Re: Can this be from the lyme? How to fix decreased perfusion

[Guest guest]

--I did't show any co infections and the last visit which was my

second appt. with the LLD he started me on a protocal for co

infections.

I did feel better treating them than with the first visit and doing

the lyme protocal.

Now I am taking very small 1/4 tab of flagyl.

For the spacey/sleepy nothing seems to help. I use to try to push

on through that feeling and it just didn't work.

Would ozone help?

Now it almost seems like the more my cervical neck hurts the worse

the spacy sleepy feels get stronger.

I didn't have that much pain in the early years of this. But the

sleepiness was so bad I cannot describe it.

I would rather have the pain than the sleepiness. The flue like is

hard to take.

Decreased perfusion is low oxygen in the brain would building up

Hemeglobin help? In the past I have had low ferritin like 8 when

normal was 11-200 then after taking iron is went up to 11.

Would taking something for inflammation help?

This might be why Ultram helps this feeing.

What is a Drs idea of fixing it?

I have never had a spect scan but did have sleep studies and eeg.

Things were not normal but not diagnostic for anything specific.

I tried all kinds of seizure drugs in the early days and now for

some strange reason neurontin is the only thing that helps this

when it works.

I can take huge doses of neurontin and it just makes me feel better.

I use to take a 2 of the 800 mg tabs 4 times a day. I cut myself

back and now I take about 2400 mg a day.

Can holding your neck wrong or having cervical neck disorders cause

this decreased perfusion?

This is a new word for me. I am so glad to have someone answer

that .

I told my local MD that I want to donate my brain to science.

First got to feeling bad summer 1987.

DX with lyme DEC 04 with IGENEX western blot 10 bands IGG and IGM.

First LLD visit May 05 .

Saw a lone star tick the other day crawling up a mans shirt that had

just walked out of the pasture.

Sandy in TN where we don't have lyme

- In , " Lizzie " <betneal@...> wrote:

>

> ---

In , eric schulman <eric_s11050@> wrote:

> HI ERIC: I THINK YOU AND GLEN FROM NJ ARE BOTH RIGHT. A SPECT SCAN

> DOES REVEAL A PATTERN OF GLOBAL DECREASED PERFUSION IN THE BRAIN

OF A

> LYME PATIENT DUE TO INFLAMATION. PERFUSION IS BY DEFINETION, BLOOD

> FLOW, AND OXYGEN IS CARRIED TO THE BRAIN VIA HEMOGLOBIN IN THE

BLOOD.

> THEREFORE DECREASED PERFUSION EQUALS DECREASED 02 IN THE BRAIN. ITS

> ONE IN THE SAME.

> I WOULD SAY TO SANDY, YES, IT IS INDEED A RESULT OF CNS

INVOLVEMENT

> DUE TO LYME DISEASE. ALMOST ALL OF US HAVE EXPERIENCED IT AT

DIFFERENT

> LEVELS AND IT IS VERY DIFFICULT TO DEAL WITH. I HAVE HAD A SPECT

SCAN

> AND IT DID REVEAL MODERATE DECREASED PERFUSION, WHICH EXPLAINED MY

> NEURO SYMPTOMS. I TRY TO KEEP MOVING AS TO GET OXYGEN TO MY BRAIN,

> EVEN IF I AM TIRED, I TRY TO TAKE A SHORT WALK. I RECENTLY STARTED

> TAKING OMEGA 3-6-9 OIL 1,000-4,000MG A DAY WHICH HAS HELPED

> TREMENDOUSLY WITH THE BRAIN FOG.

> YOU NEED TO MAKE SURE TO BE TESTED FOR ALL THE CO-INFECTIONS, AS

OTHER

> BACTERIAS AND PARASITES FROM A SINGLE TICK BITE CAN ALSO TRAVEL TO

THE

> BRAIN WITH THE Bb. ALL CO'S NEED TO BE PROPERLY TREATED. ERIC HAD A

> GOOD POINT TO MAKE SURE BEFORE YOU GO OUT AND TRY ALL THESE

DEVICES,

> TO GET INTO A GOOD LMD WHO CAN PROPERLY DIAGNOSE AND TREAT YOU.

