Re: Question for Lymies

[Guest guest]

Hi Timea,

I was going to post about my MMS experience anyway, but your post

prompted me sooner.

I have only been on small doses (up to 4 drops for a few days). My

experience was so intense that I had to take a break of a few days.

I took it on an empty stomach in the a.m. using lemon juice as an

activator. It didn't bother my stomach, but it sure bothered my sleep.

I couldn't sleep very well for two nights. That is a herx for me. I

also felt very tight, like every muscle fiber was very taut. The

pressure kept building inside (extreme tension) and only released when

I stopped MMS. There is also an electric feeling like I've been plugged

into a light socket...kind of like an extreme rifing session. There was

some kidney pain on the last day.

From what I've seen of others' posts, this is rather atypical. Many

sleep better and have more energy...I guess I had energy but it was a

very unnerving (no pun intended) type. I also experienced anxiety.

These are all herxes for me, since my nervous system is usually where

herxes occur. I also had bumps on my face, like pre-zits. Something was

coming out.

You've been on salt/c longer than I have and probably at higher doses,

so maybe you've already had a lot more Lyme die-off. I'll be interested

in hearing your experiences....and hoping they're milder! )

Avril

In , " timea_moore "

<timea_moore@...> wrote:

>

> Hello fellow Lymies

>

> Just wondering if you experience the classic HERX on MMS (as on other

> protocols eg. monthly worsening of symptoms,w/headache, etc) or is it

> different on MMS?

>

> Thanks

> Timea

>

[Guest guest]

I'll chime in too with my experiences. I have been on MMS on/off since September. I am up to 5 drops (with DMSO) in the morning and 7 at night. I get a lot neuro herxes also. Anxiety, heart palps, depression, etc. I also get some muscle soreness like I had just gotten a shot or worked out too much. If the heart palps get too severe I cut my dose back a drop or so. I also get those little bumps on my face like deep zits and some mild breakouts.

If you go slow you can avoid a lot of bad reactions. You can control the speed and severity of herxes! But overall, I do feel much better on the MMS than not. My thyroid has improved a lot and so have my adrenals.

BTW, I was on salt/c from July on-a few months before I started the MMS and I still take that too.

Good luck to you with the MMS-remember to go slow!

S

-- [ ] Re: Question for Lymies

Hi Timea,

I was going to post about my MMS experience anyway, but your post

prompted me sooner.

I have only been on small doses (up to 4 drops for a few days). My

experience was so intense that I had to take a break of a few days.

I took it on an empty stomach in the a.m. using lemon juice as an

activator. It didn't bother my stomach, but it sure bothered my sleep.

I couldn't sleep very well for two nights. That is a herx for me. I

also felt very tight, like every muscle fiber was very taut. The

pressure kept building inside (extreme tension) and only released when

I stopped MMS. There is also an electric feeling like I've been plugged

into a light socket...kind of like an extreme rifing session. There was

some kidney pain on the last day.

From what I've seen of others' posts, this is rather atypical. Many

sleep better and have more energy...I guess I had energy but it was a

very unnerving (no pun intended) type. I also experienced anxiety.

These are all herxes for me, since my nervous system is usually where

herxes occur. I also had bumps on my face, like pre-zits. Something was

coming out.

You've been on salt/c longer than I have and probably at higher doses,

so maybe you've already had a lot more Lyme die-off. I'll be interested

in hearing your experiences....and hoping they're milder! )

Avril

In , "timea_moore"

<timea_moore@...> wrote:

>

> Hello fellow Lymies

>

> Just wondering if you experience the classic HERX on MMS (as on other

> protocols eg. monthly worsening of symptoms,w/headache, etc) or is it

> different on MMS?

>

> Thanks

> Timea

>

[Guest guest]

> Just wondering if you experience the classic HERX on MMS (as on other protocols eg. monthly worsening of symptoms,w/headache, etc) or is it different on MMS? <

My youngest daughter is a Lymie but I am not. We both have experienced numerous Herxes, particularly from Salt/C, a certain radiational device we call the MKBD, and now from MMS. The Herxes are all the same to us. Mine now take longer to accumulate into a good butt-dragger since I have killed off so much infection. Same for her.

Daddybob

No virus found in this outgoing message.

Checked by AVG Free Edition.

