Re: OT: MMS irritating the bladder...or annoying the spirochetes in the bladder?

[Guest guest]

hi fifi,don't know if any of this fits you, but here is my experience with bladder 'problems'.  started having many bladder infection in early 2000's when i got reinfected and didn't know it.  lots of test etc. no one knew why my bladder infections went into kidney infections before i could even get on the abx.for the bladder infection.  think i know now.

 then when we discovered lyme, bart, babs and started abx (mistake-didn't know) i remember coming home shortly after i started rifampin, for bart, and started feeling those awful bladder infection problems, urgency, pain, etc.  dr said abx shouldn't do that.  wasn't an infection and shortly after the problem went away.

 but have had a few infections since.  last time dr gave me the typical abx, but it stopped working, think i became resistant to it.  so i asked here if anyone knew of something natural.  D MANNOSE immediately came back by about 6 people.  IT DOES WORK FOR ME

as i've been coiling for bart, i sometimes would get that infection feeling again.  the urine is not always cloudy, so don't know if it was an infection or not.  but i start the d mannose and within a day, 2 tops, it is gone.  

now, again, i can't say if it was a true infection, or if some killing was doing something.  i think i read somewhere that bart will cause bladder problems.  mms kills whatever it finds, so....  

i like the now brand powder, 3 oz.  it mixes well, cheaper,  tastes fine and i think it works faster.  when i first took it, after 2 doses, most symptoms were gone.  when i get that feeling, i take it right away to catch it early.  if it's bad, i take it 4x a day  to get a head of it, then will continue for at least 1 wk at 2x a day, sometimes longer depending on if the urine is cloudy or not. then again, i have taken it for only a few days and was fine.  i do wonder if it is just a complication of the killing of maybe bart--if i remember it correctly about bart. 

anyway, that is how i have handled those symptoms.  they can  not only be  irritating, but sometimes scary.  of course, if d mannose, didn't help, a dr visit would be in order.

here is the link for the d mannosehttp://www.swansonvitamins.com/Search?keyword=d+mannose & doSearch=true & ntt= & n=0 & ntk=Level1 & x=32 & y=8

barbara

 

Folks-

Was finally able to work up to 1/2 drop of MMS daily and then only before bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After about 10 days I noticed increasing bladder irritation that resembled a bladder infection with pressure and odor, but no burning. No amount of water or cranberry juice was resolving it and it was to the point of not being able to travel to work without fear of an accident. I figured deal pathogens would flush out with all of the water and wouldn't be causing the issue.

Finally went to the doctor to be tested for bladder infection and they found...nothing. I stopped the nightly MMS and after several days, it finally calmed down.

The thing is...during that run of MMS and even after, I felt noticeably better in terms of energy and mental clarity, so I'm going to start back up. I can pick up some Depends if it means I can remember what I was doing.

I suppose I can take MMS again till the bladder screams and then stop until it subsides, but I wish there was something I could do to calm the bladder, because that's no fun. I was wondering if spirochetes in the bladder were being killed/ " annoyed " by the MMS and if that's what was going on. As I've being coiling, I'm focusing on bladder/stomach area, because the bladder sensitivity has been an issue as the Lyme has gotten worse.

Searched the archives to see if someone has had a similar situation or has any guidance, but didn't see anything.

Off to mix up my mini-dose of MMS. What a treat to feel even a small bit better.

Thank you.

Best regards,

Fifi

[Guest guest]

Barbara, Hi.....I was intrigued by fifi's post as well but didn't have any

answers! I do believe it's bart. related and part of die-off. It can almost

feel like an infection...urine smells, cloudy, frequent urination etc. If I

lesson my treatment it calms down...if I push too hard I can tell because all

the symptom increase! Especially the smelly, putrid urine! Thanks for the

D-mannose tip! I was on that a long time ago.....can't remember why I took

it..will look into that. Thanks, JOdie L.

>

> > **

> >

> >

> > Folks-

> >

> > Was finally able to work up to 1/2 drop of MMS daily and then only before

> > bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After

> > about 10 days I noticed increasing bladder irritation that resembled a

> > bladder infection with pressure and odor, but no burning. No amount of

> > water or cranberry juice was resolving it and it was to the point of not

> > being able to travel to work without fear of an accident. I figured deal

> > pathogens would flush out with all of the water and wouldn't be causing the

> > issue.

