Colloidal Silver used to kill off Lyme

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Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/22/2008 2:42 PM (GMT -7)   
I have been put on doxy and minocycline and amoxy all to no avail for my Lyme (and now Bartonella). But none of them did the trick in the last 4 years, and not for my 5 year old either who got lyme at 11 mos and we were both treated the day we got the tick bite. We knew when we got bitten and had no delay in treatment. So the easy to catch and easy to cure is BS.
But now after only getting sicker and sicker for 4 years and 30 Dr.s later. I am getting treatment in AZ. And they are giving me colloidal silver every day. I had never even heard of it. What is stranger is that it is not harmful. The lyme does not seem to think of the silver as a enemy and because of the shape of the silver, that being of an arrow, it targets the lyme inside the cells and cuts off its oxygen supply therefore killing it.
I am getting 10 cc of it 4 times a week. IV. I was told I could even give it to my dog. I bought some on line from mesosilver and it does not have any taste to it at all. Why is there not more information about this great product? Is it because the pharm. comp.s cannot patent it and make a killing of of it? Does greed really come before lives?
I have a friend who was on it for his cancer treatment. The others methods did not work for him. Chemo and radiation. But he got silver and his cancer tumors shrunk and went away. He is fine now. So what is the deal with this colloidal silver? It has been around for 2,000 years and seemed to have worked pretty darn well for everyone before other abx were invented.

idea Well I will keep you posted on my progress with this silver. So far most of my symptoms are gone. But I am not going to through a party just yet. I still have 4 more weeks of therapy with my colloidal silver to do the trick. Only time will tell.
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


hopingToFindCure
Veteran Member


Date Joined Nov 2008
Total Posts : 759
   Posted 11/22/2008 3:26 PM (GMT -7)   
I've heard of it...I'm glad it's working! That's great. Seems like they know what they're doing and how to use it. I've seen it at health food stores, but I wouldn't want to risk it. My llmd says "it will turn you blue, and there's no remedy when that happens"...

I think he did approve of a biomat or something like that, especially in the cold.

Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/22/2008 5:52 PM (GMT -7)   
How funny, did he really say that? Or are you kidding? He must watch a lot of TV and saw the only man in the world who decided that he was going to make collidal silver in his garage, and yes, he turned blue.
That being said, I don't think that anyone else is going to be making a lab to make drugs in their garage to save 180.00 a gallon.
Did you LLMD tell you how many people die every year of anx abuse? Like hundreds of thousands. And that it is the most dangerous drug out there to abuse. They seem to love to pass out all of the abx. And of course that is the only way that Dr.s stay in buss.
I am not blue darling. But I am getting a ton of it pumped into my body 4 days a week, and I am getting much, much better.
And I am not getting immune to abx for future infections. Which was my biggest concern.
Read in line about silver. It has no negative side effects.
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


hopingToFindCure
Veteran Member


Date Joined Nov 2008
Total Posts : 759
   Posted 11/22/2008 7:13 PM (GMT -7)   
I'm glad it's working and yes, he scared me about the Colloidal Silver. He also thinks C-Salt is dangerous.

It's effective when administered the way youre getting it I'm sure. And you're not going to take it day in day out for 10 years like this guy and the other montana libertarian. sounds like they drank A LOT of this stuff to turn themselves blue.


I am glad you're improving and continue to beat this thing. I'd be there too if I could -- taking it all in to wipe this thing out once an for all. I'd have no qualms.

baileygirl76
Regular Member


Date Joined Sep 2008
Total Posts : 123
   Posted 11/22/2008 7:58 PM (GMT -7)   
Your doc is talking about the guy that was on Oprah. He and his friend drank it every day. I guess they had some machine. Well, he turned blue. It was crazy. He obviously over did it. Dr. Oz was on with him.
Good health to everyone.

Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/22/2008 9:35 PM (GMT -7)   
ha...I heard about him too. What shade of blue was he? Aqua, co balt blue....or vivid like the "Blue Man Show?"
I am surprised that they did not turn grey instead.
I read a long story about it on line. But the body passes it if it is small. I don't think that it is easy to make. It cost a lot of money to make collidal silver. The particles must be really small. They say it is also good to put on the skin and is okay to drink. I am getting it pumped into my main artery by my heart. I don't feel any side effects from it. But I am tired after the whole procedure.
I am more worried about starting Laviquin tonight. Into the mix.
This is all so confusing when you have 4 different internist all telling you something different. And then throw in all of the other Dr.s it is a blurr. I feel like a lab rat. But I will be blue if I don't try all of the options out there.
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


hopingToFindCure
Veteran Member


Date Joined Nov 2008
Total Posts : 759
   Posted 11/23/2008 6:45 AM (GMT -7)   
I don't blame you. We're all trying everything. And, yes, I hate being on antibiotics. But I don't know of any other options. I think it's keeping it at bay. But I have some side effects.