> LIZZIE.

> > I don't think that we have low oxygen to our brains as it was

> revealed on pet scan...I believe that inflammation is the culprit

and

> that takes along time to reverse as well as the sick neuron

cells...

> >

> > Glen Wolfsen <wolfsen@> wrote: Sandy:

> > I cannot answer all your questions. but from my own

experience

> > with Lyme I can say that YES, there is less oxygen to the brain

than

> should

> > be and this slows down and inhibits functions in the over all

brain.

> There

> > are many hormones in the brain that influence the neuron

> communication -

> > making one feel anxious, paranoid, bipolar, autistic, etc,

Also, when

> > there is a lot of kill-off of any Lyme or co-infections in the

brain, a

> > bi-product is amonia. Amonia gives that spacy - disorientated

> > feeling. There are some new and effective homeopathic formulas

that

> > address this condition, but I cannot give them to you on the

list, only

> > through private e-mail. If you would like to , write me at

> > mailto:wolfsen@ - Glen from NJ. (I have experienced much of

> > what you are going through. My head problems are the " last to

go: "

> in the

> > healing process.. I am still affected by Babesoisis in my brain)

> Take care

> > and write back if you like., - Glen.

> >

>

[Guest guest]

Try to hang in there Sandy. I know its hell sometimes. I would also

rather have the pain than that awful sleepy-spacy feeling. I am just

coming off a very long herx and I do not remember ever sleeping as

much as I did this time. Try to sleep as much as you can. Your body

needs rest, sleep. Maybe the flagyl which passes the blood brain

barrier is killing bacteria in your brain and you are experiencing a

brain herx which is really hellish! But a good sign the bacteira is

being killed off. I do not think holding your neck wrong is causing

the perfusion problem. I too suffer from pain in the cervical neck,

this is classic lyme neck pain. I have had lyme for 5 years and still

have bad neck pain. It is difficult to find a comfortable sleeping

position.

Patience is required, but difficult to obtain. You pose many good

questions to which I do not have answers for. I question your

treatment of 1/4 flagyl pill. At least you are on something. Maybe

there is another LMD in your area who you can see and get a second

opinion and better answer your questions.

Write to me anytime at my email address provided. Lizzie

Sandy:

> > > I cannot answer all your questions. but from my own

> experience

> > > with Lyme I can say that YES, there is less oxygen to the brain

> than

> > should

> > > be and this slows down and inhibits functions in the over all

> brain.

> > There

> > > are many hormones in the brain that influence the neuron

> > communication -

> > > making one feel anxious, paranoid, bipolar, autistic, etc,

> Also, when

> > > there is a lot of kill-off of any Lyme or co-infections in the

> brain, a

> > > bi-product is amonia. Amonia gives that spacy - disorientated

> > > feeling. There are some new and effective homeopathic formulas

> that

> > > address this condition, but I cannot give them to you on the

> list, only

> > > through private e-mail. If you would like to , write me at

> > > mailto:wolfsen@ - Glen from NJ. (I have experienced much of

> > > what you are going through. My head problems are the " last to

> go: "

> > in the

> > > healing process.. I am still affected by Babesoisis in my brain)

> > Take care

> > > and write back if you like., - Glen.

> > >

> >

>

[Guest guest]

Well, I've been lurking on this discussion and will tell you that

hyperbaric oxygen fixes this...I have a home (mild portable)

chamber...it works.

>

> --I did't show any co infections and the last visit which was my

> second appt. with the LLD he started me on a protocal for co

> infections.

> I did feel better treating them than with the first visit and doing

> the lyme protocal.

>

> Now I am taking very small 1/4 tab of flagyl.

