Chris’s Story – Cipro and Ibuprofen

Chris Landscape

I was prescribed cipro for a toenail infection on October 22nd. I went to the emergency room at 3am because it hurt so bad (the ingrown toenail). I was given a script of cipro and ibuprofin 800mg. I went to walgreens, picked the script up, asked the pharmacist if it was okay to take together and he said “yes just make sure to eat something so your stomach doesn’t hurt”

I would say what I experienced was way more than a hurt stomach. I was dizzy, anxious, bedridden and eventually suicidal and wanting to hurt other people after taking this med. Just so you know I am a very loving person, just a very traumatic thing for me I had severe chest pains 24/7. I went to the ER eight times with no luck. I was sent to the psych ward against my will once and then the second time just for being suicidal. I was so suicidal I wanted to jump eight floors from my balcony or buy a gun and shoot myself in the head. I was actually going to go to the gun store down the road, buy a gun, drive two hours away to the hills just to end my life.

I would rather have had my toe amputated instead of going through life like I did bedridden and suicidal and wanting to attack other people especially loved ones. Just think how hard that is. I am also $2500 in debt just from completely clueless doctors after literally EIGHT er visits! Just glad I have insurance as my total care was over $50,000! I too have suspicions when going to the doctor now, just wondering if they really have any idea what they’re doing. Just before leaving the ER that night the doctor told me the med (cipro) was just a generic med, made it sounded fine, just trusted what he said and went and took it. I took 20 pills over the course of two weeks.

I would have liked to known blowing my brains out was a possibility. I would have liked to known about buying a guy driving two hours away to end my life was a possibility. I would have liked to known jumping eight floors or wanting to hurt other people was a possibility as well. I would have liked to have known about the eight ER visits and two psychiatric ward visits as well. I would have liked to known about the debt as well. I would have gave it (the cipro) right back to him. I would have opted for an amputated toe instead of this mess – left me traumatized basically. I would like an explanation how I go to a fun loving uncle on October 21st to picking my prescription up on October 22nd at 3 in the morning wanting to jump eight stories or blow my brains with a gun out the day after taking this medication. I would hope doctors share my story with their patients before giving them this medicine. FORTUNATELY, I am better now and back to normal. I am no longer suicidal and living a normal life now, just lucky I guess. I would have to put this med alongside with date rape drugs or something, just completely messed up medication. Just can’t help but wonder sometimes..just take this medication off the market. I wouldn’t know if it has uses or not. I wouldn’t know as I’m not a doctor, just a computer technician. Just as a follow up, this med and the other floros are on my allergy list now, just so I never take them again.

Michelle’s Story – Cipro Induced Lupus

Michelle Lupus

The diagnostic paperwork says, “Lupus – onset 3yrs ago: Triggered by Cipro use.”

 

Michelle’s story:

July 21st.2011 a day I will never forget. The day that I had my severe adverse reaction to Cipro.  The day prior I had went to my Dr.’s office because I felt the onset of a UTI, my children were in town and I didn’t want to be laid up in pain.

The Dr. asked me if I had taken Cipro before, I said “no.”

She then said to me really fast “If you feel pain in your arms let us know”. Then headed out to see the next patient.  I took 3 pills.. a dose and a half. An hour or so after my last pill I took I was so weak to lift my finger felt heavy.  My body ached everywhere. I then became so tired … It took my husband about 10 minutes to wake me up..to even get a reaction out of me.

Ever since then I have experienced heart racing, seizure, temporary hearing loss, stinging, burning, tingling, and numbing in my arms, legs, wrists ankles fingers shoulders…everywhere.  I have been up for hours at night crying in so much pain everywhere I just wanted to die.  So weak, exhausted. I have had loud ringing in my ears, my blood pressure has elevated to 140/100. I have never had high blood pressure. I am losing about 3 pouds a week. I have a huge loss of appetite.

I feel as though acid is running thru my veins and my body is burning inside.

These are just some of the things I have experienced , certainly not all.

Prior to Cipro I was active, loved to laugh, loved to go on walks. I smiled all the time. Now I am lucky if I can walk down 3 aisles at the store without stopping. It takes so much energy just to laugh.

Cipro has robbed me of me. Sucked everything out of me.

I didnt want my kids to have to deal with me in any kind of pain while they were here, I was doing the right thing by seeing the Dr.

What they ended up seeing was me in devistating pain, tears that will not stop and wondering if I was going to make it.

