from my friends about how many people they know

who

> > have Stage IV cancer, and the cancer is either under control or in

> > remission. You are wisely seeking out those stories for your wife.

> > They are where you both need to keep your focus, there and loving

> > that new baby of yours. You don't want to look back 5 years from

now

> > and think of the time you spent in mental suffering when you

didn't

> > need to. I know you will hear the positive stories, too. Hang your

> > hat on them, not the others.

> > >

> > > Prayers and seeing you both at peace,

> > >

> > > Ellie

> > >

> > > 9a. Liver Metasis (sp)

> > > Posted by: " michigangrad96 " hpapp@ michigangrad96

> > > Date: Sun Jan 28, 2007 12:13 pm ((PST))

> > >

> > > Looking for postive information to share with my wife. We are

nine

> > > days in with the first chemo undergone. The cancer has spread to

> > the

> > > lymph nodes as well as the liver. Our baby is only 6 mo.s old,

and

> > we

> > > need something to hang on to; everything you read about this

type

> > IV is

> > > so negative. Please, someone share some success stories with me,

> > so I

> > > can relate that positivity to her. This is so hard on me, I

can't

> > > imagine what it's like on her.

> > > Namaste,

> > > Heath

> > >

> > >

> > >

> > >

> > > ---------------------------------

> > > Finding fabulous fares is fun.

> > > Let Yahoo! FareChase search your favorite travel sites to find

> > flight and hotel bargains.

> > >

> > >

[Guest guest]

Hi,

Sorry to hear about your wife's diagnosis.

I found breastcancer dot org has a discussion forum.

In it they have a section for people with metastized cancer.

You have to sign up to log into it.

I found more useful information on that board because the voice really

isn't hear about metastic cancer. At least that is how i felt.

My mom has mets in her liver. We got some good news last week, her

blood test markers were down 400 points. They are still way elavated,

but I consider good news for my mom.

I felt some more relief over their because they talk about

the different mets, what drugs their on, and good news, well and bad

news about people progress.

Connie

[Guest guest]

Hi Heath, I had stage iv BC with metastasis too, but it's move to my

bone not liver. It's in my right shoulder bone (the first BC was on

the left, I have no idea how they could move so far).

Before I had chemo my shoulder and arm was painful and I couldn't

move it. I am right handed and that made me not able to do my stuff

as usual. But after do the chemo 2 cycles, herbal therapy and acid-

alkaline diet, my condition is getting better and better. Now my

right hand can move again freely, without any pain and no pain

killer taken. My Dr. and his team were surprised, because at the

first time they didn't have much hope for me, and told me to

consider surgery (bone transplantation) or if the case getting

worse, it could be an amputation. But they didn't want me to be

handicapped so soon (I'm only 22 and working as an illustrator and

graphic designer) so they suggested me to try the chemo first to

reduce the size of cancer. They plan to gave me 3 cycles of chemo

and then do the MRI after that. If the size of cancer could be

reduced, maybe they still have to do the surgery but at last not

amputate.

Maybe my story not so good since even my condition is better I still

have no idea about how it will end, but there's still a hope.

There's nothing easy in dealing with stage iv bc because we must

prepare for the worst situation. But I believe if we still have a

hope and positive thinking, a good thing will come . And we all

fighting together, I'm having my family beside me, like your wife

having you and the baby (I hope one day I'll be able to have one

too!)

Take care,

Tyas

> > 9a. Liver Metasis (sp)

> > Posted by: " michigangrad96 " hpapp@ michigangrad96

> > Date: Sun Jan 28, 2007 12:13 pm ((PST))

> >

> > Looking for postive information to share with my wife. We are

nine

> > days in with the first chemo undergone. The cancer has spread

to

> the

> > lymph nodes as well as the liver. Our baby is only 6 mo.s old,

and

> we

> > need something to hang on to; everything you read about this

type

> IV is

> > so negative. Please, someone share some success stories with

me,

> so I

> > can relate that positivity to her. This is so hard on me, I

can't

> > imagine what it's like on her.

> > Namaste,

> > Heath

> >

> >

> >

> >

> > ---------------------------------

> > Finding fabulous fares is fun.

