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veteran floxie
8 years ago
Thank you joanneg for your reply,
well here is an update. yesterday i decided to bite the bullet and go back to my strict alkaline diet. All day i was exhausted because i did not sleep the day before. I had some sweet potato i had bought on friday and i ate that all day, not a lot since i was not very hungry. I drank water with some electrolytes and for dinner i ate an avocado.
I went to bed at 8 o clock with my usual bedtime magnesium chloride and herbal teas for sleeping, i took my regular dose of melatonin which is 1.5 mg. and i went to bed. I was very tired and in about an hour i was asleep.
I always follow my myoclonic jerks to see the pattern and strength, this time they were not that strong and less frequent, so i managed to sleep the whole night, i woke up about three times during the night but i managed to fall back asleep again. Needless to say i slept better than the day before. I attribute this to the alkaline diet.
The herpes virus affects the nerves in the spinal cord and the alkaline diet seems to help in that respect, specifically there could be many reasons for that.
So in retrospect i recommend keeping an alkaline diet which helps the body maximize its oxygen levels.
Courtney cole
8 years ago
I am on day 5 of cipro for a UTI, but am stopping. I have leg and joint pain. I am allergic to penicillins and a round of macrobid did not clear my infection. The doctor at least told me cipro has its serious detractors in the medical community, and it’s more a last line of defense. So I was warned, but didn’t understand the full scope until I looked online. I actually searched “fever day 4 of uti on cipro” because I assumed it must not be working and would be back at the urgent care a forth time with the UTI.
My temperature has been fluctuating high and low pretty quickly. The search returned much more about cipro. Is temperature fluctuation a side effect? The leg and joint pain indicated I should stop taking it. I’m kind of staggering from point A to point B then lying down, but I did that 6 days ago with the UTI. Out of breath.
It is important to note here I get frequent UTI s since an episode of KIDNEY FAILURE I was hospitalized for 2 years ago.v (6 days in) I have seen a nephrologist and am recovered but probably need a urologist. I recently moved states, and my former Dr was about to refer me to one. It is even more important to mention I was TAKING LEVAQUIN the week before my kidney failure. What I have read in the last 24 hours is truly alarming. At the time, my kidney failure was a mystery to doctors. This is what I told this new Dr 6 days ago–mystery as to why the failure occurred. I was a healthy 47 year old woman.
I also had had a GLUTATHIONE IV from a holistic center 48 hours before hospitalization. I told Drs this at the time. I now believe I must have been floxed, and then added another terrible blow with the glutathione. I see people here insisting glutathione is good. I have believe in holistic treatments from Drs with M.D., my whole life, but in that instance, with other issues at work, it almost killed me. I was out of work for a month. Please be cautious with glutathione. My mom had it with me the same day, & she passed out half way through so they removed the IV. 3 weeks later, we discovered randomly she had a-fib, which runs in the family. When they checked her blood, her creatine levels were high, like mine were in kidney failure mode, but not the super elevated status of mine. That told me the IVs harmed us both.
What I have read since yesterday has shed so much light! I don’t know what antibiotic will treat my UTI s, I hope something, as this is diminishing my life. However, I don’t need to add the possible damage of cipro. Any advice on what to do, the day you stop cipro is appreciated.
joanneg
8 years ago
Hi Lisa,
I’m sorry, I didn’t realize that it would be delayed because of the links.
Thanks for letting me know 🙂
Ahmdi
8 years ago
Hi all,
I know that fq drugs damage all human body, but when i read dq drugs damage mitochondria cells they make me feel so baddd…
I want to know which are best methods to repair mitochondria with no suppl but with diet and lifestyle 🙂
Nicole Reedy
8 years ago
Has anyone tried Prolotherapy for their tendons?!
By the way just from the above glut. conversation, it pretty much saved my life. My liver was destroyed by the 1st pill & the liver dr said it would be a year before it was back to normal. I had glut. in my myers then had my enzymes checked & my liver ultrasound at 4 months and everything was healed. My doctor was shocked! Said it had to be the glut. as it is known as the master liver healer?!
