Several of the recovery stories on floxiehope.com describe people who are mostly, but not fully, recovered. A lot of the recovery stories are from people who can see the light at the end of the fluoroquinolone toxicity tunnel, but they’re not completely out of the tunnel yet. Even though these recovery stories are not of complete recoveries, I think that they’re still valuable. The show that life can go on through and after fluoroquinolone toxicity, and they describe the physical, emotional, mental, and spiritual journey while it is still vivid and raw. Many of the people with partial recovery stories on floxiehope.com continue to improve. Life goes on–sometimes with bumps in the road/setbacks–but often toward continued recovery.
Some people who have read these partial recovery stories have asked, quite reasonably, if there are any people who FULLY recover, and return to their pre-flox capabilities. To this, I answer, “YES, I have fully recovered.” Me – Lisa – the author of the majority of the posts on this site. I have fully recovered.
When I wrote my recovery story in 2013 I was 90-something-percent recovered. I still had some autonomic nervous system issues and the fear and anger that came with getting poisoned by ciprofloxacin lingered. I wrote an update in 2014 that noted some features of my continued recovery.
Since 2014, I have continued to improve. I was physically completely healed in 2014, but the emotional journey has continued. I have worked through a lot of fear and anger since 2014. Both the fear, and most of the anger, have largely gone away.
I have healed.
I write this not to brag, or to diminish the experiences of those who don’t recover (there are some people who don’t recover, and they deserve our sympathy and support), but, as always, to give others hope. A full recovery is possible. I have fully recovered. I hope for the same for all who read this.
I recently (I got home day before yesterday at the time of writing this) visited Australia on vacation and was able to do all the things that I wanted to with ease. I went on a tour of Tasmania with a bunch of 20-something year olds and was able to keep up with them. We hiked to waterfalls and jumped off sand-dunes. It was fun! My feet didn’t hurt and I had plenty of energy to keep up with them. I was able to eat whatever I wanted. I slept decently–even on couches and in hostels. It was a good vacation. It was exactly what it would have been if I had never gotten floxed. I have recovered.
I hope that my recovery, and these pics of my vacation, give you hope that recovery, and a life that is full of activity and adventure, are possible. I posted these pictures, and others, on my facebook wall as I was touring Sydney, Melbourne and Tasmania. Several people thanked me for sharing the photos because they gave them hope that this type of travel is possible post-flox. It is possible. I had a fantastic time, and I hope that you are each able to take a similar journey, or whatever else you desire that indicates a full recovery.
All aspects of my journey through fluoroquinolone toxicity took time. I encourage you all to be patient with yourselves. I couldn’t have traveled through Australia like I did earlier this month when I was first floxed. I can do it now though, and that feels really, really, really good.
You are so right, Lisa – ‘No way in hell’; one good thing that has come about after having been floxed is our sharpened senses to the lies perpetrated by the medical community and our refusal to no longer be vulnerable to the dictates of the medical profession. I wish everyone who is considering having a colonoscopy could read about your horrific experience as you presented it here. More horror would have certainly followed if you hadn’t gotten out of there. People should know that there are alternatives: Cologuard, Fecal Occult Blood Test, and Flexible Sigmoidoscopy. Furthermore, the Colonoscopy cannot detect any cancers on the right side of the colon, it can only detect and clip the precancerous polyps that protrude out, not the flat ones, 15,000 people a year die from this procedure (1 in 1,000), the chance of colon perforation is greater than they would have you believe, the equipment in 85% of the procedures is not properly sterilized (Cidex is used because it is pennies cheaper, not peracetic acid). Therefore, contaminants and infection can easily be passed from one patient to another. More often than not, you are left with gastrointestinal problems for the rest of your life, etc. As long as the lunacy of animal testing persists, these toxic drugs put out there to an unsuspecting public will continue to kill 300,000 people a year and permanently damage and cripple more than two million. Fluoroquinolones head the list. Your recovery and success is so very inspiring, Lisa – it gives us hope that we too will get better.
Hi and thank you all for your comments. I took cipro 500mg 2x a day, July, 2015. Coming up on 1 year and I am still dealing with CNS stuff, anxiety attacks, morning hallucinations, depression and brain fog…and I’m recycling again as I write. I take paxil, a fluoride based anti depressant and Mirtazapine which I need for ocd. Every time I get upset, the anxiety is exaccerbated by s/e. I have had a lot of anger which I think is partially a result of my brain being poisoned. It is difficult to have a conversation on the phone. Listening to someone for more than a few minutes upsets me. I was never like this before. Could this be the cipro? Would appreciate any response. Thanks.