I hate waking up these days. I always think -- what's it going to be today?

Glad to know you are getting better. I may have to head west to get well too some day.

cbsoapfan
Regular Member


Date Joined Apr 2007
Total Posts : 128
   Posted 11/23/2008 7:52 AM (GMT -7)   
The guy that turned "blue," he made it in his home. It was more of a blue/grey color. He drank the stuff by the gallons AND he applied it topically (which is more than likely what caused him to turn colors). He is continuing to use it even after doctors recommended that he stop.

Now that said, my LLMD does "prescribe" colloidal silver in small doses. I took about 3 tsp a day for 4 weeks then off for 4 weeks then back on again.

Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/23/2008 1:42 PM (GMT -7)   
Well...gallons of anything daily, even water, is bad for you.
But I wouldn't even try to make my own soap or shampoo, I would turn my hair green...:>)
I only get my CS, 10 cc, 4 times a week, then with a three day break. I am also getting a lot of fluids put into me. Like Vit. C by the bag somedays.
I have noticed that after 3 straight weeks of hard IV treatment that my skin looked dull. But no one else could see it. After going home for a week it was gone. I usually have sort of glowing pinkish skin.
On the meso silver link, they have a study of a Dr. testing his urine and wasted every day to see if the silver all passed..and yuke...but it all did.
Fun homework.
Well I am not on Levaquin tablets too, 500 mg. Because they found the Bart. in my blood. Man only one night of that stuff and I did not want to get out of bed today. I had forgotten how tired abx make me. Like floored. Does it do that to you too?
Hoping what are you taking for depression or pain?
I did not feel like even getting up with all of the pain and fatique till I got on cymbalta. It really helped me. And now I use it in 30mg and then 30 mg later in the day so I can get through a whole day and till like 9 pm. I had trouble taking 60mg at one time because of chest pains. But this works for me like a charm. makes me skinny though. kills the appetite too.

yeah cbssaopfan! That is so cool that your LLMD is perscrieing silver! You actually get it??? that is great! Where do you live????
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


hopingToFindCure
Veteran Member


Date Joined Nov 2008
Total Posts : 759
   Posted 11/23/2008 1:48 PM (GMT -7)   
I take flexeril. It is a tricyclic antidepressant that blocks pain and relaxes the muscles. Take it before bedtime along with 200 mgs of doxy and 500 mgs biaxin. Yes, it's a down trip, but I do have the energy to stay up.

On the silver, did the short term memory issues resolve? Or is that a vitamin deficiency.

On another subject, I wrote the ID head at the university hospital where I live. What the hay! I want to make him aware of the disease and its impact on my little old life. Will keep you posted on that one!

I wrote the department of health. Woo Wee! They didn't want to touch that hot potato with a ten foot poll.

Oh and BTW, I let this doctor know that the ONLY doctors who treat Lyme either

a. Had/Have it themselves

-OR -

b. Have a friend or relative who had/have it!!!!


Ain't that just a shame!

Dowa
Veteran Member


Date Joined Sep 2008
Total Posts : 1120
   Posted 11/23/2008 2:32 PM (GMT -7)   
This may sound like a simple question, but if colloidal silver is SO wonderful, why the need for antibotics now?? Why doesnt the CS take care of the bart if it is so effective?? D

Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/23/2008 2:45 PM (GMT -7)   
Hoping...you go girl! raise some hell! no kidding with the Dr.s who treat it...the only ones that give a darn are the ones who get it also. Isn't that silly? But hey...here's to more Dr.s getting it.
Normally I would not wish this on anyone. But if this is what it takes...lol.

