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Sorry it's taken me a couple of days to reply back to you-esp. after

your replied to me so quickly. I was out at working at a remote

office for a few days. Anyway ... The surgeon removed a large tumor

from his colon, but didn't touch the tumors on his liver. The

surgeon was actually very grim about my dad's prognosis, so it's even

more amazing to us that he's doing so well.

The onc. only prescribed him Xeloda. (I think because my dad was

really, really scared about a port-a-cath & intravenous chemo - to

almost the point of not wanting to try chemo.) She originally

mentioned putting him on Avastin, but then decided to just try the

Xeloda on its own at first.

It's reassuring to read that the CEA readings can be very erratic

during chemo. They do have the baseline scans from when they found

the tumors, but they haven't done another one yet. The dr. wanted to

wait until he finished the 4 rounds of Xeloda and then do another

scan.

Caroline.

>

> Caroline:

> Where was the tumor that was removed? Was it in the liver? Was

that the

> only liver tumor or were there others that could not be removed?

If they

> removed all of the visible tumors, it sounds like he has done

well. You said he

> is on " chemo with Xeloda " . Is he on Folfox? I am just starting

chemo next

> week after liver resection, colon resection, and more and I am

starting on

> Folfox (Oxaliplatin, 5FU and Leucovorin with Avastin to be added

the third

> round). No Xeloda the first time. I am curious as to what other

chemo he is using

> and is doing so well on. The CEA can be misleading and it is more

important

> to look at the CT/Pet Scans. Has he had a follow up or baseline

scan since

> he began chemo?

>

>

> Hi - I don't think I've introduced myself before; I'm primarily

> a " lurker " on this board... My dad was diagnosed with stage 4

colon

> cancer (w/ mets to liver and lymph nodes) on 5/18/05. He was

> admitted to the hospital immediately and had a large tumor removed

> and part of his colon 3 days later and a permanent colostomy put

in.

> He started chemo w/ Xeloda about 3 weeks later. After the first

> round (2 weeks on, 2 weeks off), he went back to the oncologist

for a

> check-up. Although he looks really good - maintaining his weight

&

> had only some nausea and fatigue with the chemo - his CEA level

was

> still up. The onc. said that was only part of the evaluation.

Since

> he looked so good, she said that was more important and ordered

him 3

> more rounds of Xeloda. Over the weekend, he finished his 2nd

course

> of the Xeloda. He handled this course much better than the first -

> virtually no nausea & much less fatigue. He's eating much better

> this time - almost all the same foods he did before the surgery.

> And, he's been more active - taking trips to the store & swimming

in

> their pool.

>

> Here's my question - how important are the CEA levels? Dad goes

back

> in next week for another blood test evaluation, and I'm worried

about

> the impact on his spirits if the CEA levels are still increasing.

His

> spirits have been much better (thank you Zoloft!) the last few

weeks,

> and if the CEA isn't that important, I don't want him to sink into

> depression (which he's prone to.)

>

> Thanks,

> Caroline.

>

>

>

>

>

>

>

>

>

>

>

>

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Guest guest

Sorry it's taken me a couple of days to reply back to you-esp. after

your replied to me so quickly. I was out at working at a remote

office for a few days. Anyway ... The surgeon removed a large tumor

from his colon, but didn't touch the tumors on his liver. The

surgeon was actually very grim about my dad's prognosis, so it's even

more amazing to us that he's doing so well.

The onc. only prescribed him Xeloda. (I think because my dad was

really, really scared about a port-a-cath & intravenous chemo - to

almost the point of not wanting to try chemo.) She originally

mentioned putting him on Avastin, but then decided to just try the

Xeloda on its own at first.

It's reassuring to read that the CEA readings can be very erratic

during chemo. They do have the baseline scans from when they found

the tumors, but they haven't done another one yet. The dr. wanted to

wait until he finished the 4 rounds of Xeloda and then do another

scan.

Caroline.

