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Re: that lyme borelliosis thing again!

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Hi ,

 

I am seeing an LLMD right now and sometimes unfortunately you are on specific

antibiotics for over a year-- sometimes people are on them two years before they

are better. Doctors that are Lyme literate will know which antibiotics work best

and only certain antibiotics will penetrate the spirochete organism and other

co-infections which you can have. The organism changes into different cell

states and it is hard to penetrate it's cell walls and it has a tendency to hide

from certain antibiotics. There is a supplement you can get that is used to

treat malaria that will help kill the Lyme organism as well and can be ordered

from the one company that my LLMD recommends. Let me know if you are interested

and I will give you the number. I am just starting out in the whole process and

was disgusted at having regular doctors tell me there was nothing they could do

for my " MS. "   When the radiologists kept telling my the lesions on my brain

didn't look like " MS "

lesions I became suspicious that the doctors didn't know what the heck was

wrong and started investigating Lyme disease.  Samento ( Cat's Claw ) helps

some.

 

Best,

 

Subject: that lyme borelliosis thing again!

To: mscured

Date: Wednesday, June 1, 2011, 10:35 AM

 

Okay.

So " finally " one of the doctors I go to diagnozed me with lyme yesterday. So I

was on the verge of tears, as well as physical collapse, for we had 30°Celsius

temperatures yesterday and that does not enhance my physical state when I am

psychically inbalanced...

She tested me on the Electroacupuncture EAV facility and I responded positive to

borelia and auto-allergy issues, also lymphatic and nervous troubles... So

despite all those specialists havent found the borelia in my lumbar puncture,

sometimes not even in my blood, (PCR tests), I might have it after all... and I

must confess I'm in utter doubts as to whether I have 'ms' at all and am

convinced of it being just a set of symptoms so many of us fall under.

So being twice treated with anti-biotics for the lyme did nothing. I am aware

that it can " hide " from the lumbar puncture and even from the blood results.

Actually the tick bite I had last year might have trigerred a much older lyme

infection, I had residually carried perhaps for years... So my 'ms' could have

been lyme all along? That makes me sick. It could even have been causing the

lesions in spinal cord I have!

SO I am treating my lyme with special homeopatic borelia remedy, " nosode " ...

With colloidal rhodium/platine.

With chlorella and young barley.

And I am just hoping I am going to heal my 'ms' which might have been lyme all

along.

Any other easy-to-use, affordable solutions please?

Thanks so much group, for being there.

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Guest guest

Hi ,

 

I am seeing an LLMD right now and sometimes unfortunately you are on specific

antibiotics for over a year-- sometimes people are on them two years before they

are better. Doctors that are Lyme literate will know which antibiotics work best

and only certain antibiotics will penetrate the spirochete organism and other

co-infections which you can have. The organism changes into different cell

states and it is hard to penetrate it's cell walls and it has a tendency to hide

from certain antibiotics. There is a supplement you can get that is used to

treat malaria that will help kill the Lyme organism as well and can be ordered

from the one company that my LLMD recommends. Let me know if you are interested

and I will give you the number. I am just starting out in the whole process and

was disgusted at having regular doctors tell me there was nothing they could do

for my " MS. "   When the radiologists kept telling my the lesions on my brain

didn't look like " MS "

lesions I became suspicious that the doctors didn't know what the heck was

wrong and started investigating Lyme disease.  Samento ( Cat's Claw ) helps

some.

 

Best,

 

Subject: that lyme borelliosis thing again!

To: mscured

Date: Wednesday, June 1, 2011, 10:35 AM

 

Okay.

So " finally " one of the doctors I go to diagnozed me with lyme yesterday. So I

was on the verge of tears, as well as physical collapse, for we had 30°Celsius

temperatures yesterday and that does not enhance my physical state when I am

psychically inbalanced...

She tested me on the Electroacupuncture EAV facility and I responded positive to

borelia and auto-allergy issues, also lymphatic and nervous troubles... So

despite all those specialists havent found the borelia in my lumbar puncture,

sometimes not even in my blood, (PCR tests), I might have it after all... and I

must confess I'm in utter doubts as to whether I have 'ms' at all and am

convinced of it being just a set of symptoms so many of us fall under.

So being twice treated with anti-biotics for the lyme did nothing. I am aware

that it can " hide " from the lumbar puncture and even from the blood results.

Actually the tick bite I had last year might have trigerred a much older lyme

infection, I had residually carried perhaps for years... So my 'ms' could have

been lyme all along? That makes me sick. It could even have been causing the

lesions in spinal cord I have!

SO I am treating my lyme with special homeopatic borelia remedy, " nosode " ...

With colloidal rhodium/platine.

With chlorella and young barley.

And I am just hoping I am going to heal my 'ms' which might have been lyme all

along.

Any other easy-to-use, affordable solutions please?

Thanks so much group, for being there.

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My Lyme Disease was misdiagnosed as MS.

Here is a News Report entitled " Ticked " where a gal's Lyme Disease was

misdiagnosed as MS.

http://vimeo.com/2354218

She was diagnosed with MS by Boston's top four hospitals. My FIRST MS diagnosis

in 2004 was by a nationally renowned MD PhD MS clinical trial physician. My

SECOND MS diagnosis in 2006 was by a neurologist reputed to " think out of the

box " .

Finally, it was ME, the PATIENT,that figured out my sickness was likely Lyme

disease (aka borreliosis). My FIRST borreliosis diagnosis was in 2008 and based

on a test from Fry Labs, my history, and confirmed by my herxheimer reaction to

doxycycline.

My SECOND Lyme Disease (borreliosis) is based on history and a blood test from

IgeneX.

I am REALLY puny and use a 4 wheel walker to move through the house. About 2

weeks ago, switched from antibiotics to a herbal treatment described in the book

" Healing Lyme " by Buhner. The book is available through the Amazon website.

Have been learning that it is not uncommon for a " lymie " to get drastically

better, then SUDDENLY, the sickness comes back stronger than before!

I sleep a lot. Feel free to send me a note to wake me up.

>

> Okay.

> So " finally " one of the doctors I go to diagnozed me with lyme yesterday. So I

was on the verge of tears, as well as physical collapse, for we had 30�Celsius

temperatures yesterday and that does not enhance my physical state when I am

psychically inbalanced...

>

> She tested me on the Electroacupuncture EAV facility and I responded positive

to borelia and auto-allergy issues, also lymphatic and nervous troubles... So

despite all those specialists havent found the borelia in my lumbar puncture,

sometimes not even in my blood, (PCR tests), I might have it after all... and I

must confess I'm in utter doubts as to whether I have 'ms' at all and am

convinced of it being just a set of symptoms so many of us fall under.

>

> So being twice treated with anti-biotics for the lyme did nothing. I am aware

that it can " hide " from the lumbar puncture and even from the blood results.

Actually the tick bite I had last year might have trigerred a much older lyme

infection, I had residually carried perhaps for years... So my 'ms' could have

been lyme all along? That makes me sick. It could even have been causing the

lesions in spinal cord I have!

>

> SO I am treating my lyme with special homeopatic borelia remedy, " nosode " ...

> With colloidal rhodium/platine.

> With chlorella and young barley.

>

> And I am just hoping I am going to heal my 'ms' which might have been lyme all

along.

>

> Any other easy-to-use, affordable solutions please?

>

> Thanks so much group, for being there.

>

>

>

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