Re: OT - Microplasm herx and other symptoms

[Guest guest]

Hi Tammy,I am so sorry you area both going through such a rough spot.  Off the top of my head, two of the best treatments for Lyme (and possibly co-infections) are some of the cheapest.  The first being Water Purification Drops, formerly MMS1.  And of course the Salt/C treatment.

Maybe these could at least get you both functioning. Have you tried either one?Sounds like you both could use some serious thyroid and adrenal help. 

 

Hi All,

 

I see a lot about this and different types of herxing.. and WOW is all of this confusing!

 

We have both been diagnosed last January with Chronic intracellular Lyme disease and Babs.

WE see Dr. P  in Iowa every month.  We are up to three different abx's, Mepron, vit d3,

magnesium, iron.  Im on cpap hubby is on bypap

 

I feel horrible for my hubby he is going through much of what I have been through

with one big difference..

 

He sleeps 22 plus hours a day.. he just cant stay awake.  I had CFS but couldn’t sleep...

If he is up he has what we call the " Horrible Heebie Jeebies " where you cant really

tell if you feel hot or cold or both.. but you feel flushed and clammy you feel like your

skin is trying to crawl off of your body and sick to your stomach... Its just a horrible feeling

and we have had it long before we were diagnosed, so I don’t think its related to any of

our medications.. unless it would be fentanyl.. as that’s the only one we had in common

before lyme treatment.

 

Also Im wondering if high triglycerides is common with Lyme?  Mine is down to 400 from

over 700 but Pat's are over 2000!!  The doctor is sending him to a Cardiologist.  We have both

been on 500mg of flush free  Niacin   2 times a day for a long time and also prescription medication

for it.

 

I started on Black Cohosh because I wondered if the " heebie jeebies " was related to hormones

and I also began spending more time outside.  I don’t know if it was either of these but mine

got about 50% better.. 

 

Any way like I said all this stuff is so confusing to me..  Im open to suggestions and ideas??

I would love to rife but as I have said before, with Pat and I both sick and unable to work

we can hardly afford what little we do have.  So if there is any Central Iowa Lymies out there

that want to share fell free to email me privately if you wish.. mstammyt@...

 

Healing Hugs to you all!!

Tammy

 

 

[Guest guest]

Hi ,

We have not tried either of them yet.. money is a serious issue for us..

I am on t3 and t4 meds.

thanks you, and info or ideas are very welcome and appreciated!

From: H

Sent: Friday, October 08, 2010 9:44 PM

To: Lyme_and_Rife

Subject: Re: OT - Microplasm herx and other symptoms

Hi Tammy,I am so sorry you area both going through such a rough spot. Off the top of my head, two of the best treatments for Lyme (and possibly co-infections) are some of the cheapest. The first being Water Purification Drops, formerly MMS1. And of course the Salt/C treatment.Maybe these could at least get you both functioning. Have you tried either one?Sounds like you both could use some serious thyroid and adrenal help.

Hi All,

I see a lot about this and different types of herxing.. and WOW is all of this confusing!

We have both been diagnosed last January with Chronic intracellular Lyme disease and Babs.

WE see Dr. P in Iowa every month. We are up to three different abx's, Mepron, vit d3,

magnesium, iron. Im on cpap hubby is on bypap

I feel horrible for my hubby he is going through much of what I have been through

with one big difference..

He sleeps 22 plus hours a day.. he just cant stay awake. I had CFS but couldn’t sleep...

If he is up he has what we call the " Horrible Heebie Jeebies" where you cant really

tell if you feel hot or cold or both.. but you feel flushed and clammy you feel like your

skin is trying to crawl off of your body and sick to your stomach... Its just a horrible feeling

and we have had it long before we were diagnosed, so I don’t think its related to any of

our medications.. unless it would be fentanyl.. as that’s the only one we had in common

before lyme treatment.

Also Im wondering if high triglycerides is common with Lyme? Mine is down to 400 from

over 700 but Pat's are over 2000!! The doctor is sending him to a Cardiologist. We have both

been on 500mg of flush free Niacin 2 times a day for a long time and also prescription medication

for it.

I started on Black Cohosh because I wondered if the "heebie jeebies" was related to hormones

and I also began spending more time outside. I don’t know if it was either of these but mine

got about 50% better..

Any way like I said all this stuff is so confusing to me.. Im open to suggestions and ideas??

I would love to rife but as I have said before, with Pat and I both sick and unable to work

we can hardly afford what little we do have. So if there is any Central Iowa Lymies out there

that want to share fell free to email me privately if you wish.. mstammyt@...

Healing Hugs to you all!!