> >

> > Finally went to the doctor to be tested for bladder infection and they

> > found...nothing. I stopped the nightly MMS and after several days, it

> > finally calmed down.

> >

> > The thing is...during that run of MMS and even after, I felt noticeably

> > better in terms of energy and mental clarity, so I'm going to start back

> > up. I can pick up some Depends if it means I can remember what I was doing.

> >

> > I suppose I can take MMS again till the bladder screams and then stop

> > until it subsides, but I wish there was something I could do to calm the

> > bladder, because that's no fun. I was wondering if spirochetes in the

> > bladder were being killed/ " annoyed " by the MMS and if that's what was going

> > on. As I've being coiling, I'm focusing on bladder/stomach area, because

> > the bladder sensitivity has been an issue as the Lyme has gotten worse.

> >

> > Searched the archives to see if someone has had a similar situation or has

> > any guidance, but didn't see anything.

> >

> > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit

> > better.

> >

> > Thank you.

> >

> > Best regards,

> >

> > Fifi

> >

> >

> >

>

[Guest guest]

Thanks, Barbara. Will give the d-mannose a shot.

I really was thinking this was related to die-off, but thought that with all the

water I'm drinking and all the time I'm spending in the loo, that nothing was

sitting in the bladder long enough to irritate.

Best regards,

Fifi

>

> > **

> >

> >

> > Folks-

> >

> > Was finally able to work up to 1/2 drop of MMS daily and then only before

> > bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After

> > about 10 days I noticed increasing bladder irritation that resembled a

> > bladder infection with pressure and odor, but no burning. No amount of

> > water or cranberry juice was resolving it and it was to the point of not

> > being able to travel to work without fear of an accident. I figured deal

> > pathogens would flush out with all of the water and wouldn't be causing the

> > issue.

> >

> > Finally went to the doctor to be tested for bladder infection and they

> > found...nothing. I stopped the nightly MMS and after several days, it

> > finally calmed down.

> >

> > The thing is...during that run of MMS and even after, I felt noticeably

> > better in terms of energy and mental clarity, so I'm going to start back

> > up. I can pick up some Depends if it means I can remember what I was doing.

> >

> > I suppose I can take MMS again till the bladder screams and then stop

> > until it subsides, but I wish there was something I could do to calm the

> > bladder, because that's no fun. I was wondering if spirochetes in the

> > bladder were being killed/ " annoyed " by the MMS and if that's what was going

> > on. As I've being coiling, I'm focusing on bladder/stomach area, because

> > the bladder sensitivity has been an issue as the Lyme has gotten worse.

> >

> > Searched the archives to see if someone has had a similar situation or has

> > any guidance, but didn't see anything.

> >

> > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit

> > better.

> >

> > Thank you.

> >

> > Best regards,

> >

> > Fifi

> >

> >

> >

>

[Guest guest]

Hi, Susie -

Yes - Cutler's book can be very overwhelming. I ended up following a digested,

simplified version of his protocol that I found on a different web site.

Since you seem to be very sensitive *and* especially since you still have

mercury fillings left, you may wish to avoid any strong mercury detox like

Cutler's approach at this time. Some of the gentler things used in the group

may be more appropriate, along with things to bolster the immune system in

general. Feeling mercury " redistribute " in the body is pretty icky, so you

really want to wait until at least the visible fillings are out before you try

DMSA or the like.

Take care.

Fifi

> >

> > Folks-

> >

> > Was finally able to work up to 1/2 drop of MMS daily and then only before

bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After

about 10 days I noticed increasing bladder irritation that resembled a bladder

infection with pressure and odor, but no burning. No amount of water or

cranberry juice was resolving it and it was to the point of not being able to

travel to work without fear of an accident. I figured deal pathogens would

flush out with all of the water and wouldn't be causing the issue.

> >

> > Finally went to the doctor to be tested for bladder infection and they

found...nothing. I stopped the nightly MMS and after several days, it finally

calmed down.

> >

> > The thing is...during that run of MMS and even after, I felt noticeably

better in terms of energy and mental clarity, so I'm going to start back up. I

can pick up some Depends if it means I can remember what I was doing.

