*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.
Lisa’s Story
In the middle of November, 2011, I took Cipro to treat a urinary tract infection. I took 2 pills (500 mg each, I believe) a day for three days. I didn’t feel like the infection was gone, so I went back to the doctor and requested more antibiotics. He gave me macrobid and the infection subsided within a couple of days. Life went on as normal for the next couple of weeks, until December 2, 2011, at which time I got my period and started taking ibuprofen to help me to deal with the cramps.
Before I continue with my story, I would like to note that I had taken Cipro to treat a urinary tract infection approximately a year earlier. I had no notable side effects at that time. Though, looking back on things, I did develop an eyelid twitch at that time and some strange stomach cramping that came and went started then. I didn’t think anything of the eyelid twitching or the stomach cramps. I certainly didn’t think that they were tied to the Cipro. I took ibuprofen regularly after taking Cipro with no adverse effects.
On December 2, 2011 my legs started to itch. On December 4th I broke out in hives all over my body. I went to the doctor and was told to take Benadryl. I took more Benadryl than the box recommends and my hives got progressively worse. On December 5th my feet and hands swelled to the point that I couldn’t use them anymore. It was painful to walk, or even to just stand. I went back to the doctor and was put on prednisone. The prednisone suppressed the swelling and calmed the hives a bit. On December 7th my left leg went weak. For the next few weeks the following symptoms got worse and worse:
- Weakness in my legs. I could barely walk. The steps that I could take took a tremendous amount of effort and energy. I couldn’t stand for more than a minute. I had to drag a chair into the kitchen in order to cook rice because I couldn’t stand to stir the pot.
- Tightness of the tendons in my legs. I had inflammation, and possibly tears, in most of the tendons in my legs and feet. My hips, knees and ankles, to simplify things, didn’t work right.
- Loss of use of muscles / loss of strength. My muscles, especially the muscles in my legs, wouldn’t move like they used to. All of my movements were slow and deliberate.
- Brain fog. I couldn’t think straight. I felt stupid. I couldn’t concentrate. It was a struggle to do my job.
- Loss of memory. My short-term memory decreased significantly.
- Loss of peripheral vision. Large, black floaters entered my peripheral vision.
- Loss of appetite and weight.
- Loss of flexibility. I went from being able to do yoga several times a week to being unable to sit with my legs curled up under me.
- Loss of balance.
- Severe loss of energy. I felt like the plug had been pulled from my energy source. I wasn’t necessarily sleepy, I was just drained. The feeling was similar to the feeling that I have when I have a cold – weak and like I just want to collapse. Just slight exertion would drain me of my energy. Walking would make me tired for a whole day afterward.
- Dry mouth.
- Anxiety. I had an ongoing anxiety attack for the first couple of months after being floxed.
- Pain in my feet. I felt like I was walking on hot coals with every step I took.
- Loss of reading comprehension. I would read a page and have no idea what I had just read.
- Loss of social skills / connectedness. I felt anxious and scared in social situations. I lost confidence in both my physical and mental abilities. I felt very alone despite having a wonderfully supportive family.
I felt as if I had aged 20 years in just a week or two. I couldn’t move, think or eat. My body and mind were falling apart and I had no idea why. I didn’t think that the sudden decline in my health had anything to do with the Cipro. After all, I had stopped taking it a couple of weeks before my body started to fall apart. I thought that I had an autoimmune disease. My symptoms seemed similar to those of rheumatoid arthritis. I went back to the doctor and they ran every test imaginable on me. I was relieved to find out that I didn’t have an autoimmune disease, but it was somewhat frustrating to hear that all of the tests were showing that I was normal and healthy when, clearly, I was neither normal nor healthy. The doctors did not provide me with a diagnosis or a prognosis. Though I was desperately seeking a diagnosis and prognosis, I am thankful, in retrospect, that they didn’t misdiagnose me. If I had been mistakenly diagnosed as having an autoimmune disease, I may have treated it with pharmaceuticals that could have made me feel even worse.
