Re: Follicular Lymphoma Small Intestine

[Guest guest]

Read Dr Leonard Coldwells book, The Only Answer To Cancer

is a fantastic book . He has a 93% cancer cure rate

[Guest guest]

A 93% cancer cure rate? Is this documented with follow up over an extended

period? If it's true, this guy should have his face on a postage stamp.

Read Dr Leonard Coldwells book, The Only Answer To Cancer

is a fantastic book . He has a 93% cancer cure rate

[Guest guest]

This reminds me of the outstanding success rate had by the FBI in getting

convictions of those they arrest.................the secret? Only arrest those

you are guaranteed to convict. I do like the postage stamp reference! Then

there is The Cancer Industry that for many years used tricky statistics to show

their success. They used the Five Year survival as a cure even if someone died

a day after the five years, they were considered cured. ? Figures don’t

lie..........liars figure.

Joe C.

A 93% cancer cure rate? Is this documented with follow up over an extended

period? If it's true, this guy should have his face on a postage stamp.

Read Dr Leonard Coldwells book, The Only Answer To Cancer

is a fantastic book . He has a 93% cancer cure rate

[Guest guest]

Hi Greg

I'm coming up on 6 years fighting fcc-NHL. I've not needed treatment thus far

and have reversed it in many ways. You are doing some really good things below.

For curcumin (turmeric), check out:

www.lef.com

Consider joining:

www.lymphomasurvival.com

It's well worth the $25 annual fee.

The two biggest factors in my disease have been mercury amalgam fillings and

Candida.

best regards, Steve

>

> Hi,

>

> Recently diagnosed with Follicular Lymphoma B-Cell of the Small Intestine

>

> Im a 57 year old male. I understand that if you have Celliac's disease

> you are 6 times more likely to get this

>

> I was told by Oncology that I would need 6-9 treatments every 3 weeks of

Rituxin Cocktail

>

> Here are some things I have started:

>

> No Glutin

>

> Cottage cheese and flax seed fresh ground + Flax oil with berries

> (Budwig Idea) with cashews and pecans

>

> Carrot pear and apple juice 8 ox /day

>

> No desserts of fruit juices

>

> Here are some things I am considering:

>

> Essiac Tea Where do I get that Which Brand? How often?

>

> Tumeric Spice How to take that Pill Form?

>

> Any and all ideas are looked at

>

> If I do the Chemo then I need a good Natural Doctor I live in Arizona near

Phoenix

>

> Thanks for any help

>

> Greg

>

[Guest guest]

You will never see Dr Leonard Colwell on the TV, controlled by huge

corporations.

Medical  Mafia in this country  doesn't want to cure cancer, billion $

buisness 

Do your homework and read his book, at least check out his website and listen to

the radio shows

Your Health Crusader

________________________________

From: ROBERT ELLAL <rcellal@...>

Sent: Wed, December 29, 2010 3:36:45 PM

Subject: Re: [ ] Follicular Lymphoma Small Intestine

 

A 93% cancer cure rate? Is this documented with follow up over an extended

period? If it's true, this guy should have his face on a postage stamp.

Read Dr Leonard Coldwells book, The Only Answer To Cancer

is a fantastic book . He has a 93% cancer cure rate

[Guest guest]

-- " do your homework? " I asked you a simple question about documentation

about his 93% cancer cure--documentation including follow-up over years. If I

see that, I'll investigate further. I'm not going to buy this guy's book based

on " claims " and testimonials. These sites are all over the Internet. You need

documentation.

I believe in alternative therapies: I used the mind/body connection in the form

of disciplined qigong practice combined with chemotherapy. When one has Stage

four bone lymphoma that has fractured the hip and pelvis, there's no time to

waste with alternative cures that may have cured some people--but left most

dead. Documentation!

Read Dr Leonard Coldwells book, The Only Answer To Cancer

is a fantastic book . He has a 93% cancer cure rate

[Guest guest]

:

I did not mean that statement in a bad way - to do your homework,

I don't care if people buy his book or not. I am just trying to help

people out.