Version: 7.5.516 / Virus Database: 269.19.10/1241 - Release Date: 1/24/2008 9:58 AM

[Guest guest]

Hi ,

Thanks for your encouragement! I will go slow. Sometimes I think the

neuro herxes are the worst. Of course, I haven't had a good bout of

diarrhea and vomiting that some have described here...so I don't have

that for a comparison.

Avril

In , " susan "

<ssiegel5@...> wrote:

>

> I'll chime in too with my experiences. I have been on MMS on/off

since

> September. I am up to 5 drops (with DMSO) in the morning and 7 at

night. I

> get a lot neuro herxes also. Anxiety, heart palps, depression,

etc. I also

> get some muscle soreness like I had just gotten a shot or worked

out too

> much. If the heart palps get too severe I cut my dose back a drop

or so. I

> also get those little bumps on my face like deep zits and some mild

> breakouts.

>

> If you go slow you can avoid a lot of bad reactions. You can

control the

> speed and severity of herxes! But overall, I do feel much better

on the MMS

> than not. My thyroid has improved a lot and so have my adrenals.

>

> BTW, I was on salt/c from July on-a few months before I started the

MMS and

> I still take that too.

>

> Good luck to you with the MMS-remember to go slow!

>

> S

>

[Guest guest]

I am a long time lymie who has done lots of abx, and the salt/c protocol so I guess I have fewer critters to deal with now. I started the MMS in early December and I find that I herx more frequently on this protocol than on any other.I use apple cider vinegar to activate as I find I do best with this. I take my dose in the evening because it makes me drowsy. I can not say if I am sleeping any better or not. I have tried taking more doses but it just makes me sleepy so have stuck to evening dosing. I take most nights 7 - 10 drops.Yesterday I had a major herx that lasted the whole day with headache and the feeling of walking through jello. Today still a bit headachey but can think.I did use citric acid for activating but once I found out it was made from mold I stopped as I have mold sensitivities.Hope this helps,SueAvril <loullew3@...>

wrote: Hi Timea, I was going to post about my MMS experience anyway, but your post prompted me sooner. I have only been on small doses (up to 4 drops for a few days). My experience was so intense that I had to take a break of a few days. I took it on an empty stomach in the a.m. using lemon juice as an activator. It didn't bother my stomach, but it sure bothered my sleep. I couldn't sleep very well for two nights. That is a herx for me. I also felt very tight, like every muscle fiber was very taut. The pressure kept building

inside (extreme tension) and only released when I stopped MMS. There is also an electric feeling like I've been plugged into a light socket...kind of like an extreme rifing session. There was some kidney pain on the last day. From what I've seen of others' posts, this is rather atypical. Many sleep better and have more energy...I guess I had energy but it was a very unnerving (no pun intended) type. I also experienced anxiety. These are all herxes for me, since my nervous system is usually where herxes occur. I also had bumps on my face, like pre-zits. Something was coming out. You've been on salt/c longer than I have and probably at higher doses, so maybe you've already had a lot more Lyme die-off. I'll be interested in hearing your experiences....and hoping they're milder! ) Avril In , "timea_moore" <timea_moore@...> wrote: > > Hello fellow Lymies > > Just wondering if you experience the classic HERX on MMS (as on other > protocols eg. monthly worsening of symptoms,w/headache, etc) or is it > different on MMS? > > Thanks > Timea > ~~~~~~~~~~~~~~~~~~~~~~~~Please join Lyme Aware on facebook athttp://www.facebook.com/group.php?gid=4960726826

Be smarter than spam. See how smart SpamGuard is at giving junk email the boot with the All-new

[Guest guest]

Hi Avril,

Thanks for your post...your experience with MMS is exactly like

mine! I got up to 3 drops after very slowly increasing over about a

week, and it got so intense with similar symptoms of being plugged into

a light socket, extreme tightness and spasmy muscles, so tight could

hardly breathe and my usual herx, insomnia. So I stopped and just the

other day tried 2 drops and am still herxing after a few days. Sure is

helpful stuff for so many folks, and some of us just need to go extra

slow and take breaks so that our bodies can recoup! (ps, I've been on

S/C for 2 years, but have had Lyme for at least 30) Suzy

Avril wrote:

>

> Hi Timea,

>

> I was going to post about my MMS experience anyway, but your post

> prompted me sooner.

>

> I have only been on small doses (up to 4 drops for a few days). My

> experience was so intense that I had to take a break of a few days.

