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Friend, If you havent already, go to the flax seed oil group Harold

[ ] An Introduction

Hi; I just found this group and thought I'd introduce myself. My name is Klaus, I'm 48 years old, live alone with 2 cats and own my own business helping inventors with engineering, design and I build plastic injection molds for them as well as running parts. 3 years ago I lost a kidney to cancer. About a year or so ago my right thumb started hurting, the doctors told me it was arthritis. About 3 months ago they took a biopsy of a growth from the heel of my hand and found that the arthritis was actually the renal carcinoma that my kidney had left behind. Now I'm almost unable to use my right hand. I've been to Mexico, for some homeopathic and enzyme treatments. I went to the Advanced Alternatives cancer center in Reno Nevada, were they gave me a Dendritic cell vaccine and nutritional IV's. I'm still somewhat depressed. My hand seems to not be improving but, under the microscope the vaccine is doing what it's supposed to be. I know that my attitude is a big factor in my healing, but it's very hard to keep good happy thoughts without some support. The support groups around here are all supporting people that are going through chemopoisoning,or radiation, and I just don't fit in with them. I've learned some of the different alternative therapies and I may be of some help to a few people with this information. But there is so much going on outside of the establishment that I'm hoping you people can fill in the blanks for me. The one question I have at this time about this group is " Do you get together physically on occasion with group members in your area's." The reason I ask is because it sure would be nice to connect face to face with a support group. Thanks Klaus Learn more about cancer:http://home.online.no/~dusan/diseases/cancer/http://home.online.no/~dusan/diseases/cancer/faq.htmhttp://www.geocities.com/~mycleanse/http://www.geocities.com/HotSprings/1158You are receiving this email because you elected to subscribe to the egroups.

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In a message dated 3/7/01 5:02:55 PM, ygammil1@... writes:

<< Klaus,

Harold's suggestion is a good one. There is no reason not to include

flaxseed oil in every cancer protocol. Subscribe:

FlaxSeedOil-subscribeonelist

How was your dendritic vaccine made? What is being looked at under the

microscope to determine that this vaccine is working -- blood? tumor tissue?

What did the vaccine cost? What is the protocol for the vaccine?

>>

Hi ; I'm taking flax seed oil. There is only one manufacturer for

the vaccine, that's biopulse clinic in mexico, (that I know of). It was

made from a donors tumor specifically for renal cell carcinoma. You can se

the dendrites encompassing the white blood cells in the blood. The vaccine

is part of a protocol depending on which clinic you go to, either 2 or 3

weeks, they give IV's of nutrients that boost your immune system, then give

the vaccine injections, while you're there. And send you home with enough for

about about 11 weeks of injection you do yourself. This costs around $13,500

Thanks Klaus

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Klaus,

Harold's suggestion is a good one. There is no reason not to include flaxseed oil in every cancer protocol. Subscribe: FlaxSeedOil-subscribeonelist

How was your dendritic vaccine made? What is being looked at under the microscope to determine that this vaccine is working -- blood? tumor tissue? What did the vaccine cost? What is the protocol for the vaccine?

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  • 7 months later...

Welcome, , I think you made a good choice in

joining a user group. Whatever you go through or

whatever questions you have, you can pretty well be

sure that somebody here has been there, or has the

information you're looking for. Many of us felt we

hadn't gotten the information or support we needed

from drs, pharmacutical companies, etc. I have found a

lot of help and support through this group. My name is

Dave, I'm from Green Bay, WI, and I have been on the

combo since January of this year. -dz-

--- quarles@... wrote:

> Hi,

> Just joined the group. Seems like a bunch of nice

> people here. Very

> active too. :-)

>

> I was diagnosed with Hep C just a few days ago. I

> have been trying

> to get all the information I could on it off the

> net. I thought that

> joining a group would help too.

>

> I don't know how I got Hep C. I have no symptoms,

> but for a job I

> was trying to get did a physical etc. and came back

> with the news. I

> was shocked to say the least and cried for a few

> hours. Now I am

> numb sort of. I am just trying to get educated

> about it. I know I

> will learn more here.