The Dr. didnt try anything else prior to giving me Cipro, didnt tell me that it had huge risks.. didnt even give me the option to choose.

I am forever scared of Dr.’s and they’re intent from now on.. never will I trust them.

I have told everyone I know to never take this , Those closest to me have seen the devistating effects of Cipro. For I have felt pain where I never knew pain existed..

My life has done a complete change.. the life I once had is gone. The mental anguish this has given me is beyond words..

everyday something new..the pain never stops.

Note – Three years after Michelle took Cipro she was diagnosed with Lupus.  Her paperwork stating that Lupus was brought on by Cipro is pictured above.

Christopher ‘s Story – Cipro changed my life forever

Swallow This

18 months ago, my liver shut down and I was diagnosed with end-stage Liver disease.  I was in and out of the hospital 13 times and the last time I was on my back for almost 3 months.  During the most critical phase of my treatment, I was prescribed ciprofloxacin (Cipro) to fight infection of the fluid that was gathering in my abdominal cavity.  I was given the Cipro in the hospital and then upon my release was prescribed 100mg Cipro daily.  The fluid eventually ceased to be a high priority concern, but even though I was under the care of several specialists, none of them were aware of the toxicity of this drug.

I was unaware of the danger too.  I was very sickly and symptomatic but figured that it was my liver causing all of these issues.  The fluid retention was directly due to my liver failure, but some of the other symptoms began to get worse and I thought that it was what dying felt like.  I can’t list ALL of the symptoms, but here is some of what began to happen; my vision began to deteriorate and I was seeing light and shadow forms.  I got glasses but grew out of the prescription in weeks.  My hearing became distorted.  I started to have a lot of forgetfulness and confusion.  When I went places I would blank out and not know where or why I was there.  I started to find it difficult to remember how to speak, I couldn’t remember the last word I said or what I was even talking about.  I was fatigued all of the time to the point where I had to lay down during my meals.  My blood pressure was so low that I had some mini-strokes and have some permanent residue from them.   I couldn’t lift my arms above my head and it was painful to stand up.  I started getting injured a lot…in bed!  I would roll over on a pillow and something tore in my ribcage.  The pain from these injuries would last about a month and this happened 6 or 7 times.  Finally my teeth started to deteriorate and calcify as well.  This happened very suddenly.  My teeth then began cracking and breaking off at the gum line.  Eventually I lost all of my teeth.  It was the scariest thing I have ever experienced in my life.   Eventually it got to the point that I felt as if I had gone crazy and there was no return.  I began planning my funeral.

My liver numbers were getting better but I was feeling worse.  People said that I was just run-down, but after my teeth fell out, I knew something was very strange.  I started to get curious about some of the meds I was taking and found an article titled “Cipro is Poison”.  In that article, the author mentions dental damage and then I started reading about the other symptoms.  I had every single one of them.  I immediately stopped taking Cipro.  Slowly, very slowly some of the most painful symptoms began to subside a little.  My memory started to come back, eventually I stopped tearing connective tissue, I could speak better and movements became less painful.  Of course my teeth are never coming back but I took Cipro for 8 months at that dosage and I am just thankful for some of the symptoms to have ended before the damage even got worse.

I do not blame my doctors.  I have great doctors, but they were not informed or aware of the long term damage that Cipro can do.  They were too busy saving my life to do the research that should have been readily available to them.  Both the manufacturer and the FDA minimize these findings and take what is plausible and try to pin it on the other’s side.  No one will admit anything.

I am still awaiting a liver transplant, but I am healthy.  Besides my teeth, the most lingering effects of the Cipro are joint and muscle pain.  I also feel my diet had a lot to do with my recovery, but that’s another topic.  The only thing I can do at this point, is NOT TAKE CIPRO!  For when I get my transplant, I have it written into my chart that I refuse Cipro in ALL situations.  I hope this helps someone to cope as the article I read, did for me.