>

> I took it on an empty stomach in the a.m. using lemon juice as an

> activator. It didn't bother my stomach, but it sure bothered my sleep.

> I couldn't sleep very well for two nights. That is a herx for me. I

> also felt very tight, like every muscle fiber was very taut. The

> pressure kept building inside (extreme tension) and only released when

> I stopped MMS. There is also an electric feeling like I've been plugged

> into a light socket...kind of like an extreme rifing session. There was

> some kidney pain on the last day.

>

> >From what I've seen of others' posts, this is rather atypical. Many

> sleep better and have more energy...I guess I had energy but it was a

> very unnerving (no pun intended) type. I also experienced anxiety.

> These are all herxes for me, since my nervous system is usually where

> herxes occur. I also had bumps on my face, like pre-zits. Something was

> coming out.

>

> You've been on salt/c longer than I have and probably at higher doses,

> so maybe you've already had a lot more Lyme die-off. I'll be interested

> in hearing your experiences....and hoping they're milder! )

>

> Avril

>

> I

>

[Guest guest]

Hi Avril,

I know I rave about how MMS helps me sleep but there have been a few

nights at first where it was the opposite. I got jumpy legs. I have

had that occasionally before too so I recognized the symptom. It went

away so I think it was part of the herx.

By the way, anyone, would you tell me the specific thing about salt

and vitamin c. I have heard of it but not the specifics.

Thanks and happy healing,

Jill

[Guest guest]

Avril,

Your experiences are similar to mine. I had to resort to taking MMS in

the morning because of the tightness and other weird things going on

after a dose. I can't seem to get over 3 drops because then, I get

nauseated. I've been on salt/c for 3+ years. Can't make a lot of

headway there, either. On 5 doses of that.

Carmen

Avril wrote:

> Hi Timea,

>

> I was going to post about my MMS experience anyway, but your post

> prompted me sooner.

>

> I have only been on small doses (up to 4 drops for a few days). My

> experience was so intense that I had to take a break of a few days.

>

> I took it on an empty stomach in the a.m. using lemon juice as an

> activator. It didn't bother my stomach, but it sure bothered my sleep.

> I couldn't sleep very well for two nights. That is a herx for me. I

> also felt very tight, like every muscle fiber was very taut. The

> pressure kept building inside (extreme tension) and only released when

> I stopped MMS. There is also an electric feeling like I've been plugged

> into a light socket...kind of like an extreme rifing session. There was

> some kidney pain on the last day.

>

> >From what I've seen of others' posts, this is rather atypical. Many

> sleep better and have more energy...I guess I had energy but it was a

> very unnerving (no pun intended) type. I also experienced anxiety.

> These are all herxes for me, since my nervous system is usually where

> herxes occur. I also had bumps on my face, like pre-zits. Something was

> coming out.

>

> You've been on salt/c longer than I have and probably at higher doses,

> so maybe you've already had a lot more Lyme die-off. I'll be interested

> in hearing your experiences....and hoping they're milder! )

>

> Avril

>

[Guest guest]

Hi all,

First post here - just a lymie lurker so far :-)

I've been on MMS since christmas and am doing fairly well on it

(improved immune fuction) but have noticed lately that I wake in

middle of the nite and can't get back to sleep. Maybe the last 2-3

days its been the effects of the full moon or it could be the mms -

not sure. Anyways, im up to 16-18 drops m-f and lay off of it on the

weekend along with all other supps to give my body a break. Have been

on S/C now for almost 3 years with some major improvement in

digestion and other areas but still have some big issues with

cognitive function etc. I've also been on Buhners herb protocol for 1

year and actually think it impaired my cognitive function to a degree

so i've quit that altogether. I've come a long ways from where I was

3 years ago so I'm very grateful for all the protocols but I strongly

beleive the MMS will finally finish the spiro bastages off.

I have very positive feelings all the way around about MMS.

Thanks for sharing your experiences Avril and others.

Regards,

Sam

> >

> > Hi Timea,

> >

> > I was going to post about my MMS experience anyway, but your post

> > prompted me sooner.

> >

> > I have only been on small doses (up to 4 drops for a few days). My

> > experience was so intense that I had to take a break of a few

days.

> >

> > I took it on an empty stomach in the a.m. using lemon juice as an

> > activator. It didn't bother my stomach, but it sure bothered my

sleep.

> > I couldn't sleep very well for two nights. That is a herx for me.