> >

> > I suppose I can take MMS again till the bladder screams and then stop until

it subsides, but I wish there was something I could do to calm the bladder,

because that's no fun. I was wondering if spirochetes in the bladder were being

killed/ " annoyed " by the MMS and if that's what was going on. As I've being

coiling, I'm focusing on bladder/stomach area, because the bladder sensitivity

has been an issue as the Lyme has gotten worse.

> >

> > Searched the archives to see if someone has had a similar situation or has

any guidance, but didn't see anything.

> >

> > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit

better.

> >

> > Thank you.

> >

> > Best regards,

> >

> > Fifi

> >

>

[Guest guest]

Hi Susie, Fifireading what you are saying re: mercury and i have some questions. this also has a reference to mms.  these questions seem 'jumbled up' in my head so i will try to explain it all coherently. 

1)  usually with a herx i can tell when it subsides and i return to 'normal'--whatever that was.  i've been using mms for some time now and am up to 9-12 drops a day.  because i forget to take it i have gone to 3 drops at a time to get more in.  seem to handle that ok, but i also want to fall asleep.  wonder if i have killed gut bugs and now more is getting into blood stream?

2)  almost 4 wks ago, i had coiled for candida and got a larger than normal herx,  we believe it hit something else, maybe ebv.  after the candida herx, i seemed to see a decline in the herx, however, since then, i have not returned to my 'normal'.  

3)  had stopped coiling for barb and babs as i was again plateauing and decided to move onto lyme.4)  about 2 wks after the candida coiling, i coiled for lyme for the first time, for 20 seconds. 

5)  i am also tapering off valium, which can cause herx like symptoms, but have been doing this for a yr--nothing new or different.6)  also, i was filled with amalgam from early age, but since middle age all the silver is gone and crowned. when tested for heavy metal, i tested 'ok'.    was the lyme 'hiding' the mercury?

so, to recap:  mms, coiled for candida, maybe hit ebv, coiled for lyme, had lots of mercury in early life, valium tappering.  is this enough to cause not returning to 'normal?'   i feel like i am still in a herx.  always, during a herx, one of my main symptoms is an increase in those attacks i get every 30 min. i have listed several times: anxiety, air hunger, nausea (stomach distress), heart pounding, and profuse sweating.  

my body feels like it is cooking inside during the sweating.  i am  'wet' with the sweat (prior to this i had gotten the attacks down to tolerable).  the other symptoms have also intensified, including head pounding, desperate to lye down, my heart/chest pounds/hurts ( but  this all only happens during the attacks, every 30 min.--nothing in between) . 

 this is how i felt in 05 when i did doxy and flagyl, and my bp went way up and they discontinued treatment. they treated too aggressively and it took 6 months to clear the herx.  but we didn't know about detox then either.

i did some colloidal silver iv's a couple yrs ago, and experienced similar, but less intense herx (because i quite after 4 treatments) that took a while to clear. no detox then either.

i am doing enemas/colonic, with intermittent ce.  essiac tea, glucammanon, constantly drinking water. am looking into more for mercury.i have read many times about mercury problems while killing lyme.  would coiling 20 seconds 10 days ago for lyme do this much?  i don't detox well. i was having problems before i coiled for the lyme, it seemed to start with the candida treatment (which i have done before and was fine).  but it is getting worse now, not better with some of the attacks.  i know i have posted for this several times, but now wondering, as i read your post on mercury, if i have more mercury than i tested for. or am i just 'grasping at straws' here?

hmmm, just thinking.  right before, or really close to all this, i experience several days of intense pain all over that i have not experienced for yrs..  hard to sleep with it.  spring flare?

 at that point i was only coiling for bart and babs, and they both were at a point of not feeling herxes, as i had been coiling for them for some time, again, and plateauing. bart usually hits me mental/emotionally.  this is physically.

so, any suggestions?  is the mercury a significant player here possibly. i'm cautious to treat again until i can get the intensity of these attacks down, as their intensity always seem to represent a herx.  the feeling of excessive internal heat, along with heart racing, pounding, are reminiscent of the doxy/flagy treatment--which could have been from killing lyme, bart, babs, ebv, myco & chlamydia ph.

so, here is the great ?:  should i wait a little while to try and clear some more toxins?  treat again for lyme and see what happens?  try the candida coiling again and see what happens?  take my toys and go home?

barbara

 

Hi, Susie -

Yes - Cutler's book can be very overwhelming. I ended up following a digested, simplified version of his protocol that I found on a different web site.

