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Re: Dr Chia update

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Bill,

Do you know if Chia tests cfs patients for borrelia and if so what

lab? I wonder if he has seen cfs in it's Lyme disease form?

Thanks,

a Carnes

>

> i finally saw Dr Chia a couple of weeks ago and i have to say that

i

> am so happy i travelled to see him.

>

> he is very determined to not only get info out about how serious

CFS

> is, but to do the necessary research to either figure this thing

out

> himself or at least get more DRs and researchers to devote

themselves

> to our condition.

>

> he has some new papers that show more evidence of these

enteroviruses

> in PWCs and really believes that he is hot on the trail.

>

> he was very compassionate and has seen CFS in all its forms. he

knew

> all my experiences before i mentioned them to him.

>

> as for treatments he mentioned a few thing he uses like IVIG

> (expensive and hard to get ins. to pay for), interferons (same

> scenario). he has had some good repsonses to the interferon

> treatments, but it also can be hard to handle.

>

> he is trying an herb that he is very excited about called matrine,

> but it needs to be from a reliable source from China and needs some

> special paperwork to get it imported to the country.

>

> i am going to give this a shot, and i will certainly report back my

> results.

>

> i woudld suggest going to see him if you are interested in trying

> this herb. i guess it can alter certain organ functions (not sure

if

> it is kidney or liver) but i have to get bloodwork done after

taking

> it for a month to see if there are any changes.

>

> i am very hopeful, and was so glad that i made the decision to see

> him

>

> thanks

> bill

>

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Where is he?

Adrienne

Dr Chia update

i finally saw Dr Chia a couple of weeks ago and i have to say that i

am so happy i travelled to see him.

he is very determined to not only get info out about how serious CFS

is, but to do the necessary research to either figure this thing out

himself or at least get more DRs and researchers to devote themselves

to our condition.

he has some new papers that show more evidence of these enteroviruses

in PWCs and really believes that he is hot on the trail.

he was very compassionate and has seen CFS in all its forms. he knew

all my experiences before i mentioned them to him.

as for treatments he mentioned a few thing he uses like IVIG

(expensive and hard to get ins. to pay for), interferons (same

scenario). he has had some good repsonses to the interferon

treatments, but it also can be hard to handle.

he is trying an herb that he is very excited about called matrine,

but it needs to be from a reliable source from China and needs some

special paperwork to get it imported to the country.

i am going to give this a shot, and i will certainly report back my

results.

i woudld suggest going to see him if you are interested in trying

this herb. i guess it can alter certain organ functions (not sure if

it is kidney or liver) but i have to get bloodwork done after taking

it for a month to see if there are any changes.

i am very hopeful, and was so glad that i made the decision to see

him

thanks

bill

This list is intended for patients to share personal experiences with each

other, not to give medical advice. If you are interested in any treatment

discussed here, please consult your doctor.

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a

i don't know for sure. we didn't talk too much about Lyme. i have

gone down that road and didn't get too much better. so, i went to him

knowing that his focus is enteroviruses in CFS.

he is a general practicing Infectious Disease DR, so i'm sure he

knows alot about it.

still, as far as i know, he is not an LLMD and being in LA probably

doesn't focus too much on Lyme.

thanks

bill

>

> Bill,

> Do you know if Chia tests cfs patients for borrelia and if so what

> lab? I wonder if he has seen cfs in it's Lyme disease form?

>

> Thanks,

> a Carnes

>

>

> >

> > i finally saw Dr Chia a couple of weeks ago and i have to say

that

> i

> > am so happy i travelled to see him.

> >

> > he is very determined to not only get info out about how serious

> CFS

> > is, but to do the necessary research to either figure this thing

> out

> > himself or at least get more DRs and researchers to devote

> themselves

> > to our condition.

> >

> > he has some new papers that show more evidence of these

> enteroviruses

> > in PWCs and really believes that he is hot on the trail.

> >

> > he was very compassionate and has seen CFS in all its forms. he

> knew

> > all my experiences before i mentioned them to him.

> >

> > as for treatments he mentioned a few thing he uses like IVIG

> > (expensive and hard to get ins. to pay for), interferons (same

> > scenario). he has had some good repsonses to the interferon

> > treatments, but it also can be hard to handle.

> >

> > he is trying an herb that he is very excited about called

matrine,

> > but it needs to be from a reliable source from China and needs

some

> > special paperwork to get it imported to the country.

> >

> > i am going to give this a shot, and i will certainly report back

my

> > results.

> >

> > i woudld suggest going to see him if you are interested in trying

> > this herb. i guess it can alter certain organ functions (not sure

> if

> > it is kidney or liver) but i have to get bloodwork done after

> taking

> > it for a month to see if there are any changes.

> >

> > i am very hopeful, and was so glad that i made the decision to

see

> > him

> >

> > thanks

> > bill

> >

>

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Bill, if at all possible, would you contact him and ask

1. Is he testing all cfs patients for borrelia and possibly

ehrlichia , babesia and bartonella?

