woensdag 8 juli 2026

fellow floxie, Íon Mórdha has lost his fight with fluoroquinolone antibiotic toxicity.




 Today, I received the devastating news that friend and fellow floxie, Íon Mórdha has lost his fight with fluoroquinolone antibiotic toxicity.


Over the years, Ion and I exchanged countless messages, voice notes and the occasional long phonecall. He was an unwavering pillar of support for me and so many others. When I was navigating my own regressions and severe neuromuscular events, he was there with vital advice on nutrients, histamines, healing strategies and emotional support to keep me going.

​Before this toxicity stole so much, Ion loved traveling, marathons, mountain biking, and filled the world with an incredible sense of humor. He was a bright, guiding light in the fluoroquinolone injured community, and his absence leaves a profound void. He will be deeply, greatly missed.

Last year Ion sent me a short biography describing how his life changed when he became poisoned by fluoroquinolone antibiotics if you care to take a moment to read...

My name is Ian Patrick Moore. May 21st, 2022, was the day my life ended as I knew it to be. The next day, I popped the first ciprofloxacin (Cipro) pill, little did I know that it would be the last time I would enjoy the sun on my face or take a simple walk. The first dose of this antibiotic was the beginning of a nightmare, and the days following were filled with hellish symptoms, both physical and mental. My mind, once sharp and dependable, became a foggy abyss of intrusive thoughts and confusion. Simple things—like walking to the shop or reading a book felt insurmountable.

The first suicidal thought struck me like a lightning bolt. I was walking through my neighborhood, desperately trying to ground myself, when the passing train caught my eye. I thought about stepping into its path, ending the nightmare before it consumed me entirely. An old man saw my hesitation and stopped me, asking if I was okay. I lied. I told him I was just feeling “a little off.” But deep down, I knew that something had gone catastrophically wrong.

The physical symptoms began almost simultaneously. My bladder burned as if it were filled with acid, and I couldn’t sit for more than a few minutes without unbearable discomfort. The sun, which once felt warm and life-giving, now left me shivering and manic, as though my very nervous system was rebelling. I didn’t understand it at the time, but the antibiotics had crossed my blood-brain barrier, wreaking havoc on my GABA receptors and destabilizing my central nervous system.

Within weeks, I was no longer myself. My legs felt weak, as if the muscles were dissolving beneath my skin. My feet burned like they were pressed against hot coals, and the simplest tasks became Herculean. Insomnia set in, robbing me of the one thing I desperately needed to heal. My nights were filled with sweat-soaked sheets and the constant sensation of being on the edge of panic.

Food, once a source of comfort, became an enemy. Certain foods scorched my gut, while others sent me spiraling into fits of anxiety. Every meal was a gamble, and I began to dread eating entirely. The weight began to melt off me, a cruel confirmation that my body was failing to absorb the nutrients it needed.

I was once a healthy 72 kilos, fit and active. Now, I was a shell of myself—frail, emaciated, and barely holding on. No matter how much I ate or how high-calorie the meals were, my weight continued to plummet, sometimes dipping as low as 47 kilos. The contrast was staggering, and I couldn’t understand how my body could betray me so completely.

I sought help, desperately trying to find someone who could explain what was happening to me. My local GP believed me from the start. They listened, empathized, and offered their best support. I will forever be grateful for their belief in my suffering, especially when so many others doubted me. But the doctors I saw afterward seemed uninterested in my case. I went to the local A&E in Bristol, telling them about my burning feet and the suicidal thoughts that were beginning to dominate my days. Instead of understanding or compassion, I was handed another prescription for 4-6 weeks of ciprofloxacin.

When I expressed my concerns, the doctor brushed them aside. She told me about her own experience with doxycycline, how her skin had peeled off her fingers but she’d “pushed through” because the benefits outweighed the risks. Her words were hollow and cruel, a dismissal of the agony that was consuming me.

Luckily, I did not take the full 6-week prescription that the hospital doctor had prescribed. I stopped the ciprofloxacin on my own, knowing deep down that it was only exacerbating my suffering. But that act of self-preservation, while saving me from further damage, didn’t end the nightmare—it only prolonged it.

This pattern repeated itself with nearly every doctor I saw. Neurologists, gastroenterologists, rheumatologists—each one ran their tests, shrugged their shoulders, and told me there was little they could do. The few who acknowledged the possibility of fluoroquinolone toxicity offered no solutions, only confirmation that I was part of a rare, unlucky group.

By the summer of 2024, my body was no longer my own. My muscles had wasted away to the point where even sitting was excruciating. My once-strong legs, the same legs that had powered me through cycling marathons, were now swollen, weak, and useless. I couldn’t climb stairs without assistance, and walking outside felt like dragging dead weight behind me.