It seems Jason finds something wrong with just about everything!!!! I told him before he confuses & upsets people especially since so many people follow the protocol in the book Lisa promotes on this site & have talked to a few people who swear it is what worked for them.
Not saying you are wrong Mr. Jason but I have often wondered if you upset people because you charge to help them. I sure hope I have misjudged you on that one & will find out someday that you really do have the answers.
Lee
8 years ago
Question!!! Has anyone ever have round reddish purple circles come up on their skin. Looks like little blood vessels in them. Someone people answer me soon.
Nicole Reedy
8 years ago
Ryan L when you stopped the glut. did your neuropathy burning stop after you stopped the glut.? I think I remember you burning. Thank you for the prolotherapy information.
Jason, I suppose I do jump on you & maybe do not give you credit for all your research but yes I am scared & so is everyone on here or we wouldn’t be here. And if there was any real clear answer in western or eastern medicine we would not be going crazy for our life back.
I know you have had other issues besides FQ toxicity but as you said you have been fighting for 30 years. I am 66, I don’t have 30 years & have almost already lost one so at my age one is a forever!
I don’t usually come on here much anymore as my emotions can not handle it. I guess I should just leave it to all to you young ones & go crawl up and die somewhere!
Lwd
8 years ago
Hello
I’m seeking help with tight muscles. I am 26 mos out in my recovery. Around 20 mos I reinjured myself by digging a hole for plants. My neurologist diagnosed strained neck and upper back. Shortly after my injury my ND recommend EMS and it did more damage to my entire back. Now my upper back is tightening up into my neck. Any suggestions?
Nicole Reedy
8 years ago
Thanks Ryan L.
I guess I should do the 23 & me testing. I have been tested for a few different mutations but I suppose not enough.
Trying to hang on but I am getting tired as my NP feels she has done all she can as she does not do the things like Ozone & prolotherapy. I have stopped the glut. but still take NAC with my protein.
My friend in Spain is now a lot better after Ozone treatments. She did the supplements for a long time but did not see a difference. So I am moving on to the big guns NP in Vancouver & can not believe all the money two seniors are having to spend to get me out of this!
Maybe it is just as so many people say, time! So maybe in 2 or 3 years we would all get better if we did nothing, don’t know?!
I do know for someone my age I am missing a lot of life for a life that is on it’s last adventure anyway.
Ramos brian
8 years ago
I am really happy that i have been cured from (HERPES SIMPLEX VIRUS) with the herbal medicine of Dr Odinokoro, i have been suffering from this disease for the past 2 years and 7 months without solution until i came across the email of this doctor who has cured so many people with his herbal medicine, i also choose to give him a chance to help me and my husband, he told me what to do and i kindly did it, and he gave us his herbal medicine and direct me on how to use it, i also follow his instructions for use and he ask us to go for a check up after 1 week and 4days which i did, to my greatest surprise our result came out as negative, we are really happy that there is someone like this doctor who is ready to help anytime any day. To all the readers and viewers that is doubting this testimony stop doubting it and contact this doctor if you really have one and see if he will not actually help you. i am not a stupid woman that i will come out to the public and start saying what someone have not done for me and i know that there are some people out there who are really suffering and hurting their family just because of these diseases so you can to mail him on Dr. Odinokoro.
He also told me that he has cure for these diseases listed below
. HERPES SIMPLEX VIRUS.
.DIABETES
. CANCER
.HEPATITIS
S.D.B.