________________________________

From: ROBERT ELLAL <rcellal@...>

Sent: Thu, December 30, 2010

 

-- " do your homework? " I asked you a simple question about documentation

about his 93% cancer cure--documentation including follow-up over years. If I

see that, I'll investigate further. I'm not going to buy this guy's book based

on " claims " and testimonials. These sites are all over the Internet. You need

documentation.

I believe in alternative therapies: I used the mind/body connection in the form

of disciplined qigong practice combined with chemotherapy. When one has Stage

four bone lymphoma that has fractured the hip and pelvis, there's no time to

waste with alternative cures that may have cured some people--but left most

dead. Documentation!

[Guest guest]

" gvblk4msn " <gvblk4@...> wrote:

<<Follicular Lymphoma B-Cell...I was told by Oncology that I would need 6-9

treatments every 3 weeks of Rituxin Cocktail>>

For follicular non-Hodgkins lymphoma (NHL) (or any other

indolent/low-grade/slow-growing lymphoma), I would NOT do chemo, as it's highly

effective ONLY w/fast-growing/high-grade/aggressive lymphomas.

However,

“Rituxan…is a good idea though if the lymphoma has not yet turned

aggressive. The use of accompanying cytotoxic chemo actually decreases any

latency period until progression. Rituxan is not a true chemo even though it can

have side effects. I know of a number of B-cell NHL (mostly intermediate grade)

whose lives were saved by this med†Gammill, 3/1/08

If I was to do chemo for a low-grade/indolent NHL (or most any other type of

cancer), I'd get it in the form of IPT.

> No Gluten

> Cottage cheese...+ Flax oil...

Great!

> Carrot pear and apple juice 8 ox /day

very good, as long as it's fresh-squeezed

> No desserts or fruit juices

Great!

> Essiac Tea Where do I get that Which Brand?

I'd use Essiac.com and/or

Detox Plus Formula by AloeLife.com

(www.harvesthealth.com/allifterhera.html)

> Tumeric Spice How to take that Pill Form?

to achieve a cancer-healing effect, you need to take high dosages (at least

about 4g) of curcumin (turmeric extract, not whole turmeric)

>need a good Natural Doctor I live in Arizona near Phoenix

contact www.Bioimmune.com (formerly CancerOption.com); info@...;

888-663-8844 or 480-778-1618. Has a superb vit. C-based protocol for cancer (and

lymphoma's reportedly the cancer that they're most effective with)

and ask them for names of practitioners they've trained who are in your area.

Most treatments aren't very effective with low-grade/indolent lymphomas.

The most effective things I know of for NHL in general (particularly CAPITALIZED

items):

high-dose PANCREATIN (Kelley- regimen), HOXSEY, BEETS, ginger, garlic,

green tea/EGCG, pomegranate?, resveratrol, curcumin, fermented soy, asparagus,

melatonin, olive leaf/antivirals, fish oil, frankincense & myrrh essential oils,

Immupower (YoungLivingOils.com) on spine, Modifilan.com; vits. A, C, D3; IV VIT.

C (w/K3); Butyrex, NALTREXONE (LDN); IPT (only for medium- and high-grade NHL);

COLEY’S TOXINS, hyperthermia; AVOID gluten

Leonard

[Guest guest]

Hi Greg

I happened to get some test results last Thursday and posted to a few sites that

I belong to. Here is the content of those posts:

I'm about to turn 50, and had a wonderful gift today at my doctor's office. I'm

always hesitant to post good results, due to the awareness and sensitivity that

there are many undergoing treatment or experiencing setbacks. But in a way, we

all are a kind of e-family, working together to survive/battle fcc-NHL. And if

sharing what's worked for me, a data point of one, helps one other person, it's

worth posting.

I just got back from my doctor (a holistic/integrative MD). He spent an hour+

with me again, all for a $20 copay. The leukemia/lymphoma panel (flow cytometry

method) test I usually get (and was diagnosed by) had an interesting narrative:

NO IMMUNOPHENOTYPIC ABNORMALITIES DETECTED

Normally, the narrative will say something like " an abnormal cell population is

present, which comprises XX percent of the total population " .

In essence today's results mean the pathologist can't find any cancerous B cells

in my blood. Again, this doesn't mean I don't have some floating around in the

lymphatic system, but the two systems do mix. And what's going on in the blood

has reflected what I feel in the lymph nodes for the past almost 6 years. At

diagnosis, the percent of cancerous B lymphocytes in the peripheral blood was

68%.