> > Let Yahoo! FareChase search your favorite travel sites to find

> flight and hotel bargains.

> >

> >

[Guest guest]

Thank you, and good luck.

heath

>

> Hi Heath, I had stage iv BC with metastasis too, but it's move to

my

> bone not liver. It's in my right shoulder bone (the first BC was on

> the left, I have no idea how they could move so far).

>

> Before I had chemo my shoulder and arm was painful and I couldn't

> move it. I am right handed and that made me not able to do my stuff

> as usual. But after do the chemo 2 cycles, herbal therapy and acid-

> alkaline diet, my condition is getting better and better. Now my

> right hand can move again freely, without any pain and no pain

> killer taken. My Dr. and his team were surprised, because at the

> first time they didn't have much hope for me, and told me to

> consider surgery (bone transplantation) or if the case getting

> worse, it could be an amputation. But they didn't want me to be

> handicapped so soon (I'm only 22 and working as an illustrator and

> graphic designer) so they suggested me to try the chemo first to

> reduce the size of cancer. They plan to gave me 3 cycles of chemo

> and then do the MRI after that. If the size of cancer could be

> reduced, maybe they still have to do the surgery but at last not

> amputate.

>

> Maybe my story not so good since even my condition is better I

still

> have no idea about how it will end, but there's still a hope.

> There's nothing easy in dealing with stage iv bc because we must

> prepare for the worst situation. But I believe if we still have a

> hope and positive thinking, a good thing will come . And we all

> fighting together, I'm having my family beside me, like your wife

> having you and the baby (I hope one day I'll be able to have one

> too!)

>

> Take care,

>

> Tyas

>

>

>

>

> > > 9a. Liver Metasis (sp)

> > > Posted by: " michigangrad96 " hpapp@ michigangrad96

> > > Date: Sun Jan 28, 2007 12:13 pm ((PST))

> > >

> > > Looking for postive information to share with my wife. We are

> nine

> > > days in with the first chemo undergone. The cancer has spread

> to

> > the

> > > lymph nodes as well as the liver. Our baby is only 6 mo.s old,

> and

> > we

> > > need something to hang on to; everything you read about this

> type

> > IV is

> > > so negative. Please, someone share some success stories with

> me,

> > so I

> > > can relate that positivity to her. This is so hard on me, I

> can't

> > > imagine what it's like on her.

> > > Namaste,

> > > Heath

> > >

> > >

> > >

> > >

> > > ---------------------------------

> > > Finding fabulous fares is fun.

> > > Let Yahoo! FareChase search your favorite travel sites to find

> > flight and hotel bargains.

> > >

> > >

[Guest guest]

Thank you.

________________________________

From: breastcancer2 on behalf of zumbergc

Sent: Sun 1/28/2007 6:06 PM

To: breastcancer2

Subject: Re: Liver Metastasis

Hi,

Sorry to hear about your wife's diagnosis.

I found breastcancer dot org has a discussion forum.

In it they have a section for people with metastized cancer.

You have to sign up to log into it.

I found more useful information on that board because the voice really

isn't hear about metastic cancer. At least that is how i felt.

My mom has mets in her liver. We got some good news last week, her

blood test markers were down 400 points. They are still way elavated,

but I consider good news for my mom.

I felt some more relief over their because they talk about

the different mets, what drugs their on, and good news, well and bad

news about people progress.

Connie

[Guest guest]

Hi there

My name is Sharon and im from the UK, 3 and a half years ago I was diagnosed

with DCIS had surgery and radiotherapy ,then 6 months ago found it had

spread to almost my entire liver with a poor prognosis as to wether chemo

would help at this advanced stage ,I was so totally devastated as you and

your wife must be ,like you everything I read was so negative and I found it

difficult to find any success stories ,(I don't mean cures but time),which

brought me down so much but ,I finished my chemo on the 21st DEC and have

just been today for my first review ,my onc is very pleased ,my tumours

markers are down from over a thousand to 55 and she now says it indicates

that the cancer is classed as inactive for now ,scans show a significant

improvement ,much better than I dared hope for and my liver function is

normal ,I have nothing to indicate I should have any symptoms apart from the

tiredness from chemo still there ,she now intends to monitor me closely but

otherwise has told me to just get on with my life , if and when my tumour

markers begin to rise she will then use another chemo plus herceptin but for

now shes happy to see how I go .and I agree , of course she cant give me a

timescale as to when the markers may rise again ,she said she has a patient

where they stayed inactive for over 3 years and another where they rose

again after 7 mths so I don't know ,but I am feeling very positive . I wish

you and your wife all the best and please try and stay positive . Ill keep

you all in my thoughts

Love

Sharon

[Guest guest]

Sharon - you are an inspriation. Thank you for being......you!