I

> > also felt very tight, like every muscle fiber was very taut. The

> > pressure kept building inside (extreme tension) and only released

when

> > I stopped MMS. There is also an electric feeling like I've been

plugged

> > into a light socket...kind of like an extreme rifing session.

There was

> > some kidney pain on the last day.

> >

> > >From what I've seen of others' posts, this is rather atypical.

Many

> > sleep better and have more energy...I guess I had energy but it

was a

> > very unnerving (no pun intended) type. I also experienced anxiety.

> > These are all herxes for me, since my nervous system is usually

where

> > herxes occur. I also had bumps on my face, like pre-zits.

Something was

> > coming out.

> >

> > You've been on salt/c longer than I have and probably at higher

doses,

> > so maybe you've already had a lot more Lyme die-off. I'll be

interested

> > in hearing your experiences....and hoping they're milder! )

> >

> > Avril

> >

> > I

> >

>

[Guest guest]

Sue,

Thanks for relating your herx experience. I have the feeling of

wobbly jello but it's on the inside. I've described it as feeling

like I have a lava lamp (the gel inside) moving around inside of me.

It's very strange.

I am also avoiding citric acid for the same reason.

Avril

> Yesterday I had a major herx that lasted the whole day with

headache and the feeling of walking through jello. Today still a

bit headachey but can think.

>

> I did use citric acid for activating but once I found out it was

made from mold I stopped as I have mold sensitivities.

>

> Hope this helps,

>

> Sue

>

[Guest guest]

Hi Suzy,

I guess us Lymies are going to experience these weird neural

herxes...since that's where Lyme likes to hide out. Thanks for

sharing...I don't feel so alone in my experience with MMS.

Avril

>

> Hi Avril,

> Thanks for your post...your experience with MMS is exactly like

> mine! I got up to 3 drops after very slowly increasing over about a

> week, and it got so intense with similar symptoms of being plugged

into

> a light socket, extreme tightness and spasmy muscles, so tight

could

> hardly breathe and my usual herx, insomnia. So I stopped and just

the

> other day tried 2 drops and am still herxing after a few days. Sure

is

> helpful stuff for so many folks, and some of us just need to go

extra

> slow and take breaks so that our bodies can recoup! Suzy

>

[Guest guest]

Hi Carmen,

You have sure had a hard time of it! I guess we'll just have to trust

that even these small doses will have some effect eventually. I also

only made it to five doses of salt/c.

Blessings,

Avril

In , Scheible

<cln3181@...> wrote:

>

> Avril,

> Your experiences are similar to mine. I had to resort to taking

MMS in

> the morning because of the tightness and other weird things going

on

> after a dose. I can't seem to get over 3 drops because then, I get

> nauseated. I've been on salt/c for 3+ years. Can't make a lot of

> headway there, either. On 5 doses of that.

>

> Carmen

>

[Guest guest]

Hi Jill,

Salt/C is a protocol that was first used by the folks at www.lymephotos.com. You can see some "wonderful" photos there of nematodes and microfilarial worms that have come through peoples' skin, ostensibly to escape the salt/c barrage. In the January 2005 edition of the Townsend Letter there is an article describing how salt and vitamin C combine to weaken the cell of wall of pathogens, thus allowing salt to cause osmotic shock to the pathogen. The protocol is discussed in depth at Lymestrategies on .

It is similar to the MMS protocol in that it is wise to ramp up slowly because of herxing, not because of the possibility of nausea.

Hope this helps a bit, Avril

>> Hi Avril,> > I know I rave about how MMS helps me sleep but there have been a few > nights at first where it was the opposite. I got jumpy legs. I have > had that occasionally before too so I recognized the symptom. It went > away so I think it was part of the herx.> > By the way, anyone, would you tell me the specific thing about salt > and vitamin c. I have heard of it but not the specifics.> > Thanks and happy healing,> Jill>

[Guest guest]

Hi Avril,

I see what they mean about having to go slow. I've been on MMS for 10

days, and was at 2 drops x 3 daily, until I got almost liquid BM this

morning. So, I will not take any more today. Tomorrow or the next day

I plan to resume at 1 drop x 2 daily. I didn't think 2x3 would be too

much, but it was, at least for me.

I've been very sore in my kidney area. It's like the surface of my

skin over the kidney area is so sore it almost can't be touched. It

hurts when I rebound right now so I do other exercises instead.

