Ciprofloxacin and lyme disease

Common Questions and Answers about Ciprofloxacin and lyme disease

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Lyme disease symptoms may come and go and late disseminated Lyme disease may present with muscle and joint pain as well as abnormal muscle movement, muscle weakness, numbness and tingling. If the symptoms persist, further evaluation may need to be done and additional diagnostic tests may be done. Seeking another urologist's opinion may also help. Take care and do keep us posted.
My dr seems to think I have Lyme disease and began treatment since Aug 2013 for Lyme disease first treatment was 3 months and I began to feel better. The fatigue never left though :((. About amonth later began having more symptoms some similar as before and new ones(very debilitating ones). I was put back on antibiotics for 2 months with dbl the dosage as first treatment. Did not feel better some symptoms were not as severe but still present.
Treatment for Lyme is much longer than for other, more usual bacterial infections, because bacteria are most susceptible to antibiotics when reproducing -- and Lyme bacteria, like the bacteria for tuberculosis and Hansen's disease (aka leprosy), have a very very slow reproductive cycle and have to be hit over a much longer period of time than the typical sore throat.
The psychopathogenesis and aporology of a new "Medically Unexplained Symptoms" Syndrome. Environmental Health Perspectives 110:607-611, 2002. Rusk MH, Gluckman SJ. Serologic testing for Lyme disease. When—and when not—to order, and how to interpret results. Consultant 38:966-972, 1998. FDA Public Health Advisory: Assays for antibodies to Borrelia burgdorferi; limitations, use, and interpretation for supporting a clinical diagnosis of Lyme disease. July 7, 1997.
_________________ Babesiosis As with other co-infections, there is a lot of overlap of symptoms between Lyme disease and Babesiosis. An accumulation of the following signs and symptoms probably warrant testing and/or treatment of Babesiosis: ___Chills ___Fatigue and often excessive sleepiness ___High fever at onset of illness ___Night sweats that are often drenching and profuse ___Severe muscle pains, especially the large muscles of the legs (quads, buttocks, etc.
com/viewarticle/423236_2 [That excerpt is talking about doxy and anthrax---- not Lyme disease. But I've seen where some Lyme doctors do rx doxy in lieu of Cipro when the patient refuses to take Cipro or can't afford it.] All I know is that I'd never willingly take a fluroquinolone again.
Lyme, mono, STD, CBC, prostate, etc. and they all came back normal. I get weird zaps in my arms and legs which i'm guessing is nerve related. The sciatic leg and back pain has pretty much ruined my life. I used to jog and mountain bike and can no longer do that, and am struggling to get through days at work. Just when I seem to be feeling better I get run down and the symptoms come back again.
I was put on antibiotics - in the end I had courses of amoxycillin, ciprofloxacin, and then a month of doxycycline (GP was concerned I may have Lyme disease and test was not back yet). Over the next 4 months I continued to have all these symptoms. I would feel well for a couple of days and then terrible again for about a week (sometimes having to take to my bed). Over the past month the cough and sore throat have subsided mostly.
Also I have tried, salycylic shampoos, tar shampoos, jojoba oil, AND nothing seems to help. Please help me and my hair. I am a busy college student, who unfortunately does not have the time and money to deal with this.
It's a disease commonly found along with Lyme disease, and can be transmitted either from ticks or scratches from cats or other animals. It's common and can be a very stealthy disease until provoked by certain antibiotics.. and it is notorious for vision/eye problems. I have both Bartonella and Lyme, and I experienced the exact same flare of symptoms you described, but from a different antibiotic (completely different class). It isn't the antibiotic itself, it's because of the infection.
Some of my symptoms over the last 18 months are; sciatic like leg and back pain, itchy legs and genitals, rashes and little red bumps on my thighs, perineum pain, stomach pain, cloudy, concentrated and foamy urine, frequent urination, dry mouth, itchy eyes, tinnitus, groin and armpit pain, and more. I have IGG tested for herpes at 5 months, 9 months and 12 months, all negative. A herpes swab of one of the bumps which was negative. Negative gonorrhea, chlamydia, Hiv, syphilis, Lyme, mono.
He believes that a lot of neurological signs and symptoms are related to Lyme Disease. I read that you have been tested for LD, but according to a lot of the experts out there, a negative test doesn't mean that you don't have Lyme, it's just not in the sample that was tested. I looked into going to see Dr. Klinghardt--he has quite a waiting list (6 month, I believe) and is fairly expensive, but he may be worth it if he can provide answers.
