Liz’s Story of Recovery from Cipro Poisoning

Hello –

I would like to start this story by commending you for reading this and reaching out for support during this time.  I was floxed on July 8th. I had gone to an urgent care center for a suspected UTI. My urinalysis came back clear so it was sent off for a culture but the physician decided to treat me with antibiotics in the meantime. When I filled the cipro prescription and saw the black box warning I was hesitant to take it. I called the physician to discuss my concerns and was assured its prescribed all the time and she has only had one patient in 15 years complain of side effects.

Despite my own reservations I figured I was overreacting and took one of the pills. I woke up the next morning with mild aches and called the physician again. She told me to stop the medicine and said we would wait until my culture came back to determine an alternative treatment.  The good news is my culture came back clear later that week but unfortunately I was still experiencing aches that were progressively getting worse even though I had only taken one dose. I had visited the Floxie Hope website and knew that it might take a while and more symptoms could occur.

My sleep was also becoming very interrupted. The fourth night I had a panic attack around 2am and had a few hives on my stomach. I have struggled with anxiety before but the panic attack was unlike anything I had ever experienced. I had spasms in my calves and at night my hips would hurt so bad I could barely sleep.

Over the next few weeks the symptoms would come and go. I would have pain in my ankles, then it would be my hips, and the calf spasms were intermittent.  Luckily I did not have another panic attack.  Around 5 weeks after I was floxed I felt confident saying I was symptom free. Now it has been almost a full 8 weeks without symptoms. During the worst of my symptoms I did not have to miss any work since I have a desk job. The biggest disruption to my day to day was the smallest chores (dishes, laundry) would give me insane lower back pain.

Below are some things I felt helped ease symptoms and speed recovery.

1. Prayer and meditation  –  Getting your mind in the right state is over half of the battle. Do not let hopelessness overtake you. Pray a much as you can. Overwhelm yourself with the truth of who God is.  Also don’t punish yourself- I was incredibly hard on myself for taking the medicine despite my own reservations so I blamed myself or the doctor all the time. Blaming yourself or someone else doesn’t speed up your healing and only adds to mental anguish so just don’t do it.

2. Eat as good as you can. Low to no sugar. Absolutely no caffeine – it made me feel crazy. I’m just now able to tolerate caffiene again.  I incorporated spinach and almonds into my meals every day. Both are high in magnesium which helps with joints/muscles.

3. Epsom salt baths. Very relaxing and the external magnesium is great on the muscles.

4. Serene Slumber Tea by the brand Lifestyle Awareness. It’s a mix of skullcap and chamomile and was the only thing that saved my sleep. However do not take if you consider yourself to be depressed or if you are on prescription medication for a mood disorder.

5.  Tart Cherry Juice. The all natural unsweetened kind. It is phenomenal at reducing inflammation and is a great alternative to OTC painkillers which can exacerbate the symptoms.

6. STAY OFF GOOGLE. Your story will likely be different in some ways than everyone elses. Don’t scare yourself to death or try to compare your journey to others. I did find a lot of great women by searching #floxiehope on Instagram and everyone was so kind and willing to message with me on my worst days. My Instagram handle is itslizholland and if you need someone to talk to – feel free to DM me.

7. Yoga and light stretching. This may not be possible all days but do it when you can and to a point that feels comfortable to your body.

I wish you all the best and pray for healing and a peace that surpasses all understanding in the meantime. “In this world you will have trouble but take heart – I have overcome the world!” – John 16:33

* 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, affect 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.

16 thoughts on “Liz’s Story of Recovery from Cipro Poisoning

  1. L September 24, 2018 at 9:16 am Reply

    you need to educate your doctor (or sue her) since there was a warning a year ago against the use of these drugs for UTIs

    • Anna October 30, 2018 at 1:08 pm Reply

      I, too, was given Cipro 500mg for a suspected UTI , just 3 months ago. Doctors are still giving it out like candy. I ended up not even having a UTI 😦

      • L October 30, 2018 at 1:51 pm Reply

        It’s criminal. I just wrote a long letter and attached some articles, to an eye doctor who seems responsive to the information. I would suggest, since there was a warning put out about a year ago that flqs should NOT be used for UTIs, that you think about a lawsuit against the doctor and, depending on the state you live in, the pharmacy. (Pharmacy laws differ from state to state, eg here in CA they are REQUIRED to consult on a new or changed prescription. Sadly, money seems to be the only thing they will pay attention to.

  2. Tom September 24, 2018 at 12:05 pm Reply

    Hello Liz, I´m happy that you recognized the poison and stop after the first pill. I took 13×500 and after 7 months I can say that I feel better. You must not take any fluoroquinolones in the future!

    • Monica October 5, 2018 at 5:24 pm Reply

      Hey Tom well you seem positive . Can you give me a buzz . I need some help with floxing symptoms. I have severe weakness and fatigue. Want to know what helped. But I also have depersonalization and derealization really bad . Hmmmm 310-432-3381

  3. Lukasz September 24, 2018 at 5:59 pm Reply

    Welcome to our unfortunate club. Membership is free and we are rapidly expanding. In all seriousness, you’ve provided people with some excellent advice here.