>

> Caroline:

> Where was the tumor that was removed? Was it in the liver? Was

that the

> only liver tumor or were there others that could not be removed?

If they

> removed all of the visible tumors, it sounds like he has done

well. You said he

> is on " chemo with Xeloda " . Is he on Folfox? I am just starting

chemo next

> week after liver resection, colon resection, and more and I am

starting on

> Folfox (Oxaliplatin, 5FU and Leucovorin with Avastin to be added

the third

> round). No Xeloda the first time. I am curious as to what other

chemo he is using

> and is doing so well on. The CEA can be misleading and it is more

important

> to look at the CT/Pet Scans. Has he had a follow up or baseline

scan since

> he began chemo?

>

>

> Hi - I don't think I've introduced myself before; I'm primarily

> a " lurker " on this board... My dad was diagnosed with stage 4

colon

> cancer (w/ mets to liver and lymph nodes) on 5/18/05. He was

> admitted to the hospital immediately and had a large tumor removed

> and part of his colon 3 days later and a permanent colostomy put

in.

> He started chemo w/ Xeloda about 3 weeks later. After the first

> round (2 weeks on, 2 weeks off), he went back to the oncologist

for a

> check-up. Although he looks really good - maintaining his weight

&

> had only some nausea and fatigue with the chemo - his CEA level

was

> still up. The onc. said that was only part of the evaluation.

Since

> he looked so good, she said that was more important and ordered

him 3

> more rounds of Xeloda. Over the weekend, he finished his 2nd

course

> of the Xeloda. He handled this course much better than the first -

> virtually no nausea & much less fatigue. He's eating much better

> this time - almost all the same foods he did before the surgery.

> And, he's been more active - taking trips to the store & swimming

in

> their pool.

>

> Here's my question - how important are the CEA levels? Dad goes

back

> in next week for another blood test evaluation, and I'm worried

about

> the impact on his spirits if the CEA levels are still increasing.

His

> spirits have been much better (thank you Zoloft!) the last few

weeks,

> and if the CEA isn't that important, I don't want him to sink into

> depression (which he's prone to.)

>

> Thanks,

> Caroline.

>

>

>

>

>

>

>

>

>

>

>

>

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Guest guest

Unfortunately, my parents live in NM, and I live in TX, so I can't

normally be there for his dr. appointments. But, I'll mention it to

my mom so she can talk with his oncologist. At this point, my dad's

feeling so well, that we're thinking something has to be working! He

had a big problem with ascites at the beginning, but that doesn't

seem to be coming back signficantly like it was before, so we think

the chemo has to be working on the liver tumors. The main thing

we're happy about right now is that my dad's enjoying a really good

quality of life. This week, he and my mom went out for dinner and

drinks for the first time since before his surgery in May. Mom said

it was really fun - felt like back to normal again.

Thanks for all the help!

Caroline.

> > Hi - I don't think I've introduced myself before; I'm primarily

> > a " lurker " on this board... My dad was diagnosed with stage 4

> colon

> > cancer (w/ mets to liver and lymph nodes) on 5/18/05. He was

> > admitted to the hospital immediately and had a large tumor

removed

> > and part of his colon 3 days later and a permanent colostomy put

> in.

> > He started chemo w/ Xeloda about 3 weeks later. After the first

> > round (2 weeks on, 2 weeks off), he went back to the oncologist

for

> a

> > check-up. Although he looks really good - maintaining his weight

&

> > had only some nausea and fatigue with the chemo - his CEA level

was

> > still up. The onc. said that was only part of the evaluation.

> Since

> > he looked so good, she said that was more important and ordered

him

> 3

> > more rounds of Xeloda. Over the weekend, he finished his 2nd

> course

> > of the Xeloda. He handled this course much better than the

first -

> > virtually no nausea & much less fatigue. He's eating much better

> > this time - almost all the same foods he did before the surgery.

> > And, he's been more active - taking trips to the store & swimming

> in

> > their pool.