Heather’s Story – Cipro and Avelox

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Bill’s Story – Tendon Pain from Cipro Ear Drops

Bill FQWall

Hello All,My name is Bill.I,m a 60yo who lives in Australia and a victim of cipro.I went to see my doctor and was prescribed ciproxin eardrops for an ear infection.They didn,t seem to help my ear so went back to doctors and told him my shoulders were very sore and I had a strange rash on my back.He sugested I may have tendonitis.Days later I discovered the conection ,cipro and shoulder pain ,on the internet.By this time my shoulders were a real problem.One had gone all clunky and the other, my left, had waves of searing pain.Lying down was unbearable and sleep none existant.I told my doctor that I suspected cipro, and was told , very unlikely.I got a second opinion from another doctor and he treated me like a fool.There are no warnings on my medication at all and none from either doctor.9months later and it just gets worse,awfull neck pain,twitching in my shoulder,constant fatigue,no sleep,pain that makes me vocalise at night,dry mouth, unable to lift arms above my shoulder etc.I was allways active and enjoyed playing my keyboard but that is now limited .I cant believe I,ve found myself in this situation.I now sleep alone so as not to disturb my wife .We , who are poisoned, need to warn others and let it be known,DO NOT TAKE CIPRO.
My sympathy to all,Bill

Missie’s Story – Cipro Side-Effects

Missie FQWall

This is a very hard story for me to tell. It all started four months ago with what I thought was a bladder infection. I called the doctor and had him prescribe something over phone. He called in a script for Bactrim which I took for three days but it didn’t make anything better so I decided to go to the doctor. I have a urine sample. They said there was no sign of infection but they would send it out for culture. In the meantime try cipro since its a broad spectrum drug. He asked if I had a problem with quinolone drugs. I had never taken cipro before so I told him I didn’t know since this would be the first time taking it. I took it starting march 12th for three days at 250 mgs twice a day so a total of six pills. On the third day I was walking up the stairs and felt a sharp pain in my knee. I had read about tendon issues so I immediately went online and what I read horrified me. I have anxiety issues already so reading all of these stories really put me over the edge. Five days later I got burning pain in both achilles and started to get non stop muscle twitching in my calves. I went to the emergency room and was told that this can happen from cipro and I was given lidocaine pain patches which didn’t do a whole lot. I started to get burning places all over my body and pin pricking sensations. I read all of the supplements that seemed to help people and tried many of them. Over the next month or so things seemed to be getting some better. The burning pains seemed to be dying down. I was getting sharper pains in my achilles tendons but they weren’t constant. Three months in I started doing physical therapy for my tendons and that really seemed to help the pain and strengthen them. Now just this past weekend four months in I started to get intense burning mainly in my hands and arms but intermittently in random places in my body. Some of the muscle twitches are coming back. I’m beyond terrified right now that this is going to be permanent. I’m only thirty years old and newly married. I’m afraid this is going to keep me from having a family and keeping my job. I can’t believe that this is all happening from an antibiotic that I didn’t even need. I keep trying to pray and stay as positive as I can but its very very hard. I get down very easily and cry alot. Especially because once I started physical therapy I really thought things were turning a corner. I hope that I don’t have permanent nerve damage and that this doesn’t get even worse. I hadn’t wanted to post my story before because it made it all too real that this was happening to me. But I know now it is real, it is happening and there’s not much I can do but hope that things don’t get worse and improve to a point where I can live my life and have the things that have always been so important to me.

Tamara’s Story – Ciprofloxacin Effects

Tamara FQwall

I was floxed by Ciprofloxacin February 4th of this year. I took two 500 mg doses of it, and began to feel like my leg was swelling, so I discontinued use. Two days later I was in the emergency room with what they thought was a blood clot. All tests came back negative. At this point any doctors I spoke to didn’t believe it was the cipro and I even had a nurse laugh at the suggestion of it.

It was then that I decided to look into it online and it opened up an entirely new, and scary world for me. Over the first week the pain began. I was in excruciating pain, it felt like my leg was being ripped apart. I was diagnosed with “tendon issues”, maybe tendonitis from my doctor and given percocet for pain and no other options.

I began a strict eating plan and “detox” schedule. I used schizandra tincture and detox tea, as well as eating a mostly vegan, high veggie and juicing diet. I went through many “detox symptom” days. I can’t say this has helped my reaction to be less severe than it would have been, but it’s possible. I also have been able to spend the entire 7 weeks post floxing at rest. This also could add to a quicker turn around.

It’s been a long seven weeks. My main symptoms have been tendonitis from hip to toes in my right leg. I’ve also experienced insomnia, tremors, anxiety/panic attacks, muscle atrophy from not using my leg, bouts of nausea , headaches, lethargy, burning/shooting pains throughout my body.

I am a dancer, I have been for 25 years. I competed, I ran a very successful agency for performers (including performing myself) for the last 4 years. I sold my portion of my company to move back out into BC, Canada, in nature and go back to teaching dance. This has completely stolen that from me…let alone being able to do most anything most days.

