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christine,i only had 2 shots so never got to see any benefits but like i said other patients really were helped.i have had a coil since fall of 09.  i did not know i needed to treat 2x day for bart and 1x babs and i was not consistent. also, i had t

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christine,i only had 2 shots so never got to see any benefits but like i said other patients really were helped.i have had a coil since fall of 09.  i did not know i needed to treat 2x day for bart and 1x babs and i was not consistent. also, i had to stop for a while when i went through acute withdrawal from a benzo drug. so i'm sort of starting over, but it does work.  but, only since being on this forum have i learned how to do it right.  also, i do not detox well, and have a gut that does not work so i just kept recycling toxins.  i have learned the importance of detoxing.  my main problem with that is all the binders block my gut so badly, it just added to the problem.  here is where i have found many answers on how to work with this handicap.

i use the oxy powder to keep things moving.  i then added the colonics and enemas.  these two have been key for me.  i have tried the coffee enemas and they work well, however, i am trying to taper down on a benzo drug and have to be careful with caffeine, because they can cause convulsions for me right now.  i do water colonics but the coffee enemas (ce) are limited  but they really work for detox.. please look into this part of your treatment because without it progress will be extremely slow and discouraging.  i learned that from experience.  also,  i've just recently started adding mms to the enemas to boost killing.

the oral mms is really working also. i tried it transdermal and did too much and got a bad herx--but it showed me it works.  so am doing that with caution.  it just kills any bug it comes in contact with, and because most of us have bugs we don't even know of, it is a boost to the killing.  the coil is bug specific and will only kill what you program it to, and usually you are only treating one,or two bugs at any one time.  so the mms is continually, slowly bringing down the over all load, aiding the coil.  but the coil is the most powerful.  my llmd suggested the coil when i asked about rife machines.

the essiac tea is a great detoxer and really easy to do.  so i use that. also, a binder is a must and the only one i may be able to  use is the glucomannon.  i have to order it yet, and hope it works.  many are using it or clay so ask about that to get more info.

coloidal silver has had a good rep for killing.  the salt/c i have heard many get help with.  making a list and keeping a journal is great and a plus when you track your protocol to see how it works.  without it you won't know what does and doesn't work.  don't rely on memory, that doesn't work for most of us.  even keeping a journal is sometimes hard to remember.  but studying and researching which protocol you want is smart, each of us is different and respond differently.  

i have been trying to address the lyme and cos since '07 and i had not seen any real progress until i started the colonics, mms and the essiac tea.  my stomach was so bad i could not eat and went to 100#.  there were times i couldn't even stand up.  whatever i was killing just kept recycling, keeping me sick.  i'm not sure what has been the key to helping my stomach, but since i started those 3 things a couple months ago,  i have gained 10#s.  i am hungry a lot, maybe making up the nutrients.  also, i have noticed some clearing in my head.  still a long ways to go, but i see improvement.  i am anxious to add the gluc, hoping it won't add to the constipation and will bind and move toxins out. 

again, without moving the toxins out, you won't see much improvement, no matter what protocol you use.  good luck in your search for the right protocol for you.  there is a lot of good info here and great people with lots of accurate info because of their research.  if you need info about mms, essiac tea ask jim.  he is the expert on these two.  but just throw out the ?s and someone will answer.

barbara

 

Hi Barbara,

It's nice to hear from another person who has had LDA treatment. So few people have heard of it and when I try to explain I feel like I get a lot of blank stares....especially when it comes to the 3 critical days and 3 weeks before the shots begin working....

I hope you are right that once the bacteria load goes down the allergies may also.

I'm still putting together my plan to tackle this thing. I just began reading Rosner's book " Top 10 Lyme disease treatments " and found a lot I had never seen posted anywhere else.

I think I will start a binder just for treating Lymes and note any changes I see.

My first step is to start with colloidal silver.

Then I think I might try extra magnesium. The salt/vit.C thing sounds good. I have to be careful of salt, cuz I do have a slight sensitivity to it, and get hives after some sea salts.

How long have you used the doug coil? Has is seemed to help a lot?

Thank you for sharing all you did with me.

Best of health to you,

>

> > **

> >

> >

> >

> >

> > Hi Everyone,

> >

> > I just wanted to post my story, in case anyone is interested.

> >

> > I began developing food allergies 5 years ago. I traced it to 2 episodes of

> > latex exposure and extreme allergic reactions and learned that latex can

> > cross-relate to all food groups. So I thought that was my diagnosis. But a

> > lot

> > of things didn't make sense. Multiple doctors couldn't believe I was

> > reacting

> > to so many foods. I found LDA food shots and began on them 2 years ago.

> > They've kept me alive...2 years ago I was starving...reacting to every

> > food.

> > But the shots also make me develop allergies, so I'm on a see-saw diet, and

> > still don't know if I'm getting over my food allergies or just barely

> > surviving....I usually don't have enough calories to eat. Enough of that

> > part

> > of the story.

> >

> > 2 weeks ago my general practitioner out of the blue said he was going to

> > do a

> > Lyme titer test on me. That started me thinking. All along I've known I was

> > exposed to Lymes because from the time I was 12 to 18 I would often be bit

> > by

> > ticks and once I had the bulls-eye rash for about 1 1/2 weeks, then

> > developed

> > arthritis type symptoms in my knees occasionally. It went away after a few

> > years and I lived a healthy life until the food allergies.

> >

> > Well, after doing some reading, I realized it doesn't matter if the Lyme

> > titer

> > test is positive or negative, the bulls-eye rash, multiple tick bites and

> > all

> > the immunological problems I currently have point to lymes.

> >

> > Now I just need to figure out what to do about it. Unfortunately, I am

> > sooooo

> > allergic to all foods, that I doubt whether I would tolerate any of the

> > recommended herbs....or if I did, it wouldn't be long until I became

> > allergic to

> > them also.

> >

> > I think rife would be great...but I have no experience with electrical

> > things....I know someone who could give some help, but even then, to buy

> > the

> > parts for the Doug coil would be out of question.

> >

> > And, I'm still not sure if I believe that rife is very effective. I keep

> > trying

> > to find personal success stories with rife, but haven't found too many.

> > Besides, at least in my case, I would have told everyone I got over Lymes

> > as a

> > kid, but the truth is, people can think they are over it, but it's still

> > hiding

> > out.

> >

> > I think the safest and most economical approach at this point is colloidal

> > silver. I'm also afraid of developing an allergic reaction to that too,

> > since

> > I'm allergic to some metals...nickel, gold.

> >

> > Ughhh...so for the present, my goal is to try to not starve by using LDA

> > food

> > shots, which unfortunately, have been shown to work for everybody but lymes

> > patients (I think it's the way the lymes causes an immune response to the

> > shots,

> > whereas with others it doesn't) and then try to overcome lymes.

> >

> > I daily think this may be my last day.....for the present I'm at 300

> > calories a

> > day and not doing well. But the LDA shot should start working in 12 days,

> > then

> > I can slowly eat many things I'm allergic to, in moderation.

> >

> > I just started 5mg Corteff for long term treatment to help with the food

> > allergies. I know it's not recommended for Lymes, but without it I would be

> > dead from starvation....and I'm not kidding.

> >

> >

> >

> >

> >

>

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