2. What lab and what tests is he using?

If you get to chat with him please tell him that I am the patient who

tried Zadaxin for borrelia for six months. I did not help me at all.

He probably found the same with the patients he treated.

Thanks,

a

>

> a

>

> i don't know for sure. we didn't talk too much about Lyme. i have

> gone down that road and didn't get too much better. so, i went to

him

> knowing that his focus is enteroviruses in CFS.

>

> he is a general practicing Infectious Disease DR, so i'm sure he

> knows alot about it.

>

> still, as far as i know, he is not an LLMD and being in LA probably

> doesn't focus too much on Lyme.

>

> thanks

> bill

>

>

> >

> > Bill,

> > Do you know if Chia tests cfs patients for borrelia and if so

what

> > lab? I wonder if he has seen cfs in it's Lyme disease form?

> >

> > Thanks,

> > a Carnes

> >

> >

> > >

> > > i finally saw Dr Chia a couple of weeks ago and i have to say

> that

> > i

> > > am so happy i travelled to see him.

> > >

> > > he is very determined to not only get info out about how

serious

> > CFS

> > > is, but to do the necessary research to either figure this

thing

> > out

> > > himself or at least get more DRs and researchers to devote

> > themselves

> > > to our condition.

> > >

> > > he has some new papers that show more evidence of these

> > enteroviruses

> > > in PWCs and really believes that he is hot on the trail.

> > >

> > > he was very compassionate and has seen CFS in all its forms. he

> > knew

> > > all my experiences before i mentioned them to him.

> > >

> > > as for treatments he mentioned a few thing he uses like IVIG

> > > (expensive and hard to get ins. to pay for), interferons (same

> > > scenario). he has had some good repsonses to the interferon

> > > treatments, but it also can be hard to handle.

> > >

> > > he is trying an herb that he is very excited about called

> matrine,

> > > but it needs to be from a reliable source from China and needs

> some

> > > special paperwork to get it imported to the country.

> > >

> > > i am going to give this a shot, and i will certainly report

back

> my

> > > results.

> > >

> > > i woudld suggest going to see him if you are interested in

trying

> > > this herb. i guess it can alter certain organ functions (not

sure

> > if

> > > it is kidney or liver) but i have to get bloodwork done after

> > taking

> > > it for a month to see if there are any changes.

> > >

> > > i am very hopeful, and was so glad that i made the decision to

> see

> > > him

> > >

> > > thanks

> > > bill

> > >

> >

>

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thanks for the input, Bill. Dr Chia will be giving a presentation at the IACFS

conference in January.

winsomme <winsomme@...> wrote: i finally saw Dr Chia a couple of

weeks ago and i have to say that i

am so happy i travelled to see him.

he is very determined to not only get info out about how serious CFS

is, but to do the necessary research to either figure this thing out

himself or at least get more DRs and researchers to devote themselves

to our condition.

he has some new papers that show more evidence of these enteroviruses

in PWCs and really believes that he is hot on the trail.

he was very compassionate and has seen CFS in all its forms. he knew

all my experiences before i mentioned them to him.

as for treatments he mentioned a few thing he uses like IVIG

(expensive and hard to get ins. to pay for), interferons (same

scenario). he has had some good repsonses to the interferon

treatments, but it also can be hard to handle.

he is trying an herb that he is very excited about called matrine,

but it needs to be from a reliable source from China and needs some

special paperwork to get it imported to the country.

i am going to give this a shot, and i will certainly report back my

results.

i woudld suggest going to see him if you are interested in trying

this herb. i guess it can alter certain organ functions (not sure if

it is kidney or liver) but i have to get bloodwork done after taking

it for a month to see if there are any changes.

i am very hopeful, and was so glad that i made the decision to see

him

thanks

bill

__________________________________________________

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I just gotta know: does he have grren sprouts growing all over his body?

On 12/16/06, cort johnson <cortttt@...> wrote:

>

> thanks for the input, Bill. Dr Chia will be giving a presentation at the

> IACFS conference in January.

>

>

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  • 4 weeks later...

Hi Bill,

I read a post by PVLady at immunesupport.com

http://www.immunesupport.com/chat/forums/message.cfm?id=1017609 & B=FM

She also sees Dr. Chia and she said he recommends a Chinese herb

extract called Matrine ( in addition to other treatments you

mentioned). She thinks the Matrine can be ordered from BeVigour and

its called Agascoli.

Is this the same product that you take?

Does Dr. Chia still require blood work after a month of taking

it, and is that becuase you are in a study with him or because it

might cause harm?

Thanks,

Cobi

>

> i finally saw Dr Chia a couple of weeks ago and i have to say that i

> am so happy i travelled to see him.

>

> he is very determined to not only get info out about how serious CFS

> is, but to do the necessary research to either figure this thing out

> himself or at least get more DRs and researchers to devote themselves

> to our condition.

>

> he has some new papers that show more evidence of these enteroviruses

> in PWCs and really believes that he is hot on the trail.

>

> he was very compassionate and has seen CFS in all its forms. he knew

> all my experiences before i mentioned them to him.

>

> as for treatments he mentioned a few thing he uses like IVIG

> (expensive and hard to get ins. to pay for), interferons (same

> scenario). he has had some good repsonses to the interferon

> treatments, but it also can be hard to handle.

>

> he is trying an herb that he is very excited about called matrine,

> but it needs to be from a reliable source from China and needs some

> special paperwork to get it imported to the country.

>

> i am going to give this a shot, and i will certainly report back my

> results.

>

> i woudld suggest going to see him if you are interested in trying

> this herb. i guess it can alter certain organ functions (not sure if

> it is kidney or liver) but i have to get bloodwork done after taking

> it for a month to see if there are any changes.

>

> i am very hopeful, and was so glad that i made the decision to see

> him

>

> thanks

> bill

>

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the matrine i ordered was from China. it certainly is possible that

Dr Chia has found a US distributor so we don't have to order from so

far away.

i am not in the study, but i decided to order it to give it a shot. i

can't really say one way or another yet whether it is helping.

i will certainly reply back when i have some more definitive feelings.

it certainly is good news that there is a US place to get Matrine,

and i would expect if PVLady mentioned it, she probably was directed

there by Dr Chia.

i am also anxious to hear back reports from the IACFS because i know

Dr Chia was presenting there.

thanks

bill

> >

> > i finally saw Dr Chia a couple of weeks ago and i have to say

that i

> > am so happy i travelled to see him.

> >

> > he is very determined to not only get info out about how serious

CFS

> > is, but to do the necessary research to either figure this thing

out

> > himself or at least get more DRs and researchers to devote

themselves

> > to our condition.

> >

> > he has some new papers that show more evidence of these

enteroviruses

> > in PWCs and really believes that he is hot on the trail.

> >

> > he was very compassionate and has seen CFS in all its forms. he

knew

> > all my experiences before i mentioned them to him.

> >

> > as for treatments he mentioned a few thing he uses like IVIG

> > (expensive and hard to get ins. to pay for), interferons (same

> > scenario). he has had some good repsonses to the interferon

> > treatments, but it also can be hard to handle.

> >

> > he is trying an herb that he is very excited about called

matrine,

> > but it needs to be from a reliable source from China and needs

some

> > special paperwork to get it imported to the country.

> >

> > i am going to give this a shot, and i will certainly report back

my

> > results.

> >

> > i woudld suggest going to see him if you are interested in trying

> > this herb. i guess it can alter certain organ functions (not sure

if

> > it is kidney or liver) but i have to get bloodwork done after

taking

> > it for a month to see if there are any changes.

> >

> > i am very hopeful, and was so glad that i made the decision to

see

> > him

> >

> > thanks

> > bill

> >

>

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I'll put a full report on him when I do the whole conference but I must say he

was a very effective presenter - an impressive physician/researcher.

winsomme <winsomme@...> wrote: the matrine i ordered was from

China. it certainly is possible that

Dr Chia has found a US distributor so we don't have to order from so

far away.

i am not in the study, but i decided to order it to give it a shot. i

can't really say one way or another yet whether it is helping.

i will certainly reply back when i have some more definitive feelings.

it certainly is good news that there is a US place to get Matrine,

and i would expect if PVLady mentioned it, she probably was directed

there by Dr Chia.

i am also anxious to hear back reports from the IACFS because i know

Dr Chia was presenting there.

thanks

bill

> >

> > i finally saw Dr Chia a couple of weeks ago and i have to say

that i

> > am so happy i travelled to see him.

> >

> > he is very determined to not only get info out about how serious

CFS

> > is, but to do the necessary research to either figure this thing

out

> > himself or at least get more DRs and researchers to devote

themselves

> > to our condition.

> >

> > he has some new papers that show more evidence of these

enteroviruses

> > in PWCs and really believes that he is hot on the trail.

> >

> > he was very compassionate and has seen CFS in all its forms. he

knew

> > all my experiences before i mentioned them to him.

> >

> > as for treatments he mentioned a few thing he uses like IVIG

> > (expensive and hard to get ins. to pay for), interferons (same

> > scenario). he has had some good repsonses to the interferon

> > treatments, but it also can be hard to handle.

> >

> > he is trying an herb that he is very excited about called

matrine,

> > but it needs to be from a reliable source from China and needs

some

> > special paperwork to get it imported to the country.

> >

> > i am going to give this a shot, and i will certainly report back

my

> > results.

> >

> > i woudld suggest going to see him if you are interested in trying

> > this herb. i guess it can alter certain organ functions (not sure

if

> > it is kidney or liver) but i have to get bloodwork done after

taking

> > it for a month to see if there are any changes.

> >

> > i am very hopeful, and was so glad that i made the decision to

see

> > him

> >

> > thanks

> > bill

> >

>

---------------------------------

Everyone is raving about the all-new beta.

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