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Hi Nancie!

Very nice to meet you and welcome to the group! I hope you will like it here.

Email me anytime you need to chat. This illness is very difficult. And it

certainly doesn't help when you don't have a support system for you. Please

know you are in my thoughts and prayers.

Soft hugs,

Annie C.

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Nancie, welcome to our group. I do agree that having fibro is better than

having lupus and all of those other diseases that you mentioned.

I think that we do have a good group. We are, for the most part, loving,

caring and supportive. If you want to vent, please do so. We all have done

so at one time or another. Need to know something? Ask and you will usually

get an answer. There are times when members of this group, are having

flares, are to sick to answer questions or just can't use their computers and

no one answers. Please ask again.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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Nancie, welcome to our group. I do agree that having fibro is better than

having lupus and all of those other diseases that you mentioned.

I think that we do have a good group. We are, for the most part, loving,

caring and supportive. If you want to vent, please do so. We all have done

so at one time or another. Need to know something? Ask and you will usually

get an answer. There are times when members of this group, are having

flares, are to sick to answer questions or just can't use their computers and

no one answers. Please ask again.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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  • 7 months later...
Guest guest

-----BEGIN PGP SIGNED MESSAGE-----

Hash: SHA1

barbieann518 wrote:

> hi yall!

......

> located in the Orlando Florida area.

Okay I'd assumed you were in the South Easstern US just from the

greeting ;-)

> My first endo is easygoing about treatment: drugs, RAI, or surgery,

> told me to come back in 6 weeks and he'll go with whatever I want to

> do. but he's real cryptic and their clinic seems to be more of a

> diabeties place, and I guess I felt like I wanted more TLC.

Endo's aren't always big on TLC...

> So I went to a 2nd endo, he's better at the TLC stuff, but is

> encouraging RAI and wants to do it like next week.

Around here we usually prefer to give the drugs at least a year or two,

as many patients can get remission from the disease, before having

surgery or RAI and possibly(surgery)/probably(RAI) having a life on

thyroxine.

So we are likely to go with the first guy, even without the TLC.

I guess with mild symptoms it doesn't matter (did anyone prescribe

betablockers?) so much, but I don't see why you have to wait 6 weeks to

start treatment, just let em know your decision as soon as it is made.

> I hope this isn't too much info, yall seem really knowledgeable, but

> it's late, I'm tired, but I'm sure I'll have lots-o-questions for

> yall this weekend.

You making the chat on Sunday at www.mediboard.com to ask these

questions then?

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Guest guest

Hi there!!

You will love this group. I don't post often but am always reading. Most

endo's are more familiar with diabetes because that's more common than

Graves. It's not easy to find a god end who will be willing to work with you

to do the treatment you want to do. Good luck and welcome!!

in MA, USA

Diagnosed w/Graves, March 1997

Glad I refused RAI Treatment and Surgery!!!

Currently in Remission!!!

Off Meds Since June 2000

Surpressed TSH and somehwat normal thyroid levels

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Guest guest

Hi there!!

You will love this group. I don't post often but am always reading. Most

endo's are more familiar with diabetes because that's more common than

Graves. It's not easy to find a god end who will be willing to work with you

to do the treatment you want to do. Good luck and welcome!!

in MA, USA

Diagnosed w/Graves, March 1997

Glad I refused RAI Treatment and Surgery!!!

Currently in Remission!!!

Off Meds Since June 2000

Surpressed TSH and somehwat normal thyroid levels

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Guest guest

hiya Simon,

LoL...yeppers, I'm a GRITS alright!

thanks for the mediboard info

I just joined up over there, posted my test results, and I'm gonna

plan to make the Sunday chat...oh wait, I better check the scheule...

(I'll be there as long as it doesn't interfere with the Nascar

race...LoL!:).

I'm starting to think the 1st endo may the best also,

" at your service " endos apparently aren't easy to find.

Thanks again!

> > hi yall!

> .....

> > located in the Orlando Florida area.

>

> Okay I'd assumed you were in the South Easstern US just from the

> greeting ;-)

>

> > My first endo is easygoing about treatment: drugs, RAI, or

surgery,

> > told me to come back in 6 weeks and he'll go with whatever I want

to

> > do. but he's real cryptic and their clinic seems to be more of a

> > diabeties place, and I guess I felt like I wanted more TLC.

>

> Endo's aren't always big on TLC...

