*The following is an individual’s story of surviving fluoroquinolone toxicity. It is not medical advice. Please see the disclaimer at the bottom of the story. Thank you, and please be cautious with all treatments.
My Approach to Recovery from Levaquin and Avelox
December 29, 2010 at 9:46pm
As promised, here is part 2, what I did to try to recover, a little late. Sorry for the delay!
After I gave up on the mainstream medical establishment to cure me, I had to figure out what I could do with my rather limited resources and newly-won deep distrust of doctors. I did go to a few for diagnostics, but of course they couldn’t find anything except to note that my “inflamation markers” were up. Gee, thanks — I didn’t need a doctor to tell me I was feeling inflamed.
This is pretty much everything I tried to recover from quinolone antibiotics. Some of it is pretty off the wall, and none of it was horribly expensive, relatively speaking to some medical therapies. I think some of it definitely helped, as I saw a noticeable improvement right at or shortly after I tried it. Other things are harder to judge.
Did I recover because of the “placebo effect”? I don’t know, and I don’t want to. Maybe it was simply my time to get better. I tend to think they really did help me, although I’m perhaps biased. Your kilometrage will undoubtably vary, so please don’t consider this medical advice.
- Medicine
Since the day I tried to put my bottle of avelox through the wall (hurting my already aching elbow in the process), I haven’t taken any medicine except for a couple of tylenol for a really bad headache. Nothing else. Perhaps I’m judging the pharmaceutical industry harshly and overreacting, but it seems to me that meds either treat only symptoms, or end up damaging the body as much as it does the invading infection. This doesn’t seem like a good deal. And since this was my second nasty antibiotics ADR, I’m feeling pretty stupid for not doing this sooner.
Also, trawling up and down the forums at the now sadly defunct favc.info, it seemed to me that those who got better were those who avoided all western meds — and those who kept taking painkillers or other things stayed sick. I didn’t keep count, but this was my overall impression.
It is possible to live, and survive ailments, without the use of modern medicine. Our ancestors did it for millenia. We know a great deal more now about good nutrition and sanitation than they did, so why not? After floxing, I contracted pneumonia. I saw a couple of doctors, each of whom wanted to stick me with more antibiotics, steroids, and other nastiness. I ended up treating the pneumonia with little more than rest, liquids, and “alternative” herbal concoctions such as thyme, colloidal silver, iodine, osha, mullein root, andrographis, herbatussin, and other such things. (Full disclosure, this was the one time I used tylenol, but it honestly didn’t seem to help much.)
I tend to believe that, in spite of what the doctors told me, the quins do not leave the body of a floxie. Not quickly, anyway. That would help explain why we can experience “cycles” months or years after the fact. Quins are probably still lurking around in me. As a result I am determined to never take NSAIDs again — even over the counter ones such as Advil or Ibuprofen. Nor corticosteroids.
Nor any quinolone antibiotic. Except maybe in a life-or-death situation. Maybe. Maybe not even then.
- Magnesium
The most important supplement I took was magnesium. Quins apparently leach this out of your tendons and joints very fast, which is why so many floxies have had their achilles tendons snap. I don’t the quins attack these tendons more than others, but I think these have a tendency to such damage precisely because they are normally so tough.
To try to replace the magnesium, I did 800 mg of Magnesium chelate every day — not ordinary Mg, but the kind that is absorbed more easily. Basically, 200 mg with every meal, and then once at bedtime. Over time, as I felt better I tapered off. Excess magnesium can give you all kinds of intestinal fun — I used this as a gauge to tell me when I was getting too much. Excess magnesium makes me sleepy, too. Nowadays I take about 400 mg once or twice a week seems to keep down joint pain — but if I stop, the pain comes back.
- Ozone
I spent about a week scrubbing the Internet trying to find any story of anyone who had recovered from quins. I finally found one mentioned vaguely on a page that strictly speaking, didn’t exist. It took some effort to track down the lady in question.
When I finally did, she told me she’d had two experiences with levaquin. The first time was bad. The second time was in a life-or-death situation, and the outcome was far worse. She ended up in a hospital bed for three years fighting pain.
