MMS 7 Months, great progress!

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Origin1 @al sender's name: aussietickchick

Original sender's address: roseonhigh

 

Hi Edy,

I was like you for so many years. I could hardly hold my head up or

sit up in a chair. I had nurses come to shower me as I couldn't even

sit up on a chair in the shower. I recall going to a doctor and I

lay my head on his desk as I could not sit up. I asked for a test

for Lupus and he refused. He decided it was a " psychiatric " problem

and sent me for " rest " in a psyche ward! The docs in the psyche ward

said I was more rational than any of their patients and one guy

couldn't understand why my BP was only 80/50. He could see I was

sick. I checked myself out after a few days because I had 2 toddlers

to care for and the hospital had nothing to offer me.

 

I spent many family outings curled up in the back seat of the car,

trying to get the energy to join in with my family. My first husband

was so furious and resentful that I would push myself to act normal

but I was so incredibly ill for so long with no proper diagnosis or

treatment.

 

When I married Vic in 1998 I was in a wheelchair and still didn't

know why. It was so scarey to be going downhill for no good reason.

Vic had to hold me over the edge of the bath to wash my hair! Every

outing and family event was just a trauma because I had to prop my

head on my hand just to talk to people and often had to go and lie

down. But I looked really well, so most people judged and abused &

abandoned me.

When I finally got my diagnosis of Lyme after 22 years, I had to prop

my head up on my hand to sit at the computer and research

treatments. I had to shift my head from one hand to the other all

the time. I had a walking frame to help me balance as I was falling

over.

 

Now I am walking miles! My muscles are building up and I am finally

getting well.

Hang in there and do not give up. My case seemed so impossible.

Rosemary.

 

 

 

Hi Rosemary,

 

Thank you for responding. I'm not going to take the ABX as I

think that's how I got into all this trouble in the first place. I'm

only going to Shoemaker for his cholestyramine protocol as I think by

going after the lyme without detoxing I got in more trouble.

 

I know that Australia doesn't believe there's lyme there and I

used to get a product called Progurt from there and the man, who tho

very nice, that I spoke with said there was no such thing as Lyme!

He actually said, and I quote " You Americans and your lyme disease! "

He made it very clear Aussie's didn't think it existed and we're a

bit neurotic over here about it.

 

Your story sounds like mine and who knows how many others. A

hell for 31 years for me. I've spent more than half that time

bedbound and only able to crawl, but only had to be in wheelchairs in

airports and such. Can't tell you how many docs I've been to and how

many hours spent in the back seat of a car lying down all the way. I

would even have to lie down in the offices and talk to them from

there as I was just too weak to sit. There's about a zillion more

symptoms, but I'm sure you all know them, too.

 

I'm MCS now as well and can't go anywhere without a mask on and

am allergic to most foods so have lost a lot of weight. Because of

the bland diet and that I can only eat in liquified like you I use a

lot of salt, but am allergic to vit C. I'm going to try the one from

the Linus Pauling Institute as it's not make from corn and maybe I

can tolerate it. I measured the salt one day out of curiousity and

found that I'm eating about 4-5 grams a day. Good sea salt.

 

I'm so happy for you that you've improved so much. YEA!

 

Hugs onya, Edy

 

aussietickchick <roseonhigh wrote:

miracle_mineral_supplement , Edy

Rayfield

<edyrayfield@> wrote:

 

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.