Greetings

[Guest guest]

well Gillian, with a name like michael I would

have to have some gaelic blood in me ,for sure.

My great great dad came from mountmellick

to bradford in yorkshire in the 1850's.

Carroll was the name. the family still live

on the farm inCo. Leix.

I am regarded as the prodigal son!

I have simmental cows, just beef.

As as possible.

maybe we could satart an export import business

with NZ lamb and you with Irish pork bacon.

no doubt the little people would interfere.

love michael w

The great events of world history are profoundly unimportant.

The essential thing is the life of the individual.

http://www.igrin.co.nz/~mcwarr

[Guest guest]

Hi Ruth,

Welcome to our list, your story is so familiar, we pretty much hear about

relapses with LD every day. In my opinion, and I am no doctor, I would surmise

that you have Chronic Lyme disease, that is now affecting you neurologically.

Please check this website:

http://www.geocities.com/HotSprings/Oasis/6455/lyme-links.html

This is the most comprehensive information available on the internet about Lyme

disease, all in one place.

Be sure that you check out Dr ph Burrascano's treatment protocol for LD and

if possible print it out and take it to your doctor,

if he is co-operative and willing, you could begin a longer treatment of orals

or IV meds to help with those recurring symptoms.

http://www.geocities.com/HotSprings/Spa/6772/conns.txt, this is the shortest

version, 7pages, and appeared in Conn's Current Therapies, a book that

physicians are familiar with.

There is a Lyme disease support group in Arizona, contact them to see if they

know of any Lyme literate doctors (LLMD) in your area:

Arizona Lyme Disease Support Group

Carol Marter

1821 N. 87th Way

sdale, AZ 85257

602-994-5449

CarolM94@...

Please feel free to ask questions, we have a very supportive and informative

group who are very willing to help you find information as best we can. Many of

us have suffered from this disease for a long time, some get better, and then

relapse, if any are totally cured, we don't always hear as they don't post

anymore, so don't give up hope when you read all our postings.

Welcome hugs,

Marta

[Lyme-aid] Greetings

From: " Ruth Trombly " <fancylala@...>

Hello,

I just signed up for this list today and I would like to introduce myself and

tell everyone a little about my life with Lyme. I am 21 years old and I am a

computer technician. I contracted Lyme back when I was 16 and living in East

Lyme, Conn. I had two ticks, the first one had not dug in to me yet when I found

it. Four days after finding the first, I discovered a second one well buried in

my side. I had to remove it with tweezers. I told my father about it and within

a few days I was so achy that I couldn't get out of bed. I was extremely tired

and had a lot of difficulty doing simple things like typing and getting dressed.

This went away as quickly as it came on, but I was feeling worse within a few

days. I didn't have a rash so I didn't think it was Lyme. By this time my aches

were accompanied with a fever that wouldn't go away so my father took me to the

Doctor. I was told that not all people with Lyme get the rash, was perscribed

Doxycylene and given a blood test. The Dox. helped but my blood test came back

negative. About two months after finding the ticks, I moved to Arizona and I

almost immediately started feeling the aches again. Not many doctors in Arizona

had ever dealt with Lyme but I was able to take another test, this time it came

up positive. I was given a perscription for Naproxen Sodium and this helped with

the pain. For years, I continued to get occasional flare-ups of pain that would

usually go away if I stayed in bed and took pain relievers. Recently, the

flare-ups have been more frequent and more painful. This past Saturday, I

started feeling dizzy, and I noticed more floaters in my eyes. I went to work on

Monday only to realize that I was having difficulty with speaking and doing

tasks necessary to my job (typing, logging in to the phone to get voicemails,

etc). I decided to see a Doctor so I went to a walk-in clinic. While I was in

the exam room waiting for the Doctor, I fainted twice. I told her about my

history and problems with Lyme and she told me that in Ohio (where I am living

now) there were few cases of Lyme and honestly said that she had not had too

many dealings with it. She gave me some doxycyclene and told me to take

dramimine for the dizziness. Today, my dizziness has subsided but now I have the

burning pains in my neck and shoulders. I have a lot of questions about Lyme

that I have not been able to find answers to, so I am hoping to learn a lot from

this list. I am upset at the lack of information I was given when I first got

sick, and the lack of available treatment is disturbing. I wonder if anyone on

this list has had the " relapses " I described. Should I be on doxycyclene every

time I have one- and if I let them go untreated as I have in the past, will they

become worse with more symptoms in the future? Thanks for reading this and I am

looking forward to gaining some knowledge!

