*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.
YAY NICK! 🙂
fantastic
has your vision improved. mate
I had the stange leg bruises to…. that’s when I stopped at 12 tablets instead of taking the full 56..did you have any muscle loss?
Nick,
We were floxed about the same time. I took a couple more Cipro, but otherwise our stories are similar. I seem to have been hit with more psychological symptoms than musculoskeletal ones, though I had both. I’m hoping the insomnia will totally end for me soon. It comes back one to three times a month.
I’ve regained a lot of muscle too. I find that it didn’t come back just on it’s own– I had to carefully rehab every part of me. Now and then I find a muscle group I missed. At a waterpark this summer I realized my upper body isn’t as strong as it could be yet– pulling myself up out of the pool was really hard. I need to get to the gym– weights, bands and using my own body weight here are good, but there are some good machines at the gym and they have heavier weights there.
Has cardio flared your symptoms at all or brought back the insomnia?
So glad to hear you are doing so well and back to work! We can do this!
We’ll both get to 100% soon!
Ruth
Thanks for sharing Nick…my husband was floxed around the same time after taking 6 Cipro pills. He was fit and healthy, then flat on his back in excruciating pain, unable to lift his arms or leave the bed to use the bathroom. Hard to believe. He is able to work out lightly 3-5 days per week. We are thankful he is able to work and function.
Keep the faith and the gratitude. You are not alone.
Very inspiring Nick. This is good to hear especially when you are newly poisoned. It’s only been a month since floxed for me, and I’m doing everything I possibly can to help the recovery process. I started Physical Therapy, but I don’t think I am able to, nor should do any working out yet. I’m afraid of rupturing a tendon or pulling something since my muscles and joints feel so vulnerable. This whole experience is pretty terrifying. It helps to read stories like yours to get tips/ideas on healing because I have not got them from the medical community.
tara did you husband have tigh calves… that’s what I hope will go for me im at month 3
Thanks for the info! I still am not sure that my insomnia is really linked to cardio. Some times when I exerted a lot it didn’t appear. Other times I did less and it happened. Floxie symptoms cycle. All the symptoms cycle. When they do we all look for a possible cause, something we did we can just not do again to regain some control. But we don’t have control and our bodies heal as they are ready to heal. There is a much stronger connection between the insomnia and my monthly cycle than to exercise. I think if I were a young dude I’d be 100% better already. But I’m not a young dude, I’m a middle aged woman. I need to be patient with myself. I’ve come a long, long way in eight months. You’re right about stress. I love my new teaching job, but it can be stressful and that may have more to do with the insomnia than anything. I do usually feel very good after a workout. Maybe I need to workout more and stress less.
Your story is mine and I am in the process of healing myself also due to the fact that no doctors want to sway toward Cipro poisoning. Thank you for sharing your story it may help in the areas that I haven’t tried yet. My next step is to see a Neurologist.. I’m very happy for your success in feeling better Nick.
Hello Nick – I was floxed in 2006 and have recurring cycles every few months. I won’t go into details, it’s been very tough and am currently undergoing my worst cycle in probably 3 years. The reason I am posting this is your bruising sounds similar to mine. Several years ago I was taking a baby aspirin every day and got bruises on either side of my stomach. Quit the NSAIDs and it was still happening with bruises coming and going. Long story short my blood was clotting a second slower than normal human response times. Went to a hematologist who conducted many tests and was completely baffled – said what was happening to me was essentially impossible. All his tests ruled out everything but something exotic. The condition finally went away on its own after several more months. Just wondering if you had something similar in terms of the bruising component. I’m glad to hear you are doing better.
Jake
I’m also having a severe relapse. What are youre symptoms. This is after 3 years of doing really well.
Melanie,
I’m very sorry to hear of your relapse. My relapse is composed of perceptions of leg weakness and sensations in my legs – which are my typically cycle symptoms, as well as some hours of just feeling horribly ill. Some burning in shoulders. Leg weakness for this cycle (which never quite went away from last May) hit me severely in early September. Felt fluish on occasion. I got a flu shot two weeks ago. Things got much worse a few days later. Every morning I wake up my legs feel horribly weak with just unusual sensation that lasts for hours. Last night I was ready to go to the ER. Never fell asleep I felt so sick inside – my body felt way off. I’ve never felt this bad so continuously other than when I was floxed 8 years ago. Legs felt bad, body felt bad, heart rate was accelerated, like when you’re fighting a cold. This is the worst I’ve felt in years. However, the symptoms wax and wane from morning to night. I’ve had other quirky symptoms that border on the impossible, including digestive disorders and blood clotting issues. No cause has ever been found. I had none of this prior to Avelox.
When I was 18 months out I thought I was almost cured. I was back to lifting weights and running a 5k every other day. Then I had a severe relapse around my 3 year mark too…followed by roughly 2 cycles per year.
Melanie,
Exercise may contribute to cycles and kick it off again. Just a theory though because I have done hard exercise without cycling. Guess the fact is I’ll never know why my cycles start, however, I am trying to stop exercise for now.
My cycles typically last 2.5 to 3 months. x 2 per year. Not a great quality of life because I cannot plan to do something – like family vacations – without the fear that I’ll hit a bad cycle during that timeframe. Sucks as it really takes the enjoyment out of life when you’re feeling miserable.
I’m so sorry you cannot work due to this horror. How about this for ironic…my primary internist was going to give me Bactrim for persistent sinusitis and I was so scared of the side effects I read of Bactrim that another doc gave me Avelox. Figured out it was a floroquinolone and I should have thrown the bottle away but was feeling so poorly thought I’d chance it. Biggest mistake ever.
I took it to for a persistent sinus infection. Ended up having sinus surgery.
This is now going into 5 months Jake so im extremely worried that I wont heal again.
Its just as though I got floxed all over again.Cant say if it was the excersise or not really..maybe it would have happened anyways regardless.
Im trying to get back home to England to be with my Mum.I need all the support I can get.Just not sure I have the energy for such a long trip. Im in Texas.
I really need to try though
I believe you will heal up and the worst stuff will go away. Most people heal within 5 years. I’m one of the outliers, not you.
Thank you Jake
Its when youre in the middle of this stuff that you seem to lose all hope of ever feeling better again. The days drag into weeks and weeks into months and its never ending. Hard not to think the worse. I feel like now if I recover i’ll more than likely have relapses . There’s no rhyme or reason to this stuff. Ive had a lot of stress over this year plus the dieting and exercise. Probably everything went towards this cycle. I just didn’t know about floxing until I read an article on facebook right after I started this relapse…lightbulb moment…guess I’d been doing everything wrong for 3 years..eating whatever etc.
I.m glad to read about relapses but not glad people have to go through them. Once is enough for anybody expecially if it was severe and I put myself in that category so who knows if I actually will get through it again. Maybe with the support of my family if I can get home i’ll have a better chance. I wish good healing for you to Jake.I read about a lady who healed after 8 years Jake so never say never. If you ever want to E mail me feel free to do so. melglove@hotmail.com
Thanks so much for getting in touch.. it really means a lot to me.
how long was your vision bad nick…
Hi Nick,
Glad to read another flox recovery and progress. We were floxed on almost the exact same day! I was February 4th. (Tamara – my story is on here too) And so interesting how many stories I’ve read on here lately who say glutathione helped. That was my magic bullet. Anyways. Keep healing! 🙂
did they try and tell you you had ms ?