Guest guest Posted May 13, 2002 Report Share Posted May 13, 2002 Jim, If you aren't feeling relief, it would be my experience that you 1) don't have LD, 2) aren't taking a high enough dose (I know it sounds crazy). A doctor who is quite famous and active in the LD community likes tetracyclines the best against LD. And he would know. Why you are getting no relief?....good question. Before you change the regimen, try taking a blood test for the level of theraputic agent in your blood stream... Personally, I feel that Zithromax is very effective and provides all symptom relief in two hours with them never returning again if taking the correct dose (takes a few days/weeks just to get that dialed in). I take over 5gms per day...normal folk don't need that. Good luck! -Jeff L. --- naturefreak2002 <naturefreak@...> wrote: > Hi, > I have been taking tetracycline 500 mg t.i.d. for > the past three > months with no improvement. Has anyone out there > had success with > tetracycline? If so, how long did it take before > you started seeing > improvement? Was it hard on your gut and gut flora? > My gut has > barely tolerated the tetracycline the last few > months, and only by > taking MASSIVE doses of beneficial bacteria. > > My doctor is about to switch me to a combination of > Biaxin > (clarithromycin) and Plaquenil (hydroxychloroquine) > and I was > wondering if anyone has had any experience with this > combination. If > so, did it work for you? How long did it take to > see improvement? > Did you have any adverse effects? How hard was it > on your gut? > > I would REALLY appreciate any input on the above! > Thanks! > Jim > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2002 Report Share Posted May 13, 2002 Hi, Are you seeing Dr. D? This is often his protocol. The tetra I was on for 4 mos helped my brain fog, but did little else. I have found the biaxin/pla'nil combo to be the best-working one (I had also tried erithro + doxy + pla'nil). The biaxin brought out some of the Lyme symptoms (esp chest pain!) so I knew I was having a herx sometimes. And I'm better on it now than I was before I took it. (note - I had aso tried IV Claforan but couldn't tolerate it - not just a Herx but some neuro-toxic reaction that had the vertigo, etc., at intolerable levels -- so we went back to oral abx). As far as the gut thing - my nutritionist recommends a probiotic sold by Culturelle (they have a website, and I don't own stock in it LOL). I have not found the Biaxin to mess up my gut. (And, boy, the Claforan sure did!) So, I think there's reason to be hopeful. You might eventually want to pursue IV abx if you haven't already, but they also pose some risks. Some docs now use Claforan instead of Rocephin bec. Rocephin can affect the gall bladder. But claforan was really rough on the gut. Good luck. My sympathy. Feel better. Sincerely, Marie ill since 1994 dx'd CFIDS Dx'd w. Lyme Dec. of '99 by Dr. D. and improving and working on my degree Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2002 Report Share Posted May 15, 2002 Hi Jim, I'm a believer that, if you have gone through several cycles of the spirochete without losing at least one lyme symptom it is time to switch abxs. In my opinion I think, switching abx is important, if you aren't improving. What's to say you don't have a strain that can't be killed off by Tetracycline. Go for a new combination, stick with it for awhile, and if you don't see improvement, then move on.............One type of abx doesn't work on everyone...........We all react differently to medication, and there are many different strains of bacteria. Different abx kill of different bacteria, so until they can isolate every single lyme bacteria, and find the abx that can kill if off...........I think switching abx is a good treatment plan............it sounds very trial and error..........but from the cured cases I have heard about, including myself, there was no one abx that worked the best!!!!! Personally, I would got ahead with the new treatment plan. Conniek nwnj Leave no stone unturned.......and ask questions! If the answers don't agree with your gut feelngs or your research, ask more questions or see another Dr !! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 21, 2002 Report Share Posted May 21, 2002 Hi Jim, Sorry it took so long to reply. I was never on Tetracycline, but my very first treatment upon the discovery of Lyme's (after 5 yrs) was 6 weeks of Biaxin. I did great on it, but then symptoms returned about 4 weeks after I stopped it. I was then referred to LLMDs for IV Therapy. The Biaxin did not bother my stomach, but I do know it can be very hard on the stomach & some people can't tolerate it. As far as the Plaquinil, the LLMD wanted to give it to me since I continued doing poorly, even after the IV therapy. You must have an extensive eye exam prior to taking it. I was on it for a short period, but then got very sick, symtoms worsened & since I didn't know whether I was sick from the Plaquinil, the Lyme's, or whatever, I chose to stop taking it, so I can't help you out much there. I do beleive Biaxin has helped a lot of people if you can tolerate it. Hope that helps! Jeannie --- naturefreak2002 <naturefreak@...> wrote: > Hi, > I have been taking tetracycline 500 mg t.i.d. for > the past three > months with no improvement. > > My doctor is about to switch me to a combination of > Biaxin > (clarithromycin) and Plaquenil (hydroxychloroquine) > and I was > wondering if anyone has had any experience with this > combination. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2002 Report Share Posted May 24, 2002 How long were you on the IVs? I have late neuro lyme and been on IVs 4 months and herx pretty bad. my legs are failing me and my lyme doc thinks plaquenal would help damage to my immune syatem.plus I was on steroids bad move which makes lyme harder to treat. Do you think you have improved on IVs and if so how long were you on it? patty Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2002 Report Share Posted May 25, 2002 Patty: I am on IV rocephin and I am experiencing high fever for the first time in 5 years. My normal body temp is 96.2...today, I was in a deep sleep and sweating and lately I am sweating through the nights...I wonder if my natural killer cells are beginning to kick in or if this is a sign of another coinfection. I have headaches every day and seem to herx most every day if that's possible. This is my second go around with rocephin but the first time I was placed on flagyl and zithromax and doxy....I think I decompensated with so many meds because I ended up in the hospital for a week with pancreatitis and cholecystitis that the ER doctor saw my liver enzyme levels and told me he had never seen levels as high as mine. I hope and pray the rocephin helps me into remission. I have lost my kid's adolescence and two will be in college and oldest is almost 30...I just hope to be well enough to be there for my youngest who will begin highschool soon. God bless, Donna Quote Link to comment Share on other sites More sharing options...
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