Ruth Trombly

fancylala@...

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

[This message contained attachments]

[Guest guest]

I am wondering if anyone ever gets totally cured. I have known so many people

that have contracted Lyme that have been dealing with it for many years, but I

don't know anyone who has been totally cured. Anyway, I am pleased with the

friendly responses I've received from the list and I want to thank everyone.

It's comforting to know that I am by no means the only one who is fighting a

hard battle with this- and that many people find their physicians

unknowledgeable and unsure about treatments. I've looked at Dr. Burrascano's

protocol and I am going to bring it to my doctor. I would give anything to be

able to lead a normal life again, not having to miss work and such. I am

currently living in Ohio and Lyme isn't a problem here like it was in Conn. so

when I tell my boss that I can't come to work because of Lyme complications, he

looks at me like I just told him I was dying of cancer. Now that I am learning

more I feel empowered and I will do everything I can to improve.

[Lyme-aid] Greetings

From: " Ruth Trombly " <fancylala@...>

Hello,

I just signed up for this list today and I would like to introduce myself

and tell everyone a little about my life with Lyme. I am 21 years old and I am a

computer technician. I contracted Lyme back when I was 16 and living in East

Lyme, Conn. I had two ticks, the first one had not dug in to me yet when I found

it. Four days after finding the first, I discovered a second one well buried in

my side. I had to remove it with tweezers. I told my father about it and within

a few days I was so achy that I couldn't get out of bed. I was extremely tired

and had a lot of difficulty doing simple things like typing and getting dressed.

This went away as quickly as it came on, but I was feeling worse within a few

days. I didn't have a rash so I didn't think it was Lyme. By this time my aches

were accompanied with a fever that wouldn't go away so my father took me to the

Doctor. I was told that not all people with Lyme get the rash, was perscribed

Doxycylene and given a blood test. The Dox. helped but my blood test came back

negative. About two months after finding the ticks, I moved to Arizona and I

almost immediately started feeling the aches again. Not many doctors in Arizona

had ever dealt with Lyme but I was able to take another test, this time it came

up positive. I was given a perscription for Naproxen Sodium and this helped with

the pain. For years, I continued to get occasional flare-ups of pain that would

usually go away if I stayed in bed and took pain relievers. Recently, the

flare-ups have been more frequent and more painful. This past Saturday, I

started feeling dizzy, and I noticed more floaters in my eyes. I went to work on

Monday only to realize that I was having difficulty with speaking and doing

tasks necessary to my job (typing, logging in to the phone to get voicemails,

etc). I decided to see a Doctor so I went to a walk-in clinic. While I was in

the exam room waiting for the Doctor, I fainted twice. I told her about my

history and problems with Lyme and she told me that in Ohio (where I am living

now) there were few cases of Lyme and honestly said that she had not had too

many dealings with it. She gave me some doxycyclene and told me to take

dramimine for the dizziness. Today, my dizziness has subsided but now I have the

burning pains in my neck and shoulders. I have a lot of questions about Lyme

that I have not been able to find answers to, so I am hoping to learn a lot from

this list. I am upset at the lack of information I was given when I first got

sick, and the lack of available treatment is disturbing. I wonder if anyone on

this list has had the " relapses " I described. Should I be on doxycyclene every

time I have one- and if I let them go untreated as I have in the past, will they

become worse with more symptoms in the future? Thanks for reading this and I am

looking forward to gaining some knowledge!

Ruth Trombly

fancylala@...

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[This message contained attachments]

[Guest guest]

ruth

welcome to our group ....here u will find compassion, support and much

information on the disease we all share......

Reid

[Guest guest]

Ruth,

Sorry I misunderstood about where you were currently living. Ohio has plenty

of Lyme, and plenty of support groups too.

Here is the link that will take you to the list of groups in OH.

http://www.geocities.com/HotSprings/Spa/6772/ohio-patients.txt

As for anyone getting cured....yes, there are some who report a complete

cessation of symptoms, so don't lose hope. We are all different, have different

immune systems, as well as different strains of the Bb, and co-infections, thus

it is not always easy for us to find that perfect combo of meds that will help

all of us. I am glad you find the list supportive and comforting to know you

are not alone, that's why we are here together. You are lucky if your boss

equates the seriousness of LD with cancer, but I doubt that is what you meant.

I hope that you find good luck with your doctor and he is willing to follow the

Burrascano protocol, if not, contact those support groups for a Lyme literate

doctor in your area.

