*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.
On February 8th, 2014 I made a fateful decision that would change my life. I took a fluoroquinolone antibiotic called Cipro. I was having frequent urination at the time and thought that I might have a urinary tract infection. I went to my primary doctor in the morning and was waiting too long so I left. I went to my local emergency room later that evening. They took cultures and swabs and gave me zpak, cipro and pyridium. I took them all at the hospital. I should have known something was wrong that night because I had what seemed like a fever and tossed and turned all night. I was being poisoned. I didn’t connect the dots and took two more doses the next day. I felt dizzy that day but never connected anything to the Cipro. On the second morning I did a workout with weights but felt weak and actually pulled a muscle with light weight which never happens to me. I went to work and was having trouble seeing, as the lights were blinding me, and I was exhausted. I then realized that something was going wrong with my body. I looked up the side effects of Cipro and went to the emergency room. By the evening my shoulders and achilles tendons were beginning to feel sore. I discussed this with the emergency room doctors and they dismissed my concerns and just told me to stop taking the medication. I had taken four 500 mg pills of Cipro total.A day after stopping Cipro, my triceps tendons became so painful that I had to sleep with ice packs on them, they felt like they were going to explode. This felt all wrong, I knew something was off. I sneezed and threw out my back. I stopped working out because my body was killing me. My tendons began to feel like they were going to break. I felt something was wrong mentally as well. It was like I lost all of my happiness and could not concentrate. Ten days after Cipro, I decided to try to workout…that maybe this was all in my mind. I began to do some lat pulldowns and while warming up I pulled my bicep tendon so severely I could not move my arm. I then re-injured my back and was now out of work. Then the peripheral neuropathy began. My legs, arms, hands, and feet began to burn like a cold fire. Muscle twitching all over my body. I developed a rash on my groin, white growth on my tongue. Insomnia, anxiety, crying, vision problems, weakness. Most of my joints and tendons hurt me. Achilles, back, triceps shoulder, knees and hands. Burning tendonosis. Ulnar neuritis. Chronic fatigue was awful. I slept most of the day. I could not enjoy anything. I stopped listening to music or watching movies. I began seeing doctors and lots of them. Orthopedics, MRI’s, X-rays, no one could tell what was wrong. They tested me for lymes disease, MS, ALS, etc, etc. and it all came back negative. Not one doctor would admit or believe me when I told them that I believed the Cipro poisoned me and I was having fluoroquinolone toxicity. I went to physical therapy and slowly the back pain declined. I still had neuropathy and tons of tendon pain. I was taking all the supplements imaginable, every day. I started eating more. Six weeks after Cipro poisoning I began to force myself to do rehab exercises everyday in pain. I started walking in pain and doing simple band exercises. My steps felt like I had dead legs and feet. My muscles shook like I had epilepsy and couldn’t control them. During this time I developed strange bruises on my calves and arms. I slept in the sunlight outside during the day to increase my sunlight exposure. I increased my magnesium and took magnesium oil and epsom salt baths. I prayed and prayed. I had been out of work for 3 months during this rehab time. Three months of my life gone, trying to fix myself with a desperation I had never known, longing for my old life back and regretting all the times I took for granted my health. I read the FloxieHope stories every day even waking at night to reread them and tried to give myself hope. They were the only thing that kept me going when I thought I was going to die. I joined all the FQ boards and was on them religiously for awhile. I spoke to others who had recovered and read their stories daily.
I finally went to the neurologist and found out that my nerve velocity was abnormal, which was indicative of a damaged myelin sheath.
I had glutathione IVs which gave me instant mental clarity. Almost like the veil or cloud was lifted from my brain. I did this twice. I think I should do it more often. I did acupuncture and massage therapy. Acupuncture seemed to give me some much needed pain and anxiety relief. I prayed a lot during this time and renewed my spirituality.
This is a brief synopsis of the hell I lived because I can’t and don’t want to remember all of it.
It is now eight months after I took my last pill of Cipro. I have had a lot of up and down cycles. I still go through them but they seem to be much shorter in duration. The problems I still have are lessened. They decreased incrementally. I have some tendon flare ups, I have knee discomfort and some back pain. Occasionally I will get a dizzy spell or have a forgetful moment where I can’t remember words. My supplementation right now is:
vitamin c 1000mg
vit d 2000mg
b complex
coq10
alpha lipoic acid
acetyl l carnitine
l arginine
glucosmine chondroitin
collagen
magnesium oil 600mg
magnesium oxide 500mg
vit e 400mg
lots of whey protein
Within a few weeks of being floxed my IGF-1 levels skyrocketed to over 400, which was double my normal level. I believe that my body sensed the cellular disruption and began a reboot, trying to increase growth hormone in the blood stream and start up normal cellular function including tendon repair and cellular repair. My thyroid went off line and now I take armour thyroid which has helped my energy levels tremendously. Somewhere along the line I had to make a choice to stop living my life in fear. I lived every day in fear, and still fight it every day when something flares up. I had to truly not give a fuck, because I knew that if I was going to win this fight I can’t be afraid to fight.
