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Angel,

You are an inspiration to me. Please keep us posted about your progress.

Best regards,

Sharon

[ ] My experience

Hello everyone, and happy "Black Friday". (I don't know why it's called that ... just that stores open around 4 am for mass hysteria's of shopping. Which sounds pretty black. LOL! ) But the sun is out today and it's beautiful if cold here in the Pacific Northwest USA.Yesterday I took small doses of MMS from 8 am to 8 pm .... about 1-1/2 hours apart or so, 17 drops in 9 doses: no dose larger than 2 drops. I stopped taking paradophilous because I wanted to see how it felt to take MMS alone.I never got to nausea or "the runs". I did feel tired, dizzy, "negative and flat". Lacking in affect. It would/will be hard to keep this up.Today I started at 3 drops. I alternate citric acid and lemon juice as activators. It sounds to me like Jim thinks the citric acid makes a stronger dose. Today I'm taking paradophilous along with it.I'm taking MMS for cancer. I read and reread the book. The last

thing Jim says about cancer is that those not getting the results they want aren't taking enough. Then of course he recommends Indian Herb. Since that causes nausea and reactions too, I'm not ready to start that yet. I do have cesium which just arrived, but don't know about taking it with MMS ... .well actually think it's not a good idea, given differences in ph needs especially.My urine and saliva pH taking mms has gotten low -- well into the acidic range. The purpose of course of cesium is to raise the pH to at least 8. It seems things that counter low ph ... for instance taking baking soda ... can stop the action of mms. I've even stopped my coral calcium to make sure that doesn't interfere.My other question, which may be and probably is retorical, since I don't know that anyone can answer it, is that cancer is in my lymph system, and I don't know if mms can go there. Jim says it can

ANYWHERE BLOOD GOES. But blood doesn't go to the lymph system. Does anyone have ideas how to get it in there? Or what else might help?I appreicate this list. AND, I am specifically here to discuss my experience with mms and find out what others are experiencing. So many posts are not on-topic, which is a lot to "plow through" to get to mms information. This was supposed to be the "focused" list. Smile.But now that I've talked about mms, I want to tack something else on here. Last week I went to two places, a cemetery to make "arrangements" and then right to a tanning parlor to tan. The differences in the atmospheres and how they made me feel was impressive. There were experiments done (by Depak Chopra) where older people were put in environments that reminded them of their youth for 2 weeks. All their body systems improved and became 'younger". That was really brought home to me last week.

The "upbeat" music and glow at the tanning parlor (whether you believe in tanning or not) was so young and lively.Before I was diagnosed with cancer I did home health care. Hung out with sick and 'down" people. I' want to hang out in places more filled with life force.Blessings to all!Angel

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Vilik,

You would gain much helpful info by investigating this group

blacksalveandpetswithcancer/

They only deal with what works, not what rumor says works,

I think you would be interested in the tonic that's been devised.

BTW, good to hear from you again. It's been way back on Jim Lambert's

list.

Chuck

I planted some bird seed. A bird grew. Now I don't know what to feed

it.

On 11/23/2007 2:49:10 PM, Vilik Rapheles (vilik@...) wrote:

> Hello everyone, and happy " Black Friday " . (I don't know why it's

> called that ... just that stores open around 4 am for mass

> hysteria's

> of shopping. Which sounds pretty black. LOL! ) But the sun is out

> today and it's

> beautiful if cold here in the Pacific Northwest USA.

>

> Yesterday I took small doses of MMS from 8 am to 8 pm .... about

> 1-1/2 hours apart or so, 17 drops in 9 doses: no dose larger than 2

> drops. I stopped taking paradophilous because I wanted to see how it

> felt to take MMS alone.

>

> I never got to nausea or " the runs " . I did feel tired, dizzy,

> " negative and flat " . Lacking in affect. It would/will be hard to keep this

> up.

>

> Today I started at 3 drops. I alternate citric acid and lemon juice

> as activators. It sounds to me like Jim thinks the citric acid makes

> a stronger dose. Today I'm taking paradophilous along with it.

>

> I'm

> taking MMS for cancer. I read and reread the book. The last thing

> Jim says about cancer is that those not getting the results they want

> aren't taking enough. Then of course he recommends Indian Herb. Since

> that causes nausea and reactions too, I'm

> not ready to start that

> yet. I d

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Black Friday - the stores that are in the red, come out of the red

from all the sales and are in the black. Black would be a profit or

positive balance; red a negative or in the whole, a minus balance.

In Christ,

Ava

>

> Hello everyone, and happy " Black Friday " . (I don't know why it's

> called that ... just that stores open around 4 am for mass

hysteria's

> of shopping. Which sounds pretty black. LOL! ) But the sun is out

> today and it's beautiful if cold here in the Pacific Northwest USA.

>

> Yesterday I took small doses of MMS from 8 am to 8 pm .... about

> 1-1/2 hours apart or so, 17 drops in 9 doses: no dose larger than 2

> drops. I stopped taking paradophilous because I wanted to see how

it

> felt to take MMS alone.

>

> I never got to nausea or " the runs " . I did feel tired, dizzy,

> " negative and flat " . Lacking in affect. It would/will be hard to

keep this up.

>

> Today I started at 3 drops. I alternate citric acid and lemon juice

> as activators. It sounds to me like Jim thinks the citric acid

makes

> a stronger dose. Today I'm taking paradophilous along with it.

>

> I'm taking MMS for cancer. I read and reread the book. The last

thing

> Jim says about cancer is that those not getting the results they

want

> aren't taking enough. Then of course he recommends Indian Herb.

Since

> that causes nausea and reactions too, I'm not ready to start that

> yet. I do have cesium which just arrived, but don't know about

taking

> it with MMS ... .well actually think it's not a good idea, given

> differences in ph needs especially.

>

> My urine and saliva pH taking mms has gotten low -- well into the

> acidic range. The purpose of course of cesium is to raise the pH to

> at least 8. It seems things that counter low ph ... for instance

> taking baking soda ... can stop the action of mms. I've even

stopped

> my coral calcium to make sure that doesn't interfere.

>

> My other question, which may be and probably is retorical, since I

> don't know that anyone can answer it, is that cancer is in my lymph

> system, and I don't know if mms can go there. Jim says it can

> ANYWHERE BLOOD GOES. But blood doesn't go to the lymph system. Does

> anyone have ideas how to get it in there? Or what else might help?

>

> I appreicate this list. AND, I am specifically here to discuss my

> experience with mms and find out what others are experiencing. So

> many posts are not on-topic, which is a lot to " plow through " to

get

> to mms information. This was supposed to be the " focused " list.

Smile.

>

> But now that I've talked about mms, I want to tack something else

on

> here. Last week I went to two places, a cemetery to make

> " arrangements " and then right to a tanning parlor to tan. The

> differences in the atmospheres and how they made me feel was

> impressive. There were experiments done (by Depak Chopra) where

older

> people were put in environments that reminded them of their youth

for

> 2 weeks. All their body systems improved and became 'younger " . That

> was really brought home to me last week. The " upbeat " music and

glow

> at the tanning parlor (whether you believe in tanning or not) was

so

> young and lively.

>

> Before I was diagnosed with cancer I did home health care. Hung out

> with sick and 'down " people. I' want to hang out in places more

> filled with life force.

>

> Blessings to all!

>

> Angel

>

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Have you thought about taking the cesium with DMSO. Put a couple of

tablets, open a couple of capsules and place in with about 2 ounces

of DMSO. Let dissolve for a few days unless it was powder in a

capsule or powder that you are to mix with fluid prior to taking then

let stand a day.

Rub a little solution onto your skin, when your PH is low.

I read online, and then in the book DMSO Nature's Healer (I believe

the book too, I'd have to look it up). How you can take b-12, folic

acid, and multi vitamins this way. Most find that they only need to

apply this solution once a month or once every two weeks.

>

> My urine and saliva pH taking mms has gotten low -- well into the

> acidic range. The purpose of course of cesium is to raise the pH to

> at least 8. It seems things that counter low ph ... for instance

> taking baking soda ... can stop the action of mms. I've even

stopped

> my coral calcium to make sure that doesn't interfere.

>

> My other question, which may be and probably is retorical, since I

> don't know that anyone can answer it, is that cancer is in my lymph

> system, and I don't know if mms can go there. Jim says it can

> ANYWHERE BLOOD GOES. But blood doesn't go to the lymph system. Does

> anyone have ideas how to get it in there? Or what else might help?

>

Try the DMSO again while you are taking the MMS.

In Christ,

Ava

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The body has 3 main kinds of fluids: blood, tissue fluid, and lymph. The

blood is the source of these fluids and they return to the blood circulatory

system.