Hey lisa.. m so happy for you and you are doing a great job.. i was floxed exacty 1 year ago and i am 70 prcnt better now and plan to write a complete recovery story in the coming year.. i havnt tried intense workout but m able to walk for 2-3 miles without any problem and do around 100 pushups.. my job requires me to be on my feet for 10 hours a day wich i am able to manage sometimes with ease and sometimes i have to push it hard but i manage it pretty well.. all this seames to b impossible for the first few months.. i did go for many supplements early on like b12 shots and vitamin d shots.. but nw i only try to eat clean without any supplements.. the only thing that bothers me now is if a need to take an antibiotic or if i fall ill will it bring me down to the same level.. i have read your comments about safer antibiotics but just want to know have you experieced any difficulty by taking any medicine post floxing after you have recovered.. also please advice me can i take alcohol again as i havnt touched it post floxing.. awaiting you response.. cheers
How nice to see there are others ,not nice but a weird comfort I guess!
Hello Lisa, I was floxed about 4 months ago, aftes 5 days x 2 pills of Cipronex, I had swollen and aching joints and muscles in legs and hands and burning skin. After two weeks I was able to walking and working 11 hours for a day in pain and with swollen legs, it was improving. Now I’m having a relapse, maybe because of very big stress. Unfortunately with cipro problems came back my anxiety disorders and I have to quit my job. I should have an laparoscopy but I didn’t sign consent because of many drugs that they wanted to use during operation. Have you heard about floxie having operation without cross-reactivity drugs with cipro? (I’m talking about anesthetics, opioids, etc)
Your history and tips for life gave me hope and helped me with side effects, I’m very grateful, thank you!
I’ll be honest, I usually try to avoid websites like these, because I always end up crying. I am a hypochondriac, so reading stories that are worse than mine send me into a panic attack.
I am 19, just about to start college, and took 3 750 mg pills of Levaquin almost 2 months ago. Within hours of my first dose, I felt stiffness in my knees, but I tried to ignore it in case I was imagining it.
By the third day, I felt soreness in both of my Achilles, and still had aching knees. I immediately stopped the antibiotic.
These problems are still with me (thankfully the only problems, so far) and now I have minor tendon pains all over my body (Achilles tendons being the worst), along with muscle cramps, and twitches.
I will say that I am not in major pain, but definitely sore enough/uncomfortable to take 2 ibuprofen every day. Is this okay? I find that it takes the edge off, but I don’t want it to hinder my recovery.
What are the odds of me rupturing my Achilles tendon? (A major fear of mine.) I currently work on my feet for 4-8 hours everyday. Surprisingly, I find that it does not make me hurt any worse, if anything maybe better, but I don’t understand how that makes sense for tendinitis, they tell you to REST as much as possible to heal.
When would you guess that I will recover by? I find that my case is thankfully, better than most, but I don’t know if that guarantees me to recover quicker, or if at all.
I understand that everyone is different, but I would love if anyone could give me some advice/insight. Its really difficult for me to research this online as it really gets me down.
L, thanks for replying! I recently started Prozac for anxiety, and I know this is made of fluoride. Yikes. I guess I should come off of that.
I also started supplementing with Magnesium Citrate, but I swear it makes everything worse; the muscle pain, spasms, tendinitis, everything. But this goes against everything I’ve read about Magnesium..hmm.
So happy to hear of your recovery…gives us hope that just started into this horrible situation..thanks
Hi guys, I’m 23 and took 3 doses of cipro 500mg around march this year. I got an instant tingling feeling so after 3 doses stopped. That week was hell as my whole body would not stop tingling. after a couple of weeks it got better and then a couple of weeks after that I started to get tendonitis symptoms. I started taking magnesium which helped a lot and apart from a few days here and there i felt pretty much perfect.
I stopped taking magnesium citrare and then my legs have just got worse again so have obviously started magnesium straight back up and have started to get better (AGAIN).
My question is, I have read a lot of stories online that symptoms get worse, its been about 8 months now since I first took my dose, do you think I will fully recover? I don’t want to worry about things like this as im a massive worrier, i just want to make a full recovery and most stories on the internet are all doom and gloom and pretty much say that it will ruin your life and that there is nothing you can do about it,
Lisa,
(A) The low dose iron made your tendons feel a little more better? Mine are aching and burning a lot.
(B) What did the beets make feel better, tendons or something else?
Thank you and take care.
Joe J
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