I still have enlarged lymph nodes (neck and possibly groin). I haven't had a CT

scan or any other type of scan since diagnosis. So the only nodes I can monitor

are the ones in the neck which wax and wane, with no detectable net change. My

body may have encased the pre-existing cancerous cells (a theory my doctor

offered up) within these nodes, or possibly it's a stale-mate between the T

cells and pre-existing cancerous B cells (something has written about).

Hard to tell without doing a biopsy, which I have not done, nor will I, due to

the possibility of stirring things up and the significant variation in nodal

micro-environment from lymph node to lymph node. The latter which makes nodal

biopsy of fcc-NHL of limited value, in my humble opinion.

Last time my doctor talked to the Quest Diagnostics (Nichols Institute)

pathologist, he wanted to know what chemo/radiation or other treatment I was

doing. He was shocked when my doctor told him I haven't had " any treatment " .

So what do I attribute this to ? In order of importance:

1) Mercury from silver amalgams – shortly after diagnosis, I had a specialized

test done on my red blood cells by an immunologist, which showed mercury off the

chart. I also had current measurements made on my fillings which showed

electrical currents with magnitudes higher than the nervous system and brain

operate on. This is something called galvanic corrosion due to dissimilar

metals. Being an engineer, this is something I'm familiar with and is taught in

the engineering core curriculum in college. Without going into additional gory

technical detail, I decided to take this issue seriously and safely (from a

biological dentist) had my amalgams removed and did chelation for 6 months.

Doing nothing else but these two things (didn't know about TNS then) did three

things:

a. Bring my total white blood cell count from about an abnormally high of 18,000

to 9,000 (within the normal range)

b. Bring the percent cancerous cells (flow cytometry test) from 68% to about 5%

c. Corrected my hypothyroidism as mercury interferes with conversion of the

thyroid hormones T3 and T4.

2) Candida – My doctor put me on Nystatin, a prescription drug for fungal

overgrowth. I have more details if anyone is interested, but I have found a

significant correlation between pain in my lymph nodes in the groin, percent

cancerous cells, and whether or not I'm on the Nystatin. I continue to stay on a

low dose of this drug. And when I'm on the Nystatin, all sinus problems have

been resolved (and I have had serious sinus problems). Makes you wonder, at

least a little, if previous posts on this board, and Dr. Simoncini (cancer is a

fungus guy) might be onto something.

3) Flax Oil/cottage cheese/rice milk/curcumin/vitamin D3/organic berries and

many other things in my morning " super shake " – Within 3 weeks of starting this

protocol, which was parts of 's original " stain-master " breakfast – my

lymph nodes in my groin stopped hurting and regressed in size. Since I have not

had many scans, I can't quantify the reduction in size of the lymph nodes.

4) I do many other things, some supported by this site, some not. But I would

say the above 3 items represent the " 90% solution " and for the ones that are

supported by this site, quality sleep in a dark room and low dose naltrexone

have been important factors as well.

I hope the takeaway of members reading this is, as stresses, take control

and implement a dynamic observation (if one is able to and not in a threatening

situation). Each of us must find and reverse the factors that may have

contributed to our diagnosis as well as find those strategies which put fcc-NHL

in a " multitudinous crossfire " . And, I hope this demonstrates, albeit with just

one patient, that natural strategies can work, whether they are before, during

or after conventional treatment.

Best regards, Steve

[Guest guest]

When I requested Rituxan alone, I was told that that was not the " standard "

treatment, and that I could only get it as part of the total chemo treatment.

Two oncologists told me this, although I googled and found a couple of people

who had Rituxan alone and were healed. At the rituxan website, it says it is

indicated for treatment alone only in cases of a return of the NHL. They make

it pretty difficult to get it the way you want it, like everything else.

My chemo worked immediately because my NHL had turned aggressive, but it shrunk

the tumor almost instantly and I refused to continue after two treatments.

However, I still need IPT treatments to continue to eradicate the lymphoma. But

the cost and lack of insurance support makes that impossible.

