Re: Dr K's parasite protocol- after effects

[Guest guest]

and others who have done the protocol,We have not started it. I am wondering if this is because the parasites have not been wiped out and started to migrate to different parts of the body. If you consult with a doctor in Dr K's office or himself, I think that you should call to report this and ask for advice. If it is what I suspect, I wonder if the doctor will recommend a second round of the protocol. , thank you for your post. I was thinking that I should do the Fry Labs stained blood smear test to "visually" understand the parasitic load before starting the protocol. After reading your post, I think that I definitely should do so to better understand what we are facing.LiminTo 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]

Thanks Limin! I was really afraid this might be the case.. I will leave another message for our LLND (we havent seen Dr K yet).

Can you tell me the name of the specific test you are thinking of? I found the labs site, but didnt see this particular test listed. Im curious about about the price as it sounds like something both my son and I should have.

I dont feel like my son is ready for anymore meds right now (need to continue addressing liver congestion) so Im concerned about the fact that the parasites may be migrating at this pt. Please let me know if you have any other suggestions as well.

We are strictly doing phone consults as w our LLND right now and we wont be able to travel to Wash again until April or June. Im wondering if you are anyone else (especially in the SF bay area) may know ofa practicioner that utlizes muscle testing in treating lyme that we could see in the meantime.

thanks so much~

To: BorreliaMultipleInfectionsAndAutism Sent: Thu, January 20, 2011 10:45:30 AMSubject: Re: Dr K's parasite protocol- after effects

and others who have done the protocol,

We have not started it.

I am wondering if this is because the parasites have not been wiped out and started to migrate to different parts of the body. If you consult with a doctor in Dr K's office or himself, I think that you should call to report this and ask for advice. If it is what I suspect, I wonder if the doctor will recommend a second round of the protocol.

, thank you for your post. I was thinking that I should do the Fry Labs stained blood smear test to "visually" understand the parasitic load before starting the protocol. After reading your post, I think that I definitely should do so to better understand what we are facing.

Limin

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]

Just wondering if your son has taken anything for inflammation? Like Boscari or

Boluoke,

for brain inflammation? Just wondering if the parasites are moving/dying- if

they cause inflammation.

Also I do think its possible supplements need to be continued that address

Parasites,

maybe for a long time? Just wondering if others have had to address this ?

Allie

>

>

> >

> >

> >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]

this maybe a silly question but who is Dr. K and does this protocol helps autistic kids.

Also anyone in this group doing biofilm protocol ,I am going to start this for my 10 year old ASD daughter

with Dr. Usman I wanted to hear any experiences.

Thanks,Rupa

To: BorreliaMultipleInfectionsAndAutism Sent: Thu, January 20, 2011 2:35:15 PMSubject: Re: Dr K's parasite protocol- after effects

Just wondering if your son has taken anything for inflammation? Like Boscari or Boluoke,for brain inflammation? Just wondering if the parasites are moving/dying- if they cause inflammation.Also I do think its possible supplements need to be continued that address Parasites,maybe for a long time? Just wondering if others have had to address this ?Allie> > > >> >> >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]

HI Allie- prior to this particular treatment he did a short course of ivermectin and alinia - before we started w our LLND last yr and then did 3 wks on alinia a few mos ago. He isnt on anything for inflammation other than Ketotifen and Im not sure if that addresses anything more than gut inflammation... still learning. thanks so much for the information. Sounds like we do need to put him on something again soon to address those remaining.

blessings~

To: BorreliaMultipleInfectionsAndAutism Sent: Thu, January 20, 2011 11:35:15 AMSubject: Re: Dr K's parasite protocol- after effects

Just wondering if your son has taken anything for inflammation? Like Boscari or Boluoke,for brain inflammation? Just wondering if the parasites are moving/dying- if they cause inflammation.Also I do think its possible supplements need to be continued that address Parasites,maybe for a long time? Just wondering if others have had to address this ?Allie> > > >> >> >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~> >> >> >>