Guest guest Posted January 2, 2012 Report Share Posted January 2, 2012 Thank you , I will contact and I hope you will improve soon! > > > > Hi all, > > > > I've been diagnosed with chronic lyme (neuroborrelia ft. ehrlechia co-infection) a while ago, now I'm looking for treatment options. So far I've read success stories about: > > > > • Long term pharmaceutical antibiotics (oral or IV) > > • Natural antibiotics and detoxifiers (herbs, tinctures, roots, etc.) > > • Diet and lifestyle changes (avoiding sugar/grains/alcohol/tobacco) > > • Magnet and electric treatments (zapper, rife) > > > > I've done oral AB, it gives short relief after a period of herxing. Gradually symptoms return after halting AB treatment and the side effects suck (AB turns me into a pale, anxious and skinny zombie without appetite). I'm gonna try Teasel/Cat's Claw soon. I've changed to a strict SC diet which did help for a period (I suspect the baking soda used in almond bread killing off some bacteria). I'm drinking a lot of green/ginger tea and taking garlic/multiVit(B/C/D)/magnesium supplements. Seems to help a little bit. > > > > Now I'm tempted to purchase a Doug Coil from healthbartner.nl. But the machine is a whopping' 7000,- EURO! I'm a 25 y/o who recently finished studying, this is a lot of money for me. So before I go spend my life savings on a rife machine. I'd like to hear your experience/toughts/succes- and fail stories about Rifing. (mainly the Doug Coil advertised @ healthbarter.nl) I wanted to search this forum for successtories, but with the current search functionality I can't seem to find any successtories or positive reactions. Also, is there any video material out there that can convince me? ...Like a video showing the rife machine in action on a dark field microscope, blasting spiro's into oblivion? > > > > Thanks! > > > > Sincerely, > > S > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2012 Report Share Posted January 2, 2012 To be honest I recently found out and I'm kinda looking for treatment options that are known to work (ie from testimonials by REAL people like yourself ). I've been tested for Co-infections: Erlechia(sp?) was positive in the lgg, everything else negative. LLDM doctor says I probably have a neuro-lyme infection and should consider long term antibiotics, GI doctor says I probably have Chrohn disease and need to take steroids. I'm afraid steroids will give lyme a free pass to a intestine feast. D: I'm not a big fan of antibiotics, but if they're the best bet I'll go for it. Right now I'm doing Samento/Teasel/Garlic/Zeolite/Yellowcarrot supplements and avoiding sugar/grains. I'm thinking about adding colloidal silver, since MMS has a bad reputation on the internet (I see alot of people compare it to bleach and getting bad stumach problems from just a few drops :S). Silver seems to be more safe from what I've read and also has antimicrobial properties or so they say. What do you think? > > > > Hi all, > > > > I've been diagnosed with chronic lyme (neuroborrelia ft. ehrlechia co-infection) a while ago, now I'm looking for treatment options. So far I've read success stories about: > > > > • Long term pharmaceutical antibiotics (oral or IV) > > • Natural antibiotics and detoxifiers (herbs, tinctures, roots, etc.) > > • Diet and lifestyle changes (avoiding sugar/grains/alcohol/tobacco) > > • Magnet and electric treatments (zapper, rife) > > > > I've done oral AB, it gives short relief after a period of herxing. Gradually symptoms return after halting AB treatment and the side effects suck (AB turns me into a pale, anxious and skinny zombie without appetite). I'm gonna try Teasel/Cat's Claw soon. I've changed to a strict SC diet which did help for a period (I suspect the baking soda used in almond bread killing off some bacteria). I'm drinking a lot of green/ginger tea and taking garlic/multiVit(B/C/D)/magnesium supplements. Seems to help a little bit. > > > > Now I'm tempted to purchase a Doug Coil from healthbartner.nl. But the machine is a whopping' 7000,- EURO! I'm a 25 y/o who recently finished studying, this is a lot of money for me. So before I go spend my life savings on a rife machine. I'd like to hear your experience/toughts/succes- and fail stories about Rifing. (mainly the Doug Coil advertised @ healthbarter.nl) I wanted to search this forum for successtories, but with the current search functionality I can't seem to find any successtories or positive reactions. Also, is there any video material out there that can convince me? ...Like a video showing the rife machine in action on a dark field microscope, blasting spiro's into oblivion? > > > > Thanks! > > > > Sincerely, > > S > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2012 Report Share Posted January 2, 2012 Hi Meo, I'm not really familiar with protocols, I'm kinda new to lyme. The first thing I did was look up all the products that aid recovery, I ended up with samento (cat's claw), teasel, ginger, garlic, zeolite, jiajolan tea and I'm looking for a powerfull antibacterial to take along with this all. (MMS or Colloidal silver is on my mind.. what do you recommend?) What other options are there? Thanks! > > > > Hi all, > > > > I've been diagnosed with chronic lyme (neuroborrelia ft. ehrlechia co-infection) a while ago, now I'm looking for treatment options. So far I've read success stories about: > > > > • Long term pharmaceutical antibiotics (oral or IV) > > • Natural antibiotics and detoxifiers (herbs, tinctures, roots, etc.) > > • Diet and lifestyle changes (avoiding sugar/grains/alcohol/tobacco) > > • Magnet and electric treatments (zapper, rife) > > > > I've done oral AB, it gives short relief after a period of herxing. Gradually symptoms return after halting AB treatment and the side effects suck (AB turns me into a pale, anxious and skinny zombie without appetite). I'm gonna try Teasel/Cat's Claw soon. I've changed to a strict