Re: Not herxing much (was) OT: Jernigan protocol

[Guest guest]

Thanks Jim,

Lucky for me, I do not have Bart or Babs. Just LD, some viruses, and some

funguses, including candida. All much better under control now. Since I

probably was exposed to LD in the mid 1960's, it may be an older form of LD--not

the modern souped-up version. Who knows--maybe I was exposed to it even

earlier. Regardless, it was not diagnosed until 2000 and no one told me I was

crazy. They just couldn't find anything wrong with me and gave me standard

advice like " Eat less salt " , " Take aspirin " , " Get more sleep " and eventually

tried lots of strong anti-inflammatories, a couple of steroid injections, and a

hypoglycemic diet. Needless to say, the inflammatories really did a number on

me, and I crashed after the 2nd steroid injection, although the physical therapy

helped a bit. The sugar-free diet probably saved my life. Eventually I started

with Dr. Brownstein and had allergy tests and metals detox and got even sicker

(he didn't know about LD then--he does now). And finally Dr. June diagnosed me,

and Dr. B then concurred. A very long journey ... over most of my adult life.

So yes, I'm very happy that it no longer totally controls and restricts me!

I think it may have been a couple of years after diagnosis that Dr. June

introduced me to Rosner's first book and I began treatment with the GB

4000. Very difficult for a a couple more years. I think the biggest change was

after my hip replacement in 2005. There was some improvement before that, but

much more afterwards. Being able to walk really helps! Joint replacements are

a huge project, but it was definitely worth it. Doesn't seem to work too well

for those who've had a traumatic injury leading to the joint replacement--that's

much more difficult. Better to have time to prepare.

Khaya

> > >

> > > Hi Khaya,

> > >

> > > If you are not herxing much anymore, then you are not killing as many

> > > pathogens

> > > and thus are not making progress anymore..

> > >

> > > Many who own rife machines including the GB4000 at some point experience

> > > less herxing,

> > > those who buy Doug Coil machines and stop using their rife machines start

> > > herxing again.

> > > You may be able to experience more herxing by opting for the MOPA amp,

> > > which would

> > > make your system a lot more powerful.. Or a Doug Coil..

> > >

> > > Unless you feel you are close to being cured, this would be the only other

> > > reason for

> > > not herxing as much..

> > >

> > > " Lyme Disease and Rife Machines " by Rosner... pg 52

> > > >>>>If herx reactions are not occurring, the therapy is ineffective. When

> > > herx reactions are no longer

> > > experienced, progress is no longer made.. Dying spirochetes result in

> > > neurotoxin release and

> > > inflammation every single time. No neurotoxin release and inflammation and

> > > associated symptoms

> > > mean no bacterial load reduction. Herx reactions are ongoing through the

> > > entire period in which spiro's

> > > are being killed and the bacterial load is being lowered.. Just as there

is

> > > no way to get over the

> > > flu without feeling sick, there is not way to fight Lyme without having

> > > herx reactions.. <<<<

> > >

> > > 's book is an excellent read and everyone on this group should own a

> > > copy...

> > >

> > > http://www.lymebook.com/lyme-disease-rife-machines-bryan-rosner

> > >

> > > --

> > > Take care,

> > > Jim