8 years ago
Floxed by 1 prescription of Cipro four years ago, I’ve lurked on this site for about three years. My symptoms began immediately after taking the last pill of the prescription; allergic reactions to foods. Ended up in the E.R. anaphylactic 6 times before associating the problem with foods. Over the next year I experienced severe muscle and joint pain in the knees and ankles, inability to regulate body temperature, torn retina, raging Candida infection of the skin, insomnia, muscle spasms, multi chemical sensitivity, fatigue that kept me bed bound some days, depression…it’s been a life changer. I am 64 years old. It has been a long, hard journey, but there have been improvements and I’m grateful for every one. As with so many others on this forum, I found mainstream biomedicine to be less than useless, and even insulting. Traditional Chinese Medicine (acupuncture and herbs) was somewhat helpful. Some things I researched and did some “out there” treatments on my own. Got rid of the Candida in the skin (which one young E.R. Doc looked at and said, “Oh, once you have that you’ll have it forever!”) by making a slurry of powdered probiotic and water and applying it to the skin. PLEASE don’t just hop to it and try this, it worked, but gave me such severe Herx reactions I thought I would die and ended in the E.R. twice in one day. Those were interesting exchanges with the medical world also…when I told them what I had done and that what I was experiencing was a detox reaction they had no idea what I was talking about. The snide nurse I was assigned to said, “Well just what is it you’d like us to do for you!?” I replied “Just one bag of standard I.V. fluid to help flush my system would be a great kindness.” With that, she ordered it, rammed an I.V. into the back of my hand, and left. I requested and signed for a full report of that E.R. visit sent to my alternative integrative M.D. Eighty pages…can’t imagine what that all contained. If you do decide to try this, GO SLOW…only small, small amounts of probiotic at a time. Go slow seems to be key in trying anything once you’ve been floxed, and indeed, as frustrating and unfair as it is, time and lots of rest are needed. I had to retire at the age of 62 due to the unrelenting fatigue. There are still so many “can’ts”…can’t go to the pool to swim due to chlorine and the scent of sunblock, and sunblock floating in the water, can’t go out for a nice dinner due to food allergies and the ocean of fragrance in the room (ditto for concerts, church services, any event with a crowd of people in a closed space,) can’t take long energetic walks in the woods, I carry antihistamines and an epinephrine pen always. I’m so chemically sensitive I can’t use homeopathy…ONE bead of anything sends me into shock. I have to look at what I “can” that I couldn’t four years ago; I can take a one mile walk with my husband and the dog every day, I can (pretty much) keep up with the housework, I can enjoy time with my family because they do understand and go fragrance free when we get together, I can enjoy a reasonable range of foods if I stick to the low and moderate salicylate range of the Feingold program, my skin is clear, the torn retina was lasered in a timely manner with minimal damage, the pain in my legs is much less, body temperature regulates much better, I’m sleeping fairly well most nights. Are my Golden Years what I expected?…no, but I’m still here and have learned not to waste energy being bitter and angry (THAT took a long time too!!!) Please don’t think I’m just spouting sunshine, part of the reason I didn’t post sooner was that I was in a very dark place for a very long time. My next venture is getting tested for the MTHFR gene mutation. Perhaps that is why Cipro hit me so hard. In looking at the family medical history there are many who had conditions seemingly related to that gene mutation. We’ll see where that leads. I’ve switched from the cyano to the methyl forms of B vitamins, and even that caused detox like reactions, so I’m going slow and taking 1/4 of the dose every other day. Thanks to all of you on this forum for being brave and open. This poison affects DNA, so it hits everyone differently, and our paths to improvement are also very different.
Cindy Jones
8 years ago
Jason
Please share the below info that you posted.
I mentioned last page it took some time, but I estimate I have the entire Floxing and all the ADR’s ~80% figured out, there is no one else even close to that number, here, or passed. Some of my clients have consulted some of the other thought of experts around and later tell me about their disappointment in doing so, BIG bucks too, and I see the protocols and hear the advice given, and boy I am WAY too cheap ????
Cindy Jones
8 years ago
Jason where did you compile your list from may we ask?
How much does it cost?
Cindy
8 years ago
Jason Are you still participating in floxiehope?
joanneg
8 years ago
Hi Everyone,
Just letting you all know that today was the first day I used the Vitamin Patch and so far it has worked great!!
I woke to another day of “i just don’t think I can do this any more” attitude because I felt like CRAP! But in less than an hour of putting on the patch, I started to feel a little sprite or some energy or more alive, and I have continued to feel even better as the day goes by.
So, I know this is quite early to really know anything, especially since this has happened with so many other supplements that then eventually made me feel even worse. But I figured I’d let you’s know step by step how it’s going.