SC diet which did help for a period (I suspect the baking soda used in almond bread killing off some bacteria). I'm drinking a lot of green/ginger tea and taking garlic/multiVit(B/C/D)/magnesium supplements. Seems to help a little bit. > > > > Now I'm tempted to purchase a Doug Coil from healthbartner.nl. But the machine is a whopping' 7000,- EURO! I'm a 25 y/o who recently finished studying, this is a lot of money for me. So before I go spend my life savings on a rife machine. I'd like to hear your experience/toughts/succes- and fail stories about Rifing. (mainly the Doug Coil advertised @ healthbarter.nl) I wanted to search this forum for successtories, but with the current search functionality I can't seem to find any successtories or positive reactions. Also, is there any video material out there that can convince me? ...Like a video showing the rife machine in action on a dark field microscope, blasting spiro's into oblivion? > > > > Thanks! > > > > Sincerely, > > S > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2012 Report Share Posted January 6, 2012 Sanne I have met Jim while travelling ,and have been on several lyme support groups with him for years and I guarantee to you, he never sells anything.He has strong beliefs in the products that work for him and posts about those things and gives links to various sellers ,usually telling us where the least expensive place to purchase something is, but also giving links to other retailers.Swansonsvitamins is one he recommends often and they are a bigger company and dont do MLM .MMS is an awesome productI recommend myherbs.net and I am not affiliated with them, they simply sell nutramedix products and bulk chinese herbs at the best price that I have foundI hope this helpsjan Re: Rife success stories? Posted by: "Lyme_and_Rife-owner " Lyme_and_Rife-owner Date: Thu Jan 5, 2012 8:12 pm ((PST))Hi Sanne,Well ya caught me! How'd you know I was a product spokesman???!!!!Actually, if you look at my Screen Name, it does say Lyme and RifeGroup Owner, I was the one who initiated the policy of NO SELLINGon this group... AND, I am sure there are many on this group who will vouch for my validitythat I have chronic neuro Lyme, I've been a member of Yahoo Groupsfor 6 years and I can assure you if I was going to sell you something, it would cost far more than $20 you'd pay for MMS! AND, I would notgive you a list of resellers, I would give you my link only!!Trust me, I am not offended, more amused as you are the first personto ask this... :-)Believe me, I have nothing to sell and I will ban anyone I find trying to sellhere as I am strongly against anyone selling on a Lyme support group!When a seller comes to these groups, you the new member is the target.I know this, I detest this and I have thrown a few sellers off this group,they didn't even know they weren't a group member anymore as I justBan them and don't tell them... I've banned machine sellers and pillpushers, even those who claim to be a doctor!Actually, when I took over this group as Moderator, I did so with the supportof many of the long time members... And they supported me because the know me and trusted me to never allow any selling here... You see,about 150 of us came from another Lyme and rife group where the group owner/moderator allowed selling... Some of us and mainly metried to stop the selling and the moderator would not listen to us, the selling was allowed.. Even after I pointed out to him Yahooforbids selling and advertising on these groups, the selling wasstill allowed... Then one day he said the wrong thing to a well likedsenior member of Yahoo groups and our friend, and it was decided we were movingand starting our own group! This group was born that very day!!And no selling has been allowed on this group since its inception!This is extremely important to me and other senior members, itjust will not happen.. I usually try not to tell new members what kind of success I've had usingmy protocols when I am talking directly to them such as now, unless I amspecifically asked, and I am going to try not to talk about my successes to you, but if you go to this link, you can read about it yourself! About the 3rd paragraphfrom the bottom!http://health.groups.yahoo.com/group/Lyme_and_Rife/message/25469And if you'd like to go into the archives and read all of my posts, all 4259 of them, here is the link! If you find anywhere I've tried to sell anything, please do share... :-)http://health.groups.yahoo.com/group/Lyme_and_Rife/msearch?date=any & DM=------------ & DD=---- & DY=---- & DM2=------------ & DD2=---- & DY2=---- & AM=contains & AT=jim & SM=contains & ST= & MM=contains & MT= & charset=UTF-8I really don't mind your questioning me!! I just wonder why it took so long for anyone to bring this up!!Take care,Jim>> Dear Jim,> > Thank you for your detailed reply, i am really considering MMS now. I've done some research but most I've discovered is true-false discussions without many arguments> I can understand without reading chemistry books. You make MMS sound really promising. I'm just afraid of undercover product spokesmen that infiltrate groups like these and place fake testimonials and what/not... How can I be sure you're a real patient with good results from just a message? It's so hard to filter the bogus from the reality on the world wide web, and in no way do i want to offend you but I think we lymies have to be very sharp and carefull when it comes to self theraphy!> > I guess your disclaimer says it best, I have to do more research, however in gratefull for your time, experience and in deptht explanation. "Im not trying to counsel any of you to do anything really special,except to dare to think, and to dare to go with the truth ,and to dare to love completely." -R. Buckminster Fuller Quote Link to comment Share on other sites More sharing options...
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