Today I can sleep with no problems. I workout with weights three times a week. Sometime I go very heavy and sometimes I go lighter for lots of reps, depending on how I feel. I squat, bench press, and train back, shoulders, and arms. I do cardio and rehab another 3-4 times a week, this consists of sled dragging, sledgehammer swings, forearm, back, ab, and rotator cuff work. Whatever I can move I train it. I have a lot less pain. I returned to and enjoy my hobbies again. The neuropathy is only occasional and lasts for a few minutes of burning or what I call hot needles, but is still scares me. I can laugh, I can be happy. My energy is returning. My libido is normal. My good days far outnumber my bad days. On my bad days I retreat to my support system and try to regroup and refocus then reattack. I eat tons of antioxidant rich foods. I avoid processed foods and sugar. I stay away from medical doctors, and am now truly an active participant in my own health. I consider this not a recovery story but a progress story. I know that things take time to heal, I am healing. I know you have to believe, you will get better. I may have setbacks to come but I’m not done fighting. Neither should you.
** 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.
Oh OK great I apreciate the quick response I will have to try those ideas. I also plan on getting some vitamin IVs done and the glutathione I heard good things from that .as far as other symptoms go. It was mostly my Achilles tendons that were the worst hit. With crazy pains and could barely walk .now it’s a lot better .it took a lot of work tho. But still get flare ups . Lots of rest ,ice , magnesium suplements , float tanks , and laser treatment from the physiotherapist. There was articles with her laser treatment that talked about healing cipro related damage . So it’s worth a try if anyone never heard of it.
and the high dose vitamin C IV (the one you will need a blood test for—a very small percentage of the population cannot do the high dose c) is good for rebuilding collagen
Thankyou for your positive and encouraging story! Mine is similar with tension and ligament issues due to levaquin. Praying for you and all of us to recover . Karon
Nick – are you still checking this site? Since you’re a weight lifter, I was wondering if you had tried Creatine? I’m a little over 1 year out from being floxed, and started lifting again and tried HMB and Creatine. Historically, when I had used them before, HMB had a positive effect (reduced soreness) and Creatine had zero effect, so I quit using it. This time around, HMB worked as expected, but Creatine also had a big impact. I was having problems with fatigue and low energy and the Creatine seem to give me a lot of energy. Surprising to me! I tied it again because of an article I read about it’s impact on mitochondria. Of course lifting also increases the number of mitochondria, so may have been a combination. In 1.5 month I went from arms shaking doing bench with 135 lbs, to do a set of 3 with 300 lbs. On the down side, I torn something in my chest, so got an MRI today. I guess because of the floxing, I’ll have to work with lower weights, higher reps in the future. Anyway, I was just curious as to your experiences with any weight lifting supplements, and was wondering how your lifting was going.
so happy you are getting better nick. I took this demonic piece of garbage drug a month ago. It gave me insomnia for 4 days straight I was on the verge of hallucinating. I still suffer waking but go back to bed. My family doesn’t believe drugs given by doctors can do damage but cipro did for me. ***I have an auto immune disease that gives me UTI’s . I got my thyroid removed 10 years when I was 14. I am now on thyroid meds for the rest of my life. I am on synthroid the synthetic kind and switching over to the natural asap because I believe non natural drugs create auto immune problems.*** After this demonic drug cipro, i now have very bad vision. I uses glasses but now I cant see out of them. My eyes are dry as fuck now and my eyes are blood shot red. I use coconut oil to lubricate them. The drug definitely fucked up my eyes. I can no longer use contacts and now am trying a new diet; no hormone injected dairy or meat. I stopped eating bread. i make smoothies every day veg and fruit. do not add juice thats fake sugar just water. I supplement with fish oil, vitamin D, calcium, magnesium and vitamin c. I tried Chlorella for a while but it was making me have diarrhea due to …I believe interacting with my thyroid meds. Chlorella is a seaweed that detoxes medals and chemicals in you and contains many vitamins and minerals. I am going to also try flax seeds soon in my smoothies. It has been a month out post demonic cirpo and my wrist started hurting yesterday. I refuse to use NSAIDS because they will damage the body even more. I will never touch a lab made antibiotic again. My nurse literally told me I am making my side effects up and that cipro has no side effects. Please let this be a lesson to others to research the drug before you use one . I made the mistake of 3 days 500 X 2 day of this crap to alter my life. Don’t say it ruins your life because that gives it energy. God is good remain trusting in him, eat right, research and treat your body as a a ecosystem. Its like the rainforest in a way this drug is like the bad men cutting down all the trees. You need to now rebuild your ecosystem (gut and nutrients) in you. Sending prayers and positive vibes to all who are reading this . GOD bless and stay safe. Remember you are not alone in your suffering 🙂
Quick question. How did you treat rashes? Is it true that antihistamines from OTC can aggrevate symptoms?