Good luck,

Marta

From: " Ruth Trombly " <fancylala@...>

I am wondering if anyone ever gets totally cured. I have known so many people

that have contracted Lyme that have been dealing with it for many years, but I

don't know anyone who has been totally cured. Anyway, I am pleased with the

friendly responses I've received from the list and I want to thank everyone.

It's comforting to know that I am by no means the only one who is fighting a

hard battle with this- and that many people find their physicians

unknowledgeable and unsure about treatments. I've looked at Dr. Burrascano's

protocol and I am going to bring it to my doctor. I would give anything to be

able to lead a normal life again, not having to miss work and such. I am

currently living in Ohio and Lyme isn't a problem here like it was in Conn. so

when I tell my boss that I can't come to work because of Lyme complications, he

looks at me like I just told him I was dying of cancer. Now that I am learning

more I feel empowered and I will do everything I can to improve.

[Guest guest]

well howdy right back at ya from the big apple

welcome to the group!!

ro

[Guest guest]

In a message dated 21/04/01 04:43:30 GMT Daylight Time, cloudnin@... writes:

Okay, well looks like a nice group and sure did want to say howdy from

Florida Land.

Welcome Pam / Cloud !

Hope you benefit from the group. Nice post, and you will probably receive some 'feedback' from it. Just wanted to say HI !!

Mike (from the UK)

[Guest guest]

In a message dated 4/20/01 10:43:31 PM US Eastern Standard Time,

cloudnin@... writes:

<< My RA Factor and ANA test came back a high positive and from reading the

general rule i found for the PA is that most test seronegative? >>

Hi Pam - One thing about you testing positive is that most of the newer drugs

are approved for RA but not yet for PA. At least your rheumy can say you

have RA to get you on Remicade or Enbrel (when it becomes available again) so

I'd say you have some good drug options. They are very expensive, however,

and you mentioned cost. I guess if you don't have insurance they are

basically not an option.

I do think, regardless of cost, you should try to see a dermatologist. You

sound like you are describing psoriasis, but who knows - does sound like you

should have it checked out though.

Good luck,

[Guest guest]

I am new to the Enbrel conversation - why is it not available?

[Guest guest]

In a message dated 8/14/01 6:52:19 AM, imachemist@... writes:

<< My arthritis is considerably worse (can hardly

walk - taking an ANSAID) my brain is foggy and I feel fatigued much of the

time. In a nutshell - I feel like crap. Suggestions? >>

Mr. Mysterious X-

I would RUN, not walk to the nearest LLMD (lyme literate dr. in which I have

a list of them) and get yourself treated!!!!! Your moronic, ignorant drs.

SHOULD KNOW that the classic bull's eye rash, which only appears in about 30%

of the people that DO have lyme, IT IS 100% POSITIVE FOR LYME DISEASE --and

this is according to the CDC!!!!!!!!!!!!

Need help? write me, I will be away for 1 wk starting tomorrow so if you

write today, I can help. My friend, you have only experienced just the

beginning of what is going to be a nightmare!!!! (if you go on untreated with

antibiotics as well as other protocols.)

I was paralyzed from the neck down from lyme and experienced what you are

going through, but 10 times worse. My husband nearly died from lyme and 5 of

my 6 kids are chronic.

Don't waste time or $$.

sue in nj

sue massie

[Guest guest]

1. You have to be proactive. First, get copies of all your old blood tests

and files from former doctors so you can be clear to your new doctors..

2. Some labs are better than others. Find a LLMD in your area (we found

ours here in SF from searching on the net) and get good blood tests specific

for Lyme Disease. (Again, always keep copies for your own file).

3. Become knowledgable on Lyme. Lots of websites, etc. The more you know,

the more you can ask the right questions.

Unfortunately, this is a complicated and underresearched disease with

catastrophic results if left untreated. You need to be your own advocate.

[Guest guest]

Sorry to hear what you are going through - your history of exposure,

rash and symptoms are very diagnostic of lyme. Unfortunately,

doctors are not clinicians anymore and rely on blood tests to " tell

them " what to diagnose. Lyme disease is diagnosed clinically, not by

blood tests (according to the CDC)! Most doctors don't know this and

don't care. There are labs which are more accurate in their testing -

Igenex and StonyBrook are two. You may have to pay out-of-pocket for

a lyme knowledgable doctor.

My daughter also was bit and had a classic EM rash - at the time I

was ignorant of lyme and didn't take her to the doctor to see it.