>

> For the spacey/sleepy nothing seems to help. I use to try to push

> on through that feeling and it just didn't work.

>

> Would ozone help?

>

> Now it almost seems like the more my cervical neck hurts the worse

> the spacy sleepy feels get stronger.

>

> I didn't have that much pain in the early years of this. But the

> sleepiness was so bad I cannot describe it.

>

> I would rather have the pain than the sleepiness. The flue like is

> hard to take.

>

> Decreased perfusion is low oxygen in the brain would building up

> Hemeglobin help? In the past I have had low ferritin like 8 when

> normal was 11-200 then after taking iron is went up to 11.

>

> Would taking something for inflammation help?

> This might be why Ultram helps this feeing.

>

> What is a Drs idea of fixing it?

>

> I have never had a spect scan but did have sleep studies and eeg.

> Things were not normal but not diagnostic for anything specific.

>

> I tried all kinds of seizure drugs in the early days and now for

> some strange reason neurontin is the only thing that helps this

> when it works.

>

> I can take huge doses of neurontin and it just makes me feel better.

> I use to take a 2 of the 800 mg tabs 4 times a day. I cut myself

> back and now I take about 2400 mg a day.

>

> Can holding your neck wrong or having cervical neck disorders cause

> this decreased perfusion?

>

> This is a new word for me. I am so glad to have someone answer

> that .

>

> I told my local MD that I want to donate my brain to science.

> First got to feeling bad summer 1987.

> DX with lyme DEC 04 with IGENEX western blot 10 bands IGG and IGM.

> First LLD visit May 05 .

>

> Saw a lone star tick the other day crawling up a mans shirt that had

> just walked out of the pasture.

>

> Sandy in TN where we don't have lyme

>

[Guest guest]

Sandy,

I have that sleepy spacey feeling too. I've had neck and

spine pain since I got sick 20 years a go. I'm also taking Flagyl

too, the sleepy spacey feeling got really bad after I stated the

Flagyl. I'm not even up to a 1/4 tablet yet. I herx really bad from

it. My LLMD told me to start with a sliver and work my way up. I've

had really bad reactions to things, I'm very drug sensitive so he

told me to go slow.

Hang in there!!

Kathy

Sandy:

> > > > I cannot answer all your questions. but from my own

> > experience

> > > > with Lyme I can say that YES, there is less oxygen to the

brain

> > than

> > > should

> > > > be and this slows down and inhibits functions in the over

all

> > brain.

> > > There

> > > > are many hormones in the brain that influence the neuron

> > > communication -

> > > > making one feel anxious, paranoid, bipolar, autistic, etc,

> > Also, when

> > > > there is a lot of kill-off of any Lyme or co-infections in

the

> > brain, a

> > > > bi-product is amonia. Amonia gives that spacy -

disorientated

> > > > feeling. There are some new and effective homeopathic

formulas

> > that

> > > > address this condition, but I cannot give them to you on the

> > list, only

> > > > through private e-mail. If you would like to , write me at

> > > > mailto:wolfsen@ - Glen from NJ. (I have experienced much

of

> > > > what you are going through. My head problems are the " last

to

> > go: "

> > > in the

> > > > healing process.. I am still affected by Babesoisis in my

brain)

> > > Take care

> > > > and write back if you like., - Glen.

> > > >

> > >

> >

>

[Guest guest]

Don't have the answers to all your questions but I want to tell you

that I was taking 1/8 flagyl and still felt its effects so i took every

other day for a while and never built up to more than 1/4.

This is quite a roller coaster ride, this illness, isn't it???

Hang in there, it gets better, even fi it gets worse soem fo the time.

Ann

[Guest guest]

Sandy

Diflucan helped my brain fog. Flagyl --I originally thought I was

taking it slowly and increasing slowly- got up to 1 1/2 a day, got

progressively more tired (different kind of tired than normal

tiredness if this makes sense) and emotional(bad emotions-

frustration, guilt, anger,etc). Finally reread about the Flagyl and

realized I was pushing it way too fast and too much. I also got

yeast on my tongue from killing too much too fast apparently, as I

also take probiotics, Candex and Nystatin and watch what I eat.

