Guest guest Posted November 26, 2004 Report Share Posted November 26, 2004 Ive had all the bladder/kidney symptoms of lyme since I was 17, 20+ years now. I also had a cystoscopy, showing nothing. What Ive found, is its some type of secondary infection (maybe candida??) caused by the lyme throwing off the internal balance of normal bacteria, and the only thing that fixes it for me is taking quinine daily. I take 1 gram, its herbal, no prescription, mixed with peanut butter on a cracker every day, and the bladder incontinence goes away. When I forget to take it, bladder/kidney symptoms return. An MD treated me 3x in a row for kidney infection, clearly seeing cloudy urine and having it tested, and the results of the tests showed more than one bacteria -- so they threw the tests out wrongly thinking contamination--- this is incorrect. Lyme is one bacteria, yeast is another, and we all know 2 can exist at once, as evidenced by erlichia (which I had/have), chronic candida yeast infections in lyme patients, etc.... and the other four piggybackers that lyme ticks can give you. So when your tests are showing blood or urine with more than one bacteria, and the lab protocol says THROW OUT RESULT< CONTAMINATION -- this is a serious error. All your bacteria variety are showing, and you are very sick/infected, yet they figure oops, we contaminated it???? My samples were even given AT the lab, so how could that be? You might want to try quinine - its at any health food store, or available on the net thru mail order by the pound. Very cheap - twenty dollars a pound will do 10 people sharing for an entire year. Incidentally, the quinine is part of the malaria remedy that many lyme people have accidentally noticed helped their lyme -- the quinine, NOT the fever as purported by many doctors. (I guess they want to make money). Quinine is not regulated so its available to all who seek it. SALT is also the latest thing Ive found to help my sinuses, lungs, and blood pressure. Lyme sweating causes a deathly imbalance of salt- deprivation and this can cause death if not corrected. Read the other post about salt, if the moderator allows you to hear about it. SALT is necessary for life, and Morton's is not the one to use...buy it kosher, sea salt, or halite. Without salt, we die, and in USA, a myth abounds that salt has no value - poppycock -- look up SALT ARCHIVES on the net to find a huge hoarde of info about salt that's been forgotten in the states. > > Lori, > > I am about to undergo a cystoscopy ( for IC ) and desperately want > to avoid it. I doubt I have IC - and your theory is interesting re > spirochettes blocking the bladder? Where you able to find out > anything on this? > > Thanks alot, > sincerly > Carmen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2004 Report Share Posted November 26, 2004 Carmen I also the the lyme bladder. I have a video tape with Dr Mattman showing ketes in the bladder lining of all IC patients. I have taken Elmiron which helps the bladder stuff but the side effects are terrible and had to stop taking it. I found a natural product that I think will work similar to the drug by rebuiling the bladder lining. The abx I have taken for the last 5yrs didn't fix the bladder. Carmen <migragurl@...> wrote: Lori, I am about to undergo a cystoscopy ( for IC ) and desperately want to avoid it. I doubt I have IC - and your theory is interesting re spirochettes blocking the bladder? Where you able to find out anything on this? Thanks alot, sincerly Carmen Questions and/or comments can be directed to the list owner at -Owner Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2004 Report Share Posted November 26, 2004 I am wondering if I should just go ahead and cancel the operation. ( cystoscopy )( Last time )They did find infection but couldn't call it IC - aswell as oedema in my bladder wall - but they cannot 'type' the infection. I was going to go through it all again because my surgeon FORGOT to tell my MD I had bladder irriation - not just urethral irriation. So to go through it again for a neg.....welll......I'll have to think about it....Carmen > > > Lori, > > I am about to undergo a cystoscopy ( for IC ) and desperately want > to avoid it. I doubt I have IC - and your theory is interesting re > spirochettes blocking the bladder? Where you able to find out > anything on this? > > Thanks alot, > sincerly > Carmen > > > > > > > Questions and/or comments can be directed to the list owner at -Owner@Y... > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2004 Report Share Posted November 26, 2004 Hi The b;ladder [rpblem crosses the gender line. I ahve ahd severe discomfort and pain for the last several months even though routine tests PSA, DRE and ultra sound were all within range. I understand that the bladder is a favorite playground for the sprichetes. Can yu share with me the natural approach you are folowing? Many thanks qnd all god luck to you JPOhn Lucher <lucher@...> wrote: Carmen I also the the lyme bladder. I have a video tape with Dr Mattman showing ketes in the bladder lining of all IC patients. I have taken Elmiron which helps the bladder stuff but the side effects are terrible and had to stop taking it. I found a natural product that I think will work similar to the drug by rebuiling the bladder lining. The abx I have taken for the last 5yrs didn't fix the bladder. Carmen <migragurl@...> wrote: Lori, I am about to undergo a cystoscopy ( for IC ) and desperately want to avoid it. I doubt I have IC - and your theory is interesting re spirochettes blocking the bladder? Where you able to find out anything on this? Thanks alot, sincerly Carmen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2004 Report Share Posted November 28, 2004 Carmen, I had MAJOR bladder issues this time last year. I couldn't go 15 minutes without using the bathroom and would go maybe 4 times as I was trying to get out of the house with kids waiting by the door. When I did the volume test, I had to run back to the Dr. office to get an extra jug! Since my lyme treatment I can say that all of my bladder symptoms are completely GONE! It took about 6 months for it to dawn on me. Either it was the lyme or something else bacterial, but I had the referral for the urologist all ready - I just wanted to wait until after I saw the LLMD and put it off. I'm glad I did because if I had gone there would have been that testing you mentioned and if I had been diagnosed with IC there would have been more drugs and emotions. I have a good friend with IC who is at her wits end because she's miserable and not any better. She's going to get tested for Lyme. This is just my testimony regarding my bladder for what it's worth. Beth [ ] bladder tests Lori, I am about to undergo a cystoscopy ( for IC ) and desperately want to avoid it. I doubt I have IC - and your theory is interesting re spirochettes blocking the bladder? Where you able to find out anything on this? Thanks alot, sincerly Carmen Questions and/or comments can be directed to the list owner at -Owner Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2004 Report Share Posted November 28, 2004 > > Lori, > > I am about to undergo a cystoscopy ( for IC ) and desperately want > to avoid it. I doubt I have IC - and your theory is interesting re > spirochettes blocking the bladder? Hi. Can you tell me what IC means, please? I've finally realized that the on-again, off-again urinary symptoms I experience are Lyme related, or Lyme itself. The good news is that whenever I experience the symptoms now I take a product called Cran-Actin. It works wonderfully. I believe the way it works is to smooth the cells lining the bladder. Symptoms I experience are the urge to urinate, then no flow. Or sometimes, urinary urgency. While these could be considered a typical issue for a woman of my age (58), the symptoms seem always to arise when I am experiencing other symptoms in a Lyme/co-infection flare-up. Dark urine is also a symptom that sometimes appears with a tickborne illness flare-up. Hope this helps. Deanna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2004 Report Share Posted November 28, 2004 HI, it means Interstitial Cystitis. Means microscopic bleeding between the bladder walls. But I feel it's probably more the lyme bladder, and severe irritation of the bladder wall - similar but not the same. Symptoms are on good days, peeing twice per hour AT LEASt and on a bad day, by the minute.....I have to take some hectic meds to stop the pain and irritation as it feels just like a UTI.( urinary tract infection ) I get cloudy urine the day b4, and I suddenly crash into the worst depression. That is one sign I am getting sick. Weird. I also have bladder bloated feeling, bladder pain and spasms, , and shivers, hot flashes and insomnia. I tried Cranberry Capsules with little help unfortunately. Has anyone tried Moducare? Carmen > > > > Lori, > > > > I am about to undergo a cystoscopy ( for IC ) and desperately > want > > to avoid it. I doubt I have IC - and your theory is interesting re > > spirochettes blocking the bladder? > > Hi. > > Can you tell me what IC means, please? > > I've finally realized that the on-again, off-again urinary symptoms I > experience are Lyme related, or Lyme itself. > > The good news is that whenever I experience the symptoms now > I take a product called Cran-Actin. It works wonderfully. I believe > the way it works is to smooth the cells lining the bladder. > > Symptoms I experience are the urge to urinate, then no flow. Or > sometimes, urinary urgency. While these could be considered a > typical issue for a woman of my age (58), the symptoms seem > always to arise when I am experiencing other symptoms in a > Lyme/co-infection flare-up. > > Dark urine is also a symptom that sometimes appears with a > tickborne illness flare-up. > > Hope this helps. > > Deanna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2004 Report Share Posted November 28, 2004 I tried Moducare when it first came out, it bothered me because it had soy in it. Then they changed it and took out the soy and used something " soy free " can't remember what is was. I still couldn't take the new one, it still caused bloating. I don't know if they cleaned the machines and got the soy off of them or continued using the same ones. I never tried it again after that. Carmen <migragurl@...