Her blood tests were also negative so they wouldn't diagnose lyme

based on my description of the rash and tick. I was also in an HMO

and we went on the merry-go-round of HMO approved doctors which

wasted a lot of time. I had thought that I could convince at least

one doctor to treat her - after all, she's a kid and did have a

classic EM rash. We had no such luck. I have found that most

doctors will diagnose anything BUT lyme disease (including chronic

fatigue syndrome in an 11 year old?) We finally went to a

pediatrician very experienced in diagnosing and treating lyme and my

daughter is now almost symptom free. I wish you the best of luck in

getting back to health.

[Guest guest]

Have you spoken to your doctor about this? It sounds like you need to also chech

into see a neurologist.

Sheryl

Re: [ ] Greetings

>

> In a message dated 8/14/01 6:52:19 AM, imachemist@... writes:

>

> << My arthritis is considerably worse (can hardly

> walk - taking an ANSAID) my brain is foggy and I feel fatigued much of the

> time. In a nutshell - I feel like crap. Suggestions? >>

>

> Mr. Mysterious X-

> I would RUN, not walk to the nearest LLMD (lyme literate dr. in which I have

> a list of them) and get yourself treated!!!!! Your moronic, ignorant drs.

> SHOULD KNOW that the classic bull's eye rash, which only appears in about 30%

> of the people that DO have lyme, IT IS 100% POSITIVE FOR LYME DISEASE --and

> this is according to the CDC!!!!!!!!!!!!

> Need help? write me, I will be away for 1 wk starting tomorrow so if you

> write today, I can help. My friend, you have only experienced just the

> beginning of what is going to be a nightmare!!!! (if you go on untreated with

> antibiotics as well as other protocols.)

> I was paralyzed from the neck down from lyme and experienced what you are

> going through, but 10 times worse. My husband nearly died from lyme and 5 of

> my 6 kids are chronic.

> Don't waste time or $$.

> sue in nj

> sue massie

>

>

[Guest guest]

To Sheryl ;

Do you have a list of LLMD's in Northern California? The only doctor that

I know of who treats a lot of Lyme patients is Dr. S. in San Francisco.

You can email me at tmroyster@... if you prefer.

Thanks a lot.

[Guest guest]

Glad to hear from you, Patty in Alaska. More later.

Harper

[Guest guest]

Greetings

.....is this your first fast? Will it be supervised by a

knowledgeable professional? 60 days sounds a little bit too long for a

first fast. Your body needs to become accustomed to fasting. Personally, I

would go much slower starting with maybe 5 days then wait a month and fast

again for 7 days then work up to 30 days at the most. Whatever you decide,

please let us know how you are doing. Betsy

Young wrote:

> My name is Young. I am 33 years old and been very intrested in

> fasting. I would like to start with a 60 day fast. I am starting research

> into juice fasting. I plan to have a 5 day intro, 50 day juice fast, 5 day

> breaking the fast.

>

>

[Guest guest]

In a message dated 04/04/2002 10:17:17 AM Central Standard Time,

westoo@... writes:

> Young wrote:

> > My name is Young. I am 33 years old and been very intrested in

> > fasting. I would like to start with a 60 day fast. I am starting research

> > into juice fasting. I plan to have a 5 day intro, 50 day juice fast, 5 day

> > breaking the fast.

>

,

I just finished a book by the world famous Sir Winters (of jason Winters

tea fame). He says for health, it is an absolute that people

fast. He suggests a 7 day juice fast using mega dodes of colon cleamser

and enemas. But he says for the amount of days you fast that how many days it

should take to break the fast. So if you fast 50 days, you should take

a loooong time to gently break it or you might undo all the good you've done.

......just a thought from his book.

Edith

[Guest guest]

My partner and I are going to start a 7 day juice fast

beginning money and possibly continuing another week.

Do you all feel that mega doses of colon cleanser and

enemas is recommended? I did this years ago and it

worked well. I took an enema in the morning upon

rising and one in the evening along with 3 heavy doses

of colon cleanser and lots of different juices all

day. Any suggestions.

--- ejohns9525@... wrote:

> In a message dated 04/04/2002 10:17:17 AM Central

> Standard Time,

> westoo@... writes:

>

>

> > Young wrote:

> > > My name is Young. I am 33 years old and

> been very intrested in

> > > fasting. I would like to start with a 60 day

> fast. I am starting research

> > > into juice fasting. I plan to have a 5 day

> intro, 50 day juice fast, 5 day

> > > breaking the fast.

