Guest guest Posted January 26, 2010 Report Share Posted January 26, 2010 , did your wife have chronic lyme or was it newly diagnosed? Just curious. I'm working toward getting this into remission myself. Re: [ ] My Lyme " success story " > > Hi, > > I may have had it for 3 years before I started on the Buhner > protocol, but the whole story is that when I first > had symptoms in '06: rashes, joint pain, fuzziness, I went > for a Lyme > test and it came up negative, but I took 3 > weeks of oral antibiotics anyway. The problem is that I > thought I was > taking the antibiotics when I was really > taking the Ibuprofin that was prescribed along with it, because the > instructions and bottles were not in separate > bags when I got them from the pharmacy and I mixed them up. So I was > actually a month delayed in getting > on the antibiotics. They did not completely cure the symptoms so I > went to a chinese herbalist, and the itching > ceased somewhat, but I discovered a naturopath who put me on a > slightly different formula (pills instead of the horrid tasting > Chinese herbs that you have to decoct). I felt much better but still > had residual aches and pains so I went to yet another > naturopath who did kineseology with me and he said although what I > was taking helped my symptoms, they were not > in the overall picture good for me so he gave me some more stuff (L- > Thyrosine was one thing I remember) and I stopped > taking what the first naturopath was giving me (formulas called > " Clear Heat " and " Skin Balance " and the other things called > VRM 1 & 2 I believe). > > I thought I was cured of whatever had been ailing me but last winter > started feeling really tired so I went for blood tests > and sure enough, this time I tested positive for Lyme. I took > a round > of three weeks of amoxycicline and went for another > test and I STILL had it, so that's when I discovered the Buhner > protocol. I have just a few weeks left until I reach the recommended > minimum 8 month marker. I had a set back when I couldn't find a > source for the herbs (the combined pills) a few weeks ago and began > to feel > achy again. In about two weeks I regained my regular energy > level and > feeling pain free, so I am hoping I can stop at the end > of 8 months, but I am thinking now I might want to stay on > them for a > while year. My fear is when I stop taking the herbs, the critters > will come out of hiding. > > My only recourse if I still test positive after 8 months or a > year is > to go on long term IV antibiotics. Though the oral > antibiotics didn't > seem to work, maybe the intravenous will. > > > > > On Jan 24, 2010, at 11:35 AM, y093666 wrote: > > > - > > > > Thanks for your sucess story! Did you have late stage lyme > or neuro > > lyme/symptoms? How long do you think you had lyme? > > > > > ------------------------------------ > > Buy Healing Lyme: Natural Healing And Prevention of Lyme > Borreliosis And Its Coinfections by Buhner at one of > these locations: > http://tinyurl.com/3bgm5d > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 28, 2010 Report Share Posted January 28, 2010 By the time she realized what was going on it was chronic. She had a short term course (3 weeks) of antibiotics a couple of months after being infected. She thought she was done with it and then relapsed about 6 months later. > Re: [ ] My Lyme " success story " to > > , did your wife have chronic lyme or was it newly > diagnosed? Just curious. I'm working toward getting this > into remission myself. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 28, 2010 Report Share Posted January 28, 2010 Hi , Is she cured now? Thanks On Jan 28, 2010, at 2:25 PM, wrote: > By the time she realized what was going on it was chronic. She had > a short > term course (3 weeks) of antibiotics a couple of months after being > infected. She thought she was done with it and then relapsed about > 6 months > later. > > > Re: [ ] My Lyme " success story " to > > > > , did your wife have chronic lyme or was it newly > > diagnosed? Just curious. I'm working toward getting this > > into remission myself. > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2010 Report Share Posted January 29, 2010 Her lyme is in remission. We don't believe there is any cure currently for chronic lyme. The best is to have a protocol that is easy on the body that keeps it in remission. Re: [ ] My Lyme " success story " to > > > > , did your wife have chronic lyme or was it newly diagnosed? > > Just curious. I'm working toward getting this into remission myself. > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2010 Report Share Posted January 30, 2010 Thanks, . This sounds a lot like my situation. Treatment came a little too late. I am hoping some kind of cure will be found and I'm thankful it's not more severe in the meantime. What does your wife take now to keep it in remission? Thanks, On Jan 29, 2010, at 8:07 PM, wrote: > Her lyme is in remission. We don't believe there is any cure > currently for > chronic lyme. The best is to have a protocol that is easy on the > body that > keeps it in remission. > > Re: [ ] My Lyme " success story " to > > > > > > , did your wife have chronic lyme or was it newly diagnosed? > > > Just curious. I'm working toward getting this into remission > myself. > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 31, 2010 Report Share Posted January 31, 2010 I just posted a bit about. You can read more in the root folder of my free lyme resource CD. www.lyme-resource.com You can lead a person to a fact, but you can't make them think! - Re: [ ] My Lyme " success story " to > > > > > > , did your wife have chronic lyme or was it newly diagnosed? > > > Just curious. I'm working toward getting this into remission > myself. > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2010 Report Share Posted February 4, 2010 - did you you/your wife have neuro isses with lyme or were they primarily muscle-skeletal? Do you know of anyone healed from deep neuro/MS type issues with the colloidal silver, rife, salt c/ etc? > > > > > By the time she realized what was going on it was chronic. She had a > > > short term course (3 weeks) of antibiotics a couple of months after > > > being infected. She thought she was done with it and then relapsed > > > about > > > 6 months > > > later. > > > > > > > Re: [ ] My Lyme " success story " to > > > > > > > > , did your wife have chronic lyme or was it newly diagnosed? > > > > Just curious. I'm working toward getting this into remission > > myself. > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2010 Report Share Posted February 4, 2010 She had both. Yes there have been numerous anecdotal testimonies of people getting their Lyme into remission with these protocols. Note I do not say healed or cured. But in remission. She has her life back and feels she is currently functioning at 90% pre-lyme. There are others claiming they have reached 100%. Please see my free Lyme Resource CD for these reports and others. www.lyme-resource.com You can lead a person to a fact, but you can't make them think! - > Re: [ ] My Lyme " success > story " to > > > > > > > > > > , did your wife have chronic lyme or was it > newly diagnosed? > > > > > Just curious. I'm working toward getting this into remission > > > myself. > > > > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2010 Report Share Posted February 5, 2010 I know some people are having good luck with neuro symptoms using teasel and MMS. The Lyme_and_Rife group has a lot of discussion about MMS in particular. deb > > - did you you/your wife have neuro isses with lyme or were they primarily muscle-skeletal? Do you know of anyone healed from deep neuro/MS type issues with the colloidal silver, rife, salt c/ etc? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2010 Report Share Posted February 5, 2010 I'm chemical sensitive and wonder about MMS toxicity? Anyone with chemical sensititivies taking it with good luck? > > > > - did you you/your wife have neuro isses with lyme or were they primarily muscle-skeletal? Do you know of anyone healed from deep neuro/MS type issues with the colloidal silver, rife, salt c/ etc? > > > Quote Link to comment Share on other sites More sharing options...
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