I was desperate for some treatment, something to stop the downward spiral that my body, mind and spirit were in. The traditional medical doctors I saw provided no relief, treatment or healing. I started seeing an acupuncturist. He was able to stabilize my condition, calm my nerves and keep me from spiraling physically or mentally. After a few weeks feeling stable physically, I started to have days where I felt better than I had the day before. Mentally, I kept going downhill for a while, but, eventually my mental health stabilized and started to improve as well.
Eventually, with the help of my acupuncturist, I connected my symptoms to Cipro. Once the connection was made, I realized that all of my symptoms were consistent with those of others who have been poisoned by Cipro and other fluoroquinolone antibiotics. I entered the scary world of being a floxie.
For about a year, I considered myself to be sick. Though the symptoms listed above were improving, slowly but steadily, I was still sick, and a long ways from the healthy, active, energetic woman that I was before I took Cipro. After a year, I started to put “sick” in the past tense. Though I wasn’t back to the level of health that I was prior to being floxed, I was getting better and, as far as most people could tell, I was well.
Following is a list of things that I did to help me to get well, to heal. I am not a doctor. This is a description of my experience and what helped me. I hope that what helped me helps you. Everyone is different though. What helped me may not help you. One thing that I know helped me and that I know will help you is hope. I hope that the fact that I have largely recovered helps you to have hope. I hope that the other steps that I took to get well also help you to gain hope and healing.
Please feel free to contact me with any questions, comments or concerns, or to share your story.
Lisa’s Healing Tips
One of the many frustrating things about fluoroquinolne toxicity is that everyone’s body is different. Everyone’s symptoms are different and everyone’s body reacts differently to treatments. Following is a list of things that helped me. I hope that what helped me will help you, but it may not. I am including other people’s healing tips as well, in case their tips can help. Of course, please read these tips with the typical disclaimer in mind – I am not a doctor or medical professional of any kind. I am sharing my experience with the hope that others may find it to be useful. Please ask your doctor, or other trusted medical professional, for medical advice, and before taking any of my advice.
In no particular order, here are the things that helped me to heal.
- Time. With time, I have healed. Each day is better than the day before. Time will heal your wounds too. Eventually, you will get better. The poisonous reaction affecting every part of your body will eventually stop and you will begin to recover. I have heard several stories of fellow floxies having a timeline similar to mine – slow, steady recovery for about 2 years. Other people take more, or less, time to recover. Time does help though, and most people do end up getting better as time goes on. Very few people get worse and worse indefinitely. There may be bumps in the road, but time is your friend. Time will help you to return to a state of health.
Try to be patient with yourself. It will take time for your body and mind to heal. I see this whole ordeal of getting sick as a lesson in patience (and compassion, gratitude and health). Pushing yourself too hard too soon can lead to pain, frustration and injury. Try to give yourself the time necessary to heal, and, with time, your body and mind will, indeed, heal.
- Avoid NSAIDs and steroids like the plague. Both NSAIDs and steroids are contraindicated with fluoroquinolone toxicity. They will make your reactions and symptoms worse. There are some published medical articles on PubMed about the contraindication between NSAIDs/steroids and fluoroquinolones. Searching at the library or on Google will give you more detailed information than I can provide. Anecdotally, I know that my reaction was triggered by taking NSAIDs (ibuprofen that I took to help me to deal with menstrual cramps) and it was exacerbated by taking prednisone (a steroid). Please note that I did NOT take NSAIDs or steroids at the same time as Cipro. I took ibuprofen 2 weeks after I finished taking Cipro and it triggered my toxic reaction and I took prednisone 3 weeks after I had finished taking Cipro, after my reaction had started. I will never take another NSAID or steroid again.