The blood consists of the blood cells and platelets, the plasma or fluid

portion, and a variety of chemical substances dissolved in the plasma. When

the plasma, without its solid particles and some of its dissolved

substances, seeps through the capillary walls and circulates among the body

tissues, it is known as tissue fluid. When this fluid is drained from the

tissues and collected by the lymphatic system, it is called lymph. The

lymphatic system eventually returns the lymph to the blood, where it again

becomes plasma.

For good performance of the circulatory system ensure you are always well

hydrated. I can't imagine why the MMS cannot get through to most everywhere

in the body.

Phil

[ ] My experience

Hello everyone, and happy ...

My other question, which may be and probably is retorical, since I

don't know that anyone can answer it, is that cancer is in my lymph

system, and I don't know if mms can go there. Jim says it can

ANYWHERE BLOOD GOES. But blood doesn't go to the lymph system. Does

anyone have ideas how to get it in there? Or what else might help?

Angel

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If that is a cancer then it sure should. I have Lyme and internal MRSA

and it will help those. Halalujah

S

>

> Hi group,

>

> My husband has lymphoma and early AD...Does anyone know if MMS will

help these conditions? I am desperate to help him.

>

> Jeanne

>

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....maybe before it ever gets through all that getting there it get used up

reacting with stuff along the way or just breaking down on it's own. that's

why in another post i suggested a little bit might make it to the lymph

system over time. now i'm guessing that maybe to get a sufficient amount in

there to treat lymphatic cancers you have to work up to large doses taken

many times per day???

so a mag pulser might be a better option, or at least a good corollary.

> -----Original Message-----

I can't imagine why the MMS cannot get through to most

> everywhere

> in the body.

>

> Phil

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i suspect the MMS will get into the lymph system a bit over time at least,

but really have no idea how that all might work. good question.

to get at the cancers in the lymphatic system i'd get a mag pulser and a map

of the lymph system and pulse the hell out of all of it daily.

there's lots of anecdotal/testimonial " evidence " in favor of mag pulsers

helping against cancers generally, and the magnetic fields go right through

everything in the body that isn't ferrous metal.

> [ ] My experience

>

>

> Hello everyone, and happy " Black Friday " . (I don't know why it's

> called that ... just that stores open around 4 am for mass hysteria's

> of shopping. Which sounds pretty black. LOL! ) But the sun is out

> today and it's beautiful if cold here in the Pacific Northwest USA.

>

> Yesterday I took small doses of MMS from 8 am to 8 pm .... about

> 1-1/2 hours apart or so, 17 drops in 9 doses: no dose larger than 2

> drops. I stopped taking paradophilous because I wanted to see how it

> felt to take MMS alone.

>

> I never got to nausea or " the runs " . I did feel tired, dizzy,

> " negative and flat " . Lacking in affect. It would/will be hard to

> keep this up.

>

> Today I started at 3 drops. I alternate citric acid and lemon juice

> as activators. It sounds to me like Jim thinks the citric acid makes

> a stronger dose. Today I'm taking paradophilous along with it.

>

> I'm taking MMS for cancer. I read and reread the book. The last thing

> Jim says about cancer is that those not getting the results they want

> aren't taking enough. Then of course he recommends Indian Herb. Since

> that causes nausea and reactions too, I'm not ready to start that

> yet. I do have cesium which just arrived, but don't know about taking

> it with MMS ... .well actually think it's not a good idea, given

> differences in ph needs especially.

>

> My urine and saliva pH taking mms has gotten low -- well into the

> acidic range. The purpose of course of cesium is to raise the pH to

> at least 8. It seems things that counter low ph ... for instance

> taking baking soda ... can stop the action of mms. I've even stopped

> my coral calcium to make sure that doesn't interfere.

>

> My other question, which may be and probably is retorical, since I

> don't know that anyone can answer it, is that cancer is in my lymph

> system, and I don't know if mms can go there. Jim says it can

> ANYWHERE BLOOD GOES. But blood doesn't go to the lymph system. Does

> anyone have ideas how to get it in there? Or what else might help?

>

> I appreicate this list. AND, I am specifically here to discuss my

> experience with mms and find out what others are experiencing. So

> many posts are not on-topic, which is a lot to " plow through " to get

> to mms information. This was supposed to be the " focused " list. Smile.