>

> > So I went to a 2nd endo, he's better at the TLC stuff, but is

> > encouraging RAI and wants to do it like next week.

>

> Around here we usually prefer to give the drugs at least a year or

two,

> as many patients can get remission from the disease, before having

> surgery or RAI and possibly(surgery)/probably(RAI) having a life on

> thyroxine.

>

> So we are likely to go with the first guy, even without the TLC.

>

> I guess with mild symptoms it doesn't matter (did anyone prescribe

> betablockers?) so much, but I don't see why you have to wait 6

weeks to

> start treatment, just let em know your decision as soon as it is

made.

>

> > I hope this isn't too much info, yall seem really knowledgeable,

but

> > it's late, I'm tired, but I'm sure I'll have lots-o-questions for

> > yall this weekend.

>

> You making the chat on Sunday at www.mediboard.com to ask these

> questions then?

> -----BEGIN PGP SIGNATURE-----

> Comment: Using GnuPG with Mozilla - http://enigmail.mozdev.org

>

> iD8DBQE+l6vDGFXfHI9FVgYRAqxxAJ9L7P7n9Xz2Tcs/y6u6toVSvuv+1QCfWpl/

> H+NDcvXSabkB4cCEA+5k+UE=

> =WpDb

> -----END PGP SIGNATURE-----

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Guest guest

hiya Simon,

LoL...yeppers, I'm a GRITS alright!

thanks for the mediboard info

I just joined up over there, posted my test results, and I'm gonna

plan to make the Sunday chat...oh wait, I better check the scheule...

(I'll be there as long as it doesn't interfere with the Nascar

race...LoL!:).

I'm starting to think the 1st endo may the best also,

" at your service " endos apparently aren't easy to find.

Thanks again!

> > hi yall!

> .....

> > located in the Orlando Florida area.

>

> Okay I'd assumed you were in the South Easstern US just from the

> greeting ;-)

>

> > My first endo is easygoing about treatment: drugs, RAI, or

surgery,

> > told me to come back in 6 weeks and he'll go with whatever I want

to

> > do. but he's real cryptic and their clinic seems to be more of a

> > diabeties place, and I guess I felt like I wanted more TLC.

>

> Endo's aren't always big on TLC...

>

> > So I went to a 2nd endo, he's better at the TLC stuff, but is

> > encouraging RAI and wants to do it like next week.

>

> Around here we usually prefer to give the drugs at least a year or

two,

> as many patients can get remission from the disease, before having

> surgery or RAI and possibly(surgery)/probably(RAI) having a life on

> thyroxine.

>

> So we are likely to go with the first guy, even without the TLC.

>

> I guess with mild symptoms it doesn't matter (did anyone prescribe

> betablockers?) so much, but I don't see why you have to wait 6

weeks to

> start treatment, just let em know your decision as soon as it is

made.

>

> > I hope this isn't too much info, yall seem really knowledgeable,

but

> > it's late, I'm tired, but I'm sure I'll have lots-o-questions for

> > yall this weekend.

>

> You making the chat on Sunday at www.mediboard.com to ask these

> questions then?

> -----BEGIN PGP SIGNATURE-----

> Comment: Using GnuPG with Mozilla - http://enigmail.mozdev.org

>

> iD8DBQE+l6vDGFXfHI9FVgYRAqxxAJ9L7P7n9Xz2Tcs/y6u6toVSvuv+1QCfWpl/

> H+NDcvXSabkB4cCEA+5k+UE=

> =WpDb

> -----END PGP SIGNATURE-----

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Guest guest

thanks lisa! yeah, I'm thinkin' with all the endo issues posted, the

first one may be the best choice. Now I've just gotta decide on what

treatment I'm most comfortable with!

> Hi there!!

>

> You will love this group. I don't post often but am always reading.

Most

> endo's are more familiar with diabetes because that's more common

than

> Graves. It's not easy to find a god end who will be willing to work

with you

> to do the treatment you want to do. Good luck and welcome!!

>

> in MA, USA

> Diagnosed w/Graves, March 1997

> Glad I refused RAI Treatment and Surgery!!!

> Currently in Remission!!!