The heat only made things worse. My body, now hypersensitive to everything, reacted violently to even a few minutes in the sun. My skin burned, my joints ached, and the nerves in my legs and pelvis felt like they were being electrocuted. Histamine intolerance, once a concept I barely understood, now dictated every aspect of my life.

Ion Mordha

Ion, may the heavy burdens you carried so bravely in this life be finally lifted from your shoulders. May your spirit return to the wild, open trails you loved, riding free, uninhibited, and surrounded by peace. We honor the light you gave to so many of us in our darkest hours. Rest beautifully, my friend; your kindness and strength will never be forgotten. Godspeed.
Minder weergeven

Opmerkinge


donderdag 2 juli 2026

“El Levofloxacino me daño de las rodillas hacia abajo… casi no puedo caminar” Es el testimonio de Titisita,

 https://www.facebook.com/reel/903858036077518?locale=nl_NL


**English Translation:**


“Levofloxacin damaged me from the knees down… I can barely walk.”  

This is the testimony of Titisita, an elderly woman who was prescribed the antibiotic Levofloxacin. The U.S. FDA warns that Levofloxacin is contraindicated in people over 60 years of age because they have a significantly higher risk of suffering its serious adverse effects.


**Fluoroquinolones Alert** is an account run by people affected by the antibiotics Ciprofloxacin, Levofloxacin, Moxifloxacin, and Norfloxacin. Every single day, without exception, we receive new testimonies from individuals who have been seriously injured by these drugs.


The U.S. FDA and the European Medicines Agency (EMA) have issued warnings and restrictions on the use of these antibiotics due to their serious, disabling, and potentially permanent adverse effects. In 2024, the UK’s MHRA introduced a mandatory restriction on their use.


The FDA has warned that these antibiotics can cause:


• Tendinitis and tendon rupture  

• Peripheral neuropathy (nerve damage)  

• Severe muscle and joint pain  

• Muscle weakness  

• Nervous system disorders  

• Anxiety, insomnia, and neuropsychiatric symptoms  

• Disabling effects that can affect multiple body systems


One of the most concerning aspects is that reactions can appear **during** treatment or even **weeks and months after** stopping the medication.


The FDA has also stated that for common infections such as sinusitis, bronchitis, or uncomplicated urinary tract infections, the risks of fluoroquinolones may outweigh their benefits when safer alternatives are available.


Unfortunately, in Latin America, fluoroquinolones are still routinely prescribed as first-line antibiotics without any warning about their serious risks. Because of their massive and indiscriminate use, thousands of people have been seriously injured.  


**Avoid tragedies. Avoid fluoroquinolones.**
------------------------
original Spanish

“El Levofloxacino me daño de las rodillas hacia abajo… casi no puedo caminar” Es el testimonio de Titisita, una mujer mayor a las que le fue recetado el antibiótico Levofloxacino. La FDA de EE.UU advierte que el Levofloxacino esta contraindicado en mayores de 60 años debido a que tienen una probabilidad mayor de sufrir sus graves efectos adversos.
Fluoroquinolonas Alerta es una cuenta de afectados por los antibióticos Ciprofloxacino, Levofloxacino, Moxifloxacino y Norfloxacino. Todos los días y sin excepción recibimos nuevos testimonios de personas que han sido gravemente lesionadas por estos fármacos.
La FDA de EE.UU y EMA de Europa han emitido alertas y restricciones al uso de estos antibióticos debido a sus graves efectos adversos discapacitantes y posiblemente permanentes. En 2024 la MHRA de Reino Unido emitió una restricción obligatoria a su uso.
La FDA ha advertido que estos antibióticos pueden causar:
• Tendinitis y ruptura de tendones
• Neuropatía periférica (daño nervioso)
• Dolor muscular y articular severo
• Debilidad muscular
• Alteraciones del sistema nervioso
• Ansiedad, insomnio y síntomas neuropsiquiátricos
• Efectos incapacitantes que pueden afectar múltiples sistemas del cuerpo
Uno de los aspectos más preocupantes es que las reacciones pueden aparecer DURANTE el tratamiento o incluso semanas y meses DESPUÉS de haber suspendido el medicamento.
La FDA también indicó que, para infecciones comunes como sinusitis, bronquitis o infecciones urinarias no complicadas, los riesgos de las fluoroquinolonas pueden superar sus beneficios cuando existen otras alternativas más seguras.
Lamentablemente en Latinoamérica las Fluoroquinolonas aun se prescriben como antibióticos de rutina y sin advertir de sus serios riesgos. Debido a su uso masivo e indiscriminado, miles de personas hemos sido gravemente lesionadas. Evita tragedias, evita las Fluoroquinolonas.

maandag 25 mei 2026

Another Flox Kiley K Woodland



 https://www.instagram.com/reels/DYlQ5SHsX4n/



**Information on the Instagram Reel**

**Link:** https://www.instagram.com/reels/DYlQ5SHsX4n/

**Creator:** Kiley K Woodland  
**Account:** @celebratethelittlewins  
**Duration:** 57 seconds  
**Publication Date:** May 21, 2026  
**Engagement (at time of verification):** 69 likes and 6 comments

### Content Summary
This is a motivational and spiritual Reel focused on personal development and resilience. The video features Kiley K Woodland delivering an encouraging message about overcoming hardship.