Detwa

[Guest guest]

That's wonderful news, steve!!!! I am so happy for you! Please don't ever be

hesitant to post your news, I know myself I find it extremely encouraging and

inspirational, and I'm sure others do also. Sometimes it makes you feel like

that could be YOU and gives us ideas that may or may not work for us. Just the

same, its always motivating!

I've followed your story for a while but most of the things you did are out of

my reach financially. One day I'd like to get my fillings removed, ironically,

I have several on the same side of my mouth where the tumor is/was on my throat

in my lymph nodes. I believe they are connected, but who knows? It's just

something I'd like to explore whenever that opportunity arises, maybe I'll get

health insurance this year that will help pay for it.

Is Nystatin only available with a prescription? Is that something we can be

tested for first, to see if we have fungus?

>

> Hi Greg

>

> I happened to get some test results last Thursday and posted to a few sites

that I belong to. Here is the content of those posts:

>

> I'm about to turn 50, and had a wonderful gift today at my doctor's office.

I'm always hesitant to post good results, due to the awareness and sensitivity

that there are many undergoing treatment or experiencing setbacks. But in a way,

we all are a kind of e-family, working together to survive/battle fcc-NHL. And

if sharing what's worked for me, a data point of one, helps one other person,

it's worth posting.

>

[Guest guest]

Thanks Steve for your response It's encouraging

also Cudos for the links

Greg

>

> Hi Greg

>

> I'm coming up on 6 years fighting fcc-NHL. I've not needed treatment thus far

and have reversed it in many ways. You are doing some really good things below.

For curcumin (turmeric), check out:

> www.lef.com

>

> Consider joining: www.lymphomasurvival.com

>

> It's well worth the $25 annual fee.

>

> The two biggest factors in my disease have been mercury amalgam fillings and

Candida.

>

> best regards, Steve

[Guest guest]

Hi Steve

Glad you are doing well...I am heading for a Holistic dentist soon

to get a 3D Xray of my mouth to determine if there are any hidden cavitations I

have plenty of Silver fillings yet to get removed

I have read the S. Sommers book Knockout and got plenty of ideas

in there

Have you had a bone marrow Study? I am off Tuesday to get that.

Glad you found a Doc that is covered by insurance I need to find

one. I live near Phoenix about 20 miles to the East

I found a NP Oncologist in sdale but he does not have an Md

by his name so I doubt if Insurance will cover.

I have a few more miles. I am 57 and work in a power management

design group re: cell phone technology

I'll send you a PM I'd like to talk

I have no swollen nodes so the only way to detect my progress

so far is to do another Endoscopy (

Regards

Greg

" steve_lmcs " <lmcs@...> wrote:

>

> Hi Greg

>

> I happened to get some test results last Thursday and posted to a few sites

that I belong to. Here is the content of those posts:

>

> I'm about to turn 50, and had a wonderful gift today at my doctor's office.

I'm always hesitant to post good results, due to the awareness and sensitivity

that there are many undergoing treatment or experiencing setbacks. But in a way,

we all are a kind of e-family, working together to survive/battle fcc-NHL. And

if sharing what's worked for me, a data point of one, helps one other person,

it's worth posting.

>

> I just got back from my doctor (a holistic/integrative MD). He spent an hour+

with me again, all for a $20 copay. The leukemia/lymphoma panel (flow cytometry

method) test I usually get (and was diagnosed by) had an interesting narrative:

>

> NO IMMUNOPHENOTYPIC ABNORMALITIES DETECTED

>

> Normally, the narrative will say something like " an abnormal cell population

is present, which comprises XX percent of the total population " .

>

> In essence today's results mean the pathologist can't find any cancerous B

cells in my blood. Again, this doesn't mean I don't have some floating around in

the lymphatic system, but the two systems do mix. And what's going on in the

blood has reflected what I feel in the lymph nodes for the past almost 6 years.

At diagnosis, the percent of cancerous B lymphocytes in the peripheral blood was

68%.

>

> I still have enlarged lymph nodes (neck and possibly groin). I haven't had a

CT scan or any other type of scan since diagnosis. So the only nodes I can

monitor are the ones in the neck which wax and wane, with no detectable net

change. My body may have encased the pre-existing cancerous cells (a theory my

doctor offered up) within these nodes, or possibly it's a stale-mate between the

T cells and pre-existing cancerous B cells (something has written about).