Danie'l
8 years ago
I got floxed in July. I feel all my symtoms are getting worse. I have terrible brain fog and my vision is messed up. I see floaters amd black spots. I get dizzy often. Has anyone else experinced these symtoms does it ever get better. I’ve had to quit school and my job because of how bad its gotten. I just don’t know how much more I can take..
S.D.B.
8 years ago
Watch the floaters and black spots. See an ophthalmologist. I had those, and then one day the torn retina came on very quickly. First there was an increase in cobweb-ey floaters and then I saw the blood gushing within the eyeball like the color of old motor oil. Fortunately my ophthalmologist is not far away, the retinologist who did the laser treatment is in the same building and I got immediate attention. It’s another result of the connective tissue damage from fluoroquinolones.
S.D.B.
8 years ago
Nutrition is always important, but especially so after being floxed. One thing that I believe helped tremendously with the joint/cartilage/tendon-ligament/connective tissue problem is bone broth. It gives the nutritional building blocks your body needs in a gentle highly absorbable form. Just be sure to use ONLY free range grass fed organic bones. Here is an excellent link. http://www.jadeinstitute.com/jade/bone-broth-health-building.php
Stephanie
8 years ago
Rich about your jerks I have them and never took lyrica in my life I was also given a high volume of cipro and other floroquinoles the only thing that has helped is my IVs from my naturopath I’m almost two years out and still have them badly. I can tell you physical therapy made them insanely worse. I suggest going to a good naturopath that treats nervous issues or trying unda therapy I am going to be trying that in a couple of weeks
Ann
8 years ago
Has anyone felt The same. I was rushed to The ER 2 months ago. With a heart rate off 219. And since then i have trouble with really bad heart palpitations. And i can feel like a really bad pounding in my stomach, like my heart is in the stomach. So weird! Has anybody felt The same? And got that better?
I was Hurt from flagyl 1 year ago. And have so many things going on in the body. But after a half year i could see some small changes. I was still awful, but at least i could walk. But The bad headaches was still there, The really severe fatigue and dizziness and off balance and The bad neuropathy. And then 2 months ago… BAAM… And The heart was pounding like crazy and i was rushed to The hospital. And now i am back to where i was in the beginning, and are even worse. And cant function at all. That feels like a bad sign, that my health are even worse than before. Is it normal to be back to square one? I dont know how i can go on with all this. Feels like im going to die. That my body cant take this anymore soon. I also get this collapses, where i almost faint, several Times a day. Im so scared. Try not to panic, but it is so Hard. Thanks for listening.
Thank you joanneg for your reply,
well here is an update. yesterday i decided to bite the bullet and go back to my strict alkaline diet. All day i was exhausted because i did not sleep the day before. I had some sweet potato i had bought on friday and i ate that all day, not a lot since i was not very hungry. I drank water with some electrolytes and for dinner i ate an avocado.
I went to bed at 8 o clock with my usual bedtime magnesium chloride and herbal teas for sleeping, i took my regular dose of melatonin which is 1.5 mg. and i went to bed. I was very tired and in about an hour i was asleep.
I always follow my myoclonic jerks to see the pattern and strength, this time they were not that strong and less frequent, so i managed to sleep the whole night, i woke up about three times during the night but i managed to fall back asleep again. Needless to say i slept better than the day before. I attribute this to the alkaline diet.
The herpes virus affects the nerves in the spinal cord and the alkaline diet seems to help in that respect, specifically there could be many reasons for that.
So in retrospect i recommend keeping an alkaline diet which helps the body maximize its oxygen levels.
I am on day 5 of cipro for a UTI, but am stopping. I have leg and joint pain. I am allergic to penicillins and a round of macrobid did not clear my infection. The doctor at least told me cipro has its serious detractors in the medical community, and it’s more a last line of defense. So I was warned, but didn’t understand the full scope until I looked online. I actually searched “fever day 4 of uti on cipro” because I assumed it must not be working and would be back at the urgent care a forth time with the UTI.
My temperature has been fluctuating high and low pretty quickly. The search returned much more about cipro. Is temperature fluctuation a side effect? The leg and joint pain indicated I should stop taking it. I’m kind of staggering from point A to point B then lying down, but I did that 6 days ago with the UTI. Out of breath.