> >

> > Here's my question - how important are the CEA levels? Dad goes

> back

> > in next week for another blood test evaluation, and I'm worried

> about

> > the impact on his spirits if the CEA levels are still increasing.

> His

> > spirits have been much better (thank you Zoloft!) the last few

> weeks,

> > and if the CEA isn't that important, I don't want him to sink

into

> > depression (which he's prone to.)

> >

> > Thanks,

> > Caroline.

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Guest guest

Unfortunately, my parents live in NM, and I live in TX, so I can't

normally be there for his dr. appointments. But, I'll mention it to

my mom so she can talk with his oncologist. At this point, my dad's

feeling so well, that we're thinking something has to be working! He

had a big problem with ascites at the beginning, but that doesn't

seem to be coming back signficantly like it was before, so we think

the chemo has to be working on the liver tumors. The main thing

we're happy about right now is that my dad's enjoying a really good

quality of life. This week, he and my mom went out for dinner and

drinks for the first time since before his surgery in May. Mom said

it was really fun - felt like back to normal again.

Thanks for all the help!

Caroline.

> > Hi - I don't think I've introduced myself before; I'm primarily

> > a " lurker " on this board... My dad was diagnosed with stage 4

> colon

> > cancer (w/ mets to liver and lymph nodes) on 5/18/05. He was

> > admitted to the hospital immediately and had a large tumor

removed

> > and part of his colon 3 days later and a permanent colostomy put

> in.

> > He started chemo w/ Xeloda about 3 weeks later. After the first

> > round (2 weeks on, 2 weeks off), he went back to the oncologist

for

> a

> > check-up. Although he looks really good - maintaining his weight

&

> > had only some nausea and fatigue with the chemo - his CEA level

was

> > still up. The onc. said that was only part of the evaluation.

> Since

> > he looked so good, she said that was more important and ordered

him

> 3

> > more rounds of Xeloda. Over the weekend, he finished his 2nd

> course

> > of the Xeloda. He handled this course much better than the

first -

> > virtually no nausea & much less fatigue. He's eating much better

> > this time - almost all the same foods he did before the surgery.

> > And, he's been more active - taking trips to the store & swimming

> in

> > their pool.

> >

> > Here's my question - how important are the CEA levels? Dad goes

> back

> > in next week for another blood test evaluation, and I'm worried

> about

> > the impact on his spirits if the CEA levels are still increasing.

> His

> > spirits have been much better (thank you Zoloft!) the last few

> weeks,

> > and if the CEA isn't that important, I don't want him to sink

into

> > depression (which he's prone to.)

> >

> > Thanks,

> > Caroline.

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Guest guest

Caroline,

In the files of this group there is a explaination of what the CEA means.

Larry and Janet

Http://groups.yahoo.com/group/Janetrgreen

Caroline ecaroline1213@...> wrote:

Sorry it's taken me a couple of days to reply back to you-esp. after

your replied to me so quickly. I was out at working at a remote

office for a few days. Anyway ... The surgeon removed a large tumor

from his colon, but didn't touch the tumors on his liver. The

surgeon was actually very grim about my dad's prognosis, so it's even

more amazing to us that he's doing so well.

The onc. only prescribed him Xeloda. (I think because my dad was

really, really scared about a port-a-cath & intravenous chemo - to

almost the point of not wanting to try chemo.) She originally

mentioned putting him on Avastin, but then decided to just try the

Xeloda on its own at first.

It's reassuring to read that the CEA readings can be very erratic

during chemo. They do have the baseline scans from when they found

the tumors, but they haven't done another one yet. The dr. wanted to

wait until he finished the 4 rounds of Xeloda and then do another

scan.

Caroline.

>

> Caroline:

> Where was the tumor that was removed? Was it in the liver? Was

that the

> only liver tumor or were there others that could not be removed?

