Re: Dr K's parasite protocol- after effects - Doc's names

[Guest guest]

Sorry, but the policy of this forum is to not mention docs' names. You can

email someone privately to get a name. We do this for several reasons. Mainly,

Lyme forums in general do not mention docs' names because of the current debates

going on amongst medical practitioners on what is and what is not proper in

treating Lyme. Secondly, there have been divorces where the parent who does not

get custody goes after the child's doctor to discredit him/her. Downloading

posts off the Internet is often used in courts. Thus, we do not associate a

name when we speak about a practitioner. Even good things said about a

practitioner can be misused. We do posts names occasionally to publicize

Conferences and books. But, specifically what docs do is not posted with their

names. We do use initials. Usually, most know who the last initial refers to.

Sorry, for the inconvenience, but it's for the best in the long run.

Love and prayers,

Heidi N

> >

> >

> > >

> > >

> > >To those of you that are doing or have done the protocol or are

knowlegable

> > >about these sorts of things...

> > >Did you see more die-off once the protocol was over? This is what we

are

> > >experiencing and I cant figure it out. It has been approx 3 wks since we

> > >completed the 6 wks of meds and approx 2 weeks after he had finished, my

son

> > >began to experience the sharp migrating pains through his body. He had

these

> > >before occasionally, but they are now more extreme. Can anyone explain to

me

> >why

> >

> > >this would be happening? I was really concerned the other day as the sharp

> > >pains were in his head and they lasted for quite a long ! time and

became

> >more

> >

> > >of headache after a while. Thankfully the pains in his head have not

returned.

> >

> > >Since then they are occuring in the lower body  where he had

experienced

> >them in

> >

> > >the past. An extremely low dose of Quintessance seems to especially bring

them

> >

> > >out more than anything.

> > >

> > >I spoke to our LLND the other day and she was also really concerned about

the

>

> > >pains in his head and is running some blood tests etc but I didnt ask her

> >about

> >

> > >the pains in the rest of his body as they werent so prevalent at the time.

She

> >

> > >did say it was uncommon for there to be alot of die-off once the meds were

no

>

> > >longer in the body. He didnt have many symptoms when he was on the meds-

> >just 

> >

> > >liver and GB congestion.

> > >thanks for any input~

> > >

> > >

> > >

> >

>

[Guest guest]

Since practitioners are always changing biofilm protocols and they vary per

patient, I think it would be better to list the items and see if someone has

used those specific things. I have not really done much towards biofilm, but

others do speak well about it. There are also some who said that they have had

way too much die-off. So, I feel that gathering information is a good idea, so

you know what to expect. And, ask the doc what to do when the die-off symptoms

appear before you start the program so you will be prepared.

Love and prayers,

Heidi N

I couldnt answer her questions about the Biofilm protocol - so if anyone can

address her question about that.