> Off Meds Since June 2000

> Surpressed TSH and somehwat normal thyroid levels

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Guest guest

Hi,

Meds are a good first line of approach because your thyroid hormone levels

are reduced and your immune system is given a chance to heal. Meds are taken

until your immune system stops producing the thyroid antibodies causing

hyperthryoidism. Most people then end up with normal thyroid function. Having

had RAI, I wouldn't recommend it. Being hypothyroid for me is far worse than

being hyperthryoid. Take care, Elaine

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  • 2 years later...
Guest guest

If I were you, I would meet with the oncologist and ask what the

statistical likelihood of a reoccurence would be without having

chemotherapy versus a reoccurence after having the recommended chemo

treatment.

A colonoscopy can detect a new primary tumor, but the reason for the

chemo would be to reduce the chance of any stray cancer cells

metastisizing.

Your father needs to weigh the side effects of the chemo, which isn't

necessarily unmanageable, against the benefits. For a patient who is

age 78, I think you are asking a very valid question.

> Hi I am in NC.My dad had emergency surgery 3 weeks ago for a

> tumor that obstructed the colon.It was as big as his fist and it

was

> cancer -stage 2 B I think ,If I remember right.He removed 12 inches

> of colon and 12 inches of small intestine.The tumor was at the top

> of the colon, growing into the small intestine.The good news , the

> margins were clear and the lymph nodes were free from cancer.The

> surgeon beleives he got it all....However the surgeon is almost

> positive the oncologist will recomend chemo and he will need a port.

>

> Here is our delema. He are trying to decide if Chemo is right for

> him.Hes 78 years old and has always been active and vital until the

> past 4 months or so.He travels and Birdwatches .He wants to know

how

> debilitating chemo is ,How long he will be out of commission, and

> given that most men dont live past 80 years old whether it would be

> worth it.

>

> The surgeon indicated it would be a 2 year recovery from the

> chemo.Is this true?how long before he would be strong enough to

> resume his lifestyle.? Amazingly he is recovering from surgery very

> quickly and feeling stronger every day.without chemo hewill

probably

> be feeling pretty good ina couple of months.If he passes on the

> chemo , would this cancer come back?Couldnt anual colonoscopys

catch

> a reoccurrence in time to remove it?

>

> Has anyone here had to face a similar decision?Any thoughts or

> recomendations?Id appreciate allthe input we can get.

>

> IN NC

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Guest guest

If I were you, I would meet with the oncologist and ask what the

statistical likelihood of a reoccurence would be without having

chemotherapy versus a reoccurence after having the recommended chemo

treatment.

A colonoscopy can detect a new primary tumor, but the reason for the

chemo would be to reduce the chance of any stray cancer cells

metastisizing.

Your father needs to weigh the side effects of the chemo, which isn't

necessarily unmanageable, against the benefits. For a patient who is

age 78, I think you are asking a very valid question.

> Hi I am in NC.My dad had emergency surgery 3 weeks ago for a

> tumor that obstructed the colon.It was as big as his fist and it

was

> cancer -stage 2 B I think ,If I remember right.He removed 12 inches

> of colon and 12 inches of small intestine.The tumor was at the top

> of the colon, growing into the small intestine.The good news , the

> margins were clear and the lymph nodes were free from cancer.The

> surgeon beleives he got it all....However the surgeon is almost

> positive the oncologist will recomend chemo and he will need a port.

>

> Here is our delema. He are trying to decide if Chemo is right for

> him.Hes 78 years old and has always been active and vital until the

> past 4 months or so.He travels and Birdwatches .He wants to know

how

> debilitating chemo is ,How long he will be out of commission, and

> given that most men dont live past 80 years old whether it would be

> worth it.

>

> The surgeon indicated it would be a 2 year recovery from the

> chemo.Is this true?how long before he would be strong enough to

> resume his lifestyle.? Amazingly he is recovering from surgery very

> quickly and feeling stronger every day.without chemo hewill

probably

> be feeling pretty good ina couple of months.If he passes on the

> chemo , would this cancer come back?Couldnt anual colonoscopys

catch

> a reoccurrence in time to remove it?

>

> Has anyone here had to face a similar decision?Any thoughts or

> recomendations?Id appreciate allthe input we can get.