Unfortunately, NSAIDs and steroids are the drugs that are the most commonly prescribed drugs used to “treat” fluoroquinolone toxicity. This is because the combination of NSAIDs/steroids and fluoroquinolones does not always cause a toxic reaction, the toxic reaction of combining fluoroquinolones and NSAIDs/steroids can occur even when the drugs are taken weeks or months apart, doctors and other medical professionals don’t acknowledge fluoroquinolone toxicity and so they don’t look for the contraindications and because many of the symptoms of fluoroquinolone toxicity are treated with NSAIDs and steroids. The pain killing qualities of NSAIDs and the swelling reduction qualities of steroids make them the drugs of choice for treating many of the symptoms of fluoroquinolone toxicity. Don’t take them though! In my nonmedical opinion, I suggest taking non-NSAID over-the-counter pain medicine like acetaminophen (Tylenol) for pain (or marijuana – which is probably better for your liver), and antihistamines for the swelling.
Often, fluoroquinolne toxicity is misdiagnosed as an autoimmune disease. In particular, it is often misdiagnosed as rheumatoid arthritis. Many of the drugs that are used to treat rheumatoid arthritis are NSAIDs. Don’t take them.
- Acupuncture. I credit my acupuncturist with saving my life. I can only guess how I would have fared without my acupuncturist, but I imagine that I would have ended up in the emergency room, pumped full of steroids and antidepressants, having a massive anxiety attack and unable to walk. That didn’t happen though and there really isn’t any point in surmising about what could have been. I do know that acupuncture stopped my downward spiral and got me on the road to recovery. Both the acupuncture needles and the herbs that he provided gave me immense relief. I don’t know why or how acupuncture works, but I do know that it worked wonders for me.
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Supplements. I have taken more supplements than I can remember. 90% of them had no noticeable effect on my health. Here is a list of supplements that I think helped me.
Iron. I take a low dose iron supplement – only 5 mg. – daily. The brand of iron supplement that I use is Pur Absorb, but I’m guessing that other low-dose iron supplements will work equally well. Within just a couple days of starting taking the iron supplement, my energy levels increased dramatically. I could walk a mile without being exhausted afterward. In addition to improving my energy level, the iron supplement seems to make my muscles and tendons more supple and malleable. When my tendons are feeling tight, a dose of iron helps to loosen them up – within just a couple hours. Too much iron is really bad for you, so please be careful with supplementing it (ask your doctor, yada yada), but it helps me immensely.
Magnesium. I take 250 mg of chelated magnesium daily. I don’t necessarily notice that it makes me feel better, but I do notice that I feel worse when I don’t take it. My muscles twitch if I don’t take my mag.
Zinc. I take zinc when I get around to it. I remember feeling mildly better when I started taking it. It doesn’t seem to affect my health dramatically though.
Chlorophyll. I take chlorophyll about every other day. It seems to help with my energy level and mental functioning.
I also take fish oils, resveratrol, a probiotic, a joint supplement, CoEnzyme Q10, vitamin B12, chlorella, glucosamine, brewer’s yeast and some other supplements. They may help. I can’t say that I feel a difference using any of them.
- Meditate. Meditating has so many amazing, positive benefits for your brain, your life, your spirit, etc. that I can go on about it ad nauseam. Meditation helped relieve a lot of the mental symptoms of my fluoroquinolone toxicity. My anxiety, inability to concentrate, inability to connect with others, depression, loss of reading comprehension, decreased mental acuity, etc. were greatly reduced (or improved) through meditating. I meditate about 10 minutes each day. I should meditate more like 20-30 minutes a day.
Meditating helped me to gain compassion for myself and my situation. It also helped me to let go of the anger that I felt toward the pharmaceutical companies and the medical culture that allows fluoroquinolones to be on the market. The pharmaceutical companies and the medical culture are both messed up and blame of them is justified, but anger and blame were not serving me mentally, emotionally, spiritually or physically. I needed to let go of my anger and blame in order to move on with my life. Meditating helped with that.
I learned to meditate through taking a class called Mindfulness Based Stress Reduction that was offered by my health insurer. It was an excellent class based on the work of Jon Kabat-Zinn. Many Buddhism centers offer Mindfulness Based Stress Reduction or Meditation 101 classes.