I have been seeing a naturopath who has been doing myofascial release on my leg to free up tightness. (I spent the first 5 weeks with my leg in a permanent semi bent position). We have also been doing Myer’s Cocktail and Glutathione IV therapy.

As of this week, I finally have some mobility in my leg, but the anxiety and panic attacks have worsened. I know it’s been suggested that the fluoroquinolone is stored in the tissues and I figure the myofascial release has been releasing it into other parts of my body.

The worst part of this for me is facing my greatest fear of not being able to do what I love: dance.

I have hope that i will get better, and maybe sharing what I have done will help others to gain some relief.

Lastly, I hope this serves as a warning to anyone who is thinking of taking the fluoroquinolone class of antibiotics. It’s just not worth it!

The picture I have attached is of me performing last summer in front of 14,000 people…now I can’t even walk. What a shame.

Traci’s Story – Cipro Poisoning

Traci FQWall

It has almost been 3 years since I took a 30 day supply of Cipro for a UTI that has
changed my life drastically. During the course of of taking Cipro the first thing I
noticed was how incredibly weak my body felt and fatigue hit so hard I couldn’t
keep myself awake for anything. I would sleep for days, calling in sick to work,
somedays were so bad I couldn’t even manage the phone call and slept right
through the day. A couple weeks after stopping Cipro the aches and pains started
first in the top of my feet and ankles. Then my wrists and forearms as if I had some
harsh form of tendonitis. I started wrapping my wrists, arms and feet with K Tape
on a daily basis.

I had no idea what was causing these issues, but started the research on Cipro as I
had read about tendon ruptures. I went back to my doctor whom I had been seeing
for 10 years and mentioned the problems and she immediately became defensive
and made a comment about how people should not read forums and try to
diagnose themselves. Basically she made me feel like I was way off base and had
no idea what I was talking about. That was my last visit to her. Not because I knew
she was wrong, but because she didn’t listen and very clearly did not want a simple
minded patient telling her what they felt was wrong. After all she did have 7+ years
of med school.

My eye sight started going bad very quickly which for some reason I attributed to
age (I was 41) even though it was only a matter of months after an eye doctor visit.
Within the first few months after taking Cipro I had constant tingling, numbness,
brittle feeling as if I had no muscle in my body, depression that I couldn’t control,
loss of balance and running into things that were right in front of me, anxiety, panic
attacks so bad that I would not leave the house, insomnia that lasts for days at a
time, and nightmares. I started to see a holistic doctor, not covered by insurance,
but I was hoping she could find cause of pain. I didn’t mention the Cipro I had
taken a year earlier as I thought I was wrong about the cause and thought if it was
really the reason for my problems it wouldn’t be on the market. My holistic doctor
diagnosed me with fibromyalgia and chronic fatigue syndrome and wanted to run
tests to find heavy metal toxins in my system after a couple of months of taking
some supplements such as magnesium, omega-3, vitamin K, B-12, and prescription
strength vitamin D.

We also talked about stress management due to my job and I decided after 16 years
I would leave my position and went to a smaller startup company. But the
problems persisted and after three months with the new company they let me go as
I could not make it to work, I missed at least one day a week and could not control
it. I would be so exhausted from insomnia that when I tried to close my eyes I
would see faces of people shouting at me and immediately jerk back awake.

I couldn’t explain and was afraid to tell any doctor for fear that they would label me
psychotic. Again more research pointed to Ciprofloxacin-induced acute psychosis.
Not only had I left a company I had been with for my whole career and lost a great
salary and great benefits, but I’ve lost years of time with my family. I lost moments
that I will never get back. I still have up and down days, the symptoms come and
go, short term memory is horrible and embarrassing at times.

Finally a few months ago I heard FDA announced the link to peripheral neuropathy
and started reading about what Cipro has done to others I at least know I am not
crazy. Levaquin almost sounds worse. I am not about to let Bayer get away with
what has happened and I have an appointment with neurologist coming up. 3 years
and I can say symptoms showed up from first couple of weeks during treatment and
new symptoms continued over months after completing the drug. Some even a
year later.

