Re: Salt & C 3 years, MMS 7 Months, great progress!

[Guest guest]

--- Gives me chills to read this. Awesome! Bravo brave Lyme

soldier! Great encouragement for the rest of us.

cathy

In , " aussietickchick "

<roseonhigh@...> wrote:

>

> Hi Gang,

> I've had slow, but steady improvement on salt & C which took me

from

> mostly housebound, on a walking frame & dying, to traveling

overseas

> last year & not well, but actually having a life.

> Throughout my 29 year Lyme battle I've had flickery vision with

> flashing lights and blind patches. Kind of like a permanent

> migraine. It has been torturous, very disabling & stopped me

driving

> my car. I could not cope with glare or sudden changes in light &

> dark. I had to wear sunglasses a lot and also sleep with a small

> night light on. On waking, the flickering would be very bad and I

> presumed it was due to poor circulation. Eye docs and

neurologists

> could not explain it, other than a rare form of permanent migraine

or

> spasms in the tiny veins in the eyes. Magnesium did not help the

> spasms.

> I have been on 5 drops of MMS morning & night for 7 months, still

> taking 2 doses salt & C during day.

> I have to tell you, the 29 year spasms are nearly gone!!!!!!!!! I

> have slept without a night light for 2 weeks with no problem!!!!!!

I

> am driving again the last few months and finally without

> sunglasses!!!!!!!! I wake in the morning and can cope if a light

is

> turned on suddenly!!!!!!!

> ooooo!!!!!!!!!!!!!!!!

> I think the MMS is killing a virus or something that salt & C was

not

> killing. I am also walking miles every day, my cheeks are pink and

> my circulation is so much better. People everywhere are noticing

how

> much better I look. I am even feeling well enough to look for a

part-

> time job soon.

> Persevere. It is worth it.

> Rosemary.

> Lyme & co, glandular fever, fibro, CFS, etc 29 years of hell.

>

[Guest guest]

This is SO wonderful to hear! Congratulations for not giving up and for getting healthy. You are a great testament for others, and for the fact that it isn't necessary to use super high doses of MMS to kill pathogens. Slow but steady DOES work, as you are proving.

Samala,

-------Original Message-------

I have been on 5 drops of MMS morning & night for 7 months, still

taking 2 doses salt & C during day.

I have to tell you, the 29 year spasms are nearly gone!!!!!!!!!

[Guest guest]

Hi Rosemary. Someone on another list is asking how to deal with both candida and lyme. Would you mind if I removed your name and sent your post on to the other list as to what is possible?

Samala,

-------Original Message-------

Persevere. It is worth it.

Rosemary.

Lyme & co, glandular fever, fibro, CFS, etc 29 years of hell.

[Guest guest]

I've been fighting this thing for 31 years and am in almost the worst shape yet. How long did it take the salt/C to do it's work and how much do you take? I'm toying with the idea of MMS, but haven't made the plunge, yet. I've got an appt with Shoemaker and am going to go after the neurotoxins first. I fail the VCS test pretty badly and have all the symptoms of neuromediated illness.aussietickchick <roseonhigh@...> wrote: Hi Gang,I've had slow, but steady improvement on salt & C which took me from

mostly housebound, on a walking frame & dying, to traveling overseas last year & not well, but actually having a life.Throughout my 29 year Lyme battle I've had flickery vision with flashing lights and blind patches. Kind of like a permanent migraine. It has been torturous, very disabling & stopped me driving my car. I could not cope with glare or sudden changes in light & dark. I had to wear sunglasses a lot and also sleep with a small night light on. On waking, the flickering would be very bad and I presumed it was due to poor circulation. Eye docs and neurologists could not explain it, other than a rare form of permanent migraine or spasms in the tiny veins in the eyes. Magnesium did not help the spasms. I have been on 5 drops of MMS morning & night for 7 months, still taking 2 doses salt & C during day.I have to tell you, the 29 year spasms are nearly gone!!!!!!!!! I have slept

without a night light for 2 weeks with no problem!!!!!! I am driving again the last few months and finally without sunglasses!!!!!!!! I wake in the morning and can cope if a light is turned on suddenly!!!!!!!ooooo!!!!!!!!!!!!!!!!I think the MMS is killing a virus or something that salt & C was not killing. I am also walking miles every day, my cheeks are pink and my circulation is so much better. People everywhere are noticing how much better I look. I am even feeling well enough to look for a part-time job soon.Persevere. It is worth it.Rosemary.Lyme & co, glandular fever, fibro, CFS, etc 29 years of hell.

[Guest guest]

Hi ,

Please feel free to share my story with anyone who may be helped by

it.

Best wishes,

Rosemary.

>

> Hi Rosemary. Someone on another list is asking how to deal with

both

> candida and lyme. Would you mind if I removed your name and sent

your post

> on to the other list as to what is possible?

>

> Samala,

>

>

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

>

> Persevere. It is worth it.

> Rosemary.

> Lyme & co, glandular fever, fibro, CFS, etc 29 years of hell.

>

[Guest guest]

>

> I've been fighting this thing for 31 years and am in almost the

worst shape yet. How long did it take the salt/C to do it's work and

how much do you take? I'm toying with the idea of MMS, but haven't

made the plunge, yet. I've got an appt with Shoemaker and am going

to go after the neurotoxins first. I fail the VCS test pretty badly

and have all the symptoms of neuromediated illness.