It is important to note here I get frequent UTI s since an episode of KIDNEY FAILURE I was hospitalized for 2 years ago.v (6 days in) I have seen a nephrologist and am recovered but probably need a urologist. I recently moved states, and my former Dr was about to refer me to one. It is even more important to mention I was TAKING LEVAQUIN the week before my kidney failure. What I have read in the last 24 hours is truly alarming. At the time, my kidney failure was a mystery to doctors. This is what I told this new Dr 6 days ago–mystery as to why the failure occurred. I was a healthy 47 year old woman.
I also had had a GLUTATHIONE IV from a holistic center 48 hours before hospitalization. I told Drs this at the time. I now believe I must have been floxed, and then added another terrible blow with the glutathione. I see people here insisting glutathione is good. I have believe in holistic treatments from Drs with M.D., my whole life, but in that instance, with other issues at work, it almost killed me. I was out of work for a month. Please be cautious with glutathione. My mom had it with me the same day, & she passed out half way through so they removed the IV. 3 weeks later, we discovered randomly she had a-fib, which runs in the family. When they checked her blood, her creatine levels were high, like mine were in kidney failure mode, but not the super elevated status of mine. That told me the IVs harmed us both.
What I have read since yesterday has shed so much light! I don’t know what antibiotic will treat my UTI s, I hope something, as this is diminishing my life. However, I don’t need to add the possible damage of cipro. Any advice on what to do, the day you stop cipro is appreciated.
Hi Lisa,
I’m sorry, I didn’t realize that it would be delayed because of the links.
Thanks for letting me know 🙂
Hi all,
I know that fq drugs damage all human body, but when i read dq drugs damage mitochondria cells they make me feel so baddd…
I want to know which are best methods to repair mitochondria with no suppl but with diet and lifestyle 🙂
Has anyone tried Prolotherapy for their tendons?!
By the way just from the above glut. conversation, it pretty much saved my life. My liver was destroyed by the 1st pill & the liver dr said it would be a year before it was back to normal. I had glut. in my myers then had my enzymes checked & my liver ultrasound at 4 months and everything was healed. My doctor was shocked! Said it had to be the glut. as it is known as the master liver healer?!
It seems Jason finds something wrong with just about everything!!!! I told him before he confuses & upsets people especially since so many people follow the protocol in the book Lisa promotes on this site & have talked to a few people who swear it is what worked for them.
Not saying you are wrong Mr. Jason but I have often wondered if you upset people because you charge to help them. I sure hope I have misjudged you on that one & will find out someday that you really do have the answers.
Question!!! Has anyone ever have round reddish purple circles come up on their skin. Looks like little blood vessels in them. Someone people answer me soon.
Ryan L when you stopped the glut. did your neuropathy burning stop after you stopped the glut.? I think I remember you burning. Thank you for the prolotherapy information.
Jason, I suppose I do jump on you & maybe do not give you credit for all your research but yes I am scared & so is everyone on here or we wouldn’t be here. And if there was any real clear answer in western or eastern medicine we would not be going crazy for our life back.
I know you have had other issues besides FQ toxicity but as you said you have been fighting for 30 years. I am 66, I don’t have 30 years & have almost already lost one so at my age one is a forever!
I don’t usually come on here much anymore as my emotions can not handle it. I guess I should just leave it to all to you young ones & go crawl up and die somewhere!
Hello
I’m seeking help with tight muscles. I am 26 mos out in my recovery. Around 20 mos I reinjured myself by digging a hole for plants. My neurologist diagnosed strained neck and upper back. Shortly after my injury my ND recommend EMS and it did more damage to my entire back. Now my upper back is tightening up into my neck. Any suggestions?
Thanks Ryan L.
I guess I should do the 23 & me testing. I have been tested for a few different mutations but I suppose not enough.
Trying to hang on but I am getting tired as my NP feels she has done all she can as she does not do the things like Ozone & prolotherapy. I have stopped the glut. but still take NAC with my protein.
My friend in Spain is now a lot better after Ozone treatments. She did the supplements for a long time but did not see a difference. So I am moving on to the big guns NP in Vancouver & can not believe all the money two seniors are having to spend to get me out of this!