- Get off the internet. Most of the information available on the internet about fluoroquinolone toxicity is horrifying. Fluoroquinolone toxicity is horrifying. It is scary. It is completely unacknowledged by the medical community – the doctors, nurses, etc. who we go to in order to make sense of things when our body goes hay-wire – so we seek answers on the internet. Unfortunately, most internet sites devoted to fluoroquinolone toxicity do not provide a balanced picture. They show the harm and the horror of fluoroquinolone poisoning, but they don’t show the healing and hope that most people eventually experience. I am writing and distributing this in order to provide the perspective of hope and healing. Some people are permanently disabled from fluoroquinolones. My heart goes out to those people and they have every right to scream their story on the internet. However, their story is not your story. My story is not your story either. But if you’re going to look to the internet for a prognosis, it’s better to find a hopeful prognosis than one that is full of doom and gloom.
When I participated in the online forums for Floxies, I noticed that my anxiety levels increased significantly. Even after I was 90% recovered and I thought I could handle it, my anxiety levels would go up simply by reading about people being floxed. Inducing anxiety is one of the worst things that someone suffering from fluoroquinolone toxicity should do. Anxiety makes all symptoms worse. I would slowly relapse and my symptoms would get worse every time I participated in the online forums.
Of course, the people participating in the online forums are seeking to help fellow Floxies, to commiserate and to participate in a support group. It is not their fault that my anxiety levels increased when viewing their sites and/or support groups. After all, most people on those sites are trying to be helpful and supportive. However, the net result of participating in the forums for Floxies is that my anxiety levels increased and my health declined while I was on those sites. I am healthier and happier not participating in the online “support groups” than I was while I did participate in those groups. Of course, this is my experience only. Many people find solace in the Floxie community and if it helps you, great!
The people who have worked hard to create a community of Floxies to support one another should be commended. It is because of their hard work that thousands of people have realized what is going on with their bodies and that they are not alone. The community of Floxies is full of wonderful people. However, you need to do what you need to do to take care of your health and if you find that hearing other people’s stories increases your anxiety levels, get off the internet. For you.
- Diet. I lost 11 pounds in 18 days when I first got floxed. My body was going hay-wire and it seemed like an allergic reaction. I had no idea what I could possibly be allergic to so I stopped eating almost everything. I didn’t eat sugar (including fruit), gluten, dairy, soy, anything non-kosher or anything spicy, or drink any alcohol or caffeine, for a month. I only ate vegetables and organic meat. It’s a highly effective way to lose weight, but I don’t think that restricting my diet severely helped me to heal. Restricting my diet gave me a sense of control, and that’s not a bad thing when your body is self-destructing, but I don’t think that it made me feel any better physically. After a month of only eating veggies and organic meat, I started to add normal foods into my diet. As soon as I started eating an appropriate number of calories, I started to feel better. Not only was I Floxed, I was also wasting away when I wasn’t eating normally. Getting enough food is an important part of healing. Of course, it’s generally good to be on the “don’t eat junk” diet, but I didn’t find that cutting my food intake significantly helped me to feel better.
Many Floxies develop GI problems. I was lucky in that I didn’t have many GI problems. Many people seem to be helped by cutting gluten, sugar and/or junk food out of their diet.
I notice that I feel slightly worse than normal when I consume sugar and/or caffeine. I think that most people do, I am just now accustomed to paying closer attention to my body.
The only food that makes me feel noticeably better is beets. For some reason, beets make me feel great. I just boil them and eat them.
I’ve heard good things about the benefits for Floxies of eating broccoli and other cruciferous vegetables. I love broccoli so I try to eat a lot of it. Unfortunately, I can’t say that I’ve noticed that it makes me feel better.
- Swim. My tendons and muscles feel significantly better when I’m in the water, and for several hours after I finish swimming. Swimming in the ocean feels especially therapeutic. There are so many minerals and trace nutrients in the ocean, I surmise that they’re helpful for healing. Unfortunately, I don’t live near the sea, so I swim in a pool. I feel better when I do so.
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Pilates. I started doing Pilates about 7 months post-floxing. Pilates strengthens the core, something that is generally important, and gently stretches muscles, tendons and ligaments, something that is particularly important for Floxies. I started slowly and gently and didn’t push my tendons, muscles or ligaments too much. I feel that gently stretching helped my tendons, muscles and ligaments to heal and return to (close to) their pre-floxing capacity. Take it easy though.