I went through the samething with cipro posioning no one wanted to believe me doctor wise, its been three years and i cant still workout the way i did before i get tired easy when i do alot with my arms and legs my tendons hurt all over again i could not even feed my self could move my arms or legs was hospitalized 3 differnt times all diffrent hospital’s they texted me fior lyme disease aids forgieon county diseases because i was on a plane a month before that i do wounder if i will ever feel the way I did before best of luck on your recovery
Hi Nick, i had a question. I took cipro about 9 pills which was 4.5 days. I have developed tendonitis in both of my shoulders where i feel pressure in my scapula but there is no pain just tightness and numbness but i still can move my arms around. The arms at the socket just crack alot. Do you think this will heal in time or do you think surgery is necessary. I start therapy this week. This happened from June 18-june 22, 2018. Thank you. PS i am a female of 25 years of age.
Hi Nick,
I know it’s been 4 years since you were floxed. I was floxed 3 months ago. I’m improving but still have a long way to go before I’m back to my old self. Your Floxie story really helped me in my first months. Hope you are feeling well now. Thanks for sharing your story.
Sandi
I’m having a very hard time at the moment. I was floxed in October 2016, had a fairly quick recovery with some odd relapsing symptoms that popped up nearly a year later, and now, 2 years later, I am experiencing strong joint pains all over (knees, wrists and lower back are the worst). This is Day 7 of pain and only getting worse. I have not taken any steroids, NSAIDS, no hugely intensive workouts. No idea what triggered this except for some squats and lunges I did three days before this madness started. I thought most of this was behind me and am now terrified that this relapse will send me into a tailspin. I’m really looking for some support from anyone who has had a recovery and a relapse over a year later. This sucks- I hope I am not one of the unlucky few who has a supposed “recovery” only to have a disabling relapse that does not heal.
hi. how long after taking the pills you had the iv gluthatione ? i m at week 6 and still have brain fog.. 🙁
Why you take Cipro? What does the reason?
Thank you Nick for your story. So that means I’m not insane! I’ve taken Cipro for UTI’s for years without any problems. About 5 months after my mother died and 2 weeks prior to my father passing, I was given Cipro for a UTI. I took the whole 5 day course. I now regret not questioning the doctor when she per-subscribed it to me. I had past UTI’s where the doctors would not per-scribe Cipro due to a Achilles tendon rupture warning. And I did have a Achilles tendon problem at one point (still do actually) but couldn’t really prove it. I feel I probably wouldn’t have had a problem from this last time taking Cipro if it wasn’t for the GREAT amount of stress I was under just loosing a mother and soon losing a father. I truly believe the stress I was under weakened me to a point where I got floxed. I have tendinitis everywhere. I have tendons in my hands that have blown and don’t even know when it happened. I feel as I’m in a constant state of arthritis. Knees, feet, hands, elbows, shoulders, and hips are constantly stiff and sore. Vision has changed and that fog you’re talking about is real. I feel like I’m in one most everyday. I’ve had these symptoms since the middle of March 2018 after my father passed and I chalked it up to the stress of loosing both parents within 5 months of each other. I am now convinced that it was the Cipro. I’m only 48 and feel like I’m 90 most days. Your story however gives me some hope that you can overcome this at least to a point where you can function in a less painful and joyful way. Thanks again for your story.
What does the peripheral nerves feeling like a cold fire indicative of?
Hi Nick,
Thank you, I am doing very well. I had another 100% day. I have been getting lots of them and even some 125% days during the summer. I had forgotten it was possible to feel that good. I am hoping to write not just a “I healed to 100%” story but a “I healed 125%” story. I am sure that if I can have isolated days like that eventually I can feel that good all the time.
I hope you are doing equally as well or even better.
Ruth
Nick – did your peripheral neuropathy resolve fully?
Hi Nick
When do your neuropathy symptoms heal?
Hey Nick,
I have neuropathy in the feet…..and the only symptom i have is the “cold fire” and a bit of weakness. What helped with your neuropathy?
Thanks, Rajiv
Hey Nick,
What did you mean when you said ” My steps felt like I had dead legs and feet”. Thanks
Dear Nick, 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