Maybe it is just as so many people say, time! So maybe in 2 or 3 years we would all get better if we did nothing, don’t know?!
I do know for someone my age I am missing a lot of life for a life that is on it’s last adventure anyway.
I am really happy that i have been cured from (HERPES SIMPLEX VIRUS) with the herbal medicine of Dr Odinokoro, i have been suffering from this disease for the past 2 years and 7 months without solution until i came across the email of this doctor who has cured so many people with his herbal medicine, i also choose to give him a chance to help me and my husband, he told me what to do and i kindly did it, and he gave us his herbal medicine and direct me on how to use it, i also follow his instructions for use and he ask us to go for a check up after 1 week and 4days which i did, to my greatest surprise our result came out as negative, we are really happy that there is someone like this doctor who is ready to help anytime any day. To all the readers and viewers that is doubting this testimony stop doubting it and contact this doctor if you really have one and see if he will not actually help you. i am not a stupid woman that i will come out to the public and start saying what someone have not done for me and i know that there are some people out there who are really suffering and hurting their family just because of these diseases so you can to mail him on Dr. Odinokoro.
He also told me that he has cure for these diseases listed below
. HERPES SIMPLEX VIRUS.
.DIABETES
. CANCER
.HEPATITIS
Floxed by 1 prescription of Cipro four years ago, I’ve lurked on this site for about three years. My symptoms began immediately after taking the last pill of the prescription; allergic reactions to foods. Ended up in the E.R. anaphylactic 6 times before associating the problem with foods. Over the next year I experienced severe muscle and joint pain in the knees and ankles, inability to regulate body temperature, torn retina, raging Candida infection of the skin, insomnia, muscle spasms, multi chemical sensitivity, fatigue that kept me bed bound some days, depression…it’s been a life changer. I am 64 years old. It has been a long, hard journey, but there have been improvements and I’m grateful for every one. As with so many others on this forum, I found mainstream biomedicine to be less than useless, and even insulting. Traditional Chinese Medicine (acupuncture and herbs) was somewhat helpful. Some things I researched and did some “out there” treatments on my own. Got rid of the Candida in the skin (which one young E.R. Doc looked at and said, “Oh, once you have that you’ll have it forever!”) by making a slurry of powdered probiotic and water and applying it to the skin. PLEASE don’t just hop to it and try this, it worked, but gave me such severe Herx reactions I thought I would die and ended in the E.R. twice in one day. Those were interesting exchanges with the medical world also…when I told them what I had done and that what I was experiencing was a detox reaction they had no idea what I was talking about. The snide nurse I was assigned to said, “Well just what is it you’d like us to do for you!?” I replied “Just one bag of standard I.V. fluid to help flush my system would be a great kindness.” With that, she ordered it, rammed an I.V. into the back of my hand, and left. I requested and signed for a full report of that E.R. visit sent to my alternative integrative M.D. Eighty pages…can’t imagine what that all contained. If you do decide to try this, GO SLOW…only small, small amounts of probiotic at a time. Go slow seems to be key in trying anything once you’ve been floxed, and indeed, as frustrating and unfair as it is, time and lots of rest are needed. I had to retire at the age of 62 due to the unrelenting fatigue. There are still so many “can’ts”…can’t go to the pool to swim due to chlorine and the scent of sunblock, and sunblock floating in the water, can’t go out for a nice dinner due to food allergies and the ocean of fragrance in the room (ditto for concerts, church services, any event with a crowd of people in a closed space,) can’t take long energetic walks in the woods, I carry antihistamines and an epinephrine pen always. I’m so chemically sensitive I can’t use homeopathy…ONE bead of anything sends me into shock. I have to look at what I “can” that I couldn’t four years ago; I can take a one mile walk with my husband and the dog every day, I can (pretty much) keep up with the housework, I can enjoy time with my family because they do understand and go fragrance free when we get together, I can enjoy a reasonable range of foods if I stick to the low and moderate salicylate range of the Feingold program, my skin is clear, the torn retina was lasered in a timely manner with minimal damage, the pain in my legs is much less, body temperature regulates much better, I’m sleeping fairly well most nights. Are my Golden Years what I expected?…no, but I’m still here and have learned not to waste energy being bitter and angry (THAT took a long time too!!!) Please don’t think I’m just spouting sunshine, part of the reason I didn’t post sooner was that I was in a very dark place for a very long time. My next venture is getting tested for the MTHFR gene mutation. Perhaps that is why Cipro hit me so hard. In looking at the family medical history there are many who had conditions seemingly related to that gene mutation. We’ll see where that leads. I’ve switched from the cyano to the methyl forms of B vitamins, and even that caused detox like reactions, so I’m going slow and taking 1/4 of the dose every other day. Thanks to all of you on this forum for being brave and open. This poison affects DNA, so it hits everyone differently, and our paths to improvement are also very different.