Hard to tell without doing a biopsy, which I have not done, nor will I, due to

the possibility of stirring things up and the significant variation in nodal

micro-environment from lymph node to lymph node. The latter which makes nodal

biopsy of fcc-NHL of limited value, in my humble opinion.

>

> Last time my doctor talked to the Quest Diagnostics (Nichols Institute)

pathologist, he wanted to know what chemo/radiation or other treatment I was

doing. He was shocked when my doctor told him I haven't had " any treatment " .

>

> So what do I attribute this to ? In order of importance:

>

> 1) Mercury from silver amalgams � shortly after diagnosis, I had a

specialized test done on my red blood cells by an immunologist, which showed

mercury off the chart. I also had current measurements made on my fillings which

showed electrical currents with magnitudes higher than the nervous system and

brain operate on. This is something called galvanic corrosion due to dissimilar

metals. Being an engineer, this is something I'm familiar with and is taught in

the engineering core curriculum in college. Without going into additional gory

technical detail, I decided to take this issue seriously and safely (from a

biological dentist) had my amalgams removed and did chelation for 6 months.

Doing nothing else but these two things (didn't know about TNS then) did three

things:

>

> a. Bring my total white blood cell count from about an abnormally high of

18,000 to 9,000 (within the normal range)

> b. Bring the percent cancerous cells (flow cytometry test) from 68% to about

5%

> c. Corrected my hypothyroidism as mercury interferes with conversion of the

thyroid hormones T3 and T4.

>

> 2) Candida - My doctor put me on Nystatin, a prescription drug for fungal

overgrowth. I have more details if anyone is interested, but I have found a

significant correlation between pain in my lymph nodes in the groin, percent

cancerous cells, and whether or not I'm on the Nystatin. I continue to stay on a

low dose of this drug. And when I'm on the Nystatin, all sinus problems have

been resolved (and I have had serious sinus problems). Makes you wonder, at

least a little, if previous posts on this board, and Dr. Simoncini (cancer is a

fungus guy) might be onto something.

>

> 3) Flax Oil/cottage cheese/rice milk/curcumin/vitamin D3/organic berries and

many other things in my morning " super shake " Within 3 weeks of starting this

protocol, which was parts of 's original " stain-master " breakfast, my

lymph nodes in my groin stopped hurting and regressed in size. Since I have not

had many scans, I can't quantify the reduction in size of the lymph nodes.

>

> 4) I do many other things, some supported by this site, some not. But I would

say the above 3 items represent the " 90% solution " and for the ones that are

supported by this site, quality sleep in a dark room and low dose naltrexone

have been important factors as well.

>

> I hope the takeaway of members reading this is, as stresses, take

control and implement a dynamic observation (if one is able to and not in a

threatening situation). Each of us must find and reverse the factors that may

have contributed to our diagnosis as well as find those strategies which put

fcc-NHL in a " multitudinous crossfire " . And, I hope this demonstrates, albeit

with just one patient, that natural strategies can work, whether they are

before, during or after conventional treatment.

>

> Best regards, Steve

>

[Guest guest]

Thanks so Much for the information

As I understand it Rituxan is a monoclonal antibody

The Doc said It could come back in 2 years after it is treated

And i also read it can then be resistant when treated again or

can cause the cancer to morph into another form

This whole chemo thing scares the Bejesus out of me frankly

I already feel allot stronger being off the gluten

I will get tested for that soon via blood I presume Ige

Best Regards

Greg

> <<Follicular Lymphoma B-Cell...I was told by Oncology that I would need 6-9

treatments every 3 weeks of Rituxin Cocktail>>

>

> For follicular non-Hodgkins lymphoma (NHL) (or any other

indolent/low-grade/slow-growing lymphoma), I would NOT do chemo, as it's highly

effective ONLY w/fast-growing/high-grade/aggressive lymphomas.