>

> I have an appointment with my primary doctor in the

> morning. I guess

> I will find out more then.

>

>

>

>

__________________________________________________

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just stick with the group and they will send you as much info as you ask for ...I am from Louisiana and joined the group a few months ago.They are the greatest bunch of people I have ever met.It's just like we know each other so well.Hope you enjoy us..I am here mostly for moral support because I too ask many questions........

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Hey everyone!!! As you can see I am back from Beaumont..Wasn't ready to leave though.....Love it there.Hope everyone is ok and once again...WELCOME YVONNE.......hey has Diane left yet????

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Hi

Welcome to the group. You will find a lot of support and info here.

The best advice I can give you at this time is try to keep up a good

attitude and outlook on life. You will be surprised at how much that helps.

[ ] An Introduction

> Hi,

> Just joined the group. Seems like a bunch of nice people here. Very

> active too. :-)

>

> I was diagnosed with Hep C just a few days ago. I have been trying

> to get all the information I could on it off the net. I thought that

> joining a group would help too.

>

> I don't know how I got Hep C. I have no symptoms, but for a job I

> was trying to get did a physical etc. and came back with the news. I

> was shocked to say the least and cried for a few hours. Now I am

> numb sort of. I am just trying to get educated about it. I know I

> will learn more here.

>

> I have an appointment with my primary doctor in the morning. I guess

> I will find out more then.

>

>

>

>

>

>

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Ok what happened??? Did I miss some more new people?? If I did I want to tell everyone hello..I am Jan....Nice to meet you....Please feel free to contact us anytime.This is a very helpful group

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Hi Dave,

Thanks for the welcome. Well, my appointment with my doctor was

changed to this afternoon. The waiting is hard. I did call the place

where I got the diagnosis from and they are faxing over the lab work

to my doctor today. Guess I will know more then.

I have read that diet is very important with Hep C. I have found out

recently that I have some food allergies too. I'm allergic to wheat

and milk. So this limits me even more I guess. Anyone know of a

good web site that has recipes or a list of foods to eat if you have

hep C?

> > Hi,

> > Just joined the group. Seems like a bunch of nice

> > people here. Very

> > active too. :-)

> >

> > I was diagnosed with Hep C just a few days ago. I

> > have been trying

> > to get all the information I could on it off the

> > net. I thought that

> > joining a group would help too.

> >

> > I don't know how I got Hep C. I have no symptoms,

> > but for a job I

> > was trying to get did a physical etc. and came back

> > with the news. I

> > was shocked to say the least and cried for a few

> > hours. Now I am

> > numb sort of. I am just trying to get educated

> > about it. I know I

> > will learn more here.

> >

> > I have an appointment with my primary doctor in the

> > morning. I guess

> > I will find out more then.

> >

> >

> >

> >

>

>

> __________________________________________________

>

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Hi ,

Thanks for the welcome. Yes, I am trying to keep a good attitude and

just face the facts. I cried for a while at first, but then I got

busy reading about it. I will know more this afternoon when I see my

doctor too.

I have always been a pretty optimistic type person.

Know any good web sites I should check out regarding Hep C?

Thanks again.

> Hi

>

> Welcome to the group. You will find a lot of support and info here.

>

> The best advice I can give you at this time is try to keep up a good

> attitude and outlook on life. You will be surprised at how much

that helps.

>

>

> [ ] An Introduction

>

>

> > Hi,

> > Just joined the group. Seems like a bunch of nice people here.

Very

> > active too. :-)

> >

> > I was diagnosed with Hep C just a few days ago. I have been

trying

> > to get all the information I could on it off the net. I thought

that

> > joining a group would help too.

> >

> > I don't know how I got Hep C. I have no symptoms, but for a job I

> > was trying to get did a physical etc. and came back with the

news. I

> > was shocked to say the least and cried for a few hours. Now I am

> > numb sort of. I am just trying to get educated about it. I know

I

> > will learn more here.