She wasn’t expecting any results when her naturopath convinced her to try ozone therapy. Also known as “ozone autohemotherapy”, or “major autohemotherapy (MAH)”, what basically happens is that they extract 250cc of your blood, inject it with ozone gas, shake it up so that the blood absorbs as much ozone as possible, and then reinsert your ozonated blood right back into your body. There is a filter on the intake line to ensure that no undisolved gas enters your blood. I studied the blood chemistry of this a little bit, and there are some good things that this can do to bolster your immune system. I forget details, but it had something to do with converting the ozone to hydrogen peroxide in the bloodstream, which is then used natively by the immune system to kill germs without harming you. It seems like a great idea for treating all kinds of ailments.
That said, it makes no sense to me that ozone would help after a floxing. But help it did. Slowly but surely, within six weeks of her ozone therapy treatment, all her symptoms vanished completely. She told me that so long as she avoids antibiotic-fed meat, she doesn’t even get twinges anymore.
I did ten rounds of MAH, going once or twice a week. After each treatment, I would get very sleepy, and be unable to stay awake very much for about 36 hours after the treatment. After I came back around though, my head felt clearer each time. The pain was a little less each time. And most measurably, my blood pressure receded not only back to my normal levels, but even lower. My pulse rate has always been high, between 100 and 110, but after floxing it was normally around 120. After ten rounds of ozone, it was 77. I was absolutely elated.
It was during the ozone treatments that my balance started to go back to normal, and I was able to reduce my use of a cane. And within six weeks, I started having days where I felt completely normal. Not every day — but normal enough to return to normal life.
This was the furthest “out there” treatment I tried. I researched it every which way I could. I could not find any evidence of any adverse reaction, aside from some folks who felt a burning, stinging sensation when the ozonated blood goes back in. I felt this on two out of my ten treatments, and I have no explanation for it, but it was bearable, all things considered.
- Deep Breathing
Since I had no explanation why ozone was working, I wondered if maybe all I needed was more oxygen. When the ozone gas is mixed in with the blood, the blood turns from dull rust brown to bright red, as hemoglobin is supposed to do in the presence of oxygen. I certainly wasn’t getting any exercise… Could just breathing more be at least part of the answer?
I think it might just be. I was able to leave off the cane completely within two days of when I started deep breathing. The pain, balance problems, and mind fog didn’t go away completely at that point, but the change was nonetheless pretty dramatic. I took the technique from a cheesy old Tony Robbins tape. I don’t know how much of what Tony says on the tape is pseudoscience and wishful thinking, but I followed it anyway.
The procedure is pretty simple. Breathe in, via nose, for a slow count of some number. There’s no magic to this, just as much as you can hold. I count to seven heartbeats before I’m full. Apparently Tony counts to ten, but he’s also roughly the size and shape of Frankenstein’s monster.
Hold your breath for a count of four times how long it took to breathe in. I count to twenty eight heartbeats, and Tony counts to forty, the freak. Tony claims that this is the optimum amount of time for maximum oxygen absorption.
Then, slowly exhale COMPLETELY through your mouth, for a count of two times the amount of time it took you to inhale. I can’t quite manage a count of fourteen, usually making it only to twelve or thirteen. I have no clue how Tony makes it to twenty except to speculate about an extra lung, perhaps in his chin. He claims that this maximum exhale stimulates the lymphatic system to flush wastes out of cells and eventually out of the body.
Do this between ten to thirty times per day. I like to do it while driving. The way I think about it, even if this has nothing to do with recovering from quins, it can’t hurt to try.
- Acupuncture
Some floxies recommended acupuncture for pain relief. I saw enough floxies recommend this that I wanted to try it too.
The acupuncturist told me that I probably wouldn’t feel any of the needles, as he was inserting them very lightly. There was unfortunately no truth in this advertising, not for me anyway. I was very sensitive to the needle insertions. There was one area of my leg, which he told me corresponded to my heart, that felt like he was shooting me with a .22 instead of a gently inserted needle. I screamed my lungs out! He said he’d never in his ten years of acupuncture ever seen anyone react to it like this.
That’s the bad news. The good news is that my chest and kidney pains, which had been worring me a lot, cleared up. Immediately.
They came back again, although less intensely, and I went back for another PAINFUL round of acupuncture. These particular pains vanished and have not come back to this day. I’ll reluctantly go back again if I need to, but so far, so good.
Some of the other pains that the acupuncturist worked on were completely unaffected. YMMV.
- Diet
Per what I saw on favc.info and other places, I cut out all soy. This is harder than it sounds. Soy lecithin is used as a bulk filler for almost everything, including vitamins. It’s packed in everything, including canned tuna. Stuff I thought was good for me turns out to be full of soy. Crap!