Hi Edy,

I am sorry to hear of your struggles. I read Shoemaker's book and

took anti-biotics together with cholestyramine as per his protocol

for 6 months. It did not help me, but I know others who have been

helped by him & I do think he is brilliant. However, I don't like

abx and think salt & C & MMS are a better way to go for chronic Lyme.

I am in Australia and our docs believe there is no Lyme here, so I

didn't even get a diagnosis for 22 years! So, you can imagine how

sick I was. I had severe neurological Lyme. I have been in a

wheelcahir at times and used a walking frame for years. By 2005 I

believe I was dying and prayed it would be soon. I was having

trouble eating, speaking, swallowing and lived on pureed food for a

year. I was falling over as I had no balance. I was housebound as I

couldn't cope with chemicals in the air and I was too fragile to go

very far.

My doc had run out of ideas. I was scared to try salt & C, but I had

nothing to lose. My doc decided it just might work.

I began with a small dose in Feb 2005. With the very first dose I

got biting, prickling & itching all over my skin which felt like

being bitten by fleas, from the inside! To Understand this read

www.Lymephotos.com I KNEW it was working. With every dose the biting

sensations increased until I actually had visible bites on my skin

after a few days! This eventually settled down but I knew it was a

good sign.

The first 18 months on salt & C were slow, gruelling and tough, but I

had evidence of healing, so I persevered through the herxes. I had

bad headaches most days, which were only relieved by coffee enemas.

(this sounds awful, but brings instant relief.)

Last year I tried Chlorella and this also relieved the headaches

quickly. I take 1000mg 1/2 an hout before meals. I rarely do enemas

now. For much of the 3 years on salt & C I tried to take between 9-

12 doses per day, according to body weight and herxes. This can

vary. Some days I did not take any, but resumed ASAP when I could

cope.

Then I intoduced MMS 7 months ago. I began with 1 drop morning and

night and worked my way up slowly. The beauty of these treatments is

that you can adjust the doses according to how you are coping. Do

not take vitamin C within 2 hours of MMS as the C will neutralise MMS.

I am not a doctor but if I was you I would begin salt & C and just

ramp up slowly. Sny decent doc can oversee your blood pressure,

liver & kidney functions, etc.

The promoters of salt & C had been sick for years and are now symptom-

free & working. I was about as low as you can get without dying &

now I have a good life.

Do not give up as nothing is impossible. We have some wonderful

tools to kill these " critters. " Just put one foot in front of the

other and you will probably find, like many of us, that you will

slowly walk out of the woods and into the sunshine again.

Love & best wishes,

Rosemary.

[Guest guest]

Great news Rosemary! Congratulations on your improvements. I am

really pleased for you!

>

> Hi Gang,

> I've had slow, but steady improvement on salt & C which took me

from

> mostly housebound, on a walking frame & dying, to traveling

overseas

> last year & not well, but actually having a life.

> Throughout my 29 year Lyme battle I've had flickery vision with

> flashing lights and blind patches. Kind of like a permanent

> migraine. It has been torturous, very disabling & stopped me

driving

> my car. I could not cope with glare or sudden changes in light &

> dark. I had to wear sunglasses a lot and also sleep with a small

> night light on. On waking, the flickering would be very bad and I

> presumed it was due to poor circulation. Eye docs and

neurologists

> could not explain it, other than a rare form of permanent migraine

or

> spasms in the tiny veins in the eyes. Magnesium did not help the

> spasms.

> I have been on 5 drops of MMS morning & night for 7 months, still

> taking 2 doses salt & C during day.

> I have to tell you, the 29 year spasms are nearly gone!!!!!!!!! I

> have slept without a night light for 2 weeks with no problem!!!!!!

I

> am driving again the last few months and finally without

> sunglasses!!!!!!!! I wake in the morning and can cope if a light

is

> turned on suddenly!!!!!!!

> ooooo!!!!!!!!!!!!!!!!

> I think the MMS is killing a virus or something that salt & C was

not

> killing. I am also walking miles every day, my cheeks are pink and

> my circulation is so much better. People everywhere are noticing

how

> much better I look. I am even feeling well enough to look for a

part-

> time job soon.

> Persevere. It is worth it.

> Rosemary.

> Lyme & co, glandular fever, fibro, CFS, etc 29 years of hell.

>

[Guest guest]

Hi Margaret,

Salt & C has brought me a long way. I used pharmaceutical grade

salt tablets from the chemist at first. Lately I have been using

sea salt.

I believe MMS is killing things that salt & C was not killing.

Perhaps viral. Not sure. You need to listen to your body and do

what works for you. I use both salt & C & MMS. I adjust the doses,

depending on herxes and how I am coping.

All the best,

Rosemary.

>

> Rosemary --

>

> thanks for sharing your story and BB, thanks for posting the

website

> on Vitamin C and salt.

>

> As I have been learning about Morgellon's (sp?), these pictures

look

> alot like it. Have you researched Morgellon's at all?

>

> Rosemary, wondering what kind of salt you use? Do you attribute the

> salt & c mostly for your improvement? or MMS too?

>

> Thanks so much

>

> Margaret