>

> IN NC

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Guest guest

Hi , Welcome to our group here. You will find a lot of good

people here and a lot of information. I am so sorry your dad had to

go through this. I am surprised that chemo was recomended for stage 2

colon cnacer. Most of the time it is done for stage 3. But all

doctors are different. It would be best to talk to the Oncologist and

see what he recomends. It would be your fathers decison no matter

what. See what he feels after he sees the Onc. If he is otherwise

healthy the chemo may not be that hard on him. But again he must

weigh his options. Colonscopy can only detect the polops in the

colon. If the cancer returns or spreads the colonscopy would not find

it. Wishing you both the best. Ingrid

> Hi I am in NC.My dad had emergency surgery 3 weeks ago for a

> tumor that obstructed the colon.It was as big as his fist and it

was

> cancer -stage 2 B I think ,If I remember right.He removed 12 inches

> of colon and 12 inches of small intestine.The tumor was at the top

> of the colon, growing into the small intestine.The good news , the

> margins were clear and the lymph nodes were free from cancer.The

> surgeon beleives he got it all....However the surgeon is almost

> positive the oncologist will recomend chemo and he will need a port.

>

> Here is our delema. He are trying to decide if Chemo is right for

> him.Hes 78 years old and has always been active and vital until the

> past 4 months or so.He travels and Birdwatches .He wants to know

how

> debilitating chemo is ,How long he will be out of commission, and

> given that most men dont live past 80 years old whether it would be

> worth it.

>

> The surgeon indicated it would be a 2 year recovery from the

> chemo.Is this true?how long before he would be strong enough to

> resume his lifestyle.? Amazingly he is recovering from surgery very

> quickly and feeling stronger every day.without chemo hewill

probably

> be feeling pretty good ina couple of months.If he passes on the

> chemo , would this cancer come back?Couldnt anual colonoscopys

catch

> a reoccurrence in time to remove it?

>

> Has anyone here had to face a similar decision?Any thoughts or

> recomendations?Id appreciate allthe input we can get.

>

> IN NC

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Guest guest

Good Advice from ... I am nearly 64 (in Oct) and I just finished 6

mos of chemo, for Stage 3c with lymph node involvement.

Doc thinks they killed whatever was still there, but I will be checked

regularly for awhile. Due for colonoscopy in Sept.

What is important too now for you and any siblings to get tested...

Don't wait.. I knew I should have been tested several years ago

when my sister told me she had some polyps removed that were

precancerous. I put off one scope appt because at the time I was

taking care of my hubby who had non hodgkins lymphoma. He passed away in

1999. Probably a couple years ago I had noticed

some blood in my stool which I figured was from hemarrhoids, got some

prep H, used it and that was the end of it. But what if it was

from a polyp. If only I had had the scope back then, I might have

avoided the surgery and chemo that followed. So many what ifs..

Awhile back I took a survey and one of the subjects addressed was how a

doc determines whether a patient needs chemo or not.

The answer was that they don't know... In breast cancer they do alot

more examining of the cells to see if there is the slightest

chance of recurring cancer but with colon cancer they don't do that. So

theoretically a patient with your dad's diagnosis had maybe

a 50% chance of getting cancer or not getting it. When I was diagnosed

my CEA was 3.5. Pretty low but since 7 out of 12 lymph nodes showed

cancer, my doc decided that I should have chemo. I came through it okay

- they can adjust dosage somewhat to reduce severity of side effects.

I did have low potassium, and low white blood count but got pills for

the potassium and shots for the wbc count and I was pretty much okay.

Felt pretty good other than being tired as I was coming down from chemo.

During chemo felt great.. LOL. Well sorry to ramble on.

I am glad that you will abide by whatever decision your dad will make

concerning taking the chemo or not. This chemo is not as hard on

a person has some of the other chemos are. Some folks even work while

they are getting their chemo, just work around their chemo days etc.

God bless your family and will keep you in my prayers. Big hugs Jolene

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Guest guest

Good Advice from ... I am nearly 64 (in Oct) and I just finished 6

mos of chemo, for Stage 3c with lymph node involvement.

Doc thinks they killed whatever was still there, but I will be checked

regularly for awhile. Due for colonoscopy in Sept.

What is important too now for you and any siblings to get tested...

Don't wait.. I knew I should have been tested several years ago

when my sister told me she had some polyps removed that were

precancerous. I put off one scope appt because at the time I was

taking care of my hubby who had non hodgkins lymphoma. He passed away in

1999. Probably a couple years ago I had noticed

some blood in my stool which I figured was from hemarrhoids, got some

prep H, used it and that was the end of it. But what if it was

from a polyp. If only I had had the scope back then, I might have

avoided the surgery and chemo that followed. So many what ifs..