Due to one of the supplements I was taking, I also had to cut out all gluten. Wheat, rye, barley, and processed oats were off the menu. So was all forms of sugar. Oh, and peanut butter. Giving up peanut butter is HARD. I also had to cut out dairy.
It should go without saying, but antibiotic-fed meat was also verbotten. No chicken produced in the US is fed with antibiotics, so this was pretty much all the meat I’d eat. From time to time I’d eat Chipotle, whose pork is antibiotics-free, or I’d get that kind of meat from Publix. I ate a lot of eggs.
No processed food, so far as I could tell. If there was something freaky in the ingredients list, I skipped it. Also, no caffeine or alcohol, although this wasn’t really a change for me.
I drank a lot of water. I tried to take a couple of tablespoons of apple cider vinegar twice a day. I stuffed as much fresh vegetation down my gullet as I could stomach. I tried to think of food as just fuel, not something to be enjoyed. I never cheated on this diet.
The last time I tried this kind of diet, long before floxing, I lost 40 pounds and felt fantastic. This time, I lost no weight and felt like crap, although possibly less like crap than I would have had I not done this diet.
Unlike many floxies, I have no food allergies. I’m eating anything I ate before I was floxed. I think this might be because I went kind of nuts on this diet and avoided all these foods for several months.
- Other Supplements
I read somewhere online that vitamin C can bind to quins and help remove them. Since I’m of the belief that the medical literature on quins are frankly AFU, and that the stuff can stay in your body for a long time, I started taking a LOT of vitamin C. I took 10,000 mg or more of C per day for several months, spread out in three doses. Since you are supposed to combine C with vitamin E, I also took 400 iu of the latter twice a day.
Many floxies report that they’re low on vitamin D. I was already low on D; a doctor actually found me low enough to give me a vitamin D injection a couple of years back, and told me that no amount of sun would probably be enough to get me up to speed. Since floxing, I’ve taken 4-5000 IU per day of D3.
I’ve taken a lot of B-complex for a couple of years, for its antidepressant qualities, four or five times the normal quantity per day. After floxing, it stopped being an antidepressant whatsoever, but I kept taking it anyway in the hopes that it would help mend my nervous system.
I took two different brands of acidophilus, a double dose of zinc, and a multivitamin.
A nutritionist put me on some detox stuff. There were three little bottles, one for liver detox, one for lymphatic detox, and one for kidney detox. I have no idea if they worked or not, but I took them in combination with a specialized non-dairy, non-soy protein shake. This was the stuff that gave me all those dietary restrictions above, but I decided the restrictions were healthy for me anyway, so no harm done.
- Sunlight and Exercise and Rest
A lot of floxies reported nasty reactions from sunlight, rashes and weird subcutaneous streaks. On the rare occasion I got some sun, I also saw that my blood vessels became very visible and almost blue. It was freaky. I avoided the sun all summer long instead. It sucked.
It should probably go without saying, but I avoided all exercise. Not that it was hard to avoid. I was in a lot of pain, pretty much constantly. Moving was not a temptation. All in all, when I wasn’t sleeping, I was resting and trying to avoid any kind of stress. It was not easy on the people around me.
- Dealing with Idiosyncratic Complications (maybe just me, Your Mileage Will Definitely Vary):
Eight months before I had my reactions to quins, I had a different reaction to a different antibiotic, amoxycillin. Now, I’ve had amoxycillin many times over the course of my life and never had a problem before, until November 2009 when I had an ear infection. After taking this med faithfully for a week or so, my stomach became horribly inflamed to the point where anything even remotely acidic — like a slice of tomato, for instance — felt like I’d just injected Tabasco directly into my tummy. Doctors diagnosed me with a range of ailments, each worse than the one before it, before they gave up on creative guesswork and settled on a probable cause of “antibiotics ADR resulting in acute gastritis”.
Basically, they treated me as though I had too much stomach acid, and gave me medicine to suit. Unfortunately, they never checked my stomach acid levels too see if that was in fact the correct diagnosis. As it turns out, this is a relatively painless and easy test, called a gastrogram. You swallow a pH sensor with a little transmitter, measure a baseline, swallow some sodium bicarbonate, and see if your stomach acid counteracts this.
As it turns out, the symptoms for too little stomach acid are identical to the symptoms of too much stomach acid. They treated me for the wrong damn thing.