**Full text overlay / spoken message:**

> “There is beauty in the breaking. You do not need to have your entire life figured out to move forward again. Little wins...one day at a time. If you feel alone and demoralized and exhausted in your journey ahead, please know I’m right there with you. Shit sucks and it’s hard beyond anything I could even describe but I do have to believe there are so many blessings on the other side of this for both of us. Even when we can’t see it, God and our guardian angels are busy helping plan our comeback. Outlast the temporary and hold the vision..I know it’s gonna be worth it 🧚🏼‍♀️✨”

### Context
Kiley K Woodland runs the account @celebratethelittlewins, where she shares content centered on personal growth, overcoming challenges, faith, and celebrating small victories. She describes herself as a singer-songwriter, survivor, and advocate.

Would you like assistance with downloading the video, more details about her profile, or any other specific information?



donderdag 21 mei 2026

Tatiana Jones

https://www.facebook.com/tatiana.jones.710
 The list of symptoms my daughter had for several months, which medical doctors attributed to anxiety and depression because she “looked too healthy and was too young to be that sick.”







Also, most of her tests used by the health system traditionally were coming out as relatively normal, but the more comprehensive tests she took and paid out of pocket for, from independent labs, were overlooked or ignored by physicians because they didn’t order those. Those tests were showing neural inflammation and physiological changes in her brain.
Doctors disregarded those test results and her statements because she was showing more knowledge of the disease than they had ever heard of. Doctors were too proud to admit that someone else with rudimentary knowledge in general medicine was smart enough to read and understand science articles and be able to diagnose herself by the process of elimination.
And why should my daughter and other neglected people with rare, complex, and poorly understood, poorly researched illnesses take that route? When will this stop? What about people not as witty as my late daughter? Do they stay in the dark for the rest of their lives trusting ignorant doctors’ opinions just because they have an MD title attached to their names? The health system of this country is in deep, murky water.
There are now non-medical companies in existence that are playing the role of “patient advocates,” helping people navigate between various health specialists, health insurance policies, claim rejection appeals, referrals, and complex terminology of test results doctors do not take the time to explain. (Solace Health as an example)
Shame, shame, shame! We need to take our right to accessible, affordable, and fair healthcare back! Who is with me?
***
List of symptoms Lena had
Intestinal failure and a hypersensitive gut requiring intravenous feeding
Severe weight loss
Severe stomach pain
Nerve pain (neuropathic pain)
Body pain including constant burning, itching, crawling, and throbbing sensations
Unpredictable muscle spasms affecting limbs, head, and body
Post-Exertional Malaise
Profound exhaustion
Painful swelling of hands, feet, and face
Head pain
Severe Migraines
Ear pain
Tinnitus
Dizziness
Eye pain
Visual disturbances
Blackouts
Loss of proprioception [a reduced or absent ability to sense the position, movement, or orientation of your body parts without looking at them]
Loss of mobility, eventually becoming wheelchair-bound and then completely confined to bed
Loss of function
Persistent infections
Severe cognitive dysfunction affecting speech, memory, word recall, interpretation, concentration, and processing
Slurred speech
Muscle dysfunction and weakness
Nausea and vomiting
Swallowing difficulties
Numbness and pins and needles
Loss of temperature control and temperature sensitivity, overheating, and shivering
Extreme hypersensitivity to light, touch, sound, smell, and movement
Hypoglycaemia
Intolerance to heat and cold
POTS - postural orthostatic tachycardia syndrome
Sleep disturbance

Breathing problems and air hunger
Remembering Lena Jones with endless motherly Love 🌺❤️🌹💐🌹❤️🌺










vrijdag 30 januari 2026

Kovács Magdolna Júlia : prescribed a drug combination: Savulin + Cataflam + Fromilid Uno.