Since you seem to be very sensitive *and* especially since you still have mercury fillings left, you may wish to avoid any strong mercury detox like Cutler's approach at this time. Some of the gentler things used in the group may be more appropriate, along with things to bolster the immune system in general. Feeling mercury " redistribute " in the body is pretty icky, so you really want to wait until at least the visible fillings are out before you try DMSA or the like.

Take care.

Fifi

> >

> > Folks-

> >

> > Was finally able to work up to 1/2 drop of MMS daily and then only before bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After about 10 days I noticed increasing bladder irritation that resembled a bladder infection with pressure and odor, but no burning. No amount of water or cranberry juice was resolving it and it was to the point of not being able to travel to work without fear of an accident. I figured deal pathogens would flush out with all of the water and wouldn't be causing the issue.

> >

> > Finally went to the doctor to be tested for bladder infection and they found...nothing. I stopped the nightly MMS and after several days, it finally calmed down.

> >

> > The thing is...during that run of MMS and even after, I felt noticeably better in terms of energy and mental clarity, so I'm going to start back up. I can pick up some Depends if it means I can remember what I was doing.

> >

> > I suppose I can take MMS again till the bladder screams and then stop until it subsides, but I wish there was something I could do to calm the bladder, because that's no fun. I was wondering if spirochetes in the bladder were being killed/ " annoyed " by the MMS and if that's what was going on. As I've being coiling, I'm focusing on bladder/stomach area, because the bladder sensitivity has been an issue as the Lyme has gotten worse.

> >

> > Searched the archives to see if someone has had a similar situation or has any guidance, but didn't see anything.

> >

> > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit better.

> >

> > Thank you.

> >

> > Best regards,

> >

> > Fifi

> >

>

[Guest guest]

Fifi,

I don't even know if I am going to get the last mercury out of one of my teeth

because that is one of the only teeth that is not bothering me at all.

Everytime I've had the mercury removed from teeth, I ended up getting caps &

then they seem to go right into root canals. I'm in a no-win situation. Thank

you for your help.

Susie

> > >

> > > Folks-

> > >

> > > Was finally able to work up to 1/2 drop of MMS daily and then only before

bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After

about 10 days I noticed increasing bladder irritation that resembled a bladder

infection with pressure and odor, but no burning. No amount of water or

cranberry juice was resolving it and it was to the point of not being able to

travel to work without fear of an accident. I figured deal pathogens would

flush out with all of the water and wouldn't be causing the issue.

> > >

> > > Finally went to the doctor to be tested for bladder infection and they

found...nothing. I stopped the nightly MMS and after several days, it finally

calmed down.

> > >

> > > The thing is...during that run of MMS and even after, I felt noticeably

better in terms of energy and mental clarity, so I'm going to start back up. I

can pick up some Depends if it means I can remember what I was doing.

> > >

> > > I suppose I can take MMS again till the bladder screams and then stop

until it subsides, but I wish there was something I could do to calm the

bladder, because that's no fun. I was wondering if spirochetes in the bladder

were being killed/ " annoyed " by the MMS and if that's what was going on. As I've

being coiling, I'm focusing on bladder/stomach area, because the bladder

sensitivity has been an issue as the Lyme has gotten worse.

> > >

> > > Searched the archives to see if someone has had a similar situation or has

any guidance, but didn't see anything.

> > >

> > > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit

better.

> > >

> > > Thank you.

> > >

> > > Best regards,

> > >

> > > Fifi

> > >

> >

>

[Guest guest]

Hi Susie,

Did you see my recent post on Modified Citrus Pectin (MCP) for removing metals?

This is a very gentle metal remover and MCP is also very healthy for us...

If you didn't see it, I can repost!!

MMS will oxidize metals, but it is not selective as it oxidizes both pathogens

and metals,

which ever it happens to come in contact with...

MCP is a dedicated heavy metal remover.

Take care,

Jim

> >

> > Folks-

> >

> > Was finally able to work up to 1/2 drop of MMS daily and then only before

bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After

about 10 days I noticed increasing bladder irritation that resembled a bladder

infection with pressure and odor, but no burning. No amount of water or

cranberry juice was resolving it and it was to the point of not being able to

travel to work without fear of an accident. I figured deal pathogens would

flush out with all of the water and wouldn't be causing the issue.

