RE: 5 Year Anniversary with no formal treatment

[Guest guest]

Great post Steve. These are the stories we all need to hear and remember. Thank

you!!! Val

From: " steve_lmcs "

Greetings,

I have reached a major milestone this month as it's been 5 years since

diagnosis. Not sure how accurate it was but I recall reading back then, that

only 50% of people diagnosed with fcc-NHL reach the 5 year mark. I also remember

after reading that, that I was determined to " beat the odds " . My rationale back

then, as it has been for these past 5 years, is that when two oncologists (and

all the traditional research) tell me that the exact cause is unknown, and there

is no cure, that my best chances would be looking into areas that traditional

medicine does not address or consider.

Great strides have been made in three areas. The first is that I was diagnosed

via a flow cytometry blood test which provides the percent cancerous cells in

the peripheral blood in addition to the various surface proteins or CD marker

levels. My percent cancerous B lymphocytes were 65% at diagnosis and now hover

between 0 and 5%. The second improvement is regression of some lymph nodes and

reduction of pain in groin nodes. The third is getting my elevated white blood

cell and lymphocyte count into the normal range.

The further I go on this journey, the more I am convinced, actually, the more I

know in my heart – that the two biggest causes or factors in my disease were

mercury due to amalgam fillings and a systemic overgrowth of Candida.

Additionally, the number one TNS was the incorporation of flax oil and cottage

cheese with curcumin back in 2008. I experienced the SR of the groin nodes

within 3 weeks of starting that protocol. And another critical TNS is sleep. The

stubborn Italian in me refused to admit that I needed more than 4 hours a sleep

a nite and that sleeping was not the sign of a sluggard. It took a long time but

I now realize the importance of deep sleep in a dark room and it has been a

significant factor in reversing the disease.

What's left for me ? I still have enlarged but stable, waxing and waning nodes

in the neck, and I have low platelet levels. I will refine my protocol as

needed, to continue driving towards full reversal of this disease.

I write this in the hopes that all members continue searching for the factors

that have played a role in their cancer and, and as is my motto, never let go of

the will to live.

Sincerely, Steve

[Guest guest]

Steve,

Your story is absolutely wonderful and such an encouragement to those who feel

alternative medicine will  not cure them...you are living proof that it does.

I'm so happy for you and will share your story every chance I get.

Best regards,

Sandy

http://buyingkefirgrains.blogspot.com/

http://heavenly-haiku.blogspot.com/

From: steve_lmcs <lmcs@...>

Subject: [ ] 5 Year Anniversary with no formal treatment

Date: Sunday, April 4, 2010, 8:53 PM

 

Greetings,

I have reached a major milestone this month as it's been 5 years since

diagnosis. Not sure how accurate it was but I recall reading back then, that

only 50% of people diagnosed with fcc-NHL reach the 5 year mark. I also remember

after reading that, that I was determined to " beat the odds " . My rationale back

then, as it has been for these past 5 years, is that when two oncologists (and

all the traditional research) tell me that the exact cause is unknown, and there

is no cure, that my best chances would be looking into areas that traditional

medicine does not address or consider.

Great strides have been made in three areas. The first is that I was diagnosed

via a flow cytometry blood test which provides the percent cancerous cells in

the peripheral blood in addition to the various surface proteins or CD marker

levels. My percent cancerous B lymphocytes were 65% at diagnosis and now hover

between 0 and 5%. The second improvement is regression of some lymph nodes and

reduction of pain in groin nodes. The third is getting my elevated white blood

cell and lymphocyte count into the normal range.

The further I go on this journey, the more I am convinced, actually, the more I

know in my heart – that the two biggest causes or factors in my disease were

mercury due to amalgam fillings and a systemic overgrowth of Candida.

Additionally, the number one TNS was the incorporation of flax oil and cottage

cheese with curcumin back in 2008. I experienced the SR of the groin nodes

within 3 weeks of starting that protocol. And another critical TNS is sleep. The

stubborn Italian in me refused to admit that I needed more than 4 hours a sleep

a nite and that sleeping was not the sign of a sluggard. It took a long time but

I now realize the importance of deep sleep in a dark room and it has been a

significant factor in reversing the disease.

What's left for me ? I still have enlarged but stable, waxing and waning nodes

in the neck, and I have low platelet levels. I will refine my protocol as

needed, to continue driving towards full reversal of this disease.

I write this in the hopes that all members continue searching for the factors

that have played a role in their cancer and, and as is my motto, never let go of

the will to live.

Sincerely, Steve

[Guest guest]

Thank you all for your online and offline words of encouragement. I should

clarify that TNS is targeted natural strategy, a term that the owner of a

lymphoma group that I belong to uses.

best regards, steve

[Guest guest]

Good Morning Steve! Congratulations. I am so pleased to hear of someone

beating the system! I do the Flax oil & cottage cheese (BP) and would like

to add the curcumin to my diet. Can you enlighten me as to how you take it?