 In December 2020, a general practitioner (let his name be Bobby) – not my own GP, I only went to him because I could not reach my regular doctor – without any examination, based solely on my single sentence that

“I have been coughing for a long time, but my lung capacity is good,”
prescribed a drug combination: Savulin + Cataflam + Fromilid Uno.
This combination is professionally contraindicated and is listed in drug–drug interaction databases as a high-risk, potentially life-threatening combination.
After prescribing the medication, Bobby asked me to come back to him, and when I reported the severe symptoms that appeared after taking the drugs (which started with an anaphylactic shock), he stated that he was not obliged to continue treating me and told me to find another doctor. In practice, he abandoned me.
After that, I tried to ask for help by email, describing my symptoms and deterioration in detail. In my desperation, I used phrases such as
“you killed me” and “you destroyed my life.”
(Bobby then started spreading claims about me, saying that I was paranoid and schizophrenic. In May 2022, he even called one of my acquaintances by phone and told them that he would “get rid of me” and “destroy me,” and that I was schizophrenic.
I have written evidence of this: my acquaintance wrote down that the doctor called them and said these things.
Naturally, the police were not interested.
My acquaintance has never been questioned.)
The doctor selected only those phrases from my emails such as “you destroyed my life” and “because of you I became disabled,” and submitted only these to the police.
The detailed descriptions of side effects and health damage were ignored.
Instead of receiving help, he filed a complaint against me for harassment, defamation, and insult.
As a consequence, I was arrested and photographed (mugshotted), questioned as a suspect, and had to appear at the police station.
This is the beginning of my story.
After the medication-induced injury, within one year I achieved approximately 60–70% improvement. I consciously protected myself: I did not run or jump to avoid deterioration. However, real recovery did not occur, because fluoroquinolones affect the body at a cellular level (interfering with DNA), so my condition stagnated for a year.
Then came my second health injury (October 25, 2022): an ENG examination that was not an examination at all, but a procedure involving severe electrical exposure, which I consider an execution.
No doctor was present, only a medical assistant, despite the fact that international protocols require a physician’s presence.
Why was there no doctor present in my case?
An important fact is that Bobby, one month before the examination, became my GP again without my knowledge or consent, and therefore saw my referral for the ENG test.
After the procedure:
my body convulsed every 20 minutes for weeks,
my nose and tongue became numb,
two thick, symmetrical red stripes appeared under my breasts, which disappeared only after a year,
the “electric current” ran through my brain for almost two years,
a cavernoma appeared, which I did not have before,
my right leg below the knee suffered nerve and vascular damage, my knee remains sensitive to this day,
I still feel the electricity in my foot, as if it were plugged into a socket,
bowel function became paralyzed; since then I can only remove stool manually. The stool presses on the nerves, causing horrific pain. When the bowels are empty, there is no nerve pain in the rectal area, therefore this is not spinal in origin.
A video showing my condition after the examination:
What electrical current can cause:
To this day, the hospital refuses to release the most important evidence:
the strength of the electrical current applied by the medical assistant, whose qualification and certification have never been verified.
No medical assistant is allowed to perform an ENG test without a doctor present.
After my second injury, I made the mistake of writing emails to Bobby several times, calling him a “spineless worm.”
Third health injury – April 2023
Out of nowhere, a man with an unusual name (Patryck Gold) appeared, presenting himself as a physiotherapist and chiropractor. He claimed that he had seen my post-ENG video and offered to help me improve my condition for free.
I told him clearly that I must not be pulled or jerked, yet that is exactly what he did.
He forcefully yanked my electrically injured foot toward himself and pulled my thigh upward while I was standing.
He knew how to cause damage, as he practices combat sports.
My body, already damaged by electricity, suffered additional injuries from the jerking: pelvic, ankle, and foot contusions.
Since then, I have become mobility-impaired.
After the incident, I realized that his appearance was not accidental. His only goal was to cause further damage. That is why he lied about being a chiropractor and physiotherapist, so that I would not resist him touching me.
He did not come to steal or for sexual reasons – that is clear.
I asked him whether he knew the medical assistant who had caused the electrical injury. He immediately blocked me, although he had been messaging me intensively before.
He blocked me because I realized what was really going on – this is obvious.
Since then, I walk like a 100-year-old, cannot bend or squat, cannot lift more than one kilogram, everything feels unbearably heavy.
The purpose of these additional injuries was clearly to blur and merge the physical damages, making accountability impossible.
I am not writing this to seek pity, but to show how the system works.
About the authorities’ “work,” an entire novel could be written.
The person in the picture is me.

Kovács Magdolna Júlia 

dinsdag 27 januari 2026

Myti M. J. van Staveren-de Jonge




 https://www.linkedin.com/in/myti-m-j-van-staveren-8a1282153/

Myti M. J. van Staveren-de Jonge

 She/Her  Derdegraads connectie
FQAD: Ik houd graag mijn kennis up to date. LinkedIn is daarvoor een prima medium. Mijn interesses o.a. : FQAD (Fluoroquinolone Associated Disability Syndrome)), Long Covid, ME, CVS.
Amsterdam, Noord-Holland, Nederland  

Info