> >

> > Finally went to the doctor to be tested for bladder infection and they

found...nothing. I stopped the nightly MMS and after several days, it finally

calmed down.

> >

> > The thing is...during that run of MMS and even after, I felt noticeably

better in terms of energy and mental clarity, so I'm going to start back up. I

can pick up some Depends if it means I can remember what I was doing.

> >

> > I suppose I can take MMS again till the bladder screams and then stop until

it subsides, but I wish there was something I could do to calm the bladder,

because that's no fun. I was wondering if spirochetes in the bladder were being

killed/ " annoyed " by the MMS and if that's what was going on. As I've being

coiling, I'm focusing on bladder/stomach area, because the bladder sensitivity

has been an issue as the Lyme has gotten worse.

> >

> > Searched the archives to see if someone has had a similar situation or has

any guidance, but didn't see anything.

> >

> > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit

better.

> >

> > Thank you.

> >

> > Best regards,

> >

> > Fifi

> >

>

[Guest guest]

Jim,

No, I didn't see the post on MCP, but are you sure it eliminates the mercury

from the body rather than recirculate it?

Susie

> > >

> > > Folks-

> > >

> > > Was finally able to work up to 1/2 drop of MMS daily and then only before

bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After

about 10 days I noticed increasing bladder irritation that resembled a bladder

infection with pressure and odor, but no burning. No amount of water or

cranberry juice was resolving it and it was to the point of not being able to

travel to work without fear of an accident. I figured deal pathogens would

flush out with all of the water and wouldn't be causing the issue.

> > >

> > > Finally went to the doctor to be tested for bladder infection and they

found...nothing. I stopped the nightly MMS and after several days, it finally

calmed down.

> > >

> > > The thing is...during that run of MMS and even after, I felt noticeably

better in terms of energy and mental clarity, so I'm going to start back up. I

can pick up some Depends if it means I can remember what I was doing.

> > >

> > > I suppose I can take MMS again till the bladder screams and then stop

until it subsides, but I wish there was something I could do to calm the

bladder, because that's no fun. I was wondering if spirochetes in the bladder

were being killed/ " annoyed " by the MMS and if that's what was going on. As I've

being coiling, I'm focusing on bladder/stomach area, because the bladder

sensitivity has been an issue as the Lyme has gotten worse.

> > >

> > > Searched the archives to see if someone has had a similar situation or has

any guidance, but didn't see anything.

> > >

> > > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit

better.

> > >

> > > Thank you.

> > >

> > > Best regards,

> > >

> > > Fifi

> > >

> >

>

[Guest guest]

he reis what we do for my husband kidneys and bladder

pershley tea + mms every hour +mms on the skinwith dmaso on thecritcal part :on his kidneys area

+some dct clack kidney cleanse pills +cranberry and mannose .

the all togoether makes a good job for my sweety

Kindly Marie

To: Lyme_and_Rife Sent: Tuesday, April 10, 2012 11:54 AMSubject: Re: OT: MMS irritating the bladder...or annoying the spirochetes in the bladder?

Fifi,I don't even know if I am going to get the last mercury out of one of my teeth because that is one of the only teeth that is not bothering me at all. Everytime I've had the mercury removed from teeth, I ended up getting caps & then they seem to go right into root canals. I'm in a no-win situation. Thank you for your help.Susie> > >> > > Folks-> > > > > > Was finally

able to work up to 1/2 drop of MMS daily and then only before bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After about 10 days I noticed increasing bladder irritation that resembled a bladder infection with pressure and odor, but no burning. No amount of water or cranberry juice was resolving it and it was to the point of not being able to travel to work without fear of an accident. I figured deal pathogens would flush out with all of the water and wouldn't be causing the issue. > > > > > > Finally went to the doctor to be tested for bladder infection and they found...nothing. I stopped the nightly MMS and after several days, it finally calmed down.> > > > > > The thing is...during that run of MMS and even after, I felt noticeably better in terms of energy and mental clarity, so I'm going to start back up. I can pick up some Depends if it means I can remember what I was doing.