I’ve reported adverse reaction to FDA, signed petitions to remove the drugs from
the market, and participated in a study over a year ago with a college that
contacted me after a post I left on http://www.askapatient.com, and I’ve contacted a
lawyer and I plan to be an advocate every day of my life especially after reading
about how many others have been impacted, lost their lives, or completely disabled
on the various support groups on the internet. I don’t want to delay any longer, I
want to make sure no one ever goes through this. I am no longer ashamed and that
is because of these support boards and stories from others that are so helpful. I
appreciate every single person that has came forward to tell what these drugs have
done to them. Don’t ever let a doctor make you feel stupid when you ask questions
about medicines or symptoms. Some have such ego problems or just completely
uninformed that they don’t take the time to listen. You know your body better than
anyone.

Laurie G’s Story – Levaquin and Cipro Effects

Laurie G FQWall

I am a 42 year-old female living in San Antonio, TX. I was a daily runner, in great health, and own my own Service Dog training company for wounded warriors and civilians with disabilities. In mid 2011, I was prescriped Levaquin for an upper respiratory infection. I had a classic swollen tongue-type reaction. The doctors noted this, took me off the Levaquin, and started me on something else. In December of 2011, I went to the military ER for a bad UTI. Despite my big red band that said severe allergy to Levaquin, I was given Cipro. I asked the doctor THREE times if he was sure I could take this. I then asked the PHARMACIST three times if I could take it. (My husband, and AF Officer, was with me the entire time). I went home, took two doses of the Cipro, and my life has never been the same. I was in such excruciating lower back pain, pain down my buttocks, and down my legs into my ankles that I was probably at the ER at least 6 times during the next three months to be put on IV Dilaudid or Morphine just to dull the pain. Then, I was sent home with Vicodin. The episodes would come any time I did a lot of physical activity, so I had to stop running. I also had to lessen my hours as a dog trainer (for which I received my Masters) because of the pain. Fortunately, I had a neurologist at the military medical center who had heard of fluoroquinolone toxicity. I had many, many workups done, and also consulted with Dr. Jay Cohen in San Diego. We sued the military hospital and they settled with us for a paltry $95,000 – of which we got $75,000. I am writing this because I just got home at 5 am this morning from yet another run to the ER with excruciating low back pain – so bad that my husband had to carry me. That makes probably over 15 visits to the ER in the past two years for exactly the same pain. It is indescribable. The effect it has had on my life, my career, everything – words could never express. If I could go back and write that doctor a personal note to let him know that his “tiny”mistake changed the course and quality of my life with two pills, I would.

Catherine’s Story – Cipro Poisoning

Catherine FQWall

I was floxed almost 2 years ago in 2012. I am 60 years old now. I was given 4 rx’s of Cipro/Ciprofloxacin (including 3 days of IV Cipro. in the hospital over a 4 week period, in 2012. The 1st Rx was given on May 21st and the last on June 24th …….when I became officially disabled. My last workday was June 21st, 2012. I was very active up until I was poisoned by Cipro. I went through the police academy at age 51 and became a Master Officer. Before this, I worked for 23 years in shipping / receiving . I worked as a jail officer for 7 years, with excellent reviews, and raises. I walked as many as 3000 stair steps a day in addition to regular walking. Before this, I worked for 23 years in shipping / receiving . I hiked the Blue Ridge Parkway as a hobby, enjoyed hunting and fishing, did trail rides with horses, liked gardening and tending to my yard/mini farm, etc… Sad to report they are things I haven’t been able to do today,

as a result of the Cipro toxicity. Continue reading

Jeff’s Story – Cipro Poisoning

Jeff FQwall

july 8 th 2008… 10 days of levaquin and the 8 days of cipro after being misdiagnosed.. My life has been ruined by these poisions.. I feel like I want to die nearly every day for almost five years now.

For the first year or so there were voices telling me to kill myself… That was about how long I stuttered as well.

me now… Shortness of breath ( some days worse than others) , severe brain fog , extreme muscle pain , 7 ruptured tendons , tendonitus , daily head aches , horrible vertigo , eye pain , joint pain…all of them , neuropathty , degeneritive discs , tennitus… So loud it wakes me up , memory loss , vision loss…. Liver and kidney damage

 

Eric’s Story – Cipro Poisoning

Eric FQwall

02/10/13

So, if I had a time machine…I would travel only once into the past. I would not revisit my youth. I would not undo any relationships, or resolve any issues of unrequited love. I would not try to right many wrongs, or turn my failures into successes. I would not say goodbye to those who were lost, that I hope to one day see again.

No…what I would do is…set that motherf***ing dial, for the exact moment that those drug pushing, poison peddling, whore-mongering, non-hippocratic-oath-observing, big pharma ass kissing, slow to learn and quick to earn, pathetically useless bastards, when they first asked me to take an FQ for my health and physiological betterment…and simply say, “No thanks… BITCH!!” “Now ask me again…GO AHEAD ASK ME AGAIN!! I DARE YOU – I DOUBLE FUC***ING DARE YOU!!!”