Anyway I backed off the Flagyl completely for at least 3 days, then

restarted with 1/8 and very gradually (5-6 days each time) increased

it til now I'm taking 1/2 a day and have stayed there. I have alot

more respect for it. My husband on the other hand increased to 2 a

day and had no problems he thought- altho I noticed his coughing was

a bit more, so got him to decrease to 1 a day.

The neck stiffness has gotten progressively much better for me- so

far have taken Doxy, Ceftin, Azithro and now the Flagyl, along with

many supplements.

HTH Rose Marie

Sandy:

> > > > > I cannot answer all your questions. but from my

own

> > > experience

> > > > > with Lyme I can say that YES, there is less oxygen to the

> brain

> > > than

> > > > should

> > > > > be and this slows down and inhibits functions in the over

> all

> > > brain.

> > > > There

> > > > > are many hormones in the brain that influence the neuron

> > > > communication -

> > > > > making one feel anxious, paranoid, bipolar, autistic, etc,

> > > Also, when

> > > > > there is a lot of kill-off of any Lyme or co-infections in

> the

> > > brain, a

> > > > > bi-product is amonia. Amonia gives that spacy -

> disorientated

> > > > > feeling. There are some new and effective homeopathic

> formulas

> > > that

> > > > > address this condition, but I cannot give them to you on

the

> > > list, only

> > > > > through private e-mail. If you would like to , write me

at

> > > > > mailto:wolfsen@ - Glen from NJ. (I have experienced much

> of

> > > > > what you are going through. My head problems are

the " last

> to

> > > go: "

> > > > in the

> > > > > healing process.. I am still affected by Babesoisis in my

> brain)

> > > > Take care

> > > > > and write back if you like., - Glen.

> > > > >

> > > >

> > >

> >

>

[Guest guest]

Oh Jill, if it were only that simple! I am thrilled for you that it

has helped. I know of so many, including myself who did this HBOT

treatment. It helped some for a while but the neuro symptoms came

back. It didn't help me at all. I did a month in Chico. It is a very

expensive treatment that most insurence does not cover. Your portable

unit must have cost quite a bit of money. Good investment if it is

working!

> >

> > --I did't show any co infections and the last visit which was my

> > second appt. with the LLD he started me on a protocal for co

> > infections.

> > I did feel better treating them than with the first visit and doing

> > the lyme protocal.

> >

> > Now I am taking very small 1/4 tab of flagyl.

> >

> > For the spacey/sleepy nothing seems to help. I use to try to push

> > on through that feeling and it just didn't work.

> >

> > Would ozone help?

> >

> > Now it almost seems like the more my cervical neck hurts the worse

> > the spacy sleepy feels get stronger.

> >

> > I didn't have that much pain in the early years of this. But the

> > sleepiness was so bad I cannot describe it.

> >

> > I would rather have the pain than the sleepiness. The flue like is

> > hard to take.

> >

> > Decreased perfusion is low oxygen in the brain would building up

> > Hemeglobin help? In the past I have had low ferritin like 8 when

> > normal was 11-200 then after taking iron is went up to 11.

> >

> > Would taking something for inflammation help?

> > This might be why Ultram helps this feeing.

> >

> > What is a Drs idea of fixing it?

> >

> > I have never had a spect scan but did have sleep studies and eeg.

> > Things were not normal but not diagnostic for anything specific.

> >

> > I tried all kinds of seizure drugs in the early days and now for

> > some strange reason neurontin is the only thing that helps this

> > when it works.

> >

> > I can take huge doses of neurontin and it just makes me feel better.

> > I use to take a 2 of the 800 mg tabs 4 times a day. I cut myself

> > back and now I take about 2400 mg a day.