Hugs!

Ellen

>

> Hi there

> My name is Sharon and im from the UK, 3 and a half years ago I was

diagnosed

> with DCIS had surgery and radiotherapy ,then 6 months ago found it

had

> spread to almost my entire liver with a poor prognosis as to

wether chemo

> would help at this advanced stage ,I was so totally devastated as

you and

> your wife must be ,like you everything I read was so negative and

I found it

> difficult to find any success stories ,(I don't mean cures but

time),which

> brought me down so much but ,I finished my chemo on the 21st DEC

and have

> just been today for my first review ,my onc is very pleased ,my

tumours

> markers are down from over a thousand to 55 and she now says it

indicates

> that the cancer is classed as inactive for now ,scans show a

significant

> improvement ,much better than I dared hope for and my liver

function is

> normal ,I have nothing to indicate I should have any symptoms

apart from the

> tiredness from chemo still there ,she now intends to monitor me

closely but

> otherwise has told me to just get on with my life , if and when my

tumour

> markers begin to rise she will then use another chemo plus

herceptin but for

> now shes happy to see how I go .and I agree , of course she cant

give me a

> timescale as to when the markers may rise again ,she said she has

a patient

> where they stayed inactive for over 3 years and another where they

rose

> again after 7 mths so I don't know ,but I am feeling very

positive . I wish

> you and your wife all the best and please try and stay positive .

Ill keep

> you all in my thoughts

>

> Love

>

> Sharon

>

>

[Guest guest]

Thank you Sharon. Your story is inspiring. This diagnoses has so few postives

to hold on to that examples such as yours provide light in a very dark place.

Keep up the good fight!

Heath

________________________________

From: breastcancer2 on behalf of sharon

Sent: Mon 1/29/2007 9:31 AM

To: breastcancer2

Subject: Re: Liver Metastasis

Hi there

My name is Sharon and im from the UK, 3 and a half years ago I was diagnosed

with DCIS had surgery and radiotherapy ,then 6 months ago found it had

spread to almost my entire liver with a poor prognosis as to wether chemo

would help at this advanced stage ,I was so totally devastated as you and

your wife must be ,like you everything I read was so negative and I found it

difficult to find any success stories ,(I don't mean cures but time),which

brought me down so much but ,I finished my chemo on the 21st DEC and have

just been today for my first review ,my onc is very pleased ,my tumours

markers are down from over a thousand to 55 and she now says it indicates

that the cancer is classed as inactive for now ,scans show a significant

improvement ,much better than I dared hope for and my liver function is

normal ,I have nothing to indicate I should have any symptoms apart from the

tiredness from chemo still there ,she now intends to monitor me closely but

otherwise has told me to just get on with my life , if and when my tumour

markers begin to rise she will then use another chemo plus herceptin but for

now shes happy to see how I go .and I agree , of course she cant give me a

timescale as to when the markers may rise again ,she said she has a patient

where they stayed inactive for over 3 years and another where they rose

again after 7 mths so I don't know ,but I am feeling very positive . I wish

you and your wife all the best and please try and stay positive . Ill keep

you all in my thoughts

Love

Sharon

[Guest guest]

here is my story ...my name is lily ..I was diagnost on april 2006

con IV stage ....nodes (4)from 23 and liver (5 small tumors) after 12

quemo's I think was taxotere, carboplatin and herceptin ....my ct

scan dont show anything ...I have macept an my right breast and they

removed my nodes ...from 23 (4 was positv) ...I hav 3 kids 17 years

old , 3 and half and 1 year and 2 month old ....exatly like your I '