I presume this is caused by stress to my kidneys due to die off / dead

pathogens, or excretion of heavy metals or something, or both.

Tony

(or you can call me Joe - it's up to you)

>

> Hi ,

>

> Thanks for your encouragement! I will go slow. Sometimes I think the

> neuro herxes are the worst. Of course, I haven't had a good bout of

> diarrhea and vomiting that some have described here...so I don't have

> that for a comparison.

>

> Avril

[Guest guest]

I just wanted to say that my herx symptoms passed by late morning and this afternoon I was buzzing around all strong and fast. Turns out this was a good herx as I feel better than I did before the herx.Avril <loullew3@...> wrote: Sue, Thanks for relating your herx experience. I have the feeling of wobbly jello but it's on the inside. I've described it as feeling like I have a lava lamp (the gel inside) moving around inside of me. It's very strange. I am also avoiding citric acid for the same reason.

Avril > Yesterday I had a major herx that lasted the whole day with headache and the feeling of walking through jello. Today still a bit headachey but can think. > > I did use citric acid for activating but once I found out it was made from mold I stopped as I have mold sensitivities. > > Hope this helps, > > Sue > ~~~~~~~~~~~~~~~~~~~~~~~~Please join Lyme Aware on facebook athttp://www.facebook.com/group.php?gid=4960726826

All new -

Get a sneak peak at messages with a handy reading pane.

[Guest guest]

Well I " complained " that I got up to 6 drops quickly with no

effect..... Yesterday it hit me and it hit me hard with a terrible

headache which I still have this morning.

Interestingly, my husband started MMS as well 3 days ago. He is

supposed to be healthy and got up to 10 drops. Today he is in bed

with runny nose and feeling really weak. Who knows what the hell MMS

is killing in his body????

Sue,

>

> Thanks for relating your herx experience. I have the feeling of

> wobbly jello but it's on the inside. I've described it as feeling

> like I have a lava lamp (the gel inside) moving around inside of

me.

> It's very strange.

>

> I am also avoiding citric acid for the same reason.

>

> Avril

>

> > Yesterday I had a major herx that lasted the whole day with

> headache and the feeling of walking through jello. Today still a

> bit headachey but can think.

> >

> > I did use citric acid for activating but once I found out it was

> made from mold I stopped as I have mold sensitivities.

> >

> > Hope this helps,

> >

> > Sue

> >

>

>

>

>

>

>

> ~~~~~~~~~~~~~~~~~~~~~~~~

> Please join Lyme Aware on facebook at

> http://www.facebook.com/group.php?gid=4960726826

>

> ---------------------------------

> All new -

> ---------------------------------

> Get a sneak peak at messages with a handy reading pane.

>

[Guest guest]

I have severe Neuro-Lyme and have been taking MMS since Jan. 9th. I

just came through a major (7-day) " herx " on MMS. It has been similar

to previous herxes from abx or herbs: body pains, headache, joint

pain in hips/knees/shoulder, extreme irritability, crying jags,

slurred speech...

My muscles twitch constantly but I noticed that this got much worse

during the herx. I do get the nausea and loose stools from MMS (but

not abx or herbs). This has been the biggest difference.

BB~Ellen

>

> Hello fellow Lymies

>

> Just wondering if you experience the classic HERX on MMS (as on other

> protocols eg. monthly worsening of symptoms,w/headache, etc) or is it

> different on MMS?

>

> Thanks

> Timea

>

[Guest guest]

PS - I've found that inversion therapy is a real help to my health. I

invert for a minimum of 5 minutes once in the AM, and if I feel like

it, 5-10 more minutes in the PM. It does a lot for my circulation,

mental outlook, and mood. It decongests the liver and exercises the

heart. It helps detox toxic pockets in the GI tract and the effects of

gravity. It drains the lymph fluids and lots of other things. I

wouldn't want to go one day without inverting before breakfast!

It's not for everyone though. People with high BP, stroke, heart

trouble, fractures, obesity, glaucoma, etc., should not invert unless

they get permission from their doctor.

Joe

> Hi Avril,

>

> I see what they mean about having to go slow. I've been on MMS for 10

> days, and was at 2 drops x 3 daily, until I got almost liquid BM this

> morning. So, I will not take any more today. Tomorrow or the next day

> I plan to resume at 1 drop x 2 daily. I didn't think 2x3 would be too

> much, but it was, at least for me.