> >

> > Can holding your neck wrong or having cervical neck disorders cause

> > this decreased perfusion?

> >

> > This is a new word for me. I am so glad to have someone answer

> > that .

> >

> > I told my local MD that I want to donate my brain to science.

> > First got to feeling bad summer 1987.

> > DX with lyme DEC 04 with IGENEX western blot 10 bands IGG and IGM.

> > First LLD visit May 05 .

> >

> > Saw a lone star tick the other day crawling up a mans shirt that had

> > just walked out of the pasture.

> >

> > Sandy in TN where we don't have lyme

> >

>

[Guest guest]

Hi Lizzie,

I agree with Jill the way to increase perfusion to the brain is to

essentially put it back. In the case of lyme you would have to use

HBOT similtaneously with the appropiate Abx therapy for your co

infection. I am a believer in Hyperbaric Oxygen however mHBOT has

also been used by many with good success.

If you are in my area, NJ, and are interested in getting Hyperbaric

Oxygen please email me privately. I offer the therapy at a very

affordable price...

Best Regards,

Sudylo RN/CHT

http://www.geocities.com/boejr1/index.html

> > >

> > > --I did't show any co infections and the last visit which was

my

> > > second appt. with the LLD he started me on a protocal for co

> > > infections.

> > > I did feel better treating them than with the first visit and

doing

> > > the lyme protocal.

> > >

> > > Now I am taking very small 1/4 tab of flagyl.

> > >

> > > For the spacey/sleepy nothing seems to help. I use to try to

push

> > > on through that feeling and it just didn't work.

> > >

> > > Would ozone help?

> > >

> > > Now it almost seems like the more my cervical neck hurts the

worse

> > > the spacy sleepy feels get stronger.

> > >

> > > I didn't have that much pain in the early years of this. But

the

> > > sleepiness was so bad I cannot describe it.

> > >

> > > I would rather have the pain than the sleepiness. The flue

like is

> > > hard to take.

> > >

> > > Decreased perfusion is low oxygen in the brain would building

up

> > > Hemeglobin help? In the past I have had low ferritin like 8

when

> > > normal was 11-200 then after taking iron is went up to 11.

> > >

> > > Would taking something for inflammation help?

> > > This might be why Ultram helps this feeing.

> > >

> > > What is a Drs idea of fixing it?

> > >

> > > I have never had a spect scan but did have sleep studies and

eeg.

> > > Things were not normal but not diagnostic for anything

specific.

> > >

> > > I tried all kinds of seizure drugs in the early days and now

for

> > > some strange reason neurontin is the only thing that helps

this

> > > when it works.

> > >

> > > I can take huge doses of neurontin and it just makes me feel

better.

> > > I use to take a 2 of the 800 mg tabs 4 times a day. I cut

myself

> > > back and now I take about 2400 mg a day.

> > >

> > > Can holding your neck wrong or having cervical neck disorders

cause

> > > this decreased perfusion?

> > >

> > > This is a new word for me. I am so glad to have someone

answer

> > > that .

> > >

> > > I told my local MD that I want to donate my brain to science.

> > > First got to feeling bad summer 1987.

> > > DX with lyme DEC 04 with IGENEX western blot 10 bands IGG and

IGM.

> > > First LLD visit May 05 .

> > >

> > > Saw a lone star tick the other day crawling up a mans shirt

that had

> > > just walked out of the pasture.

> > >

> > > Sandy in TN where we don't have lyme

> > >

> >

>

[Guest guest]

Yes, I did two rounds of treatments in multichambers in clinics. They

*are* very expensive, plus it was a lot of travel, and there's no

doubt, you may lose the benefits over time. That's why I got the

portable chamber. Because a year after my last round of 2 months of

clinic treatments, I was back to baseline. My portable is sitting

right here by my desk and I simply don't know how I'd function without

it, and I do it about once a week for an hour. It is so stress-free

for me to be able to use it when I want for how long I want. I don't

know if , the nurse, is on , I think she is, but she

bought her own *real* chamber. That requires professional training and

fireproofing etc. Hers go to deeper depths than mine but I find that

mine (1.3 ata) really works just fine. I wish more docs would get the

portables as they really are much cheaper and the cost to patients

would be reasonable.