>

> But now that I've talked about mms, I want to tack something else on

> here. Last week I went to two places, a cemetery to make

> " arrangements " and then right to a tanning parlor to tan. The

> differences in the atmospheres and how they made me feel was

> impressive. There were experiments done (by Depak Chopra) where older

> people were put in environments that reminded them of their youth for

> 2 weeks. All their body systems improved and became 'younger " . That

> was really brought home to me last week. The " upbeat " music and glow

> at the tanning parlor (whether you believe in tanning or not) was so

> young and lively.

>

> Before I was diagnosed with cancer I did home health care. Hung out

> with sick and 'down " people. I' want to hang out in places more

> filled with life force.

>

> Blessings to all!

>

> Angel

>

>

>

>

>

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Yes Bob. Some will be used up so only a little MMS may be left to target the

problem you're concerned about. Do recall that MMS is thought to promote the

immune systems (IS) efforts. I believe the IS can be prompted by your

intent/desire to attend to your problem but then there is the matter of

supplying the nutrients that the IS will need.

I think that if you were to make some green juice from freshly harvested

wheat or barley grass, edible green leaves of garden plants. Extract it with

a blender in a vitamin C solution, and strain out the solids in a cloth.

Drink it while still very fresh but " chew " it thoroughly as you do so. Don't

have other foods from refined or processed sources then (this saves your

body from having to sort out damaged nutrient components).

The green juice contains everything that the plant requires for it's own

grown. This is, I've found, great for getting the best from the immune

system.

The MMS and IS do destroy pathogens, but we need to recall Hulda 's

work and her finding that as you kill a pathogen you often have a release of

pathogens carried by the one just destroyed. This is why Hulda advises you

when using a zapper to use the zapper again 20 minutes later (indeed 2 times

in all). Jim Humble says to go slow too.

I made the mistake of having the MMS too much and too quickly. When I

shortly restart I am going to take it slowly (- I just hope I actually keep

to that!).

Do keep yourself well hydrated. If you begin to feel " off " maybe you should

drink some more water?

Phil

bob Larson wrote - RE: [ ] My experience

....maybe before it ever gets through all that getting there it get used up

reacting with stuff along the way or just breaking down on it's own. that's

why in another post i suggested a little bit might make it to the lymph

system over time. now i'm guessing that maybe to get a sufficient amount in

there to treat lymphatic cancers you have to work up to large doses taken

many times per day???

so a mag pulser might be a better option, or at least a good corollary.

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Hi ,

You're right it is Alzheimer's...I hate saying it so I just use the initials. Has anyone at all been helped for this condition by using MMS? I will probably try it because I've tried everything else. What exactly is it and where do I get it?

thanks for the support. If this is off topic, please email me privately.

Jeanne

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Hi Jeanne,

I was just listening to an interview with Jim H. and he was talking

about Alzheimer's. Jim said that not a lot of people have used it for

this disease so there is not a lot of data. He said that these

patients have a high spirochete count in their brains and a high

metal level like a Lyme patient. Because MMS does oxidize both of

these he feels that this can be eradicated, but like Lyme it can take

a much longer time (Lyme can take a year).

S

>

> Hi ,

>

> You're right it is Alzheimer's...I hate saying it so I just use the

initials. Has anyone at all been helped for this condition by using

MMS? I will probably try it because I've tried everything else.

What exactly is it and where do I get it?

>

> thanks for the support. If this is off topic, please email me

privately.

>

> Jeanne

>

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  • 2 years later...

Hi Tess. 

     I so enjoyed your post today.  Your Aunt sounds so wonderful.  RA

treatments have come a long way, thank goodness.  I know what your Aunt was

dealing with each day.  I had a great-aunt who was totally crippled with RA. 

As her condition got worse, she could not longer come to my house for all the

holidays.  Getting into my Grandfathers car was too hard for her.  From then

on we went to their house in Boston for every holiday.  She lived to be 88 but

very rarely left the house.  She was a very sweet, special lady.

 

     I am happy that the RA meds. you take are doing so good for you.  Now

you have a life.  I know how tired we do get, but it is a small price to pay to

have our RA under control and in a medicine induced remission.  I am very

thankful for that.

 

     Glad to see you psoting today.  I hope your RA meds. keep working so

well for you.