> >

> > I have an appointment with my primary doctor in the morning. I

guess

> > I will find out more then.

> >

> >

> >

> >

> >

> >

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I don't, I'm sure somebody does here. In general

though, eating healthy is the main thing. Minimize red

meats and iron. Good luck with your appointment.

-dz-

--- quarles@... wrote:

> Hi Dave,

> Thanks for the welcome. Well, my appointment with my

> doctor was

> changed to this afternoon. The waiting is hard. I

> did call the place

> where I got the diagnosis from and they are faxing

> over the lab work

> to my doctor today. Guess I will know more then.

>

> I have read that diet is very important with Hep C.

> I have found out

> recently that I have some food allergies too. I'm

> allergic to wheat

> and milk. So this limits me even more I guess.

> Anyone know of a

> good web site that has recipes or a list of foods to

> eat if you have

> hep C?

>

>

>

>

> > > Hi,

> > > Just joined the group. Seems like a bunch of

> nice

> > > people here. Very

> > > active too. :-)

> > >

> > > I was diagnosed with Hep C just a few days ago.

> I

> > > have been trying

> > > to get all the information I could on it off the

> > > net. I thought that

> > > joining a group would help too.

> > >

> > > I don't know how I got Hep C. I have no

> symptoms,

> > > but for a job I

> > > was trying to get did a physical etc. and came

> back

> > > with the news. I

> > > was shocked to say the least and cried for a few

> > > hours. Now I am

> > > numb sort of. I am just trying to get educated

> > > about it. I know I

> > > will learn more here.

> > >

> > > I have an appointment with my primary doctor in

> the

> > > morning. I guess

> > > I will find out more then.

> > >

> > >

> > >

> > >

> >

> >

> > __________________________________________________

> >

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The one I have found most helpful is

www.hepatitis-central.com They have quite a bit of

varied information. -dz-

--- quarles@... wrote:

> Hi ,

>

> Thanks for the welcome. Yes, I am trying to keep a

> good attitude and

> just face the facts. I cried for a while at first,

> but then I got

> busy reading about it. I will know more this

> afternoon when I see my

> doctor too.

>

> I have always been a pretty optimistic type person.

>

> Know any good web sites I should check out regarding

> Hep C?

>

> Thanks again.

>

>

>

>

> > Hi

> >

> > Welcome to the group. You will find a lot of

> support and info here.

> >

> > The best advice I can give you at this time is try

> to keep up a good

> > attitude and outlook on life. You will be

> surprised at how much

> that helps.

> >

> >

> > [ ] An Introduction

> >

> >

> > > Hi,

> > > Just joined the group. Seems like a bunch of

> nice people here.

> Very

> > > active too. :-)

> > >

> > > I was diagnosed with Hep C just a few days ago.

> I have been

> trying

> > > to get all the information I could on it off the

> net. I thought

> that

> > > joining a group would help too.

> > >

> > > I don't know how I got Hep C. I have no

> symptoms, but for a job I

> > > was trying to get did a physical etc. and came

> back with the

> news. I

> > > was shocked to say the least and cried for a few

> hours. Now I am

> > > numb sort of. I am just trying to get educated

> about it. I know

> I

> > > will learn more here.

> > >

> > > I have an appointment with my primary doctor in

> the morning. I

> guess

> > > I will find out more then.

> > >

> > >

> > >

> > >

> > >

> > >

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Hi Jan

Glad you had a good time.

Re: [ ] Re: An Introduction

Hey everyone!!! As you can see I am back from Beaumont..Wasn't ready to leave though.....Love it there.Hope everyone is ok and once again...WELCOME YVONNE.......hey has Diane left yet????

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Looks like I missed one too

Re: [ ] Re: An Introduction

Ok what happened??? Did I miss some more new people?? If I did I want to tell everyone hello..I am Jan....Nice to meet you....Please feel free to contact us anytime.This is a very helpful group

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Hi , and welcome to the family. I am Dennis from New Hampshire and

do a lot of stuff outside.