>

> Oh Jill, if it were only that simple! I am thrilled for you that it

> has helped. I know of so many, including myself who did this HBOT

> treatment. It helped some for a while but the neuro symptoms came

> back. It didn't help me at all. I did a month in Chico. It is a very

> expensive treatment that most insurence does not cover. Your portable

> unit must have cost quite a bit of money. Good investment if it is

> working!

>

[Guest guest]

> > > >

> > > > --I did't show any co infections and the last visit which was

> my

> > > > second appt. with the LLD he started me on a protocal for co

> > > > infections.

> > > > I did feel better treating them than with the first visit and

> doing

> > > > the lyme protocal.

> > > >

> > > > Now I am taking very small 1/4 tab of flagyl.

> > > >

> > > > For the spacey/sleepy nothing seems to help. I use to try to

> push

> > > > on through that feeling and it just didn't work.

> > > >

> > > > Would ozone help?

> > > >

> > > > Now it almost seems like the more my cervical neck hurts the

> worse

> > > > the spacy sleepy feels get stronger.

> > > >

> > > > I didn't have that much pain in the early years of this. But

> the

> > > > sleepiness was so bad I cannot describe it.

> > > >

> > > > I would rather have the pain than the sleepiness. The flue

> like is

> > > > hard to take.

> > > >

> > > > Decreased perfusion is low oxygen in the brain would building

> up

> > > > Hemeglobin help? In the past I have had low ferritin like 8

> when

> > > > normal was 11-200 then after taking iron is went up to 11.

> > > >

> > > > Would taking something for inflammation help?

> > > > This might be why Ultram helps this feeing.

> > > >

> > > > What is a Drs idea of fixing it?

> > > >

> > > > I have never had a spect scan but did have sleep studies and

> eeg.

> > > > Things were not normal but not diagnostic for anything

> specific.

> > > >

> > > > I tried all kinds of seizure drugs in the early days and now

> for

> > > > some strange reason neurontin is the only thing that helps

> this

> > > > when it works.

> > > >

> > > > I can take huge doses of neurontin and it just makes me feel

> better.

> > > > I use to take a 2 of the 800 mg tabs 4 times a day. I cut

> myself

> > > > back and now I take about 2400 mg a day.

> > > >

> > > > Can holding your neck wrong or having cervical neck disorders

> cause

> > > > this decreased perfusion?

> > > >

> > > > This is a new word for me. I am so glad to have someone

> answer

> > > > that .

> > > >

> > > > I told my local MD that I want to donate my brain to science.

> > > > First got to feeling bad summer 1987.

> > > > DX with lyme DEC 04 with IGENEX western blot 10 bands IGG and

> IGM.

> > > > First LLD visit May 05 .

> > > >

> > > > Saw a lone star tick the other day crawling up a mans shirt

> that had

> > > > just walked out of the pasture.

> > > >

> > > > Sandy in TN where we don't have lyme

> > > >

> > >

> >

>

[Guest guest]

Hi, I have a few thoughts about this.

First, if you had a coinfection like babesia that might need to be

treated first. has some studies showing that some strains of

babesia may do okay in oxygen--I'm not convinced that organisms other

than yeast, and maybe something like psuedonomas or very aerobic

organisms, flourish much in higher oxygen, but in any case, that might

be an issue.