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Healing arts. I love to dance. I’m not a good dancer, but I love to do it. About 16 months post-floxing I started to dance again. Dance has been healing for me. I feel spiritual, strong and joyful when I dance. I’m not sure if it’s the dancing itself that I find to be healing, of if it’s the joy that I feel when I dance that is healing. Either way, it helps. I surmise that other forms of expression would have similar healing qualities. If you love to sing, sing. If you love to paint, paint. If you love to write, write.
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Attitude tips.
Try not to compare yourself to how you used to be. I used to hike 20 miles in a day. I can’t do that anymore, but I can hike 3 miles today and I couldn’t do that when I first got floxed. Compare yourself to how you were yesterday, not to how you were before you got floxed.
Do something – anything – to work toward healing, every day. Walk a little further than you did yesterday. Meditate. Take an Epsom Salt bath. Get an acupuncture treatment. Do a puzzle. Whatever makes you feel good – do it. Every little step helps.
Don’t kill yourself. Have hope. You will get better.
You’re not crazy. You’re sick. Have hope. You will get better.
You’re not stupid. You’re sick. Have hope. You will get better.
Try not to identify yourself as sick. The mind is a powerful thing so try to stay positive. It’s hard, I know. But try, because it’s worth it.
You will have bad days. They will pass. This all will pass. It is not permanent. You are strong – present tense. You were knocked down, but you weren’t killed. You will get better.
Don’t quit your job. Try to maintain as much normalcy in your life as you can.
It is not your fault. Even if you knew better, even if you demanded the most powerful drug possible from your doctor, even if you self-medicated, even if you coerced your doctor into giving you the fluoroquinolone antibiotic, even if the infection that you were treating was something that you got because of doing something stupid, or from sex, even if you continued to take it after you started to get sick, even if you floxed your child/parent or other loved one – IT IS NOT YOUR FAULT. You are sick. You are poisoned. You are not to blame for your sickness or for the fact that you are poisoned. Who to blame is a discussion that I don’t want to get into because I want this to be positive, but it is not you. You are not to blame. You are a victim. It is not your fault.
Lisa’s Life now
Life is good. I don’t consider myself to be sick any more. I’m not quite up to my pre-floxing capacity in a couple of areas. I don’t have the endurance, energy, strength or flexibility that I used to. However, I’m pretty close to my pre-floxing capacity in those, and other, areas. I’m about 99% better. Not being capable of intense exercise since December, 2011 has left me a bit out of shape, but I’m working toward being able to exercise intensely again and my stamina, strength, energy, etc. are increasing. I can’t hike 15 miles with a backpack on quite yet (something I could do before I was floxed), but I am capable of most physical and mental activities that would put me in the “normal” or “not sick” categories.
I can work full-time. I am grateful for the fact that I have a job that is not too demanding physically or mentally because I was able to hold onto it through my worst times. My boss and coworkers were wonderfully understanding and they claim not to have noticed that I couldn’t think straight for about a year. I even got a promotion about a year post-floxing!
I can do Pilates 4 times a week, swim 2 times a week, dance once a week and walk daily.
When I was unable to walk a block I told myself that I would consider myself to be “better” when I could dance all night in heels (my feet hurt like hell when I was sick), I can do that now. I never liked high heels, but I can wear them now.
My memory isn’t quite what it used to be, but it’s good enough to do well at my job and to maintain my relationships.
In many ways, I’m a different person than I was before I got floxed. This has been perplexing for me and my loved ones, but it’s not an altogether negative thing. I’m a much more spiritual person than I was before I got sick. I was a pretty firm Atheist before I was floxed. Now, through meditation, dancing, believing in alternative therapies that focus on energy, etc., I’m finding some spiritual outlets that I didn’t have, need or want in the past.
I have become a more compassionate and patient person. I now empathize with people who have mystery diseases. I used to have the attitude that I now find so frustrating in medical professionals – that if there isn’t a way to diagnose or treat an ailment, it doesn’t exist. Now I know that people are genuinely suffering and that there is a real cause for their pain – regardless of whether or not it is acknowledged by the medical community. My heart goes out to those in pain.
