I wrote my recovery story about a year ago. A lot changes in a year, so I thought I’d write an update.
I was pretty well recovered when I wrote my story. In most areas, I was about 95% of my pre-flox capacity. I could do most of the physical and mental things that I needed and wanted to do to with relative ease. I could walk, hike, do pilates, swim, dance, work, have good conversations with my friends, maintain relationships, etc. I was healthy enough and life was good. I would have felt fine about staying in the condition that I was a year ago indefinitely.
It has been a nice surprise that I have continued to get better. Little things have improved/gone back to how they were pre-flox.
I started sweating again. I was kind of enjoying not sweating, but it’s good to have that part of my autonomic nervous system working normally again.
I stopped being cold all the time. I had a hard time feeling warm for a long time after taking cipro. Sometime in the last year my body has gone back to its normal – being “hot blooded” (I’m Swedish).
I feel like I felt pre-flox when drinking coffee and alcohol. It’s difficult for me to describe how I felt different after having caffeine or alcohol while I was sick – but it just felt different – and now it feels normal again.
I went through a period of nausea in the last year. For a couple of months, I couldn’t eat without feeling nauseous. I’m not sure if the nausea was because of a break-up that I went through right before it started (lots of people don’t eat for a while after a break-up), if it was a floxing symptom, or if it was a combination – my digestive tract shuts down now when I go through a period of stress. Whatever the source, it went away when I started supplementing hydrochloric acid (HCL – stomach acid).
I also had some issues with feeling a tightness in my chest that went away when I started supplementing HCL.
My mental capacity is as good as it was before I got floxed. It may even be better than it was pre-flox. I had no interest in biochem before I started researching how fluoroquinolones work – now I read biochem articles for fun, and they’re making me smarter. Also, my writing has gotten better – which is nice.
My energy, endurance, flexibility and strength have continued to improve. It’s difficult to tell if I am capable of as much physical activity now as I was before I got floxed for a couple of reasons. First, I am a bit out of shape. I have an office job so I sit for 8 hours a day. That’s not good for anyone’s physical fitness. Getting floxed certainly didn’t help, as it left me completely sedentary for a while and semi-sedentary for a while after that. Second, I was in really excellent physical condition before I got floxed. I’m not sure how fair it is to compare myself to how I was 2.5-3.5 years ago because I was really fit at that point in my life. Anyhow, those are details. My point is that I’m doing well physically. I can keep up with my boyfriend (who has never touched a fluoroquinolone) while hiking, swimming, etc.
I still struggle a bit with my motivation. I felt like cipro stole my “give a damn.” I’m very passionate about exposing the dangers of fluoroquinolones, and about helping people through fluoroquinolone toxicity, but I still struggle to “give a damn” about other areas of my life. It’s getting better though.
My level of fearfulness has subsided over the last year. (It had actually improved tremendously a year ago when I wrote my story – it was horrible when I first got floxed – I was terrified.) It has taken a long time for me to convince myself that this isn’t going to kill me. I can’t say that the fear about the consequences of the cellular damage done is completely gone. But I can say that I feel good right now. It’s not going to kill me today. Today, I’m doing well.
Diet – I am not on any specific diet. I avoid junk food but other than that, I eat whatever. Food does affect how I feel, but I don’t think that it affects how I feel any more than it did before I got floxed.
Supplements – I’ve switched out my supplements a bit. I still take iron (Pur Absorb 5 mg/day) and I still think that it helps me a lot. I also think that magnesium (250 mgs. Chelated mag/day) helps me. Lecithin helped to clear my brain fog. Hydrochloric acid (HCL) helped to get rid of my nausea and heartburn. I also take a fish-oil supplement, chlorella, glucosamine, vitamin D3, vitamin K2, coenzyme Q10 and a probiotic.
Food Supplements – These supplements are actually food, so I’m putting them into a different category from the supplements. I think that all of them have helped me a lot. Brewer’s yeast – it’s full of B vitamins, amino acids, trace minerals and has things like uridine and iodine in it that are helpful. I think that brewer’s yeast has helped me a lot. Cod liver oil – full of good fats. Raw crushed garlic – for the thiamine and other nutrients. Beets – they make me feel better (nitric oxide??) – do NOT get scared when you pee/poo purple after eating beets.
Exercise – I still find pilates, swimming and walking to be very therapeutic. I haven’t been as diligent in sticking with them this year as I was the year before.
Meditation – I still think that meditation is a wonderful thing for everyone to do. I have gotten horribly lazy about doing it myself.
Acupuncture – I go to my acupuncturist about once a quarter now. I was going at least once a month previously.
Staying off the internet – I’ll give myself a big fat F- on this one. Being involved in floxie stuff over the internet doesn’t induce anxiety for me any more though – so I don’t think that it’s unhealthy for me that I concentrate on it too much.
Having a positive attitude – I think that I’m still doing pretty well with this one. It has been wonderful and touching to have a group of positive people commenting on this site – letting their fellow floxies know what they know – and everyone encouraging each other and having faith in the notion that this too shall pass. I thank everyone who has supported a floxie through their time of need with a positive attitude and/or words of wisdom.
As I have gotten healthier and healthier, I have become less diligent about doing the things that helped me to get to a place of health. It would probably be better for my continued health if I was more diligent about sticking with them. Oh well. I think that it’s relatively normal to get lazy about doing the things that you did to get healthy once you have reached a point where you feel healthy enough.
I consider myself to be 99-100% recovered.
I am very, very, very lucky.
