FAQ/Help |
Calendar |
Search |
Today's Posts |
|
![]() |
#1 | ||
|
|||
Member
|
I have taken alot of Cipro & Macrobid over the years for chronic bladder infections. I'd say I take them about 6 times a year. But I had not taken any for several months before my SFN symptoms began. Could you have gotten all over sfn so long after taking the antibiotics or does it come on quickly after you had just taken them?
|
||
![]() |
![]() |
![]() |
#2 | |||
|
||||
Wisest Elder Ever
|
It is hard to say.... both drugs are known PN causers.
I have a thread above about this in the Subforum with links. But knowing you used two drugs, I'd concentrate on supplements that support mitochondrial functions if you hope to enhance any healing that might be possible: acetyl carnitine lipoic acid CoQ-10
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
|
|||
![]() |
![]() |
"Thanks for this!" says: | rose_thorn98 (11-08-2010) |
![]() |
#3 | |||
|
||||
Member
|
Quote:
I had heard that those types of medicines could cause PN, but I didn't know they were antibiotics. Because of my PN pain, I had a spinal cord stimulator trial two weeks ago. After the trial, what did they give me as an antibiotic? Levaquin! A fluoroquinolone! How frustrating. I had an allergic reaction to it. I was only on it for 4 days, but why would doctors give that out to someone with PN if it has been shown to cause PN? Stupid.
__________________
. ♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥ My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems. |
|||
![]() |
![]() |
![]() |
#4 | ||
|
|||
Junior Member
|
They definitely do cause neuropathy...Its been 20 months since I took Levaquin and it has not resolved. I do not know if it ever will but these are bad drugs only to be taken in a life or death circumstance.
|
||
![]() |
![]() |
![]() |
#5 | ||
|
|||
Member
|
|
||
![]() |
![]() |
![]() |
#6 | ||
|
|||
New Member
|
I took Cipro 3 months ago and my peripheral neuropathy began approx 8 days later. since then, i have done a lot of research on fluoroquinolone toxicity, and it seems that these symptoms can show up immediately, as in after one pill, or much later after the drug has been discontinued, as in a year later. also, you can take the drugs prior to having a reaction like that. best to all of you for quick healing.
|
||
![]() |
![]() |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
What antibiotics can we take? | Myasthenia Gravis | |||
Antibiotics | Peripheral Neuropathy | |||
Antibiotics and MS question | Multiple Sclerosis | |||
Antibiotics with MG | Myasthenia Gravis | |||
Antibiotics and PD | Parkinson's Disease |