  4. Nancy Vogel October 7, 2018 at 1:51 pm Reply

    hi Liza–so glad you are better. My story was almost identical…No apparant UTI…1 pill…although when I read the warnings the pharmacist said not to worry also. I’m at 5 months and still struggling with symptoms although they are less severe. Anxiety is a
    \ part of ME also. What happens is MY anxiety triggers a full nervous system reaction It is teaching me to try to stay calm and stress free. Thanks for your post!

  5. L October 11, 2018 at 3:01 pm Reply

    well good thing you stopped when you did. (I started having PN, eyes full of floaters and flashing lights after just ONE pill. I went on to take 4 and it devasted me body wide, and I lost more than a year of my life completely. BUT I also had it with prednisone.) think the fact that your conditions have been fewer and far between is a good thing. Something like the eye twitch—that could be from pretty much anything ,so I wouldn’t necessarily blame that on the cipro. As for the other pains, they certainly could be. And I am not so sure that Bactrim is a great one to take either. One thing I would definitely do is make sure you are taking a good magnesium supplement as much as 800 mg a day for now if you can tolerate it, and /or epsom salts, a good probiotic and avoid ALL NSAIDS, steroids.

  6. Anna October 30, 2018 at 1:14 pm Reply

    I was given CIpro, I only took one pill. I am still struggling 3.5 months later. Tingling, numbness, pain, stiffness, twitching in ankles, knees, legs. Frozen shoulder causing numbness and tingling down the arm. Left foot and left eye brow twitch on and off. ALso, the worst was my eye reaction, which sent me to the ER. After the first pill, within 48 hours I developed pain and tightness behind the eyes, with severe light sensitivity. Eye doctor determined the eye itself to be healthy, so he guesses it’s autoimmune inflammation or trochleitis, tendinitis of the orbital area. My under eye muscle is noticeably inflamed too. I just started 150mcg of kelp supplement, which is basically Iodine, and meant for detoxing from fluoride toxicity. I already take Magnesium, but I really doubt it helps, I am starting to think it has been a placebo for me. I think Mag maybe useful early on, within the first month of a floxing, but after that I dunno

  7. Marianne November 4, 2018 at 7:45 pm Reply

    Hi LIz, thank you for sharing. I am new to this .. didn’t even know this condition existed and still not 100% if I’ve been floxed? I’ve been ill for 10 months after taking a 5 day course of levofloxin. I have cystic fibrosis and needed something for my chest infection. Since then I’ve been on it for another 5 weeks (2 weeks once, and 3 weeks the 2nd time). I took it again cause I was so ill and we just figured it was a chest infection …. grrr!!! Anywho sounds like the damage was already done in the first 5 days. To add injury to injury or whatever the saying is I take daily 600 mg of ibuprofen for chronic inflammation and of course was taking it during the course of levofloxin. I’m reading now that this increases the chances of developing fluoroquinolon toxicity. I see that you suggested tart cherry juice. Thanks for the tip. I’ve picked it up and had my first glass today while going through a painful time. So when you say that ibuprofen can make the symptoms worst is it still considered dangerous to take them (I’m not on levo now and NEVER EVER EVER WILL BE AGAIN!). Unfortunately the chronic inflammation causes just as much pain as the symptoms from fluoroquinolone.

    • L November 4, 2018 at 9:23 pm Reply

      some things you might want to look into are serrpeptase, NAC, MSM. They all help with congestion. I would also look around for an integrative MD….

  8. Dan Jervis February 23, 2019 at 8:46 am Reply

    I am so grateful for your improvement, I wish I had only taken a few 500mg doses but I took 120 24 years ago. A sinus infection was ver stubborn and it didn’t even touch the infection. It had to be surgically removed. The doctor said, “I’m just using a bigger sledge hammer on you.” Suffering is an understatement for the last 1/3 of my life but I can’t give up because of m wife, son and grandson who need me. For 23 years I have wondered if I could make it another year. I am still alive.

  9. Dan Jervis March 2, 2019 at 10:25 am Reply

    Dear Liz, Please consider sending your story to CBS 60 Minutes.
    Our stories need to be heard, Dan

    • L March 2, 2019 at 10:47 am Reply

      I hope people do contact as many institutions out there as they can…TV shows, magazines, newspapers, etc. But I will tell you that I have contacted dozens, and one big problem, especially with the TV shows is that a lot of their ad revenue comes from big pharma…and not just in the ubiquitous drug ads you see. Take Bayer for example…they own Dr Scholls (will never buy again); of course Bayer aspirin; Afrin, Alka Seltzer; Claritin; Coppertone; Roundup since they took over Monsanto; and dozens more.

    • Katrina March 9, 2019 at 10:56 am Reply

      Dan what do you still have left or struggling with the most ?

  10. Roxanne May 3, 2019 at 9:45 am Reply

    It’s wonderful that your recovery came in 8 weeks. It’s probably a blessing you only took the one pill. Yes you’re right we are all different, but do experience some of the same side effects. What is so irritating to me is how doctors are so confident that you won’t have a problem with this med. As said, we are all different!! They shouldn’t assume it’s safe for everyone.

Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

This site uses Akismet to reduce spam. Learn how your comment data is processed.

%d bloggers like this: