OT?: what is the relation between Lyme and gluten sensitivity??

[Guest guest]

Hi all

I am about to do all the testing per Dr Shoemaker's list in the back of Mold

Warriors. To

remind you of my health issues: mercury poisoning, Crohn's Disease for over 20

years

(supposedly but I question that diagnosis), MCS, am exploring the possibility of

mold

illness. I am eating gluten the past 3 days to make sure I get an accurate

result for gliadin

antibodies since I have been grain-free pretty much for 4 years.

I am also currently doing a sea salt/vitamin c protocol for killing parasites

and gut bugs

that a lot of Lymies are doing with great success (see

LymeStrategies if

interested). Up till now I did not suspect Lyme at all. Since starting to eat

gluten, I have the

following symptoms: insomnia (literally up all night), migratory muscles

pains/spasms,

worse diarrhea, gas, weird hypoglycemic episodes including very clammy skin on

calves

with a sort of " menthol " -like feeling on skin. I never had any of these symptoms

before

(except for diarrhea and gas of course), even when I've eaten gluten in the

past.

My thought was that the Lyme bug likes gluten and feeds on/multiplies with it.

And then

the sea salt/vit c kills the organisms, causing major die-off and so what I am

experiencing

could be the die-off symptoms. Or is there any way this whole experience has

activated a

very latent/dormant long term Lyme infection??

Anyone have any ideas about this? Dr. Schaller??

Thanks!

[Guest guest]

julie, i have a pharmacist friend with crohns.....he uses probiotics, & says

he feels MUCH better. he also know the crohns is r/t fungal invasion.

just fyi.....take care,

victoria

[] OT?: what is the relation between Lyme and gluten

sensitivity??

> Hi all

> I am about to do all the testing per Dr Shoemaker's list in the back of

> Mold Warriors. To

> remind you of my health issues: mercury poisoning, Crohn's Disease for

> over 20 years

> (supposedly but I question that diagnosis), MCS, am exploring the

> possibility of mold

> illness. I am eating gluten the past 3 days to make sure I get an accurate

> result for gliadin

> antibodies since I have been grain-free pretty much for 4 years.

>

> I am also currently doing a sea salt/vitamin c protocol for killing

> parasites and gut bugs

> that a lot of Lymies are doing with great success (see

> LymeStrategies if

> interested). Up till now I did not suspect Lyme at all. Since starting to

> eat gluten, I have the

> following symptoms: insomnia (literally up all night), migratory muscles

> pains/spasms,

> worse diarrhea, gas, weird hypoglycemic episodes including very clammy

> skin on calves

> with a sort of " menthol " -like feeling on skin. I never had any of these

> symptoms before

> (except for diarrhea and gas of course), even when I've eaten gluten in

> the past.

>

> My thought was that the Lyme bug likes gluten and feeds on/multiplies with

> it. And then

> the sea salt/vit c kills the organisms, causing major die-off and so what

> I am experiencing

> could be the die-off symptoms. Or is there any way this whole experience

> has activated a

> very latent/dormant long term Lyme infection??

>

> Anyone have any ideas about this? Dr. Schaller??

> Thanks!

>

>

>

>

>

>

>

> FAIR USE NOTICE:

>

>

>

[Guest guest]

hi victoria

what does " r/t fungal invasion " mean?

do you know what probiotics he uses? i use acidophilus and bifidus. i have tried

many over

the years. my guess is that crohns is usually from a bioorganism and everyone

has a

different mix, so everyone reacts positively and negatively to different things.

probiotics

have never made a huge difference for me, but i have taken them for about 3-4

years now.

but i have heard stories of others who are essentially " cured " overnight of

their symptoms

once they take them.

thanks julie

> julie, i have a pharmacist friend with crohns.....he uses probiotics, & says

> he feels MUCH better. he also know the crohns is r/t fungal invasion.

>

> just fyi.....take care,

> victoria

[Guest guest]

r/t is related to......

and i think, if i recall right, he goes to www.treeoflife.com to get his

probiotics. can't tell ya more, though.

sorry

v.

[] Re: OT?: what is the relation between Lyme and

gluten sensitivity??

> hi victoria

> what does " r/t fungal invasion " mean?

>

> do you know what probiotics he uses? i use acidophilus and bifidus. i have

> tried many over

> the years. my guess is that crohns is usually from a bioorganism and

> everyone has a

> different mix, so everyone reacts positively and negatively to different

> things. probiotics

> have never made a huge difference for me, but i have taken them for about

> 3-4 years now.

> but i have heard stories of others who are essentially " cured " overnight

> of their symptoms

> once they take them.

>

> thanks julie

>

>> julie, i have a pharmacist friend with crohns.....he uses probiotics, &

>> says

>> he feels MUCH better. he also know the crohns is r/t fungal invasion.

>>

>> just fyi.....take care,

>> victoria

>

>

>

>

>

>

> FAIR USE NOTICE:

>

>

>