If they

> removed all of the visible tumors, it sounds like he has done

well. You said he

> is on " chemo with Xeloda " . Is he on Folfox? I am just starting

chemo next

> week after liver resection, colon resection, and more and I am

starting on

> Folfox (Oxaliplatin, 5FU and Leucovorin with Avastin to be added

the third

> round). No Xeloda the first time. I am curious as to what other

chemo he is using

> and is doing so well on. The CEA can be misleading and it is more

important

> to look at the CT/Pet Scans. Has he had a follow up or baseline

scan since

> he began chemo?

>

>

> Hi - I don't think I've introduced myself before; I'm primarily

> a " lurker " on this board... My dad was diagnosed with stage 4

colon

> cancer (w/ mets to liver and lymph nodes) on 5/18/05. He was

> admitted to the hospital immediately and had a large tumor removed

> and part of his colon 3 days later and a permanent colostomy put

in.

> He started chemo w/ Xeloda about 3 weeks later. After the first

> round (2 weeks on, 2 weeks off), he went back to the oncologist

for a

> check-up. Although he looks really good - maintaining his weight

&

> had only some nausea and fatigue with the chemo - his CEA level

was

> still up. The onc. said that was only part of the evaluation.

Since

> he looked so good, she said that was more important and ordered

him 3

> more rounds of Xeloda. Over the weekend, he finished his 2nd

course

> of the Xeloda. He handled this course much better than the first -

> virtually no nausea & much less fatigue. He's eating much better

> this time - almost all the same foods he did before the surgery.

> And, he's been more active - taking trips to the store & swimming

in

> their pool.

>

> Here's my question - how important are the CEA levels? Dad goes

back

> in next week for another blood test evaluation, and I'm worried

about

> the impact on his spirits if the CEA levels are still increasing.

His

> spirits have been much better (thank you Zoloft!) the last few

weeks,

> and if the CEA isn't that important, I don't want him to sink into

> depression (which he's prone to.)

>

> Thanks,

> Caroline.

>

>

>

>

>

>

>

>

>

>

>

>

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Guest guest

Caroline & Karima:

My mother in law lives in Taos but has lived in various other places in New

Mexico for many years (Santa Fe & Costilla). Santa Fe became too big for her

and she built a beautiful home on a golf course in Taos where it is more

peaceful. She still travels into Santa Fe once a week. She loves it.

Where are your parents, Caroline?

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Caroline & Karima:

My mother in law lives in Taos but has lived in various other places in New

Mexico for many years (Santa Fe & Costilla). Santa Fe became too big for her

and she built a beautiful home on a golf course in Taos where it is more

peaceful. She still travels into Santa Fe once a week. She loves it.

Where are your parents, Caroline?

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Guest guest

That is wonderful to hear that your dad is feeling so good and able to

get out with your mom and enjoy life a bit. Makes all the difference in

the world.

I still have not heard about my scan, grrr. I expect my Onc will call me

today or I will call someone next week.

I can't expect them to remember all the people and reasons to call them,

BUT he should remember to go over all his patients records before

the weekend.

Where in Texas are you? I am in central Texas next door to Fort Hood...

What part of NM are your folks. My sis used to live across border in

Hobbs, what God forsaken territory that was, well west Texas is too..

She lives in AZ now. Anyway I am going to have to call about my back

as well, as it is still giving me cause to complain. Should have been

back to normal by now.. Grrr. I am afraid it will affect my breathing (

I have COPD as well), hurts like heck to sneeze but not as bad as it

was.. I just don't want any problem with my breathing to mess me up. As

it is I don't feel right going job hunting just yet, want to make sure I

am ALL well before I do that. Why is your dad so afraid of the Port A

Cath and intraveneous chemo? I have had no problem with my cath, I

hardly know it is there anymore. My chemo was not bad at all. Had some

instances where I was quite tired after I completed a chemo cycle, but

over all felt pretty darn good - the drugs esp Decadron - helped my

breathing (a steroid) as well as took my aches and pains away from my

hips and knees which are now back again, and may also play a part in my

breathing now. I am worrying now more than I did during chemo. Not about

the cancer but about everything else...LOL.. Go figure.

