*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.
Mark W 06/29/2012
I am a 35 year old math professor. I took Cipro 500mg twice per day for a UTI over 4 days from May 11th to May 15th 2010. After 8th pill I had a horrible reaction. Usual symptoms, cramping, burning, muscle twitching, brain fog, nightmares, felt like I was being dried out and like my head was being twisted in a vice. Could barely walk for months afterwards. I felt utterly destroyed and thought I would never recover. I also thought my career as a research mathematician was over and that I would end up permanently disabled and unable to cope with any sort of stress or responsibility. I read all sorts of horrifying stories online about cipro damage which utterly smashed my morale. One promise I did make was that if I ever recovered, I would post it somewhere to give hope to those who may feel now as I felt then. My heart goes out to all of you. I am now happy to say that I am running, biking, lifting weights and playing football (“soccer” to you Americans) regularly. Getting better has been a long and difficult road involving physical therapy, acupuncture and copious amounts of magnesium (both oral and topical) and vitamins B, D and E. Whether or not some or all of these therapies were placeboes is impossible to say. They certainly felt like they helped. All I know is that, bar some minor aches and pains, I am much much better. NEVER EVER GIVE UP.
** 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.
So good to hear. Thank you for posting this.
Glad to hear you recovered Mark. It’s been 9 months since I took a 7 day course of cipro (500mg x2 a day) and I still can’t work more that 50 yards without my achilles feeling like they are going to snap. I also lost 30 lbs of muscle. Just skin and bones now. How were you doing in terms of walking/running around the 9th month?
My symptoms decreased substantially when I began to double dose PQQ and CoQ10. I believe cipro mimics PQQ in the body and poisons the sites it catalyzes. Cipro is essentially PQQ with a Fluorine group and a few extra carbons.
Dear Mark, 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
WE NEED OUR STORIES TO BE HEARD, Dan
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