Charcot-Marie-Tooth Disease (From Cipro Drug)

[jaminhealth]

Oh about 13 yrs ago my daughter who was still trusting of MD's and their drugs, took Cipro (has black box warning) and she knew nothing,. but that Idiot MD knew and pushed G.D. drugs on her.

Her feet deformaties started to come on some yrs after on Cipro and she had no clue and now we find out that ligament damage is major with Cipro and that class of FLUORIDE LOADED drugs..... She saw 3 foot specialists back then and none every mentioned CMT and the drugs of course......

Over the years it all got worse and now at 59 she is so sadly damaged and now with the help of her holistic minded daughter is finding all this info. And seeking help to get theur her life.

https://www.hnf-cure.org/patience-r...neurotoxic-drugs-charcot-marie-tooth-disease/

Anyone know this Disease and the terrible pharma drugs of the Fluoroquine class (Cipro, Levaquin et al)?

Fluoroquinolones are antibiotics --- And SHOULD BE TAKEN OFF THE MARKET

Please share all you may know of this disease and even the drugs. Thanks...

 

[Tammy7]

I'm sorry to hear about your Daughter's challenges as a result of the antibiotic. I have heard many a horror story related to the class of antibiotics known as Fluoroquinolones and I agree strongly that this class of antibiotics should be taken off the market. I have made it very clear to my Dr. and have it in my file at my local hospital that I'm never to be given Fluoroquinolones. I put down that I'm allergic to them.

I think you will find more info by joining support groups that specifically talk about this.

 

[jaminhealth]

I'm sorry to hear about your Daughter's challenges as a result of the antibiotic. I have heard many a horror story related to the class of antibiotics known as Fluoroquinolones and I agree strongly that this class of antibiotics should be taken off the market. I have made it very clear to my Dr. and have it in my file at my local hospital that I'm never to be given Fluoroquinolones. I put down that I'm allergic to them.

I think you will find more info by joining support groups that specifically talk about this.

Thanks and I don't have a group to go to and discuss this topic. Do you have one to
recommend? Thanks..

 

[Tammy7]

I don't know of any personally but I did a quick search on the internet and lots of things came up. Google Fluoroquinolones facebook support groups. Or google Floxed support groups on-line. Google My Quin Story also. I'm sure redditt has discussions on this topic also.

 

[jaminhealth]

Thank you and I'll dig deeper when I can.....there is a lot of info I found but an actual support forum or a forum of health issues with CMT as a subforum......j


Sadly from the beginning of the CMT my daughter was so in the dark and the 3 docs she initially saw were no HELP with what she had going on., She had no clue about the Cipro connection, a pharmaciist at the homeopathic pharmacy we go to, asked her if she took Cipro ---- Bingo..... she was in denial for a while too ....so many issues in her young years.