So there is that connection again between the immune system and flare ups of MS Now ciprofloxacin is an all-purpose antibiotic and the word hasn't yet gotten out. So I tend to see a lot of patients whose MS begins when they're being prescribed something like Cipro. Is this true for the other floxacins? There are cousins of Cipro that are available, there's oxfloxacin and levofloxacin. We're not sure yet, but if I had MS I'd avoid any drug that had the word floxacin in it.
Allergynerd, I hate to use Youtube as a link, but the International Lyme And Associated Disease Society had a 2011 conference in Canada and someone put videos on youtube. PLEASE, search for 2011 ILADS Conference-Dr Horowitz -Updates on diagnosis and treatment. There you will find him talking about Babesia and Bartonella species that they have never seen before and no tests had been developed for them, so people test neg on Bart and Babs.
Just as an example, fluoroquinolone antibiotics (ciprofloxacin, marketed in Spain as Baycip and with more names, levaquin, floxin, tequin) cause permanent and irreversible neuropathies in severe cases, and very systemic neuropathies that mimick Lyme, Multiple Sclerosis, Gulf War Syndrome, Sj
These didn't help, I then started to develop other symptoms, ringing in the ear every day to this date, pins needles in hands and feet and muscle twitching all over my body. If I sneeze or close my eyes up tightly and re open my eye twitches everytime uncontrollably.
I have noticed the same thing today..Can't remember it happening before today...I do have high bp and NF(tumor disease...use yahoo and enter NF and tumors if you are wondering "what is NF?"..
Basing on yours and my experiences I figure out that this kind of disease tends to move from the genitalia to another organ... the brain! With this i don't want to hurt anyone but i just want to express this impression i have that the persistence of symptoms and the misdiagnosis (I'm of the sector and i can tell you that doctors are just unable to say "I don't know what is happen to you") could lead to an obsessive mood.
I have thought about shingles since I had this two years ago, but I should still have some immunity and I have no skin blisters or anything else. I have also considered Lyme and other tick borne diseases as well as a spider bite, but the symptoms aren't typical. I think these are most likely. I will see my doctor by Monday if this continues. I am wondering about mold, fungus, parasites and viruses. I very much doubt this is neurological and a disease such as MS.
think about the next scared 15 year old kid who all of a sudden has this problem and doesn't know where to turn, he may never think to look on the internet for our posting of the cure, so it is OUR job to spread the word on how to diagnose, treat, and cure this disease. It is our job to make sure the medical community sees that these symptoms ARE POSSIBLE, etc.
I just stumbled across this site that looks to have a potential diagnosis/solution. (www.hillderm.com/skin-disease-treatments/itchy-ears.shtml) They call it Chronic Eczematous External Otitis and recommend prescription ear drops called DermOtic Oil. I have no idea how good the info is, but I'm going to check it out. I'm also going to look into the food allergy idea, as I'm the type that wants to know what caused this in the first place.
Kissing, breathing etc can all transmit many things flu, kissing disease and many others.. Though immune could be down etc and your stress levels high can have created a cocktail of symptoms etc.. Relax yourself fully and work it out ,though if you have had something bad happen prior to all these symptoms like a break up, loss of job etc consider this aspect ... See a counsellor. Hope this helps I am no doctor just telling you what I did when came down with many of the above symptoms..
So does celiac and Hashimoto's (low thyroid), and celiac and Addison's Disease (adrenal glands). Do a Google search for JFK and celiac-- there's convincing evidence he was a celiac with Addison's. I am very familiar with this association because I'm close to someone who has celiac, lupus, and diabetes, all autoimmune issues. Just because you have one doesn't mean you'll have the other. But it can happen. Your body is fighting against itself and all sorts of wild things can happen.
Hi Everyone. This is my first post. I started having problems about 5 years ago. It was occasional problems such as mild sinus pain/pressure and headache with mild eye strain. Each year it has gotten worse. Over the course of the past 5 years I have seen multiple doctors across different specialites: Ears, Nose & Throat, Neurologist, Allergist, and my Intern. I have had MRI's and CT scans. This year has been the worst so far. I have already gotten 2 sinus infections.
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