 

Hugs,

 

Barbara

From: mercycove@... <mercycove@...>

Subject: [ ] My experience

Date: Sunday, August 29, 2010, 3:54 PM

 

Hi All...I was diagnosed with RA and PsA after years of other dx including lupus

and mixed connective tissue disease.  I have been on many treatments from old

to new.  When my rheumatologist encouraged me to try the biologics, I was

scared of side-effects.  But I was so sick, in pain, and troubled mobility,

and with a sed rate over 100 and C Reactive Protein way high.  Several

biologics either just did not work, or stopped working, or I became very sick on

them.  But we kept trying. Since 2003 I have been on weekly injections of

methotrexate and Humira.  75% of the time I feel good with fatigue being the

most difficult to deal with.  For me, any potential risk of adverse

side-effects did not measure up to feeling like a functioning person most of the

time again.

My beloved Aunt June had RA for 40+ years  We were diagnosed at the same age

(39).  The damage to her hands and feet from RA was devastating.  All she had

for treatments most of her life were gold shots and anti-inflammatories.  I

often wonder how much better her life would had been if she had had the

treatments we now have.  She was a great lady who handled things with much

grace, but she had so much pain and crippling.  At age 80 or so she developed

nodules in her lung.  Two years later she had surgery for lung cancer (never

smoked).  She died at age 83.  She was brave and tenacious and how I wish she

had been blessed with better treatment.

I know I don't speak up much here (not like I did a few years ago : ) but I just

wanted to share my experience.

Love...

Cheryle, in Oregon...aka Tess

[ ] RESEARCH - Prompt aggressive treatment improves outcomes

in RA

 

Medscape Medical News

August 26, 2010

Prompt aggressive treatment improves outcomes in RA

Prompt aggressive treatment is the strongest predictor of remission in

patients with rheumatoid arthritis (RA), regardless of the presence of

poor prognostic factors, according to a new study published in the

August issue of Arthritis Care & Research.

" In the past, the treatment of RA aimed at a reduction of disease

activity to a low disease activity state due to a lack of effective

treatment, " write Wanruchaa Katchamart, MD, from the University of

Toronto, Canada, and colleagues. " With the advent of biologic agents,

the ultimate goal of treatment in RA is now remission in the early

stage of the disease before patients develop permanent deformities,

functional disability and RA-related systemic morbidity and

mortality. "

According to the article, biologic agents can suppress inflammation

and halt radiographic progression, but they also can cause adverse

effects that lead to discontinuation of the medication. In addition,

they are costly. Therefore, being able to identify factors that

predict remission early in the disease would help physicians tailor

their treatment plans to individual patients.

The aim of this study was to summarize the potential predictors of

remission in RA patients.

The researchers reviewed 18 prognostic studies that used multivariate

analysis to identify predictors of remission. They found a number of

independent predictors of remission, including baseline clinical and

laboratory characteristics and genetic markers, as follows:

• Male sex

• Young age

• Late-onset RA (occurring past the age of 65 years)

• Short disease duration

• Nonsmoker

• Low baseline disease activity

• Mild functional impairment

• Low baseline radiographic damage

• Absence of rheumatoid factor and anticitrullinated peptide

• Low serum level of acute-phase reactant, interleukin 2, and receptor

activator of nuclear factor κ B ligand (RANKL) at baseline

• MTHFR 677T alleles and 1298C alleles in the methotrexate-treated patients

• Magnetization transfer ratio 2756A allele ± either the SLC 19A180A

allele or the TYMS 3R-del6 haplotype in the methotrexate plus

sulfasalazine combination-treated patients

• Early treatment with nonbiologic disease-modifying antirheumatic

drug (DMARD) combinations

• The use of anti–tumor necrosis factor (anti-TNF)

• The concurrent use of DMARDs in the anti-TNF-treated patients

• Moderate or good response to treatments at the first 6 months

" Although all of the studies included in this review investigated an

independent association using multivariate analysis, the hypotheses of

these studies were usually based on the unreal assumption that the

association between the prognostic factors and RA remission is direct

and isolated, " the study authors write. " This model may be inadequate

to explicitly describe the complex relationship between prognostic

factors and remission for multifactorial and unclear mechanisms of a

disease condition like RA. "

These relationships need to be explored further in phase 3 trials to

better understand the complex prognostic pathways or processes of RA,

the authors conclude.

One author was supported by a Canadian Institutes of Health Research

Clinician Scientist Award; another holds a Canada Research Chair in

Knowledge Transfer for Musculoskeletal Care and has received

consultant fees, speaking fees, and/or honoraria from Schering, Roche,

Biogen Idec, PESI Healthcare, Wyeth, Abbott, and Abbott Canada.

Arthritis Care Res. 2010;62:1128-1143.

http://www.medscape.com/viewarticle/727525

Not an MD

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