> wrote: HI, it means Interstitial Cystitis. Means microscopic bleeding between the bladder walls. But I feel it's probably more the lyme bladder, and severe irritation of the bladder wall - similar but not the same. Symptoms are on good days, peeing twice per hour AT LEASt and on a bad day, by the minute.....I have to take some hectic meds to stop the pain and irritation as it feels just like a UTI.( urinary tract infection ) I get cloudy urine the day b4, and I suddenly crash into the worst depression. That is one sign I am getting sick. Weird. I also have bladder bloated feeling, bladder pain and spasms, , and shivers, hot flashes and insomnia. I tried Cranberry Capsules with little help unfortunately. Has anyone tried Moducare? Carmen > > > > Lori, > > > > I am about to undergo a cystoscopy ( for IC ) and desperately > want > > to avoid it. I doubt I have IC - and your theory is interesting re > > spirochettes blocking the bladder? > > Hi. > > Can you tell me what IC means, please? > > I've finally realized that the on-again, off-again urinary symptoms I > experience are Lyme related, or Lyme itself. > > The good news is that whenever I experience the symptoms now > I take a product called Cran-Actin. It works wonderfully. I believe > the way it works is to smooth the cells lining the bladder. > > Symptoms I experience are the urge to urinate, then no flow. Or > sometimes, urinary urgency. While these could be considered a > typical issue for a woman of my age (58), the symptoms seem > always to arise when I am experiencing other symptoms in a > Lyme/co-infection flare-up. > > Dark urine is also a symptom that sometimes appears with a > tickborne illness flare-up. > > Hope this helps. > > Deanna Questions and/or comments can be directed to the list owner at -Owner Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2004 Report Share Posted November 29, 2004 Carmen and all- I have not been on this board in a long, long time but have been here for 8yrs. I use Arginex and Cataplex ACP with bladder/urine problems and it works within a few hours!!! Arginex is a kidney detoxifier and is ALL natural (beet pulp and rice bran). It contains the enzyme arginase, which detoxes the arginine (which builds up in the kidneys as a by-product of protein metabolism). I know that protein and fat digestion are 2 of lymies worst problems. Cataplex ACP supports blood, epithelial, connective tissues and is used for general resistance for infections. Both are from Standard Process (Drs. sell them only, I do have them but this is NOT a sales pitch!!!). Arginex runs $24 and Cataplex ACP is $9. I have had tremendous success with my lyme clients with this protocol~~ It sure is cheaper and less painful on the body than surgery and is ALL natural. Just a suggestion. sue massie, CNHP 732 933-4011 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2004 Report Share Posted November 29, 2004 TY Sue - by the time I get through the waiting list I am hope my symptoms will have improved! Carmen > > Carmen and all- > I have not been on this board in a long, long time but have been here for > 8yrs. > I use Arginex and Cataplex ACP with bladder/urine problems and it works > within a few hours!!! Arginex is a kidney detoxifier and is ALL natural (beet pulp > and rice bran). It contains the enzyme arginase, which detoxes the arginine > (which builds up in the kidneys as a by-product of protein metabolism). I know > that protein and fat digestion are 2 of lymies worst problems. Cataplex ACP > supports blood, epithelial, connective tissues and is used for general > resistance for infections. > Both are from Standard Process (Drs. sell them only, I do have them but this > is NOT a sales pitch!!!). Arginex runs $24 and Cataplex ACP is $9. > I have had tremendous success with my lyme clients with this protocol~~ > > It sure is cheaper and less painful on the body than surgery and is ALL > natural. > Just a suggestion. > > sue massie, CNHP > 732 933-4011 > > > Quote Link to comment Share on other sites More sharing options...
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