Dowa, hey, I have no idea why I got the Levaquine this week too. They are also upping all of my other stuff next week. One would think it would start off hard and lighten up but no...it is the other way around. I am also going to get abx in a bag as well. I am getting nailed...lol.
I have not taken a lot of abx in the past almost 5 years. my intern told me that 60 days of doxy was more than enough and they for 4 years he just sent me to specialist for my heart and brian and mind. the pain was too much. so he gave me celebrex. ******.
I finally went to germany and got treatment there. But that really did not help me either.
so here I am. all rather new to this abx and all of these drugs. a newbie to all of the stuff really.
I ask alot of questions at the clinic..and then...duhhhhh. I will take a note book with me..and write down what I hear....I will tell them it is for DR, DOWA....:>)))))
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/23/2008 3:00 PM (GMT -7)   
Hoping, my short term memory is a lot better. I can find things now. I am not getting lost. But I have no stress in my life right now. so...it is hard to tell with my strict routine and hotel service you know. I no longer am able to work and I do need to do bills...lol. I don't seem to take car of things the way I use to at all.
I am pretty low key now. with the exception of my 5 year old here with me. But she has always been a easy going child. thank goodness. I don't really have bad days now.
But I do feel moody. And not really wanting to deal with anyone outside of my box...lol
I have a lot on my mind and I really worry to much now. about what is going to happen to my kids if this does not work, and where I should live etc. Move back to Texas,my home, or stay in Florida, near my x. It is too much to decide all right now. But it weights heaving on me. My girls have diff. dads that live in diff. states and I want to keep the girls together. So it is important for me to figure things out while I do have my mind.
I am lucky to have a great x who loves both of my girls and he and his wife have been helping me a lot. It is hard for people to understand how this all happened to some one like me. I was a very assertive, aggressive, developer and very active and sharp, but after the one bite...forget it...it all changed drastically for me.
Along with the really scary depression and the suicidal thoughts I became my worse enemy. I had never been depressed before. But it hit me right after the bite.
So on ward forward. No? One day at a time. That is the only way that I can do this. But I still worry about what is going to happen at the end of my therapy in 4 weeks and if this stuff does not all re surface. So.....
I guess if I end up in a old folks home...I will be the hottest one there...lol
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


Dowa
Veteran Member


Date Joined Sep 2008
Total Posts : 1120
   Posted 11/23/2008 3:32 PM (GMT -7)   
Marie: Who did you  see in Germany and what therapy did they do there? I am asking because a friend of mine with Lyme just emailed me today about maybe going there and I am wondering if it is the same doc or treatment. If it did not help you, I want to warn her. Most of us will try just about anything...you know. I am so glad you are seeing improvment. Go get em!!  D

cbsoapfan
Regular Member


Date Joined Apr 2007
Total Posts : 128
   Posted 11/23/2008 3:39 PM (GMT -7)   
I'm in North Carolina. Now I was on other stuff when I was on the Colloidal Silver too. I'm not on CS anymore, but some other stuff. IV stuff that I'd rather not get into b/c it's pretty controversial. All I know is that I am getting better and that's all that matters.

Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/23/2008 7:13 PM (GMT -7)   
Dowa,
I loved the Dr. in Wursburg. Dr. Schartz. He has had a great success rate with cronic lyme. And he told me to repeat it up to three times. But I had problems. I was on 200 mg of mino. and 100 of hydrochoroqine...sp??? and did those both twice a day...I think...
Look on the old post I put it down somewhere.
And did that for 50 days, then did fluconal, 200 mg, for 50 days.
But he said that some people had to do it up to 3 times for cronic. I just don't seem to handle the abx so well. But it was much better than the LLMD in FLL who put me on 1,200 of doxy that landed me in the hosp.
So?????
I liked him, he had lyme he was very understanding. There are some new clips about him on line at the essex house in NYC.
He told me that he had about 70% success rate.
But he is old and was talking about retirement. So?
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/23/2008 7:14 PM (GMT -7)   
CBS,....tap on me directly. On the letter on the far left side. I hear you.
Marie
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


hopingToFindCure
Veteran Member


Date Joined Nov 2008
Total Posts : 759
   Posted 11/23/2008 7:34 PM (GMT -7)   
Marie - Your comment about the doctors was hilarious!

Thanks for making me laugh.

If you are able to get away during your time in Scottsdale I highly recommend Frank Lloyd Wright's Taliesin West.

Also, that hotel that he designed is worth seeing as is the Wrigley Mansion.

BTW, if you can get away for a weekend, Sedona has a lot of healing type places that are totally worth exploring! You never know what you might stumble on in Sedona. They are into energy fields or something like it. You'll see people in the hills of Sedona doing different things.

Take care!

king1234
Regular Member


Date Joined Nov 2006
Total Posts : 491
   Posted 11/23/2008 7:38 PM (GMT -7)   
That is great you sound like you have come along way. How long have you been at this facility? I cannot stand ax, they scare me..