> >

>

> ,

> I just finished a book by the world famous Sir

> Winters (of jason Winters

> tea fame). He says for health, it is an absolute

> that people

> fast. He suggests a 7 day juice fast using mega

> dodes of colon cleamser

> and enemas. But he says for the amount of days you

> fast that how many days it

> should take to break the fast. So if you fast 50

> days, you should take

> a loooong time to gently break it or you might undo

> all the good you've done.

> .....just a thought from his book.

> Edith

>

>

>

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________

[Guest guest]

charles92808@... writes:

> My partner and I are going to start a 7 day juice fast

> beginning money and possibly continuing another week.

> Do you all feel that mega doses of colon cleanser and

> enemas is recommended? I did this years ago and it

> worked well. I took an enema in the morning upon

> rising and one in the evening along with 3 heavy doses

> of colon cleanser and lots of different juices all

> day. Any suggestions.

>

,

Some people highly recommend using a colon cleanser along with a juice fast

and others feel that the juice fast is cleansing enough in itself. So it's

really an individual choice. I have done a number of fasts in varying

lengths and have never used a colon cleanser along with a longer one, so I

can't really tell you anything from personal experience.

Can you share a little more about what your objectives are in doing this

fast? That might help with some answers. thanks.

in health,

rachel~

" Live your dreams now. Life is not a dress rehearsal. "

[Guest guest]

APEX6872@... writes:

> My name is Young. I am 33 years old and been very intrested in

> fasting. I would like to start with a 60 day fast. I am starting research

> into juice fasting. I plan to have a 5 day intro, 50 day juice fast, 5 day

> breaking the fast.

>

Hello

That's quite an undertaking for your first fast! I would concur with what

others have written about the usual recommendation of building up to a longer

fast and about the importance of pre-fast preparation and post-fast

transitioning back into regular food. I think you would want to plan for

much longer than five days. I also think that when planning a longer fast

it's good to be sensitive to what the body actually needs, as the body

doesn't recognize numbers of days like we do. When I did my most lengthy

fast I had thought I would go to 70 days, but ended up starting the

transition after 67 days. So please just be aware of what your particular

needs might be.

having said that, though, I will wish you well in your endeavor and encourage

you to be VERY aware of your body during this time and any signals that it

might be sending you of what it needs in order to do the cleansing it's

trying to do.

What prompted you to try fasting and how did you arrive at that particular

number of days?

in health,

rachel~

" Live your dreams now. Life is not a dress rehearsal. "

[Guest guest]

basically to have more energy and have good health.

Your suggestions are most helpful.

--- Rachd1961@... wrote:

> APEX6872@... writes:

> > My name is Young. I am 33 years old and

> been very intrested in

> > fasting. I would like to start with a 60 day fast.

> I am starting research

> > into juice fasting. I plan to have a 5 day intro,

> 50 day juice fast, 5 day

> > breaking the fast.

> >

>

> Hello

> That's quite an undertaking for your first fast! I

> would concur with what

> others have written about the usual recommendation

> of building up to a longer

> fast and about the importance of pre-fast

> preparation and post-fast

> transitioning back into regular food. I think you

> would want to plan for

> much longer than five days. I also think that when

> planning a longer fast

> it's good to be sensitive to what the body actually

> needs, as the body

> doesn't recognize numbers of days like we do. When

> I did my most lengthy

> fast I had thought I would go to 70 days, but ended

> up starting the

> transition after 67 days. So please just be aware

> of what your particular

> needs might be.

>

> having said that, though, I will wish you well in

> your endeavor and encourage

> you to be VERY aware of your body during this time

> and any signals that it

> might be sending you of what it needs in order to do

> the cleansing it's

> trying to do.

>

> What prompted you to try fasting and how did you

> arrive at that particular

> number of days?

>

> in health,

> rachel~

> " Live your dreams now. Life is not a dress

> rehearsal. "

>

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________

[Guest guest]

Karla,

I read my messages on line. I go to the message # where I left off,

open it, then click on message index. Then after this is open click

on expand messages. I then read all the messages until I get to the

bottom of the page, end of the lot, or run out of time. Maddie

> A heardy hello to you all as I am just new to your group.

> I have a question about the management of the board.

> Is there a way to read the postings with out the advertisements

> interferring with the messages. Since it is easier to follow the

> threads while reading the message board outside of email, I like

to

> do that hate the advertisments and being redirected to the

messages.

>

> also... I am wondering why the kirkman labs enzymes are so much

> different ( cost wise and also ingtrediant wise ) from the Houston

> products.