watching my diet...organic as much I can affor it and fiber ...no red

meat no chichen only chichen or turkey organic ....plus I taking one

antioxidant thing liquid from my country it call birm ....i living in

charlotte north carolina .....go to church every sunday pray every

night and try to be so busy so I can no think too much .....i wish

they can do a 'quemo soul " or quemo mind " ......but i think the worst

part of all this is mind .....Oh I almost forget i dont used white

sugar anymore only honey o brawn sugar ....my doctor said that in my

case is hard to get cure but no imposible ...is only in God

Hands...in april I'm going to have a year from diagnost date

plus I watching news waiting for the new drugs to get aproved from

the goverment ....is the one that is good for us HERS2 .but is pill

and cover all body ...dont remember the name .....

>

[Guest guest]

Thank you for your story. It sounds so positive compared to what else you can

read. That's what we need. Good luck and keep on fighting the good fight.

Namaste,

heath

lilyschachner lilyschachner@...> wrote:

here is my story ...my name is lily ..I was diagnost on april 2006

con IV stage ....nodes (4)from 23 and liver (5 small tumors) after 12

quemo's I think was taxotere, carboplatin and herceptin ....my ct

scan dont show anything ...I have macept an my right breast and they

removed my nodes ...from 23 (4 was positv) ...I hav 3 kids 17 years

old , 3 and half and 1 year and 2 month old ....exatly like your I '

watching my diet...organic as much I can affor it and fiber ...no red

meat no chichen only chichen or turkey organic ....plus I taking one

antioxidant thing liquid from my country it call birm ....i living in

charlotte north carolina .....go to church every sunday pray every

night and try to be so busy so I can no think too much .....i wish

they can do a 'quemo soul " or quemo mind " ......but i think the worst

part of all this is mind .....Oh I almost forget i dont used white

sugar anymore only honey o brawn sugar ....my doctor said that in my

case is hard to get cure but no imposible ...is only in God

Hands...in april I'm going to have a year from diagnost date

plus I watching news waiting for the new drugs to get aproved from

the goverment ....is the one that is good for us HERS2 .but is pill

and cover all body ...dont remember the name .....

>

---------------------------------

Want to start your own business? Learn how on Yahoo! Small Business.

[Guest guest]

Hi Lily,

Thank you for sharing your story. It sounds like you are staying

positive and doing healthy things for your body.

I take it you are her2+?

I think Laptinab is approved for stage 4 women.

take care,

[Guest guest]

yes ,I m hers2 and that is the drog lapatinid or something like

that ....I did'n hear anything on the news yet ...

>

> Hi Lily,

>

> Thank you for sharing your story. It sounds like you are staying

> positive and doing healthy things for your body.

>

> I take it you are her2+?

> I think Laptinab is approved for stage 4 women.

>

> take care,

>

[Guest guest]

lily,

The mind will drive you nuts. I have spent the last 10 months on the

internet searching for the best ways to cure this thing..

Some days I am very very up... and some days I feel helpless..

Like you said prayer is the best medicine.. if for nothing else.. to have

strength to get out of bed every morning and begin a new day..and to say thanks

for giving us that Day...

Kiss your children and hug them a lot... my kids and grandkids have been my

salvation.. and my husband too.. this is the first time in 35 years that I can

remember not being the 'Strong One " for the family.. I actually collapsed

one day into my husbands arms and just sobbed.. and he let me stay there and

just held me.. like I said.. the first time in 35 years of marriage that I had

ever done that.. funny how much we find out during all of this..

I will pray for you too..Hugs for you too...

Cheryl

[Guest guest]

Lilly,

It is nice to meet you... You have a wonderful, miraculous story to share,

thank you.. It makes those of us who aren't stage IV yet see that there is a

light when/if we get there. I am happy that everything is going well so far.

Your children rely on you and I truly believe everything is up to God as well.

May you keep the path of healthiness and happiness.