I wish luck, healing and recovery for all of you! I know that a complete recovery is not possible for everyone, and, well, read this about partial recoveries – https://floxiehope.com/2014/03/05/redefining-recovery/. I like the quote at the end of it, “Healing doesn’t mean the damage never existed. It means the damage no longer controls our lives.” If a full recovery isn’t possible, I wish you a recovery in which the damage no longer controls your life.
I am incredibly grateful for everything that I have gained in the last year. This site has reached more people, and touched more lives, than I could have possibly imagined a year ago. More people have read, and cared about, my healing story than I ever could have imagined. I hope that it has helped you. I hope that this follow-up, letting you know that the improvements have continued for me, give you even more hope for your own healing.
Xoxo
-Lisa
Hi Lisa. I sent you an email could you please take a look at it and respond back to me if you can. Thanks.
Did anyone get inflammation after cipro?
Thank you so much for sharing your story. Elizabeth
lisa. Any suggestions on what to do or take if toxic neuropathy is part of this too as well as neurally mediated hypotension? My “healthy” vitamins are high. Never took supplements. B6 and k are high. Others get low??? So confusing. No pain. Mostly dizzy nauseau numbness and tingly. Plus, serious brain fog. Thank you in advance for any suggestions.
I have been diagnosed with viral arthritis by a rheumatologist. Although I have a suspicion that it might be the cipro poisoning. I am currently on prednisone to “get rid of the inflammation that’s causing the pain.” There’s really no way to know for sure which it is. I have heard that prednisone could either benefit those that have cipro poisoning or in most cases hurt them more. Because I have no way of knowing for sure if what I have is viral arthritis or cipro poisoning I have decided to continue to take the prednisone to see. Has anyone been diagnosed with viral arthritis or have taken prednisone?
Hi Lisa!
Do you still take the HCL?
Good for u Lisa. Im completely off the forums myself I only saw this bc one my fb friends posted it. This time last year I was dying, not exaggerating literally dying. Internally bleeding, awake for mths lost 70lbs was a wreck mentally an out of work for 7mths. I am happy ro report brain fog, anxiety, energy, stomach, mood all that has returned to normal. Started getting better around 7mths im now at 14mths and consider myself 99-100%. I do not like talking to anyone about it do not like reading anymore non positive stories and although I am better I just want to forget what happened to me, which considering what I went thru is fair. U helped me alot with ur positiveness and ur supplement ideas n I did do ozone glut an vit ivs which could’ve helped but who knows. I couldnt keep down a cracker last yr n now can eat whatever I want n dont have ne reactions. I to consider myself extremely lucky. I should write a recovery story but honestly I just dont care nemore. Which when u heal I feel most ppl will tell u they feel that way. Thank u for all ur help an im very grateful to have found u on the internet! Happy bday btw 🙂
Lisa….thanks for starting this site..I am so glad I found it…so good to hear that you are so much better…I am using a lot of the supplements that you & others have tried…I think they are helping me…My story is nothing compared to what most of you have & are going through…I am so sorry for all of you…I pray for your healing….We will help each other out and come through this stronger people….
Hi Lisa,
Wishing you a very Happy Birthday☺. I am very grateful to you and all who post. I took cipro just over a year ago and I am coming up on one year of symptoms this month. I have spent 10 months in physical therapy, finding that my shoulder has tendenosis, tendon fibers altered via mri in June. This was confirmation of being floxed. Could not use left arm for months. I now have more functionality, thank goodness. Did have a major setback in Aug, hamstring injury, pt and I suspect a tendon. Both legs in hamstring ache, tingle etc since. Hamstring pull is slowly healing, Have used icing primary and occasionally infrared sauna. Only 2 1/2 doses nasids last winter and stopped because of your site. Also suspect floride treatments could have affected back in Aug, Thanks to postings here. I also battle ankle pain n tingling, thank goodness for magnesium and mag oil. Have upped my intake of iron in my diet, have to minimizing supplements cause I react to many. Thanks again for all the tips.
Thank you soo much for all your work and hope Lisa. I know you have responded to me before but I was wondering if you heard from anyone who made the mistake of getting a b12 shot and actually making some symptoms better but going from chronic fatigue to wired energy and insomnia? Any info would be sooo much appreciated. Xoxo thanks again, Melissa
Lisa, what exactly was your treatment? Did you do any iv glutathione? Have you heard anything about that? Thanks for your insight
Tina
I, too, am doing well at almost 2 years post-flox. I am so extremely grateful and blessed and consider myself lucky! Thank you for always being that positive encouragement on my shoulder. Your posts and the help of others on the FB pages and Floxiehope saved my life! God bless you!
im in 3 years being floxed my 1year half has no improvementand get worsen to the point my hair and skin does not look like before ..im constipated and my gut was not moving at all ..and i try plant based diet mostly on raw foods for one and half year and only this thing get my hair get back to thin and my skin like before ..i forgot being floxed im in a raw foods so everday gives me hopes this diet helps me .. i learn to dream again and to hope i stop blaming ..i stop looking for my old days everyday i became positive although theres still have up and downs i still have this pain tho but actually the way i think and i felt stronger than before ..im almost liviing a normal life and im look like 5 year younger ..as im intense doing juicing lots of raw veg and fruits..nuts and seeds..have a speedy recovery for us
sorry its thick not thin
So glad you are doing well!
So non severe pain aside would it be beneficial to exercise or detrimental to recovery? I’ve done nothing for 4 months and if anything I just want to get out and about again
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