Is it a capsule or an organic herb I can buy at the store? How much per

day. And do you take it by itself or incorporated in food /drink? I'll use

anything I can in my arsenal to beat this darn cancer.

And Thank you for sharing, it gives me hope.

Toni D.

From: steve_lmcs

Sent: Sunday, April 04,

Greetings,

I have reached a major milestone this month as it's been 5 years since

diagnosis. Not sure how accurate it was but I recall reading back then, that

only 50% of people diagnosed with fcc-NHL reach the 5 year mark. I also

remember after reading that, that I was determined to " beat the odds " . My

rationale back then, as it has been for these past 5 years, is that when two

oncologists (and all the traditional research) tell me that the exact cause

is unknown, and there is no cure, that my best chances would be looking into

areas that traditional medicine does not address or consider.

Great strides have been made in three areas. The first is that I was

diagnosed via a flow cytometry blood test which provides the percent

cancerous cells in the peripheral blood in addition to the various surface

proteins or CD marker levels. My percent cancerous B lymphocytes were 65% at

diagnosis and now hover between 0 and 5%. The second improvement is

regression of some lymph nodes and reduction of pain in groin nodes. The

third is getting my elevated white blood cell and lymphocyte count into the

normal range.

The further I go on this journey, the more I am convinced, actually, the

more I know in my heart - that the two biggest causes or factors in my

disease were mercury due to amalgam fillings and a systemic overgrowth of

Candida. Additionally, the number one TNS was the incorporation of flax oil

and cottage cheese with curcumin back in 2008. I experienced the SR of the

groin nodes within 3 weeks of starting that protocol. And another critical

TNS is sleep. The stubborn Italian in me refused to admit that I needed more

than 4 hours a sleep a nite and that sleeping was not the sign of a

sluggard. It took a long time but I now realize the importance of deep sleep

in a dark room and it has been a significant factor in reversing the

disease.

What's left for me ? I still have enlarged but stable, waxing and waning

nodes in the neck, and I have low platelet levels. I will refine my protocol

as needed, to continue driving towards full reversal of this disease.

I write this in the hopes that all members continue searching for the

factors that have played a role in their cancer and, and as is my motto,

never let go of the will to live.

Sincerely, Steve

[Guest guest]

Steve, congratulations! Will you please clarify flax oil and cottage

cheese with curcumin. Do you mean the mix of flax oil with cottage cheese (the

Budwig diets)? And add curcumin to the mix?

Thanks.

In a message dated 4/4/2010 10:56:16 P.M. Eastern Daylight Time,

valheieck@... writes:

Great post Steve. These are the stories we all need to hear and remember.

Thank you!!! Val

From: " steve_lmcs "

Greetings,

I have reached a major milestone this month as it's been 5 years since

diagnosis. Not sure how accurate it was but I recall reading back then, that

only 50% of people diagnosed with fcc-NHL reach the 5 year mark. I also

remember after reading that, that I was determined to " beat the odds " . My

rationale back then, as it has been for these past 5 years, is that when two

oncologists (and all the traditional research) tell me that the exact cause is

unknown, and there is no cure, that my best chances would be looking into

areas that traditional medicine does not address or consider.

Great strides have been made in three areas. The first is that I was

diagnosed via a flow cytometry blood test which provides the percent cancerous

cells in the peripheral blood in addition to the various surface proteins or

CD marker levels. My percent cancerous B lymphocytes were 65% at diagnosis

and now hover between 0 and 5%. The second improvement is regression of

some lymph nodes and reduction of pain in groin nodes. The third is getting

my elevated white blood cell and lymphocyte count into the normal range.

The further I go on this journey, the more I am convinced, actually, the

more I know in my heart – that the two biggest causes or factors in my

disease were mercury due to amalgam fillings and a systemic overgrowth of

Candida. Additionally, the number one TNS was the incorporation of flax oil and

cottage cheese with curcumin back in 2008. I experienced the SR of the groin

nodes within 3 weeks of starting that protocol. And another critical TNS

is sleep. The stubborn Italian in me refused to admit that I needed more

than 4 hours a sleep a nite and that sleeping was not the sign of a sluggard.

It took a long time but I now realize the importance of deep sleep in a

dark room and it has been a significant factor in reversing the disease.

What's left for me ? I still have enlarged but stable, waxing and waning

nodes in the neck, and I have low platelet levels. I will refine my protocol

as needed, to continue driving towards full reversal of this disease.

I write this in the hopes that all members continue searching for the

factors that have played a role in their cancer and, and as is my motto, never

let go of the will to live.

Sincerely, Steve

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