Love

Michele

lilyschachner lilyschachner@...> wrote:

here is my story ...my name is lily ..I was diagnost on april 2006

con IV stage ....nodes (4)from 23 and liver (5 small tumors) after 12

quemo's I think was taxotere, carboplatin and herceptin ....my ct

scan dont show anything ...I have macept an my right breast and they

removed my nodes ...from 23 (4 was positv) ...I hav 3 kids 17 years

old , 3 and half and 1 year and 2 month old ....exatly like your I '

watching my diet...organic as much I can affor it and fiber ...no red

meat no chichen only chichen or turkey organic ....plus I taking one

antioxidant thing liquid from my country it call birm ....i living in

charlotte north carolina .....go to church every sunday pray every

night and try to be so busy so I can no think too much .....i wish

they can do a 'quemo soul " or quemo mind " ......but i think the worst

part of all this is mind .....Oh I almost forget i dont used white

sugar anymore only honey o brawn sugar ....my doctor said that in my

case is hard to get cure but no imposible ...is only in God

Hands...in april I'm going to have a year from diagnost date

plus I watching news waiting for the new drugs to get aproved from

the goverment ....is the one that is good for us HERS2 .but is pill

and cover all body ...dont remember the name .....

>

[Guest guest]

Thank you.

BEEHIVEHOLLOW@... wrote: lily,

The mind will drive you nuts. I have spent the last 10 months on the

internet searching for the best ways to cure this thing..

Some days I am very very up... and some days I feel helpless..

Like you said prayer is the best medicine.. if for nothing else.. to have

strength to get out of bed every morning and begin a new day..and to say thanks

for giving us that Day...

Kiss your children and hug them a lot... my kids and grandkids have been my

salvation.. and my husband too.. this is the first time in 35 years that I can

remember not being the 'Strong One " for the family.. I actually collapsed

one day into my husbands arms and just sobbed.. and he let me stay there and

just held me.. like I said.. the first time in 35 years of marriage that I had

ever done that.. funny how much we find out during all of this..

I will pray for you too..Hugs for you too...

Cheryl

[Guest guest]

thank you nice to meet you all ..I dont write too much because english is no my

first language ..however I read all of your email's well I 'm taking herceptin

and tamoxifen......and on feb 7 i going to hav another ct scan all body (I doing

every 3months ) .......and my mother is with me helping me with the kid's

.......my husband righ beside me ......is true some day's I'm ok some days the

little things can put me so down...) but my mother pull me up ........and try

to be busy .......and when I'm on my house try to eat healthy ...and keep my

routine sleep the same hours, eat almost the same food ..fruit and vegetables in

the morning (only juice) beet and carrot , green pepper and fruit everyday

everyday ....like 4 glass of juice ....dont like but if I dont drink it I fell

bad .....weak ...so those juice make my days plus my prayers

take care your self with the very very best ways

Lily

__________________________________________________

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[Guest guest]

Lily,

Your English is just fine. Please continue to post and share with us. I will

keep you in my prayers.

Hugs

nne

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

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Re: Re: Liver Metastasis

thank you nice to meet you all ..I dont write too much because english is no

my first language ..however I read all of your email's well I 'm taking

herceptin and tamoxifen......and on feb 7 i going to hav another ct scan all

body (I doing every 3months ) .......and my mother is with me helping me with

the kid's ......my husband righ beside me ......is true some day's I'm ok some

days the little things can put me so down...) but my mother pull me up

.........and try to be busy .......and when I'm on my house try to eat healthy

....and keep my routine sleep the same hours, eat almost the same food ..fruit

and vegetables in the morning (only juice) beet and carrot , green pepper and

fruit everyday everyday ....like 4 glass of juice ....dont like but if I dont

drink it I fell bad .....weak ...so those juice make my days plus my prayers

take care your self with the very very best ways

Lily

__________________________________________________

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[Guest guest]

Dear Lily,

I just had to post something about your message. Like nne said,

your English is just fine; I had no trouble at all understanding your

words and I sure have no trouble understanding that you are one of

us. This disease is our common thread no matter where we are from or

what language we speak. We all look at the same moon and sun and we

are sisters together in our struggles. It is my fervent prayer that

someday no woman, anywhere, anytime has to fight this disease and

live what we all are living. Peace to you Lily.

>

> Lily,

> Your English is just fine. Please continue to post and share with

us. I will keep you in my prayers.