> > > > > > I suppose I can take MMS again till the bladder screams and then stop until it subsides, but I wish there was something I could do to calm the bladder, because that's no fun. I was wondering if spirochetes in the bladder were being killed/"annoyed" by the MMS and if that's what was going on. As I've being coiling, I'm focusing on bladder/stomach area, because the bladder sensitivity has been an issue as the Lyme has gotten worse. > > > > > > Searched the archives to see if someone has had a similar situation or has any guidance, but didn't see anything.> > > > > > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit better.> > > > > > Thank you.> > > > > > Best regards,> > > > > > Fifi> > >>

>>

[Guest guest]

I for got the MMS2 twice a day

kindly marie

To: Lyme_and_Rife Sent: Tuesday, April 10, 2012 11:54 AMSubject: Re: OT: MMS irritating the bladder...or annoying the spirochetes in the bladder?

Fifi,I don't even know if I am going to get the last mercury out of one of my teeth because that is one of the only teeth that is not bothering me at all. Everytime I've had the mercury removed from teeth, I ended up getting caps & then they seem to go right into root canals. I'm in a no-win situation. Thank you for your help.Susie> > >> > > Folks-> > > > > > Was finally

able to work up to 1/2 drop of MMS daily and then only before bed, since it was knocking me out. (Yes, I'm a lightweight...I know!) After about 10 days I noticed increasing bladder irritation that resembled a bladder infection with pressure and odor, but no burning. No amount of water or cranberry juice was resolving it and it was to the point of not being able to travel to work without fear of an accident. I figured deal pathogens would flush out with all of the water and wouldn't be causing the issue. > > > > > > Finally went to the doctor to be tested for bladder infection and they found...nothing. I stopped the nightly MMS and after several days, it finally calmed down.> > > > > > The thing is...during that run of MMS and even after, I felt noticeably better in terms of energy and mental clarity, so I'm going to start back up. I can pick up some Depends if it means I can remember what I was doing.

> > > > > > I suppose I can take MMS again till the bladder screams and then stop until it subsides, but I wish there was something I could do to calm the bladder, because that's no fun. I was wondering if spirochetes in the bladder were being killed/"annoyed" by the MMS and if that's what was going on. As I've being coiling, I'm focusing on bladder/stomach area, because the bladder sensitivity has been an issue as the Lyme has gotten worse. > > > > > > Searched the archives to see if someone has had a similar situation or has any guidance, but didn't see anything.> > > > > > Off to mix up my mini-dose of MMS. What a treat to feel even a small bit better.> > > > > > Thank you.> > > > > > Best regards,> > > > > > Fifi> > >>

>>

[Guest guest]

Jim,

Thanks for the link.

Susie

> > > > >

> > > > > Folks-

> > > > >

> > > > > Was finally able to work up to 1/2 drop of MMS daily and then only

before bed, since it was knocking me out. (Yes, I'm a lightweight...I know!)

After about 10 days I noticed increasing bladder irritation that resembled a

bladder infection with pressure and odor, but no burning. No amount of water or

cranberry juice was resolving it and it was to the point of not being able to

travel to work without fear of an accident. I figured deal pathogens would

flush out with all of the water and wouldn't be causing the issue.

> > > > >

> > > > > Finally went to the doctor to be tested for bladder infection and they

found...nothing. I stopped the nightly MMS and after several days, it finally

calmed down.

> > > > >

> > > > > The thing is...during that run of MMS and even after, I felt

noticeably better in terms of energy and mental clarity, so I'm going to start

back up. I can pick up some Depends if it means I can remember what I was

doing.

> > > > >

> > > > > I suppose I can take MMS again till the bladder screams and then stop

until it subsides, but I wish there was something I could do to calm the

bladder, because that's no fun. I was wondering if spirochetes in the bladder

were being killed/ " annoyed " by the MMS and if that's what was going on. As I've

being coiling, I'm focusing on bladder/stomach area, because the bladder

sensitivity has been an issue as the Lyme has gotten worse.

> > > > >

> > > > > Searched the archives to see if someone has had a similar situation or

has any guidance, but didn't see anything.

> > > > >

> > > > > Off to mix up my mini-dose of MMS. What a treat to feel even a small

bit better.

> > > > >

> > > > > Thank you.

> > > > >

> > > > > Best regards,

> > > > >

> > > > > Fifi

> > > > >

> > > >

> > >

> >

>