Re: new member Sharee

[Guest guest]

HI Sharee,

I have tryed all the treatment of the earth first on my husban dI could not save from his ALS then on my when it wen to me

finally the definitive answer were th efoolowing protcol

each part if I woudl fail to do it would bring me back to paralysis so it need egally each one

silver 1cup or two a day I made myself for one year then 1/2 a cup

welchol up to 3 per meal to began with then 2 then 1 per meal over time decreasing

to avoid constipation up to 5 magnsium citrate the strongest dosage I would find

the coil I stayed at 5 second sfor one year ans it worked due to violent herx the coil every 2 to 3 weeks

3colonics per week for 4 months then 2 per week for 1 year then 1 perweek for one year and now one per month since 2 months

the paralysis took 3 month to go from the time I had all this then it was very fragil for one year now I seldon feel the sensation fo pralsysi anymore with a strong herx . for the general health howere i stagnated one year and then progressed extremely slowly.

4 month of rocefine IV did nto do neither the protcol of dct B I tryed for two month and I could not handle due to my gut

KIndly Marie

To: "Lyme_and_Rife " <Lyme_and_Rife > Sent: Sunday, August 12, 2012 9:53 AMSubject: Re: new member

Hi Sharee,

I come form where you are went out of the weel chair and grave I will post today for you what i did to get outof past progressing paralysis that were first diagnosed as MS then as ALS . I did all the reatement of the hearth before I fond the right combination fo rme and it was not antibiotics

Talk to you later to day I am in a hurry now

Kinldy marie

To: "Lyme_and_Rife " <Lyme_and_Rife > Sent: Friday, August 10, 2012 11:51 PMSubject: new member

Hi all,

I have just recently been diagnosed with Lyme disease, after 20 years of symptoms and been misdiagnosed with motor neuron disease (like ALS) for 10 years. Sadly and luckily there is only one doctor in Western Australia where I live that will treat people with chronic Lyme. He has just given me abx for babesia which scares me because I don't know how he diagnosed me with it, he doesn't explain thing very well and it probably didn't help that I had a emotional breakdown in his office. I have never had abx for lyme or babesia before and after doing research and reading lots of post here I'm really worried about starting them and potentially making everything thing worse.

The problem is that after reading the posts of this group I am not sure how to get hold of some of the things you guys talk about. Like essiac tea does anyone know where I can get it from, I don't think mountain rose herbs sends to Australia.

Also trying to get a rife machine, I've sent some email inquiries about doug coils but haven't had responses as yet. I'm not sure if I can get one sent her. Does anyone know who is the best person to contact about one.

it is really hard getting advice or help in australia because lyme is not well known about and 95% of health practitioners and doctors either don't know about or deny it exists here. But I definitely got bitten in western australia however I don't remember, what I do remember is that my life completely changed at 15 and I just thought it was puberty.

So any help or advice for me as I start the treatment for Lyme would be appreciated

Thx so much

Sharee

[Guest guest]

Hi Sharee,

Here are treatments I had that helped very much by slowing the paralysis or by getting out of paralysis temporarly/ Hoever there were not definitive results

Gerovital 5 cc 3 time a week IM gives strenght good mood and remove part my paralysis in one day but it comes right back

ozone IM IV or rectal insufflation I felt better and it was slowing the paralsysis

armor thyroid removed temporary my paralysis

MMS1+MMS2 +Dmso th elife threatening protocol changed my ALS back into a fast progressive MS and helped me stand while I di dnto

have the ozone IV every day my dct being in hollydays

the most beautifull one being stem cell from placenta after the birth of the baby . on ehour later i was walking a gain and I felt grater and grater the two following weeks then the paralysis came back slowly ythe second month and all th ebenefit was lost . it made me gain two preciosou month thought to fight

Kindly Marie

To: "Lyme_and_Rife " <Lyme_and_Rife > Sent: Tuesday, August 14, 2012 3:27 AMSubject: Re: new member Sharee

HI Sharee,

I have tryed all the treatment of the earth first on my husban dI could not save from his ALS then on my when it wen to me

finally the definitive answer were th efoolowing protcol

each part if I woudl fail to do it would bring me back to paralysis so it need egally each one

silver 1cup or two a day I made myself for one year then 1/2 a cup

welchol up to 3 per meal to began with then 2 then 1 per meal over time decreasing

to avoid constipation up to 5 magnsium citrate the strongest dosage I would find

the coil I stayed at 5 second sfor one year ans it worked due to violent herx the coil every 2 to 3 weeks

3colonics per week for 4 months then 2 per week for 1 year then 1 perweek for one year and now one per month since 2 months

the paralysis took 3 month to go from the time I had all this then it was very fragil for one year now I seldon feel the sensation fo pralsysi anymore with a strong herx . for the general health howere i stagnated one year and then progressed extremely slowly.

4 month of rocefine IV did nto do neither the protcol of dct B I tryed for two month and I could not handle due to my gut

KIndly Marie

To: "Lyme_and_Rife " <Lyme_and_Rife > Sent: Sunday, August 12, 2012 9:53 AMSubject: Re: new member

Hi Sharee,

I come form where you are went out of the weel chair and grave I will post today for you what i did to get outof past progressing paralysis that were first diagnosed as MS then as ALS . I did all the reatement of the hearth before I fond the right combination fo rme and it was not antibiotics

Talk to you later to day I am in a hurry now

Kinldy marie

To: "Lyme_and_Rife " <Lyme_and_Rife > Sent: Friday, August 10, 2012 11:51 PMSubject: new member

Hi all,

I have just recently been diagnosed with Lyme disease, after 20 years of symptoms and been misdiagnosed with motor neuron disease (like ALS) for 10 years. Sadly and luckily there is only one doctor in Western Australia where I live that will treat people with chronic Lyme. He has just given me abx for babesia which scares me because I don't know how he diagnosed me with it, he doesn't explain thing very well and it probably didn't help that I had a emotional breakdown in his office. I have never had abx for lyme or babesia before and after doing research and reading lots of post here I'm really worried about starting them and potentially making everything thing worse.

The problem is that after reading the posts of this group I am not sure how to get hold of some of the things you guys talk about. Like essiac tea does anyone know where I can get it from, I don't think mountain rose herbs sends to Australia.

Also trying to get a rife machine, I've sent some email inquiries about doug coils but haven't had responses as yet. I'm not sure if I can get one sent her. Does anyone know who is the best person to contact about one.

it is really hard getting advice or help in australia because lyme is not well known about and 95% of health practitioners and doctors either don't know about or deny it exists here. But I definitely got bitten in western australia however I don't remember, what I do remember is that my life completely changed at 15 and I just thought it was puberty.

So any help or advice for me as I start the treatment for Lyme would be appreciated

Thx so much

Sharee