>

> I've been very sore in my kidney area. It's like the surface of my

> skin over the kidney area is so sore it almost can't be touched. It

> hurts when I rebound right now so I do other exercises instead.

> I presume this is caused by stress to my kidneys due to die off / dead

> pathogens, or excretion of heavy metals or something, or both.

>

> Tony

>

> (or you can call me Joe - it's up to you)

>

[Guest guest]

Hi Sam,

Thanks, fellow Lymie, for posting such an encouraging MMS report!

Avril

In , " Sam " <dudehorner@...>

wrote:

>

> Hi all,

>

> First post here - just a lymie lurker so far :-)

>

I've come a long ways from where I was

> 3 years ago so I'm very grateful for all the protocols but I

strongly

> beleive the MMS will finally finish the spiro bastages off.

>

> I have very positive feelings all the way around about MMS.

>

> Regards,

>

> Sam

>

[Guest guest]

Sorry about the headache.

I don't think you can know for sure that it is from the MMS.

Hope you feel better soon.

What are you and your hubby treating?

Kathy

Sue,

> >

> > Thanks for relating your herx experience. I have the feeling of

> > wobbly jello but it's on the inside. I've described it as

feeling

> > like I have a lava lamp (the gel inside) moving around inside of

> me.

> > It's very strange.

> >

> > I am also avoiding citric acid for the same reason.

> >

> > Avril

> >

> > > Yesterday I had a major herx that lasted the whole day with

> > headache and the feeling of walking through jello. Today still

a

> > bit headachey but can think.

> > >

> > > I did use citric acid for activating but once I found out it

was

> > made from mold I stopped as I have mold sensitivities.

> > >

> > > Hope this helps,

> > >

> > > Sue

> > >

> >

> >

> >

> >

> >

> >

> > ~~~~~~~~~~~~~~~~~~~~~~~~

> > Please join Lyme Aware on facebook at

> > http://www.facebook.com/group.php?gid=4960726826

> >

> > ---------------------------------

> > All new -

> > ---------------------------------

> > Get a sneak peak at messages with a handy reading pane.

> >

>

[Guest guest]

The Salt and Vitamin C Treatment

The Essential Treatment is basically

1.Body weight in pounds/10 = total daily consumption in grams, so

& #61601; 1 gram of Salt, and

& #61601; 1 gram of Vitamin C

& #61601; for each 10 pounds of body weight. Use pure salt (sodium chloride)

without any additives such as

& #61601; aluminum

& #61601; silica, or

& #61601; iodine

2.If you use powdered salt or Vitamin C be aware that

& #61601; 1 teaspoon (tsp) = 5 grams, thus

& #61601; 1 tablespoon (tbs) = 15 grams.

3.One should space out these into three or more doses each day. For

example, a 150 pound individual would swallow 15 grams of each in total

as

& #61601; 5 grams of each in the morning,

& #61601; 5 grams of each at midday and

& #61601; 5 grams of each in the evening.

4.Total daily consumption should not exceed 18 grams of each per day.

5.Drink lots of water. 6.High doses can be very hard on the stomach.

Experiment; start with lower doses, such as 3 grams each 5 times a day

to get your daily total. Again, drink plenty of water.

Treatment protocol developed by individuals at lymephotos.com © 2006-

2007 lymephotos.com

--- In , " Jill " <datjat1@...>

wrote:

>

> Hi Avril,

>

> I know I rave about how MMS helps me sleep but there have been a few

> nights at first where it was the opposite. I got jumpy legs. I have

> had that occasionally before too so I recognized the symptom. It

went

> away so I think it was part of the herx.

>

> By the way, anyone, would you tell me the specific thing about salt

> and vitamin c. I have heard of it but not the specifics.

>

> Thanks and happy healing,

> Jill

>

[Guest guest]

tony,

it could also be that you have had problems with your kidneys in the

past. I and many others have had reacurrences of symptoms of past

problems. some of the problems were 40 years ago (although that

couldn't of been me cause that would mean I am old) regardless

anytime we are having issues with our kidneys, it is good to

rehydrate.

JUSTMYOPINION

> >

> > Hi ,

> >

> > Thanks for your encouragement! I will go slow. Sometimes I think

the

> > neuro herxes are the worst. Of course, I haven't had a good bout

of

> > diarrhea and vomiting that some have described here...so I don't

have

> > that for a comparison.