I had to become more compassionate and patient with myself as well.
I like some things that I didn’t like before I was floxed and I don’t like some things that I used to like a lot. I hated swimming for the first 32 years of my life. Now I love it and consider it to be an important aspect of my healing. I used to like working out in an intense way that got me dripping with sweat. Now I like to do exercises like Pilates that are focused, slow and deliberate. I used to love hiking, camping and backpacking. I miss loving those things so I’m going to try to get back into them, but I’m not sure that they’re my passions any more. Drinking used to be one of my favorite pastimes. My tolerance for alcohol is shot now and I don’t really enjoy it any more. I missed it for a while even though I knew that it was for the best that I wasn’t drinking like a fish. My appetite has changed as well. I used to be able to eat a lot of food and I loved to eat. I still eat, of course, but I don’t eat as much as I used to and I don’t eat with as much gusto. This is probably a good thing seeing as I’m not into exercising intensely any longer.
Even though I would do just about anything to turn back time and not take Cipro, the place that I am in life isn’t bad, and I probably would be someplace different if I hadn’t gotten sick. It sucks that I had to gain empathy for people who suffer from pain, mystery ailments and debilitating fatigue, but it’s probably a good thing that I now have more empathy. I would like to think that I’m a better person from going through this. I’m not a stronger person, but maybe I am a better person.
I hope that my tips and words of advice are welcome and helpful. Please feel free to contact me if you have any questions or concerns.
** 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.
Ashley, there is a doctor in Michigan named Dr. Wycoff who may be able to help you. He does ultraviolet blood iradiation, among other treatments, that I think would help floxies. I almost got it myself but never made it up there. I know people who had good results from the treatments. Google Wycoff Wellness Center.
This really seems to be the next big thing for us:
https://youtu.be/ZKiKVWDac7k?t=41m58s
Check out what Joe Rogan says about a German sports medicine doc I really think this could cure those suffering from tendon issues!
What you guys think?
martha, are you still out ther? dan
hi martha, great to hear your better!! i am still dealing with issues, mostly muscle spams, nerve stuff in general. take care. dan.
Lisa, just an update on me. The brain fog lasted about five months from May until Oct, I only made it because I felt like you were on one shoulder and Ruth was on the other. I kept telling myself, Lisa said it would get better with time, over and over again, it was my mantra. I spent over $300 on supplements that was suggested by one of your floxies, but none seemed to help. I did up the green juice and went strictly antibiotic free meats, could not go completely vegan. The flu shot set me back for two weeks but I am OK now. Still have the pain in my back and neck and am on my second round of PT. It was suggested to me to try aquatic therapy and have found some places that do that so when my double vision goes away, I am going to try that. I am working on my genealogy and that keeps my mind off the pain, also I am painting bookmarkers for the library. God Bless Everyone and hoping everyone will have a healthy New Year. Kris T
hello good year 2016 for all of you
what the best help for sleeping
thank you
good 2016 to all of you
what is the best ways to improve sleep
thank you
Claude, I have been using a natural sleep aid called Tranquil Sleep. By Stress Relax. It has L-Theanine and Melatonin in it. I got mine at the health food store. Mine are chewable tablets and recommended by a Dr Michael Murray. It says to chew two tablets but I find one is enough. kris T
Hi All,
I was also one of the victim of Cipro. I also posted some of the questions to forum and got reply from Lucero and kris T.
I took Cipro on April 2015 for UTI for 2 a day for 7 days and then i have been experiencing all weird thing around my body.