Hope things went well with the dr. It's a long road and we all have to keep

out spirits up. This group is good that way. I don't drink cow's milk

anymore but use soy milk on my cereal and have come to really like it.

Where are you from?

Don't be scared - and remember - we're always here to help.

Dennis

[ ] Re: An Introduction

> Hi Dave,

> Thanks for the welcome. Well, my appointment with my doctor was

> changed to this afternoon. The waiting is hard. I did call the place

> where I got the diagnosis from and they are faxing over the lab work

> to my doctor today. Guess I will know more then.

>

> I have read that diet is very important with Hep C. I have found out

> recently that I have some food allergies too. I'm allergic to wheat

> and milk. So this limits me even more I guess. Anyone know of a

> good web site that has recipes or a list of foods to eat if you have

> hep C?

>

>

>

>

> > > Hi,

> > > Just joined the group. Seems like a bunch of nice

> > > people here. Very

> > > active too. :-)

> > >

> > > I was diagnosed with Hep C just a few days ago. I

> > > have been trying

> > > to get all the information I could on it off the

> > > net. I thought that

> > > joining a group would help too.

> > >

> > > I don't know how I got Hep C. I have no symptoms,

> > > but for a job I

> > > was trying to get did a physical etc. and came back

> > > with the news. I

> > > was shocked to say the least and cried for a few

> > > hours. Now I am

> > > numb sort of. I am just trying to get educated

> > > about it. I know I

> > > will learn more here.

> > >

> > > I have an appointment with my primary doctor in the

> > > morning. I guess

> > > I will find out more then.

> > >

> > >

> > >

> > >

> >

> >

> > __________________________________________________

> >

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We believe she has. She said she was sending her last

message before leaving. -dz-

--- Jannewilms42@... wrote:

> Hey everyone!!! As you can see I am back from

> Beaumont..Wasn't ready to leave

> though.....Love it there.Hope everyone is ok and

> once again...WELCOME

> YVONNE.......hey has Diane left yet????

>

__________________________________________________

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I have also switched to using soy milk, I am not

really allergic, but I have a lactose intolerance. Now

I wouldn't want to go back to regular milk, although

soy is a little more expensive. I still must confess

to a weakness for a little ice cream now and then.

-dz-

--- Dennis <dhuber@...> wrote:

> Hi , and welcome to the family. I am Dennis

> from New Hampshire and

> do a lot of stuff outside.

> Hope things went well with the dr. It's a long road

> and we all have to keep

> out spirits up. This group is good that way. I

> don't drink cow's milk

> anymore but use soy milk on my cereal and have come

> to really like it.

> Where are you from?

> Don't be scared - and remember - we're always here

> to help.

>

> Dennis

__________________________________________________

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Hi,

Someone told me of a great recipe---a tofu smoothie. She said it

made her lose weight, dropped her cholesterol 90 in a year and tastes

good.

She said take tofu, soy milk and any fruit you want and put in a

blender. I have not tried it yet, but will soon. It sounds pretty

good. Should be healthy.

> > Hi , and welcome to the family. I am Dennis

> > from New Hampshire and

> > do a lot of stuff outside.

> > Hope things went well with the dr. It's a long road

> > and we all have to keep

> > out spirits up. This group is good that way. I

> > don't drink cow's milk

> > anymore but use soy milk on my cereal and have come

> > to really like it.

> > Where are you from?

> > Don't be scared - and remember - we're always here

> > to help.

> >

> > Dennis

>

>

> __________________________________________________

>

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It sounds good. I have never really had tofu. All I

know is that it is in some way derived from soy. Some

things a juicer is not good for, though. I don't have

a good blender. I tried bananas once and that was a

disaster. -dz-

--- quarles@... wrote:

> Hi,

>

> Someone told me of a great recipe---a tofu smoothie.

> She said it

> made her lose weight, dropped her cholesterol 90 in

> a year and tastes

> good.

>

> She said take tofu, soy milk and any fruit you want

> and put in a

> blender. I have not tried it yet, but will soon.

> It sounds pretty

> good. Should be healthy.

>

>

>

__________________________________________________

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