> 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

> Re: Re: Liver Metastasis

>

>

> thank you nice to meet you all ..I dont write too much because

english is no my first language ..however I read all of your email's

well I 'm taking herceptin and tamoxifen......and on feb 7 i going to

hav another ct scan all body (I doing every 3months ) .......and my

mother is with me helping me with the kid's ......my husband righ

beside me ......is true some day's I'm ok some days the little things

can put me so down...) but my mother pull me up ........and try to be

busy .......and when I'm on my house try to eat healthy ...and keep

my routine sleep the same hours, eat almost the same food ..fruit and

vegetables in the morning (only juice) beet and carrot , green pepper

and fruit everyday everyday ....like 4 glass of juice ....dont like

but if I dont drink it I fell bad .....weak ...so those juice make my

days plus my prayers

> take care your self with the very very best ways

>

> Lily

>

> __________________________________________________

> Correo Yahoo!

> Espacio para todos tus mensajes, antivirus y antispam ¡gratis!

> Regístrate ya - http://correo.espanol.yahoo.com/

>

>

[Guest guest]

Lily;

Your story is such an inspiration to me! Thank you for sharing. I pray that

God will keep you and touch you with healing power.

I will keep you in my prayers as well as your family and your mom. This is

never easy.

Take care.

Jan K

Lily Loor-Schachner lilyschachner@...> wrote:

thank you nice to meet you all ..I dont write too much because english

is no my first language ..however I read all of your email's well I 'm taking

herceptin and tamoxifen......and on feb 7 i going to hav another ct scan all

body (I doing every 3months ) .......and my mother is with me helping me with

the kid's ......my husband righ beside me ......is true some day's I'm ok some

days the little things can put me so down...) but my mother pull me up

.........and try to be busy .......and when I'm on my house try to eat healthy

....and keep my routine sleep the same hours, eat almost the same food ..fruit

and vegetables in the morning (only juice) beet and carrot , green pepper and

fruit everyday everyday ....like 4 glass of juice ....dont like but if I dont

drink it I fell bad .....weak ...so those juice make my days plus my prayers

take care your self with the very very best ways

Lily

__________________________________________________

Correo Yahoo!

Espacio para todos tus mensajes, antivirus y antispam ¡gratis!

Regístrate ya - http://correo.espanol.yahoo.com/

[Guest guest]

Hello Namaste,

This is her husband writting (with intervention of the wife ). My name is

. We have a 3 year old angel and a 1 year old little bear (whom can

already turn the door knobs). We also have a teenager who thinks she lives in

orange county ( as on TV ) with a phone permanently attached to her ear. No

fault to her! Had I been a teenager at this time I think I would have been just

as bad with, perhaps, a little more geek-tronics.

I wanted to share a few words about our situation. For example, today, she was

given a clean bill of health from a CT Scan taken yesterday. While we are not

declared as being in remission this is third consectutive scan where nothing was

found. It a sliver of light in all this darkness.

We wanted to share this with you becuase when this began we searched all over

for any sign of success or survival. We found good results in Spain, where her

brother lives, and in Ecuador which is her home country.

At this time, we are keeping healthy as much as possible and have been active,

again, in all parts of our lives that we were prior to the start of this road.

Included in our activities is prayer and giving thanks to God for good health.

We (she... ) would like you to know that she's currently using Herceptin

and the results have been good.

Well, I can't think anythink else...

We'll keep everyone in the groups in our prayers.

& Lily

Thank you for your story. It sounds so positive compared to what

else you can read. That's what we need. Good luck and keep on fighting the good

fight.

Namaste,

heath

lilyschachner wrote:

here is my story ...my name is lily ..I was diagnost on april 2006

con IV stage ....nodes (4)from 23 and liver (5 small tumors) after 12

quemo's I think was taxotere, carboplatin and herceptin ....my ct

scan dont show anything ...I have macept an my right breast and they

removed my nodes ...from 23 (4 was positv) ...I hav 3 kids 17 years

old , 3 and half and 1 year and 2 month old ....exatly like your I '

watching my diet...organic as much I can affor it and fiber ...no red

meat no chichen only chichen or turkey organic ....plus I taking one

antioxidant thing liquid from my country it call birm ....i living in

charlotte north carolina .....go to church every sunday pray every

night and try to be so busy so I can no think too much .....i wish

they can do a 'quemo soul " or quemo mind " ......but i think the worst

part of all this is mind .....Oh I almost forget i dont used white

sugar anymore only honey o brawn sugar ....my doctor said that in my

case is hard to get cure but no imposible ...is only in God

Hands...in april I'm going to have a year from diagnost date

plus I watching news waiting for the new drugs to get aproved from

the goverment ....is the one that is good for us HERS2 .but is pill

and cover all body ...dont remember the name .....