One of the very few doctors I do trust speculates that it was the antacid medicine that somehow screwed up my body’s ability to make its own stomach acid very well. In any case, a lack of stomach acid can keep you from processing much of the food you put into it, and extracting nutrients such as protein, or even magnesium.
As a result, the most important non-flox-related supplement I now take is an HCl tablet. I take two with every meal, and I take care to take one every time I take a Magnesium tablet. I mention this here because I think that possibly the reason I felt the effects of the quins so strongly was because perhaps I was already magnesium deficient, from months of poor digestion. I might not be the only one. And possibly taking the HCl tablets along with the Mg has helped to get that mineral where I need it more quickly and efficiently. It was an integral part of my recovery regime that I put together, and I still take these tablets with every meal.
The deeper point here is, try to be aware of what else might be going on in your body that is different from others, and try to see if it is somehow related to your flox issues.
That’s it. If I recall anything else I tried — possible, since my memory of that period is really fuzzy — I’ll tack it in here. Meanwhile if anybody has any questions please feel free to post.
** The story above is truthful, accurate and told to the best of the ability of the writer. It is not intended as medical advice. No person who submits his or her story, nor the people associated with Floxie Hope, diagnoses or treats any illness. The story above should not be substituted for professionally provided medical advice. Please consult your doctor before trying anything that has been mentioned in this story, or in any other story on this site. Please also note that people have varying responses to the treatments mentioned in each story. What helps one person may not help, and may even hurt, another person. It is important that you understand that supplements, IVs, essential oils, and all other treatments, effect people differently depending on the millions of variables that make each of us unique. Please use appropriate caution and prudence, and get professional medical advice.
Thanks for sharing Bill, and sry about your plight. Lots of good advice in both your Part 1 and part 2.
Wa wondering how many people above or in this entire Forum have been tested for a Genetic born mutation called Ehlers Danlos Syndrome all types??? Seems to me all the
things that help like vitamin C large doses plus Vitamin D3 & Magnesium are all used in patients diagnosed with Ehlers Danlos Syndrome ir is also related to Syncope and/or
P.O.T.S. plus some can have Chiari and/or Stenosis numerous complications involved it could be that antibiotics make EDS worse…See Wikepedia Ehlers Danlos Syndrome I am
now awaiting to see if I will be tested by a Geneticist soon it is a chronic condition type 4 is the Vascular type…Some have attached ear lobes some have thin upper lips some thin
noses some with small ears with lobes…Hypermobility some are stiff most have elasticity skin they used to call this ‘rubber man’ illness it runs in families passed on from Mother or
Father…It may not be the medicines it could be your genetics that makes one unable to take these medicines…Some say radiation which has not yet been proven as ‘Replicated Science’ *Anything is possible until proven/replicated until then everything is presumed…Remember this ASSUME has 3 words…
Genetics almost certainly plays a part in why certain people are more affected by FQs than others. For example, under-methylation due to MTHFR mutations (among many others) comes to mind. But this doesn’t necessarily indicate EDS. All of these conditions: Lyme, EDS, CFS, Fibromyalgia, FQTS, etc are difficult to diagnose and can masquerade as other conditions. So I suppose that EDS is one of the many difficult-to-impossible to diagnose syndromes that might explain the symptoms that floxies have. You’ve posted numerous times about this in this forum and I’m not sure what you’re hoping to achieve by continuing to do so.
Great info. Lucky me I ran across your website by accident (stumbleupon).
I’ve saved as a favorite for later!
Bill: Your writing is beautiful, and your story, incredible! Thanks so much. Diet rules! What we put in our system is how it functions, oftentimes…for most ailments, diseases and illness anyway. Many thanks, once again, and nothing but a road of health and feeling great ahead, for you, friend.
Hi Bill,
Not sure if you still come here or not. I was recently floxxed in July and your story seems to be the only one on here to do with Avelox. I too took Avelox and am experiencing the symptoms you describe.
I wanted to ask you about a particular symptom to do with my vision. Basically it feels as though my eyes don’t line up straight. When i read or look at the TV my vision is very weird and I cant stand to look at it. Which is really bad as my main job involves computing all day and I loved to watch the tv and play games as a hobby and now i cant even look at the screen,
If I look at a person or try to have a conversation i can focus on a persons face but the surroundings appear all trippy blurry and spaced out, making me feel really anxious and uneasy.
Did you or anyone else that still comes to this thread experience these symptoms? Did they ever go away.