I surely hope you dad continues to feel well, that is a really good sign

far as I am concerned. Will remember you all in my prayers. Jolene

Caroline wrote:

> Unfortunately, my parents live in NM, and I live in TX, so I can't

> normally be there for his dr. appointments. But, I'll mention it to

> my mom so she can talk with his oncologist. At this point, my dad's

> feeling so well, that we're thinking something has to be working! He

> had a big problem with ascites at the beginning, but that doesn't

> seem to be coming back signficantly like it was before, so we think

> the chemo has to be working on the liver tumors. The main thing

> we're happy about right now is that my dad's enjoying a really good

> quality of life. This week, he and my mom went out for dinner and

> drinks for the first time since before his surgery in May. Mom said

> it was really fun - felt like back to normal again.

>

> Thanks for all the help!

> Caroline.

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Guest guest

Jolene, I am so sorry that your back is acting up again. I think it

has been going on for too long now. Perhaps you need to get it

checked to make sure it is not a pinched nerve or something like

that. I am adding a Prayer for your back as well. Do hope you get

some relief from the back soon. Ingrid

>

> > Unfortunately, my parents live in NM, and I live in TX, so I can't

> > normally be there for his dr. appointments. But, I'll mention it

to

> > my mom so she can talk with his oncologist. At this point, my

dad's

> > feeling so well, that we're thinking something has to be

working! He

> > had a big problem with ascites at the beginning, but that doesn't

> > seem to be coming back signficantly like it was before, so we

think

> > the chemo has to be working on the liver tumors. The main thing

> > we're happy about right now is that my dad's enjoying a really

good

> > quality of life. This week, he and my mom went out for dinner and

> > drinks for the first time since before his surgery in May. Mom

said

> > it was really fun - felt like back to normal again.

> >

> > Thanks for all the help!

> > Caroline.

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Guest guest

Jolene, I am so sorry that your back is acting up again. I think it

has been going on for too long now. Perhaps you need to get it

checked to make sure it is not a pinched nerve or something like

that. I am adding a Prayer for your back as well. Do hope you get

some relief from the back soon. Ingrid

>

> > Unfortunately, my parents live in NM, and I live in TX, so I can't

> > normally be there for his dr. appointments. But, I'll mention it

to

> > my mom so she can talk with his oncologist. At this point, my

dad's

> > feeling so well, that we're thinking something has to be

working! He

> > had a big problem with ascites at the beginning, but that doesn't

> > seem to be coming back signficantly like it was before, so we

think

> > the chemo has to be working on the liver tumors. The main thing

> > we're happy about right now is that my dad's enjoying a really

good

> > quality of life. This week, he and my mom went out for dinner and

> > drinks for the first time since before his surgery in May. Mom

said

> > it was really fun - felt like back to normal again.

> >

> > Thanks for all the help!

> > Caroline.

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Guest guest

Jolene, I am so sorry that your back is acting up again. I think it

has been going on for too long now. Perhaps you need to get it

checked to make sure it is not a pinched nerve or something like

that. I am adding a Prayer for your back as well. Do hope you get

some relief from the back soon. Ingrid

>

> > Unfortunately, my parents live in NM, and I live in TX, so I can't

> > normally be there for his dr. appointments. But, I'll mention it

to

> > my mom so she can talk with his oncologist. At this point, my

dad's

> > feeling so well, that we're thinking something has to be

working! He

> > had a big problem with ascites at the beginning, but that doesn't

> > seem to be coming back signficantly like it was before, so we

think

> > the chemo has to be working on the liver tumors. The main thing

> > we're happy about right now is that my dad's enjoying a really

good

> > quality of life. This week, he and my mom went out for dinner and

> > drinks for the first time since before his surgery in May. Mom

said

> > it was really fun - felt like back to normal again.

> >

> > Thanks for all the help!

> > Caroline.

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