Re: Is there anyone here with cancer?

[Guest guest]

Sorry I know you are looking for someone who is using this

for cancer and I only know of one person but I think it's a different

kind of cancer.

JH says to take it for awhile and go and have more Xrays done and see

if the tumors have shrunk. He is looking for stories like yours so we

are all waiting to hear more success stories. He also recommends

another product. I believe it was an Indian Herb but I'm not sure.

Best Regards

Sharon

>

> Is anyone on this list battling cancer w/MMS? From what I'm

seeing, there are mostly other

> conditions on this particular list.

>

> I've been reading in JH's book and he mentions, several times, to

only stay on high doses for

> a couple of weeks until you see an improvement, then go down to

maintenance dose. My

> problem is that I've never felt pain or sickness as a result of

cancer ... so I will have no way to

> see improvement. The tumors were in my abdomen, so I can't exactly

see them. I feel like

> I'd be really flailing around in the dark, which is why I'd really

love to talk to someone who is

> using this with cancer ...

>

> xxoo

>

>

[Guest guest]

Hi,

I am using MMS for Lyme but my husband is using it for protate

cancer. Like you, he can't see his cancer and won't go back to the

specialist for a couple of months. However, I can say that he is

looking much better. His skin is a healthy pink color instead of the

horible yellow tinge that it has been for many years. He is really

tired, but there are signs of healing.

We also have another friend, who has been battling an

agressive tumor on his neck for many years. A few months ago he

submitted to radiotherapy, but then they found a tumor on his lung.

He had this removed and then more spots were found on the other

lung. He was looking pretty sick until recently. He has been on MMS

for a few months and is looking and feeeling so much better. His

website is www.healingcancerandsickness.com He can answer your

questions. Please also read

http://www.miraclems.com/testimonies.html

All the best,

Rosemary.

>

> Is anyone on this list battling cancer w/MMS? From what I'm

seeing, there are mostly other

> conditions on this particular list.

>

> I've been reading in JH's book and he mentions, several times, to

only stay on high doses for

> a couple of weeks until you see an improvement, then go down to

maintenance dose. My

> problem is that I've never felt pain or sickness as a result of

cancer ... so I will have no way to

> see improvement. The tumors were in my abdomen, so I can't exactly

see them. I feel like

> I'd be really flailing around in the dark, which is why I'd really

love to talk to someone who is

> using this with cancer ...

>

> xxoo

>

>

[Guest guest]

Thank you, Rosemary! So what kind of a dose is your hubby on? To my

understanding, from

what I read, us cancer folks should be on 15 drops,twice a day?

xxoo

> >

>

[Guest guest]

Hi ,

I have Stage 4 breast cancer, extensive mets to bones and 5 lung mets. I've been using the MMS for a couple of weeks now. I have had increased energy and generally feeling good since I started. I also am doing oral Xeloda chemo. Wish I could say it was without side effects, but I've had to stop the treatment twice because of horrific side effects. I ended up in the hospital with appendicitis brought on by the awful irritation of severe diarrhea. I am on my third try at another reduced dose to see if I can tolerate it. Currently I am on day 5 and the last 2 times the side effects hit full force on day 7 or 8.

I did reach my threshold for the time being with the MMS last night at 15 drops. For the first time I got nauseous and vomited and also had diarrhea which I still have today. Though, I do have to say there are no cramps so I've felt decent today, but not as good as I did before the vomiting episode last night. Today I did not take any MMS but will go back to 10 drops tomorrow.

I also am a member of the Budwig diet mailing list. I do not follow the diet completely, but I do make flaxseed oil/cottage cheese smoothies quite regularly.

I very much hope the MMS works; this is a hard disease to live with. The uncertainty of what the future holds and the possibility of more pain and suffering rarely leaves my mind. By the way, I am 48 years old and was diagnosed from the get go stage 4 in March of 06.

Regards,

Carla

Crystal, MI

   If You're going through hell.......

keep going!

.......Winston Churchill

-- [ ] Is there anyone here with cancer?

Is anyone on this list battling cancer w/MMS? From what I'm seeing, there are mostly other conditions on this particular list. I've been reading in JH's book and he mentions, several times, to only stay on high doses for a couple of weeks until you see an improvement, then go down to maintenance dose. My problem is that I've never felt pain or sickness as a result of cancer ... so I will have no way to see improvement. The tumors were in my abdomen, so I can't exactly see them. I feel like I'd be really flailing around in the dark, which is why I'd really love to talk to someone who is using this with cancer ... ;)xxoo

[Guest guest]

Carla,

I admire your resolve

and love the Churchill quote!