How is Bill as of now
Hi Bill. I read your story and was wondering how many days past getting floxed did you start taking ozone.
Im rather skeptical about the ozone in this scenario as reading through literature it seems quinolone toxicity is mediated by free radical injury and ozone means a lot of free radicals. Thats why it seems anti oxidants play a role in relieving side effects.
Id think it may work fine much later if you have detoxed the quinolones from your system with tamarind or any other way.
I think i may have developed quinolone toxicity with very miniscule doses of oflox as i was on ozone for other health issues already.
If ozone truly is the answer i should not have developed symptoms while being on ozone already.
I worked as a pharmaceutical chemist for 20 years. I will not touch most pharmaceuticals or any Western meds which are OTC (over the counter). I know too much. The industry is completely corrupt and the FDA and AMA are all one big happy family with Big Pharma. They lies about so-called “side effects” (I call them unwanted toxic effects). If you keep your bodies in balance with TCM (Traditional Chinese Medicine) and/or Ayurveda, you won’t experience “infections”. Even if a body does have an infection, there are way more effective ways to deal with it than anti-biotics. By the way, anti-biotic is a fitting terms for these poisons. Biotic refers to living things, so anti-biotic is against living things anti-life!
Bill, So I had a terrible reaction to cipro in 2013. Lots of cns issues, headache, panic, heart palpitations. Vertigo, brain fog, week, feeling hypoglycemic etc. symptoms slowly got better. Then I got pregnant and had a boy in 2015. No issues while pregnant. Ffw to now. October 2016 pinched a nerve and took prednisone and Advil. November, almost exact 4 weeks after those old feelings are back!!! I’m so bummed. Could the prednisone cause a relapse?? I’m so angry.
Bill, Can you please describe your balance issues but very preciesly, because i am experiencing bug balance and keeping straight problems, like i am in a boat feeling all the time, when i walk, stand upright. please how you managed the balance issues?
hello,
I ve been floxed 10 years ago with Izilox. I recovered then felt again with food containing quinolone. I tried to detox with glutathion but all came back, maybe too much release or a problem of evacuation because of cytochrome p450.
I will tell you what i did to recover and it ‘s working even if i m ‘not 100%, i can live like others except avoiding sports but will be possiblle after the healing process.
-First you have to limit the oxidative stress with anti-oxydative. I take quercetin(2g per day) and it ‘s fantastic. It reduces oxydative stress but also bind to the same site of FQ so they can ‘t less affect your body even if in it.
– Vitamine C at high dose is also a key of healing process, it helps detox and participte to the building of collagen via the hydroxylation of the proline which is an important amino acid in collagen and studies shown that quinolones affect the hydroxylation of the proline and that can be a really important part of the side effects felt by people because if collagen is poor or bad quality, it leads to desease like floxed have. Of course you can take collagen alone . i wanted to take hydroxyproline directly because your body can ‘t do it like before but each time i tested collagen from animals, i got a rollback so i stick to amino acid now.
-FQ affect the mitochondria and lead to a lack of atp. you have to boost your mitochondria replication because floxed cells are non efficient and you have to replace them. For that you have to take PQQ, vit B3 (niacinamide).
-You also have to protect your cells from quinolones and R.O.S. Vit E and resveratrol have shown to protect the cells.
So , to feel better you have to take:
– Vit. C, E
– Quercetin
– PQQ
– niacinamide (vit B3)
– l-proline (collagen if you have non contaminated source)
– resveratrol
very important. You have to take activated charcoal in cure of 15 days ( because everyday it lead to insufficiencies because activated charcoal absorb the good and the bad,4 hours minimum after supplements) because studies have shown that the fq are widely evacuated by the bile .
I hope my message will help some people and if you have others tips to give me, it will be welcome.
I am a 46 yr old nurse , I’ve been struggling since March 2018 after taking Cipro and Avelox, I’m about to give up hope , I started ozone on 7/28/18. My legs spasm now arms since the ozone Tx if u would please reach out to me . I am taking mag along with vitamins every day . I’m so desperate for help
Dear Bill, I am Dan Jervis, the last one on the long list. Would you please consider sharing your story to CBS 60 Minutes? 60m@cbs.news.com
OUR STORIES NEED TO BE HEARD, Dan
Where did you go for the ozone treatments?
Bill, could you give us an update of how you are doing? I have the same massive increase in hunger, what did you find helped that? Thanks.
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