1) Pain in my neck
2) pain in my finger joint and numbness now and then in my both hand
3) pain in my right shoulder and down muscle of right shoulder
4) dry mouth
5) high BP
6) Chest Pain
7) Cold feet
8) burning sensation on all over body
9) Gastroenterology issues
These are the major thing i was experiencing and i went to see doctors many times and they said that you have all side effects which will go away with time and you dont have to take too much medication to counter one issue. she said just give sometime and put your mind out of all this then you will see huge difference. I was having more of this impact since i was working from home all the time and half time my focus was only in and around this and thus i was noticing more issues.
today post 9 months i am out of all issues apart from point 9 which is more due to my life style. i went to endoscopy and came to know that i am having hiatal hernia which is causing shortness of breath sometime which i have to deal with it with making change in life style apart from that i am again back to normal and trying to do all thing normally the way i was doing before.
in nut shell what i am trying to say is we all can come back to normal and honestly i have not taken any of the big medication or any of the vitamin and all. i just change my focus from being alone at home, i started working from office sometimes and started meeting people and just forget about all this issues though it was reminding me all the time in back of my mind. Now i am not thinking about anything at all what has happened i just forget it as bad time of life.
please make sure that you dont think much about it and then you should be good. please avoid any unnecessary medication since it may end up damaging something else.
I still suspect that due to this stress and all i end up getting Hiatal Hernia which is not good and still i am doing my excercise just to keep myself fit and fine. i only took medication for my dry mouth since after CIPRO i was having fungal infection in my mouth for that i took Clotrimazol and Fluconzol which my doc gave me for 21 days both and then i came back to normal.
I must say please keep faith in you and make sure that you have someone around you who will not allow you to keep thinking about what is wrong in you.
God bless all.
MR
Did anyone have tinnitus and if so how long did it take to go away? 4 months out and am still having muscle spasms and insomnia. I can not take anything makes me sick.
Tami
Tami, I have always had tinnitus so I can’t say about that issue. My muscle spasms lasted for five months before going away. I could not take any of the supplements that Ruth Recommended, like you they made me sick or dizzy, I could not even take the magnesium. I just had to wait it out. Have you tried Sleepy Time Tea for the insomnia? Or I take a sleep aid called Tranquil Sleep which has Suntheanine and Melatonin in it. But I only take one to a half a tablet. The worst thing for me after taking Cipro was the brain fog and just not feeling like myself. That lasted for months along with the muscles spasms. Every now and then I get a spasm when I wake up in the morning, but its not nearly as bad as it used to be. It helped me to get a therapist to talk things out. I must emphasize that no one on this website is a dr, so you will have to try whats best for you, through trial and error. Kris T
Hi lisa
I saw that you took chlorella. Im also on it now. Did it help you? How much did you take? Regards Ann
I’m sorry that u had such a nightmare after taking cipro. Only a very few professionals would know and recognize what’s ur problem and diagnosis. It’s called systematic mycosis, since the antibiotics are mycotoxins, a byproducts of mold and they are the most toxic yet most ignored and unknown toxins and the root causes of most diseases. I’d be happy to give u more info and resources, please contact me. Ur dieter and lifestyle changes are all good, except brewer yeast which is an oil on the fire, i do not recommend it.
Lisa, now that you have recovered, what supplements do you still take besides the chlorella? I had problems taking all the ones Ruth Recommended although I know that everyone is different. I did the nutritional end of it also, no sugar and antibiotic free meats for five months, but by the six month, I was in the chocolate area in my grocery and Katy Bar The Door, I ended up with a dozen chocolate chip cookies! My two remaining problems, the back pain and the double vision but I just get through each day at a time. Kris T
I just found this post and read it with both a sense of relief and panic. It’s 3.30am and once again I can’t sleep. Stepping back about 7 months ago I was given a prescription of cipro to try and tackle a suspected prostatitis issue. After 8 days use I had developed acute pain in my left elbow and weakness. So much so I stopped the pills and refused to take the remaining 3 weeks+ It took a couple of weeks to calm down and I figured that was it. Since then I had various issues, fatigue, sleep problems, aches and pains but didn’t put 2 and 2 together. I noticed I’d get burning sensations on my skin, headaches, stiff joints. Anyway about 6 weeks ago, some 5 or more months since the last pill, I woke up with a tightness and soreness in my left calf. This hasn’t improved and I have a tingling and slight burning sensation also now. It doesn’t hurt to press in but it’s constant. I’ve also experienced what I can only describe as a heavyness like walking is hard work. Since I’d done no exercise for a long time I initially thought maybe it was just my fitness but 6 weeks later it’s no better, possibly worse. I’m now wondering if this could be a delayed reaction to the cipro and I’m starting to panic! What do you think? Could this start 5 or more months after? I had a cold in December and remember taking ibuprofen but couldn’t say fir sure that was before this started.