Ah yes, if WE only had a time machine…of this I am most certain. Continue reading

Mirella’s Story – Cipro Poisoning

Mirella FQWall

Hello everyone! I would like to share my story. I am from Mexico, and was given cipro xr 9 months ago for a UTI. Only had 3 500 mg pills. and I got floxed. I had panic attacks, coudn´t eat at all, survived for a month with water and ice in my lips. Lost 35 pounds in a month, diarrhea for 3 months, throwing up the water I drank, mental confusion, pain all over my body. Had multiple tests done here in Mexico and the USA, and apparently for the drs. I just had anxiety…jaja what a joke! MRI, scans, blood tests, brain scans because they thought it was MS or an autoinmune disease. Had to go to ER almost every week. I cried all day long, insomnia, couldn´t express myself well….like the words where not flowing…thought that I was dying every moment…I was scared, depressed, tired. Then I started getting bruises in my legs and small red dots in my hands. One of my toe nails fell, as well as my hair. The list can go on and on, but there is HOPE! Yesterday for the first time in 9 months I went walking 1 mile!!!

I send all my love and prayers!! You´ll get better!! Hang in there!

Thank you for reading and sorry if my english is not very clear. Cipro slows my mind sometimes!!

Jessica’s Story – Cipro and Levaquin

Jessica FQWall

Jessica Reid 01/24/13

My Name is Jessica Reid, 24 with a wonderful family of a husband, and 3 wonderful children. My life was Blessed! I started having some dizzy issues, went to a doctor i was told i could trust at the time i had no Health insurance… I wished i would of NEVER WENT! I was misdagionsed and put on 10 antibotics of the course of 4 months! One being Leaqvin (750MG)10 pills, but ionlt took 9. The whole time i had brain fog, Hallunications, Heart papls,Ear pain, Worse headaches, Tingling, Numbness, bruning pain. I called the doctor and i was told everything i had was “Anxiety” which i believe was BS! ive never had health problems before. After that i started getting pain in my back legs bathroom problems, i was told i had a uti! So i was put on CIPRO! 500mg 2x day for 10days… I got worse and worse by the 6th day i couldnt take it anymore, I ended up in the hospital, i was told i never had ANY infections and was put on all the antibotics for NO REASON. I was told to stop and to never take anitbotics again and that i may have a nerve diease. She was thinking MS,Lupus.My thryiod went to a 6.8 to 8.1 than back down to a 2.5, never had problems like that before. I also at this time had very bad bowel problems but was told it was normal due to all the anitbotics and my gut would get better. I found out that i had C-Diff for 4 months since starting antibotics and of course they wanted to feed me Falgyl also, got strep throat and they begged me to take another anitbotic. I have never been on drugs and hate taking them… They had me on xannx, Tried to get me Amritplyine? Celexa, and others.. I refused i would take 4 pills and stop. It just made me WORSE. Ive had and still have Nightsweats, Heart papls, eye pains, blurry eyes, stomach pains, Kidney pains, Ribcage pains, Pretty much muscle pain throughout my body, bone pain throughout my body, and nerve pain (tingling burning and throbbing) my ears pop all the time and my left one goes out than my face gets numb. I have Carple tunnel that ive never had! My life was taken from me! I LOVE being mother and wife! My life is around them.. Now i have to miss going to the school events, running aorund with my kids, pushing them on the playgrounds. I use to workout 2x a day 45mins now i cant do it anymore. I push myself to do 15mins x2 a day now but afterwards im screaming in pain.. Ive tried supplements, Espom baths, Detox pills, proboitics, And right now i have stoped all Redmeat and eat Organic Free Anitbotic Chicken and rice. I have no clue where to go from here. I would have ended things but my Family keeps me going. No doctors believe me. And i cant get justice but everyday im left crying in pain. I wonder if it will kill me? or will it ever go away? Please someone give me some good advice and tips. I was thinking of Ozone treatment, but ive heard scary stories about it. So im not 100%. Anyone has any advice please feel free to email me!!! I am sorry for everyone that is going through this. I hate the FDA and i hate Doctors now! I dont trust them with anything! So its hard for me now to listen to the ones that wanna see whats wrong with me.. I pray for all of us. Thanks for listening to my story!