> However,

> “Rituxan…is a good idea though if the lymphoma has not yet turned

aggressive. The use of accompanying cytotoxic chemo actually decreases any

latency period until progression. Rituxan is not a true chemo even though it can

have side effects. I know of a number of B-cell NHL (mostly intermediate grade)

whose lives were saved by this med†Gammill, 3/1/08

>

> If I was to do chemo for a low-grade/indolent NHL (or most any other type of

cancer), I'd get it in the form of IPT.

>

> > No Gluten

> > Cottage cheese...+ Flax oil...

> Great!

>

> > Carrot pear and apple juice 8 ox /day

> very good, as long as it's fresh-squeezed

>

> > No desserts or fruit juices

> Great!

>

> > Essiac Tea Where do I get that Which Brand?

> I'd use Essiac.com and/or

> Detox Plus Formula by AloeLife.com

> (www.harvesthealth.com/allifterhera.html)

>

> > Tumeric Spice How to take that Pill Form?

> to achieve a cancer-healing effect, you need to take high dosages (at least

about 4g) of curcumin (turmeric extract, not whole turmeric)

>

> >need a good Natural Doctor I live in Arizona near Phoenix

> contact www.Bioimmune.com (formerly CancerOption.com); info@...; 888-663-8844

or 480-778-1618. Has a superb vit. C-based protocol for cancer (and lymphoma's

reportedly the cancer that they're most effective with)

> and ask them for names of practitioners they've trained who are in your area.

>

> Most treatments aren't very effective with low-grade/indolent lymphomas.

> The most effective things I know of for NHL in general (particularly

CAPITALIZED items):

> high-dose PANCREATIN (Kelley- regimen), HOXSEY, BEETS, ginger, garlic,

green tea/EGCG, pomegranate?, resveratrol, curcumin, fermented soy, asparagus,

melatonin, olive leaf/antivirals, fish oil, frankincense & myrrh essential oils,

Immupower (YoungLivingOils.com) on spine, Modifilan.com; vits. A, C, D3; IV VIT.

C (w/K3); Butyrex, NALTREXONE (LDN); IPT (only for medium- and high-grade NHL);

COLEY’S TOXINS, hyperthermia; AVOID gluten

>

> Leonard

>

[Guest guest]

Hi Greg,

Essiac tea one can buy at Mountain Rose Herbs, same for Turmeric. Turmeric is

best taken with olive oil or better coconut oil if the weather is warm and

allows to oil to be fluid.

Best regards,

Jan P.

Phu Kiao

Thailand

________________________________

From: gvblk4msn <gvblk4@...>

Sent: Wed, December 29, 2010

Hi,

Recently diagnosed with Follicular Lymphoma B-Cell of the Small Intestine

Im a 57 year old male. I understand that if you have Celliac's disease

you are 6 times more likely to get this

I was told by Oncology that I would need 6-9 treatments every 3 weeks of Rituxin

Cocktail

Here are some things I have started:

No Glutin

Cottage cheese and flax seed fresh ground + Flax oil with berries

(Budwig Idea) with cashews and pecans

Carrot pear and apple juice 8 ox /day

No desserts of fruit juices

Here are some things I am considering:

Essiac Tea Where do I get that Which Brand? How often?

Tumeric Spice How to take that Pill Form?

Any and all ideas are looked at

If I do the Chemo then I need a good Natural Doctor I live in Arizona near

Phoenix

Thanks for any help

Greg

[Guest guest]

The blood test is not that accurate unless you are in the advanced stages of the

disease and have been eating gluten. Since you have been off gluten you may

test negative (even though you are celiac) since your body won't currently be

making antibodies against gluten since you haven't been consuming it. It is

best to use a gene and stool panel from

https://www.enterolab.com/StaticPages/TestInfo.aspx If you are on a budget then

I would just order the stool gluten panel for $99. If you include the gene test

it would cost $249. Best of luck to you, please do not rely on the blood test

it gives so many false negatives.

You wrote:

> I already feel allot stronger being off the gluten

> I will get tested for that soon via blood I presume Ige

>

> Best Regards

>

> Greg

>

[Guest guest]

Thanks for this input I was wondering how accurate the blood test would be

> > I already feel allot stronger being off the gluten

> > I will get tested for that soon via blood I presume Ige

> >

> > Best Regards

> >

> > Greg

> >

>