Discussion in 'Health News and Research unrelated to ME/CFS' started by MarcNotMark, Apr 15, 2018 at 9:03 PM.
I will go to my grave knowing that I did not have ME/CFS until three days after starting on a "skookum" dose of Penicillin. That is when my ME kicked in, and within the year, allergies and Chronic Sinusitis.
Same here. I was having some bowel problems and a few allergies and intollerances. I then was prescribed cipro for a misdiagnosed bowel infection and that triggered my ME. It made me sick as a dog and i wanted to stop using it but the physician kept pushing me i had to finish the course or she would drop me as a patient.
I've never been the same since.
Now i have no more life. Thank you.
Hi @Thinktank, welcome to the forum. I'm sorry to hear you have had such a devastating effect from this drug.
There is a support/advocacy group
I too think that Fluoroquinolones may have played a part in my getting ME.
Welcome @Thinktank and great to see you over here. You know my story already but a neurotoxic reaction to Levaquin was the very beginning of my entire illness and the first trigger in a series of hits to my immune system. Hoping for the day that Levaquin is banned from the planet.
@Trish , thank you.
@Gingergrrl , nice to see you here. Yup, your story is a prime example of the damage that these fluoroquinolones can achieve.
I didn’t know fluoroquinolones caused psychiatric and sensory disturbances along with the physical problems. Why on earth are they still allowed to sell them.
Because they are an enormous money maker for Ortho-McNeil/Johnson & Johnson. They are one of the top drugs in the US (maybe worldwide, I am not sure) which shows that they are given out like candy if a drug that you take for seven days is given as frequently as a med that someone would take daily (365 days/year).
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