All the best,

Ballady

>

> Hi ,

> I have Stage 4 breast cancer, extensive mets to bones and 5 lung

mets. I've

> been using the MMS for a couple of weeks now. I have had increased

energy

> and generally feeling good since I started. I also am doing oral Xeloda

> chemo. Wish I could say it was without side effects, but I've had

to stop

> the treatment twice because of horrific side effects. I ended up in the

> hospital with appendicitis brought on by the awful irritation of severe

> diarrhea. I am on my third try at another reduced dose to see if I can

> tolerate it. Currently I am on day 5 and the last 2 times the side

effects

> hit full force on day 7 or 8.

>

> I did reach my threshold for the time being with the MMS last night

at 15

> drops. For the first time I got nauseous and vomited and also had

diarrhea

> which I still have today. Though, I do have to say there are no

cramps so I

> ve felt decent today, but not as good as I did before the vomiting

episode

> last night. Today I did not take any MMS but will go back to 10 drops

> tomorrow.

>

> I also am a member of the Budwig diet mailing list. I do not follow the

> diet completely, but I do make flaxseed oil/cottage cheese smoothies

quite

> regularly.

>

> I very much hope the MMS works; this is a hard disease to live with.

The

> uncertainty of what the future holds and the possibility of more

pain and

> suffering rarely leaves my mind. By the way, I am 48 years old and was

> diagnosed from the get go stage 4 in March of 06.

>

> Regards,

> Carla

> Crystal, MI

>

>   

> If You're going through hell.......

> keep going!

> .......Winston Churchill

> -- [ ] Is there anyone here with cancer?

>

> Is anyone on this list battling cancer w/MMS? From what I'm seeing,

there

> are mostly other

> conditions on this particular list.

>

> I've been reading in JH's book and he mentions, several times, to

only stay

> on high doses for

> a couple of weeks until you see an improvement, then go down to

maintenance

> dose. My

> problem is that I've never felt pain or sickness as a result of

cancer ...

> so I will have no way to

> see improvement. The tumors were in my abdomen, so I can't exactly

see them.

> I feel like

> I'd be really flailing around in the dark, which is why I'd really

love to

> talk to someone who is

> using this with cancer ...

>

> xxoo

>

>

[Guest guest]

Carla, have you, by any chance, gotten any of that Indian Herb that JH talks

about for

people with cancer? I know that he said if you keep hitting the wall and can't

get past it,

to try this Indian Herb and even another product, which he mentions on his

website (and

book). He gives the contact info for these folks on his website too.

I know his website sez that, with cancer, you can tell if it's gonna help or not

by hitting

that wall (which was 15 drops for you), backing off, then taking a running start

at it again.

If you can't get past the 15-drop dose, he recommends those two other things.

Just

something to consider ... or course, what do I know? I'm not even taking MMS

yet! LOL

Also, I wonder if it's not playing so nicely with the chemo ... talk about a

major pathogen

to have to kill!

xxoo

--- In , " Carla "

<ccarter48818@...>

wrote:

>

> Hi ,

> I have Stage 4 breast cancer, extensive mets to bones and 5 lung mets. I've

> been using the MMS for a couple of weeks now. I have had increased energy

> and generally feeling good since I started. I also am doing oral Xeloda

> chemo. Wish I could say it was without side effects, but I've had to stop

> the treatment twice because of horrific side effects. I ended up in the

> hospital with appendicitis brought on by the awful irritation of severe

> diarrhea. I am on my third try at another reduced dose to see if I can

> tolerate it. Currently I am on day 5 and the last 2 times the side effects

> hit full force on day 7 or 8.

>

> I did reach my threshold for the time being with the MMS last night at 15

> drops. For the first time I got nauseous and vomited and also had diarrhea

> which I still have today. Though, I do have to say there are no cramps so I

> ve felt decent today, but not as good as I did before the vomiting episode

> last night. Today I did not take any MMS but will go back to 10 drops

> tomorrow.

>

> I also am a member of the Budwig diet mailing list. I do not follow the

> diet completely, but I do make flaxseed oil/cottage cheese smoothies quite

> regularly.

>

> I very much hope the MMS works; this is a hard disease to live with. The

> uncertainty of what the future holds and the possibility of more pain and

> suffering rarely leaves my mind. By the way, I am 48 years old and was

> diagnosed from the get go stage 4 in March of 06.

[Guest guest]

Hi ,

He tries to take about 15 drops twice per day. This varies according

to how he is coping.

Regards,

Rosemary.

>

> Thank you, Rosemary! So what kind of a dose is your hubby on? To my

understanding, from

> what I read, us cancer folks should be on 15 drops,twice a day?

>

> xxoo

>

>

> > >

> >

>

[Guest guest]

I have based my treatment upon the following testimonial that I found

when dosing once a day proved to be to debilitating for me. It is

comments from a cancer patient:

GP Tells Family Their Daughter only Had 2-3 Weeks to Live

Delwyn was originally diagnosed with breast cancer at the age of just

26. It quickly spread to her bones, hips, spine and lung. Her  liver

was in bad shape also.