“Could this start 5 or more months after?”
Yes Chris, unfortunately it can start 5 months after as a delayed reaction and judging by your story I’m pretty sure that your current side effects are Cipro related.
Mark
Chris, you are going to have to stay off of the ibuprofen, this is what starts most of the bad side effects from Cipro. Try to take tylenol and go to Ruth’s story and she can suggest some supplements for you to take. Magnesium make help some of the spasms, but I had problems taking Magnesium so I supplemented with foods high in Magnesium. Also Epsom Salt baths are good and try the Magnesium spray which I found at a health food store. Kris T
Chris, most people on this website did not get “mild symptoms”. I would suggest you read everyone’s story. I think we all suffered differently. My symptoms were more in my back, most have pains in their legs. I had terrible brain fog for months, but I had been on so many antibiotics besides the Cipro, I am wondering if my problems stemmed from all of them, a stubborn UTI which they called re-occurring because it would not go away. I scream at myself every day at not stopping Cipro when I got the first leg spasm, but I thought I only have four days left of the med, so I kept taking it. Then I stopped it but started to take the stronger version of it and I am sure that is was completely screwed me up! I feel almost normal now, except I still have double vision and back pain. Kris T
Greetings all,
I am joining the ranks as one who is also experiencing cipro side effects. I took 2 a day for 5 days (was perscibed for 7days). First 3 days just noticed being “weird in the head”, short term memory terrible, ear popped and rang once, anxiety. 4th day had pain in lower back radiating down both legs, thought maybe I had body aches from infection and took tylenol, unaware of the micro print of the “rare” side effects. 5th day had same back/leg pain, took tylenol again…by end of the day had tremors(like when one comes out of anesthesia from surgery), chills, major anxiety, leg muscel tightness, rapid heart beat, and finally realized I was experiencing side effects.. .looked at the fine print and really freaked out. I stopped taking the cipro, next day muscles seized up especially in legs and felt like I had just finished a marathon on verge of cramping and chills continued. Over the next few weeks muscles continued tightening in both arms and legs. Like most of us, went online to get some answers and just found gloom and doom; but became more aware of what seems to me to be more than “rare” side effects. I was most desperate for any accounts of recovery or hope. I went to my Dr. (Who was not the prescriber). She didn’t know much about it so called she call pharmisist who said they never saw side effects last this long and said it wasn’t. I told my dr I totally disagreed with that opinion, she took my remaining bottle of cipro and left. A strange interaction to say the least, and left me very discouraged. More weeks have past (almost a month now) and have added stomach pain, blk. stool (indicating bleeding), extreme muscle fatigue/tightness, joint pain, numb. tounge, m ajor energy level drain (like when have flu), memory problems, popping joints, dizziness, anxiety, sleep disturb (5hr max), chills/cold feet hands/temp sensing issues, rash, labored breathing, urination level not typical, communication difficulties, and a few others.
My main reason in posting this is in hopes to share our struggles and if I find something that helps my symptoms to share any remodies I might find. I also wanted to share how much it means that Lisa took the time to start this blog in order to give others hope through this trial. It was a great encouragement to me personally, as we all know there isn’t much posted online about recovery accounts. I am just starting this journey, but I have faith that God will use this to help refine me. Already by her sharing, I found beets to help me feel more enery also (the canned didn’t, but baked raw beets did). So thank you Lisa for that tip too!
God Bless – Lindy
Lisa,
After how long did you notice your muscle strength/tightness and energy to start to improve? I forgot to mention in my first entry I also was taking IB prof PM (1 capsule) at night during and after until I read your warnings a few days ago and stopped. So thanks for that advise also. Side note: I have random muscel twitches also (leg/arms)..
thanks,
Lindy