>

> Has anyone advise on which is the better enzyme compound to use in

> terms of what they include in their individual recipes of tablets?

> I can see tha the Kirkman labs enzymes seem to list alot more

> individual components, but that does not make them better, maybe

jsut

> more costly.

> Thanks for having this mesage board also!

[Guest guest]

Dear Darcy,

This really angers me. Your doctor says you have only six months and

yet still gives you radiation. To me, this is criminal behaviour....to give

chemo and/or radiation when they know it will not work!! Thank goodness

you are not buying it. But be careful, probably unknowingly, your doctor

is seeing to it that the six month prognosis will come true. NO CANCER

IS INCURABLE!!!!!!!!!!

Please research the following websites - you won't be sorry. You need

to start this protocol ASAP.

Cantron is an electrolyte; a liquid which you take 1/4 tsp every four hours.

I cured myself of lung cancer with it and personally know a lot of people who

have been successful with it. It works on all cancers by lowering the

energy

level (voltage) in the cancer cells to a point where they cannot

divide/spread/grow. Then the immune system does the rest.

ENTELEV / CANCELL / CANTRON HOME PAGE / These sites

explain about Cantron:

http://www.best.com/~handpen/Cancell/cancell.htm

Technical - How it works:

http://www.best.com/~handpen/Cancell/how.htm

Cantron Testimonials:

http://www.geocities.com/cantron_2000/testimonials.html

Medical Research Products / Manufactures and sells Cantron and protocol

(Lots of info on this site)

http://www.cantron.com/

My doctor who walked me through to wellness - a real angel.

http://cancerchoices.com/wellness_program.htm

http://cancerchoices.com/testimonies.htm

Dr.Maras is available for consultations 4:00PM to 6:00PM,

EDT, Monday thru Thursday. The telephone number is: 561-792-7077

or email him at : jmaras@...

If I can answer any questions or be of any help, let me know.

I highly recommend you get with Dr. Maras D.O.

Hank

In a message dated 6/30/02 11:46:03 AM Eastern Daylight Time,

darceshipman@... writes:

> Dear Group,

>

> I just joined this group and wanted to check in. My name is Darcy.

> I live in Korea and am kind of out of the loop on alternative cancer

> treatment. My American trained doctors here are " against " any kind

> of healing through diet or supplements, although otherwise they

> are/seem competent in my treatment which so far has been chemotherapy

> for the first time (6 years ago) and now radiation. I would like to

> share what I am doing to boost my immune system but at the same time

> I am pretty confused about what's right to take and what's not. I

> have a lot of questions.

>

> Anyway, since this is my first time in a group just wanted to say Hi!

> and let you know I'm out here and in need to connect with other

> people with cancer. My cancer, by the way, is adenocarcinoma and

> according to my doctor " incurable " . He's given me " 6 months...maybe. "

> But I'm not buying it!

>

> Hope to hear from you soon.

> Darcy

[Guest guest]

Darcy you could try looking on this group to..........mostly about using

cottage cheese and flaxseed oil to help with cancer.Terry

FlaxSeedOil2

>From: " darceshipman " <darceshipman@...>

>Reply-

>

>Subject: [ ] greetings

>Date: Sun, 30 Jun 2002 15:45:08 -0000

>

>Dear Group,

>

>I just joined this group and wanted to check in. My name is Darcy.

>I live in Korea and am kind of out of the loop on alternative cancer

>treatment. My American trained doctors here are " against " any kind

>of healing through diet or supplements, although otherwise they

>are/seem competent in my treatment which so far has been chemotherapy

>for the first time (6 years ago) and now radiation. I would like to

>share what I am doing to boost my immune system but at the same time

>I am pretty confused about what's right to take and what's not. I

>have a lot of questions.

>

>Anyway, since this is my first time in a group just wanted to say Hi!

>and let you know I'm out here and in need to connect with other

>people with cancer. My cancer, by the way, is adenocarcinoma and

>according to my doctor " incurable " . He's given me " 6 months...maybe. "

>But I'm not buying it!

>

>Hope to hear from you soon.

>Darcy

>

>

>

>

[Guest guest]

Bye see you soon. WIll miss you like crazy till your back. [ ] Greetings Hello, everyone: Just to let you know: I'll be unsubscribing for awhile. I finally got my new hard drive in and it's a bit of a job 'unpacking' the old files and getting up to speed with the new settings. So, I'll be gone for awhile; will return when I get things sorted out. Best wishes to all,