Tammy

[Guest guest]

Actually, I recently got some WPD for $9.99. Can't remember which source: it was in the right hand column of the google MMS/WPD listings, complete with citric acid, even though I prefer using Bragg's apple cider vinegar. ∞, LA person can pick up WPD for $20 - enough to last several months starting with one drop/day and building up.Salt/C could be started for not much more (depending on the C one purchases and the salt). An initial purchase should last 1-3 months depending on how quickly one increases dosage.These are both strong anti-microbials and can kill a lot of pathogens.I'm glad you are getting some thyroid help. :-) Hi ,We have not tried either of them yet.. money is a serious issue for us..I am on t3 and t4 meds.thanks you, and info or ideas are very welcome and appreciated!From: HSent: Friday, October 08, 2010 9:44 PMTo: Lyme_and_Rife Subject: Re: OT - Microplasm herx and other symptoms Hi Tammy,I am so sorry you area both going through such a rough spot. Off the top of my head, two of the best treatments for Lyme (and possibly co-infections) are some of the cheapest. The first being Water Purification Drops, formerly MMS1. And of course the Salt/C treatment.Maybe these could at least get you both functioning. Have you tried either one?Sounds like you both could use some serious thyroid and adrenal help. Hi All, I see a lot about this and different types of herxing.. and WOW is all of this confusing! We have both been diagnosed last January with Chronic intracellular Lyme disease and Babs.WE see Dr. P in Iowa every month. We are up to three different abx's, Mepron, vit d3,magnesium, iron. Im on cpap hubby is on bypap I feel horrible for my hubby he is going through much of what I have been throughwith one big difference.. He sleeps 22 plus hours a day.. he just cant stay awake. I had CFS but couldn’t sleep...If he is up he has what we call the " Horrible Heebie Jeebies" where you cant reallytell if you feel hot or cold or both.. but you feel flushed and clammy you feel like yourskin is trying to crawl off of your body and sick to your stomach... Its just a horrible feelingand we have had it long before we were diagnosed, so I don’t think its related to any ofour medications.. unless it would be fentanyl.. as that’s the only one we had in commonbefore lyme treatment. Also Im wondering if high triglycerides is common with Lyme? Mine is down to 400 fromover 700 but Pat's are over 2000!! The doctor is sending him to a Cardiologist. We have bothbeen on 500mg of flush free Niacin 2 times a day for a long time and also prescription medicationfor it. I started on Black Cohosh because I wondered if the "heebie jeebies" was related to hormonesand I also began spending more time outside. I don’t know if it was either of these but minegot about 50% better.. Any way like I said all this stuff is so confusing to me.. Im open to suggestions and ideas??I would love to rife but as I have said before, with Pat and I both sick and unable to workwe can hardly afford what little we do have. So if there is any Central Iowa Lymies out therethat want to share fell free to email me privately if you wish..mstammyt@... Healing Hugs to you all!!Tammy

[Guest guest]

awesome!

 

Actually, I recently got some WPD for $9.99. Can't remember which source: it was in the right hand column of the google MMS/WPD listings, complete with citric acid, even though I prefer using Bragg's apple cider vinegar. ∞, L

A person can pick up WPD for $20 - enough to last several months starting with one drop/day and building up.

Salt/C could be started for not much more (depending on the C one purchases and the salt).  An initial purchase should last 1-3 months depending on how quickly one increases dosage.These are both strong anti-microbials and can kill a lot of pathogens.

I'm glad you are getting some thyroid help. :-)On Sat, Oct 9, 2010 at 2:51 PM, Tammy Hotmail  wrote:

 Hi ,

We have not tried either of them yet.. money is a serious issue for us..I am on t3 and t4 meds.thanks you, and info or ideas are very welcome and appreciated!

From:  HSent: Friday, October 08, 2010 9:44 PM

To: Lyme_and_Rife Subject: Re: OT - Microplasm herx and other symptoms

 Hi Tammy,I am so sorry you area both going through such a rough spot.  Off the top of my head, two of the best treatments for Lyme (and possibly co-infections) are some of the cheapest.  The first being Water Purification Drops, formerly MMS1.  And of course the Salt/C treatment.

Maybe these could at least get you both functioning. Have you tried either one?Sounds like you both could use some serious thyroid and adrenal help.  

On Fri, Oct 8, 2010 at 6:36 PM, Tammy Hotmail  wrote:

 Hi All,

 I see a lot about this and different types of herxing.. and WOW is all of this confusing! 

We have both been diagnosed last January with Chronic intracellular Lyme disease and Babs.WE see Dr. P  in Iowa every month.  We are up to three different abx's, Mepron, vit d3,

magnesium, iron.  Im on cpap hubby is on bypap I feel horrible for my hubby he is going through much of what I have been through

with one big difference.. He sleeps 22 plus hours a day.. he just cant stay awake.  I had CFS but couldn’t sleep...

If he is up he has what we call the " Horrible Heebie Jeebies " where you cant reallytell if you feel hot or cold or both.. but you feel flushed and clammy you feel like your

skin is trying to crawl off of your body and sick to your stomach... Its just a horrible feelingand we have had it long before we were diagnosed, so I don’t think its related to any of

our medications.. unless it would be fentanyl.. as that’s the only one we had in commonbefore lyme treatment. 

Also Im wondering if high triglycerides is common with Lyme?  Mine is down to 400 fromover 700 but Pat's are over 2000!!  The doctor is sending him to a Cardiologist.  We have both

been on 500mg of flush free  Niacin   2 times a day for a long time and also prescription medicationfor it. 

I started on Black Cohosh because I wondered if the " heebie jeebies " was related to hormonesand I also began spending more time outside.  I don’t know if it was either of these but mine

got about 50% better..  Any way like I said all this stuff is so confusing to me..  Im open to suggestions and ideas??

I would love to rife but as I have said before, with Pat and I both sick and unable to workwe can hardly afford what little we do have.  So if there is any Central Iowa Lymies out there

that want to share fell free to email me privately if you wish..mstammyt@...

 Healing Hugs to you all!!Tammy