>

Lily

__________________________________________________

Correo Yahoo!

Espacio para todos tus mensajes, antivirus y antispam ¡gratis!

Regístrate ya - http://correo.espanol.yahoo.com/

[Guest guest]

Hello and Lily,

I'm so glad the scans are good! I just finished a year of Herceptin.

It's been touted as a miracle drug that offers hope for an aggressive

type of cancer. I also am a member of her2support.org, where many stage

iv women are on herceptin permanently with NED.

Lily, I hope you continue to get good news. , you are a

supportive husband - and family is so important for us in facing any

challenge.

take care,

[Guest guest]

Thank you so much for the insight. We are off to the oncologist today for the

third chemo tx. She is on taxol and doxil right now. I honestly don't know if

it's the proper protocol. We are going to UCLA as soon as we can get in. What

exactly is herceptin?

Thanks again,

Heath

Lily Loor-Schachner lilyschachner@...> wrote:

Hello Namaste,

This is her husband writting (with intervention of the wife ). My name is

. We have a 3 year old angel and a 1 year old little bear (whom can

already turn the door knobs). We also have a teenager who thinks she lives in

orange county ( as on TV ) with a phone permanently attached to her ear. No

fault to her! Had I been a teenager at this time I think I would have been just

as bad with, perhaps, a little more geek-tronics.

I wanted to share a few words about our situation. For example, today, she was

given a clean bill of health from a CT Scan taken yesterday. While we are not

declared as being in remission this is third consectutive scan where nothing was

found. It a sliver of light in all this darkness.

We wanted to share this with you becuase when this began we searched all over

for any sign of success or survival. We found good results in Spain, where her

brother lives, and in Ecuador which is her home country.

At this time, we are keeping healthy as much as possible and have been active,

again, in all parts of our lives that we were prior to the start of this road.

Included in our activities is prayer and giving thanks to God for good health.

We (she... ) would like you to know that she's currently using Herceptin and

the results have been good.

Well, I can't think anythink else...

We'll keep everyone in the groups in our prayers.

& Lily

Thank you for your story. It sounds so positive compared to what else you can

read. That's what we need. Good luck and keep on fighting the good fight.

Namaste,

heath

lilyschachner wrote:

here is my story ...my name is lily ..I was diagnost on april 2006

con IV stage ....nodes (4)from 23 and liver (5 small tumors) after 12

quemo's I think was taxotere, carboplatin and herceptin ....my ct

scan dont show anything ...I have macept an my right breast and they

removed my nodes ...from 23 (4 was positv) ...I hav 3 kids 17 years

old , 3 and half and 1 year and 2 month old ....exatly like your I '

watching my diet...organic as much I can affor it and fiber ...no red

meat no chichen only chichen or turkey organic ....plus I taking one

antioxidant thing liquid from my country it call birm ....i living in

charlotte north carolina .....go to church every sunday pray every

night and try to be so busy so I can no think too much .....i wish

they can do a 'quemo soul " or quemo mind " ......but i think the worst

part of all this is mind .....Oh I almost forget i dont used white

sugar anymore only honey o brawn sugar ....my doctor said that in my

case is hard to get cure but no imposible ...is only in God

Hands...in april I'm going to have a year from diagnost date

plus I watching news waiting for the new drugs to get aproved from

the goverment ....is the one that is good for us HERS2 .but is pill

and cover all body ...dont remember the name .....

>

Lily

__________________________________________________

Correo Yahoo!

Espacio para todos tus mensajes, antivirus y antispam ¡gratis!

Regístrate ya - http://correo.espanol.yahoo.com/