Awhile back I took a survey and one of the subjects addressed was how a

doc determines whether a patient needs chemo or not.

The answer was that they don't know... In breast cancer they do alot

more examining of the cells to see if there is the slightest

chance of recurring cancer but with colon cancer they don't do that. So

theoretically a patient with your dad's diagnosis had maybe

a 50% chance of getting cancer or not getting it. When I was diagnosed

my CEA was 3.5. Pretty low but since 7 out of 12 lymph nodes showed

cancer, my doc decided that I should have chemo. I came through it okay

- they can adjust dosage somewhat to reduce severity of side effects.

I did have low potassium, and low white blood count but got pills for

the potassium and shots for the wbc count and I was pretty much okay.

Felt pretty good other than being tired as I was coming down from chemo.

During chemo felt great.. LOL. Well sorry to ramble on.

I am glad that you will abide by whatever decision your dad will make

concerning taking the chemo or not. This chemo is not as hard on

a person has some of the other chemos are. Some folks even work while

they are getting their chemo, just work around their chemo days etc.

God bless your family and will keep you in my prayers. Big hugs Jolene

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Guest guest

Jolene, thanks for the info. Im glad to hear chemo isnt all that bad. I hope

your cancer can be wiped out.

IN NC

Jolene Ehret jehret@...> wrote:

Wilkins

http//:www.juiceplus.com/+lw55887

The Children's Research Foundation Children 6-15 FREE for 3 years

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

Start your day with Yahoo! - make it your home page

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Guest guest

Jolene, thanks for the info. Im glad to hear chemo isnt all that bad. I hope

your cancer can be wiped out.

IN NC

Jolene Ehret jehret@...> wrote:

Wilkins

http//:www.juiceplus.com/+lw55887

The Children's Research Foundation Children 6-15 FREE for 3 years

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

Start your day with Yahoo! - make it your home page

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Guest guest

Jolene, thanks for the info. Im glad to hear chemo isnt all that bad. I hope

your cancer can be wiped out.

IN NC

Jolene Ehret jehret@...> wrote:

Wilkins

http//:www.juiceplus.com/+lw55887

The Children's Research Foundation Children 6-15 FREE for 3 years

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

Start your day with Yahoo! - make it your home page

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  • 4 years later...
Guest guest

I'm new here and wanted to say " Hi. "

I found the SCD doing research for a diet for IBS (with C not D). I've had

bronchitis and required antibiotics at least a couple of times a year all my

life. I have developed allergies to three major classes of antibiotics and my

doctor recommended immunotherapy shots to get over the allergies to the

antibiotics because there are so few they can give me and it could be life

threatening if I develop any more allergies or encounter a resistant bacterial

infection.

I have had pneumonia three times, sinusitis twice, and strep twice in the last

eighteen months alone. I am so sick and tired of being sick and tired. I read

Elaine's book and it made so much sense. I've been on a vicious cycle of

illness, antibiotics and more illness. I knew I had to try the SCD. So here I

am.

Also, I was recently diagnosed with ADD-inattentive and I am hoping it will help

me with that too. My doctor said I was self medicating with caffeine and carbs.

I bought all the SCD cookbooks I could find on Amazon and I am learning a lot

from reading all your old posts! Thanks so much, everyone!

My best, Clichy Rose

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Guest guest

Hi Clichy,

Welcome and hope you feel better soon.

PJ

>

> I'm new here and wanted to say " Hi. "

>

> I found the SCD doing research for a diet for IBS (with C not D). I've had

bronchitis and required antibiotics at least a couple of times a year all my

life. I have developed allergies to three major classes of antibiotics and my

doctor recommended immunotherapy shots to get over the allergies to the

antibiotics because there are so few they can give me and it could be life

threatening if I develop any more allergies or encounter a resistant bacterial

infection.

>

> I have had pneumonia three times, sinusitis twice, and strep twice in the last

eighteen months alone. I am so sick and tired of being sick and tired. I read

Elaine's book and it made so much sense. I've been on a vicious cycle of

illness, antibiotics and more illness. I knew I had to try the SCD. So here I

am.

>

> Also, I was recently diagnosed with ADD-inattentive and I am hoping it will

help me with that too. My doctor said I was self medicating with caffeine and

carbs.

>

> I bought all the SCD cookbooks I could find on Amazon and I am learning a lot

from reading all your old posts! Thanks so much, everyone!

>

> My best, Clichy Rose

>

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