----------------------------------------------------------------------
33 yr old female/GERD dx 3/07/Migraines with Aura/IBS
SYMPTOMS  migratory joint/bone pain, extreme joint cracking, feet buzzing/vibrating, right eye pain,mid spine soreness (like a constant bruise) fatigue and dizzy spells, bumps and indents on nails. 
New as of Aug-muscle twitching throughout my bod NONSTOP DAILY EVERYWHERE. 
 TESTS-BloodCBC,ANA,Sed rate,Lupus,RA, Vit D,Anti nuc,Calcium.TSH T3 -Too many to list -all CLEAR
 Scans/xraysUltra sound of stomach organs,Sig/colonoscopy (mid way through),MRI of head and spine, full body bone scan-ALL CLEAR
LYME-TESTED POS BAND 31 AND IND ON 34 41 IGM THROUGH IG IN PALO ALTO, GIVEN CLINCAL DX ON 11/17-ON DOXY, ZITHRO, FLAGYL
 
 
 
 
 
 


Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/23/2008 8:18 PM (GMT -7)   
Thanks hoping...I will check it out for sure. I feel fine except for these new darn cramps...lol
I know it is the abx...geezzz...I am going to try to get out taking these somehow..why don't they just put it in my port...that is what it is for..no?
whine whine whine...
I would say something else..but I ALWAYS get in trouble...lol
My and my mouth...l:>)

Hey King....
I got here 6 weeks ago. And took a week off to go home to take my kids out for holloween and to show off my gorgeous port...lol.
It was the first time I felt good out in 4 years.
I felt like a new person after week one. My fever was gone. I had been sweating my ass off for 4 mos. non stop. And the headache..that I just tried to ignore...it was non stop...I lived in shades and my house was a walk in meat locker and was dark....loved it.
I was not eating. Hard to eat with acute nausea from the migrain..no?
So....then I could not even remember a thing and my suicidal thoughts were getting scary. It was like...I want icecream..no I want to die...I mean it just did not mean anything to me. I was going blank and thought that would be better than being in a mental institute...besides the occomodations suck. and there would be not hot guys there..lol
so..I got a call one day from a women I do not know and she told me about envita. I called that day. I had a nice chat with vanessa, I called my travel agent, I called my x and I got on the next plane with my favorite dying dog. and out we came.
he has lyme too so he would hang and sleep with me all day. my toto.
But I feel good. It is just weird to be back into my self. I am raw with emotion and I am going to rock the boat and the CDC so get ready for me boys....I am on a mission! If this CS is the trick then I will be thrilled for everyone who is suffering and going broke on abx that are not working. If this is what works then it will be so fantastic! I will buy it for all of my stupid hardvard grad dr.s and tell them to shove it!
If I have to stay on this stuff to stay well I am ok with that. I had bought some on line and it tastes like water. So no big deal. I have no plans to make it in my garage...lol
Have you had bells palsy yet?
all of my fancy test came back clear as well...why do they bother? to rule out althzmers I guess...but this lyme can cause that for sure...it was with me.
If this sc works and it is all natural then these things will be like mc donalds soon...they will be everywhere!
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


king1234
Regular Member


Date Joined Nov 2006
Total Posts : 491
   Posted 11/23/2008 9:26 PM (GMT -7)   
Out of curiousity did you test positive the first time you had labs done? That is what is confusing in my condition as noted in my signature...
----------------------------------------------------------------------
33 yr old female/GERD dx 3/07/Migraines with Aura/IBS
SYMPTOMS  migratory joint/bone pain, extreme joint cracking, feet buzzing/vibrating, right eye pain,mid spine soreness (like a constant bruise) fatigue and dizzy spells, bumps and indents on nails. 
New as of Aug-muscle twitching throughout my bod NONSTOP DAILY EVERYWHERE. 
 TESTS-BloodCBC,ANA,Sed rate,Lupus,RA, Vit D,Anti nuc,Calcium.TSH T3 -Too many to list -all CLEAR
 Scans/xraysUltra sound of stomach organs,Sig/colonoscopy (mid way through),MRI of head and spine, full body bone scan-ALL CLEAR
LYME-TESTED POS BAND 31 AND IND ON 34 41 IGM THROUGH IG IN PALO ALTO, GIVEN CLINCAL DX ON 11/17-ON DOXY, ZITHRO, FLAGYL
 
 
 
 
 
 


Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/23/2008 9:58 PM (GMT -7)   
The day I piked the tick off my butt was the day I hit the floor. My Dr. In MV did not question what I had, I already had the so called flu, neck pain, fever and fatique, and I was so weak. I could barely drive to the Dr. I was not able to see very well. He did my blood work and it came back negative. I was like....so your test cannot find it huh?
It was years of taking blood from myself and my baby and none one came up positive...ever. Then I found IGNEX and it finally showed up, along with the CDC's primitive test.....and by then it had grown big time.
I guess the CDC thinks that by telling everyone that they do not have lyme that we are supposed to not die. Just not do it. Why don't they spend time finding out what does work for this big problem we have here. Because it is not going to go away. And everyone that is not going to be able to work will cost the gov. so much more than they every imagined.
This big lie has gone on long enough.
The CDC needs to pull their head out. Get with the program and address this public health issue.
Maybe a class action law suit for fraud would get their attention....like the tobacco companies.
What they are doing is criminal.
They are lying. Plain and simple. And it is costing us the lives of our families and our friends and our children.
When the test come back negative. Our children are refused treatment of any kind.
They are criminal.
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


king1234
Regular Member


Date Joined Nov 2006
Total Posts : 491
   Posted 11/23/2008 10:26 PM (GMT -7)   

Thank you for sharing your story. I guess I was curious about the labs as I am still not 110% convinced I have lyme, and I soley feel this way due to my labs. All my symptoms point to this and I have had SO many other tests done as you see in my signature--one of my drs called me a medical mystery, another said I needed a psych and that it was all in my head, another stress, and another said well I dont know what is wrong but I am sure it will surface when you get worse. I only tested pos on 31 IGM and IND 34 41 with Ige in Palo Alto. I am on doxy now, and add the other meds this week, then will retest.

Why does the CDC not acknowledge what lyme specialists and some labs do? It doesnt make sense why they wouldnt? Whats the issue with it all?


----------------------------------------------------------------------
33 yr old female/GERD dx 3/07/Migraines with Aura/IBS
SYMPTOMS  migratory joint/bone pain, extreme joint cracking, feet buzzing/vibrating, right eye pain,mid spine soreness (like a constant bruise) fatigue and dizzy spells, bumps and indents on nails. 
New as of Aug-muscle twitching throughout my bod NONSTOP DAILY EVERYWHERE. 
 TESTS-BloodCBC,ANA,Sed rate,Lupus,RA, Vit D,Anti nuc,Calcium.TSH T3 -Too many to list -all CLEAR
 Scans/xraysUltra sound of stomach organs,Sig/colonoscopy (mid way through),MRI of head and spine, full body bone scan-ALL CLEAR
LYME-TESTED POS BAND 31 AND IND ON 34 41 IGM THROUGH IG IN PALO ALTO, GIVEN CLINCAL DX ON 11/17-ON DOXY, ZITHRO, FLAGYL
 
 
 
 
 
 


Martha's Vineyard
Veteran Member


Date Joined Jul 2008
Total Posts : 1119
   Posted 11/24/2008 12:22 AM (GMT -7)   
Read lab 257. It will give you a lot of insight to who is trying to cover who's ass. As long as the Dr. Saphiro and DR. Steere give false info. to the CDC. Then the CDC can lie and say that there is not a horrific outbreak in this country, the big lie about the easy to catch, when the blood test lie, and the big lie about the easy to cure, cause they don't have a cure. so the insurance companies can all say that they do not have to cover you, because you cannot prove you are sick and then when you finally do prove it....they lie and say that 2 weeks will cure you. and anything beyond that in treatment is illegal.
it is all about money.
Like everything else in this country it seems.
It is becoming a world wide problem and fast. There needs to be something that humans can put on themselves. And quickly. If we can get it again and again from mosquitos. Or I wonder if at some point maybe we become immune to it. Who knows. It is a bit frightening I think. especially for kids. The main group that is getting it is 5-12. And it is really hard on them. It must be the cause of all of the cancers that are effecting our young.
2004 in Martha's Vineyard me and my two daughters then 11 mos and 6 all got Lyme Disease. This was only known to us because we found the tiny ticks on us and we got very ill. My dog also got lyme and he went lame.
We have fought it for 4 years to no avail.
We all got it again this summer is Texas.
I am now in treatment in Scottsdale Arizona at Envita.

"The eyes cannot see for for what the mind does not know."


KO-LD
Veteran Member


Date Joined Aug 2007
Total Posts : 887
   Posted 12/11/2009 1:37 PM (GMT -7)   
HI All,
I was looking for info on Ionic Silver (CS), does anyone have any updates on what they think. or any stories to tell?  Thanks, KO
01 Tingling in fingers/toes both sides, not tested at that time for LD
07 Summer pos. WB, diag with LD, neg for co-infections thru Igenex
Abx - Doxy 100mg 2x/day for 3 weeks (before diagnosis)
Amoxicillin 1gm 2x/day for 1 month
Amoxicillin 1gm 3x/day with Probenecid 500mg 2x/day  5 months 
Dr. Zhang's protocol stopped after 6 months symptoms returned.  Started Buhner's protocol May 2009

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