 Four weeks ago she was confined to bed, had to urinate in a glass

bottle, and weighed only 45 kg.

 On October 3rd  2007 was a black day for the family. She had not

eaten for 3 days and her Doctor met with the family and said  they

needed to make a decision as to whether to pull the feed tubes out of

her or not.  She had 2 – 3 week to live.  In emergency hospital, the

family had arranged her funeral and cemetery plot

 She started on the MMS and 10 days later the cancer  markers

continued to increase but her strength and energy started to return.

She was walking and even drove a short distance around the paddock at

her parents Park. 

It is now November 1st  2007 and her cancer markers are on the way

down, falling even 40 points in the past week and still falling

(Measuring her CA.15-3 scores). She is driving better than she was 6

months ago, She has no pain, is able to dress herself, her kidneys

and liver are in better condition. Is now sleeping and walking better

than 4 months ago.

 Her Doctor saw her last week and simply could not believe how well

she looked.  She has no pain and has reduced all of her medications.

 Delwyn and her family acknowledge God's leading and provision of her

treatment and the timing of it all at deaths door. Yes it is early

days but she is 6 months ahead of where she was just 4-5 weeks ago.

Delwyn has a good diet of vegetable juices, berries and raw foods

which help enormously in keeping her body alkaline as well as

nourishing her cells to re-build stronger and healthier**.  There is

no doubt that the MMS in this case has been foundational in cleansing

the body of pathogens, mould, fungus, viruses and bacteria that have

been so prolific and allowing the cancer to grow and spread.

**         She practices the 8 natural health laws:  Nutrient,

Exercise, Water, Sunshine,       Temperance, Air, Rest and Trust in

God

Helen (Delwyn's Mum) Warrigal

Delwn's Protocol: 

Day 1               2 drops every 1 hours 6 or 7 times a day

Day 2               3 drops every hour      "

Day 3               4 drops every hour      "

Day 4               5 drops every hour      "

Day 5               6 drops every hour      "

Day 6               7 drops every hour      "

Still 5 weeks later 7 drops every 1hour 6-7 times a day.

http://www.miraclems.com/testimonies.html

11/26/2007

Testimonies of those using MMS

Page 2 of 8

Initially she could not keep anything down, just kept throwing up,

juice the drops everything for about 3 days.

When she got nausea she would eat a dry biscuit or banana

She has been having fever baths every 2 days raising her temp to 38

deg (bath 41 deg) with half a cup of Bicarb of soda

That is basically it.  She is now off all medications and doing very

well

The diarrhea and vomiting are good signs that the body is simply

eliminating what it does not need.

Have a listen to MMS Simplified at www.miraclems.com/interviews.html

>

> Hi ,

> I have Stage 4 breast cancer, extensive mets to bones and 5 lung

mets. I've

> been using the MMS for a couple of weeks now. I have had increased

energy

> and generally feeling good since I started. I also am doing oral

Xeloda

> chemo. Wish I could say it was without side effects, but I've had

to stop

> the treatment twice because of horrific side effects. I ended up

in the

> hospital with appendicitis brought on by the awful irritation of

severe

> diarrhea. I am on my third try at another reduced dose to see if I

can

> tolerate it. Currently I am on day 5 and the last 2 times the side

effects

> hit full force on day 7 or 8.

>

> I did reach my threshold for the time being with the MMS last

night at 15

> drops. For the first time I got nauseous and vomited and also had

diarrhea

> which I still have today. Though, I do have to say there are no

cramps so I

> ve felt decent today, but not as good as I did before the vomiting

episode

> last night. Today I did not take any MMS but will go back to 10

drops

> tomorrow.

>

> I also am a member of the Budwig diet mailing list. I do not

follow the

> diet completely, but I do make flaxseed oil/cottage cheese

smoothies quite

> regularly.

>

> I very much hope the MMS works; this is a hard disease to live

with. The

> uncertainty of what the future holds and the possibility of more

pain and

> suffering rarely leaves my mind. By the way, I am 48 years old and

was

> diagnosed from the get go stage 4 in March of 06.

>

> Regards,

> Carla

> Crystal, MI

>

>   

> If You're going through hell.......

> keep going!

> .......Winston Churchill

> -- [ ] Is there anyone here with

cancer?

>

> Is anyone on this list battling cancer w/MMS? From what I'm seeing,

there

> are mostly other

> conditions on this particular list.

>

> I've been reading in JH's book and he mentions, several times, to

only stay

> on high doses for

> a couple of weeks until you see an improvement, then go down to

maintenance

> dose. My

> problem is that I've never felt pain or sickness as a result of

cancer ...

> so I will have no way to

> see improvement. The tumors were in my abdomen, so I can't exactly

see them.

> I feel like

> I'd be really flailing around in the dark, which is why I'd really

love to

> talk to someone who is

> using this with cancer ...

>

> xxoo

>

>