> >

> > Avril

>

[Guest guest]

Hi Kathy

I am treating lyme and co. My headache is from die off so somewhat it

is a good sign. I missed mms for 3 days, headache gone.Took 3 drops

yesterday....today headache is back plus my throat started to hurt.

But that is die off symptom as well. I started taking chlorella to

get rid of the die off toxins quicker, hopefully it will help reduce

my headaches.

My hubby has recurrent sinus infection which we thought was some kind

of allergy. But after starting the mms he developed flu like symptoms

for about 4 days, so maybe it wasn't allergy, but some bug was

causing his sinus invection....we will see.

Timea

Sue,

> > >

> > > Thanks for relating your herx experience. I have the feeling

of

> > > wobbly jello but it's on the inside. I've described it as

> feeling

> > > like I have a lava lamp (the gel inside) moving around inside

of

> > me.

> > > It's very strange.

> > >

> > > I am also avoiding citric acid for the same reason.

> > >

> > > Avril

> > >

> > > > Yesterday I had a major herx that lasted the whole day with

> > > headache and the feeling of walking through jello. Today

still

> a

> > > bit headachey but can think.

> > > >

> > > > I did use citric acid for activating but once I found out it

> was

> > > made from mold I stopped as I have mold sensitivities.

> > > >

> > > > Hope this helps,

> > > >

> > > > Sue

> > > >

> > >

> > >

> > >

> > >

> > >

> > >

> > > ~~~~~~~~~~~~~~~~~~~~~~~~

> > > Please join Lyme Aware on facebook at

> > > http://www.facebook.com/group.php?gid=4960726826

> > >

> > > ---------------------------------

> > > All new -

> > > ---------------------------------

> > > Get a sneak peak at messages with a handy reading pane.

> > >

> >

>

[Guest guest]

I (another Lymie) also tend to get headaches after taking MMS and I

don't usually get headaches.

Ballady & #9824;

Sue,

> > > >

> > > > Thanks for relating your herx experience. I have the feeling

> of

> > > > wobbly jello but it's on the inside. I've described it as

> > feeling

> > > > like I have a lava lamp (the gel inside) moving around inside

> of

> > > me.

> > > > It's very strange.

> > > >

> > > > I am also avoiding citric acid for the same reason.

> > > >

> > > > Avril

> > > >

> > > > > Yesterday I had a major herx that lasted the whole day with

> > > > headache and the feeling of walking through jello. Today

> still

> > a

> > > > bit headachey but can think.

> > > > >

> > > > > I did use citric acid for activating but once I found out it

> > was

> > > > made from mold I stopped as I have mold sensitivities.

> > > > >

> > > > > Hope this helps,

> > > > >

> > > > > Sue

> > > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > > ~~~~~~~~~~~~~~~~~~~~~~~~

> > > > Please join Lyme Aware on facebook at

> > > > http://www.facebook.com/group.php?gid=4960726826

> > > >

> > > > ---------------------------------

> > > > All new -

> > > > ---------------------------------

> > > > Get a sneak peak at messages with a handy reading pane.

> > > >

> > >

> >

>

[Guest guest]

I sometimes get headaches from mms, and I don't have lymes, just hcv.

[ ] Re: Question for Lymies

I (another Lymie) also tend to get headaches after taking MMS and Idon't usually get headaches.Ballady & #9824; Sue,> > > > > > > > Thanks for relating your herx experience. I have the feeling > of > > > > wobbly jello but it's on the inside. I've described it as > > feeling > > > > like I have a lava lamp (the gel inside) moving around inside > of > > > me. > > > > It's very strange.> > > > > > > > I am also avoiding citric acid for the same reason.> > > > > > > > Avril> > > > > > > > > Yesterday

I had a major herx that lasted the whole day with > > > > headache and the feeling of walking through jello. Today > still > > a > > > > bit headachey but can think.> > > > > > > > > > I did use citric acid for activating but once I found out it > > was > > > > made from mold I stopped as I have mold sensitivities.> > > > > > > > > > Hope this helps,> > > > > > > > > > Sue> > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > ~~~~~~~~~~~~ ~~~~~~~~~ ~~~> > > > Please join Lyme Aware on facebook at> > > > http://www.facebook .com/group. php?gid=49607268 26> > > > > > > > ------------ --------- --------- ---> > > > All new - > > > > ------------ --------- --------- ---> > > > Get a sneak peak at messages with a handy reading pane.> > > >> > >> >>

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