Regarding the eyes, yes I had the issue with the eyes. You need to

keep your eyes closed in the chamber. Deckoff , when she

ran a hyperbaric center, figured that out herself from a few lines in

a textbook. The cornea is permeable. Keeping your eyes open while in a

100% oxygen environment (either a monochamber, or a multichamber with

hood) means you are getting huge amounts of oxygen under pressure into

the eye. If your vitreous membrane is not in good shape (which could

be in part age which damages it in all of us which is why eventually

everybody gets cataracts, and could also be oxidative damage from

infections like lyme which do migrate into the optic nerve and maybe

the eye), it will allow some of that oxygen straight into the lens

which does not like oxygen (whereas the retina needs lots of oxygen),

and apparently also it may be that the pressure temporarily changes

the shape of the lens. So the combo effects vision but I think it is

mainly the oxygen and they don't understand that. This occurs at deep

depths like 2.4 ata that are the clinic depths that are routine. Why

they do 2.4 ata, it's never been proven you need that much

oxygen...but anwyay...that's an old argument and one that isn't worth

going into here.

So if you decide to do it again, keep your eyes closed. One of Dr

Deckoff ' patients started to have the myopia and then when she

kept her eyes closed during sessions it reversed and she did about 4

months of daily treatments and twice weekly treatments for another year.

I have tried to explain this to other clinic owners, and they don't

listen. They smile and shrug. But really, people *should* keep their

eyes closed.

> Hi : I was on IV Rocephin at the time I did HBOT 3 years ago. I

> did HBOT 2x a day for 30 days. I did not feel better after 30 days and

> was offered to stay another two weeks for free, but my eyesight had

> got so bad from the 100% oxygen that I could no longer make the drive

> from the apt I rented to the chamber. My eye sight never recovered and

> I am now required to wear glasses. Has this happened to anyone else? I

> really went into it with high hopes, it just didn't work for me. I

> would like to know if anyone has used HBOT and had permanent success?

> I know of some that had initial success, but symptoms came back.

> Thanks Lizzie

>

[Guest guest]

How do you know the neck pain is from Lyme? I have Lyme and Fibro

or Lyme with Fibro, etc. I also had neck surgery-3 discs out. My

surgeon said the pain was from the Fibro.

I get spasms. I get lots of spasms in my back too. My lyme dr. said

he does not think my back spasms are from Lyme. He said it is just

me, he does not know what causes it. My whole back is in one big

spasm now........

Thanks-

In , " Kathy " <aiden424@...> wrote:

>

> Sandy,

> I have that sleepy spacey feeling too. I've had neck and

> spine pain since I got sick 20 years a go. I'm also taking Flagyl

> too, the sleepy spacey feeling got really bad after I stated the

> Flagyl. I'm not even up to a 1/4 tablet yet. I herx really bad

from

> it. My LLMD told me to start with a sliver and work my way up.

I've

> had really bad reactions to things, I'm very drug sensitive so he

> told me to go slow.

>

> Hang in there!!

> Kathy

>

>

>

> Sandy:

> > > > > I cannot answer all your questions. but from my

own

> > > experience

> > > > > with Lyme I can say that YES, there is less oxygen to the

> brain

> > > than

> > > > should

> > > > > be and this slows down and inhibits functions in the over

> all

> > > brain.

> > > > There

> > > > > are many hormones in the brain that influence the neuron

> > > > communication -

> > > > > making one feel anxious, paranoid, bipolar, autistic, etc,

> > > Also, when

> > > > > there is a lot of kill-off of any Lyme or co-infections in

> the

> > > brain, a

> > > > > bi-product is amonia. Amonia gives that spacy -

> disorientated

> > > > > feeling. There are some new and effective homeopathic

> formulas

> > > that

> > > > > address this condition, but I cannot give them to you on

the

> > > list, only

> > > > > through private e-mail. If you would like to , write me

at

> > > > > mailto:wolfsen@ - Glen from NJ. (I have experienced much

> of

> > > > > what you are going through. My head problems are

the " last

> to

> > > go: "

> > > > in the

> > > > > healing process.. I am still affected by Babesoisis in my

> brain)

> > > > Take care

> > > > > and write back if you like., - Glen.

> > > > >

> > > >

> > >

> >

>