Jason
Please share the below info that you posted.
I mentioned last page it took some time, but I estimate I have the entire Floxing and all the ADR’s ~80% figured out, there is no one else even close to that number, here, or passed. Some of my clients have consulted some of the other thought of experts around and later tell me about their disappointment in doing so, BIG bucks too, and I see the protocols and hear the advice given, and boy I am WAY too cheap ????
Jason where did you compile your list from may we ask?
How much does it cost?
Jason Are you still participating in floxiehope?
Hi Everyone,
Just letting you all know that today was the first day I used the Vitamin Patch and so far it has worked great!!
I woke to another day of “i just don’t think I can do this any more” attitude because I felt like CRAP! But in less than an hour of putting on the patch, I started to feel a little sprite or some energy or more alive, and I have continued to feel even better as the day goes by.
So, I know this is quite early to really know anything, especially since this has happened with so many other supplements that then eventually made me feel even worse. But I figured I’d let you’s know step by step how it’s going.
I got floxed in July. I feel all my symtoms are getting worse. I have terrible brain fog and my vision is messed up. I see floaters amd black spots. I get dizzy often. Has anyone else experinced these symtoms does it ever get better. I’ve had to quit school and my job because of how bad its gotten. I just don’t know how much more I can take..
Watch the floaters and black spots. See an ophthalmologist. I had those, and then one day the torn retina came on very quickly. First there was an increase in cobweb-ey floaters and then I saw the blood gushing within the eyeball like the color of old motor oil. Fortunately my ophthalmologist is not far away, the retinologist who did the laser treatment is in the same building and I got immediate attention. It’s another result of the connective tissue damage from fluoroquinolones.
Nutrition is always important, but especially so after being floxed. One thing that I believe helped tremendously with the joint/cartilage/tendon-ligament/connective tissue problem is bone broth. It gives the nutritional building blocks your body needs in a gentle highly absorbable form. Just be sure to use ONLY free range grass fed organic bones. Here is an excellent link. http://www.jadeinstitute.com/jade/bone-broth-health-building.php
Rich about your jerks I have them and never took lyrica in my life I was also given a high volume of cipro and other floroquinoles the only thing that has helped is my IVs from my naturopath I’m almost two years out and still have them badly. I can tell you physical therapy made them insanely worse. I suggest going to a good naturopath that treats nervous issues or trying unda therapy I am going to be trying that in a couple of weeks
Has anyone felt The same. I was rushed to The ER 2 months ago. With a heart rate off 219. And since then i have trouble with really bad heart palpitations. And i can feel like a really bad pounding in my stomach, like my heart is in the stomach. So weird! Has anybody felt The same? And got that better?
I was Hurt from flagyl 1 year ago. And have so many things going on in the body. But after a half year i could see some small changes. I was still awful, but at least i could walk. But The bad headaches was still there, The really severe fatigue and dizziness and off balance and The bad neuropathy. And then 2 months ago… BAAM… And The heart was pounding like crazy and i was rushed to The hospital. And now i am back to where i was in the beginning, and are even worse. And cant function at all. That feels like a bad sign, that my health are even worse than before. Is it normal to be back to square one? I dont know how i can go on with all this. Feels like im going to die. That my body cant take this anymore soon. I also get this collapses, where i almost faint, several Times a day. Im so scared. Try not to panic, but it is so Hard. Thanks for listening.