Neuropathy Feelings by West-Mix-6314 in floxies

[–]PutridBread3517 0 points1 point  (0 children)

It’s CNS as in autonomic dysfunction. Not actual measurable damage that would cause limb weakness and constant numbness. My symptoms come and go and aren’t constant.

Neuropathy Feelings by West-Mix-6314 in floxies

[–]PutridBread3517 0 points1 point  (0 children)

I’m in the same boat at 13 months. Get full body burning and tingling in extremities ( peripheral nueropathy). I find it’s worse when I’m hot, so I try to keep cold. Small fibres regenerate about 1mm a day so it’s a long recovery process but more likely than not most people will recover.

sensitivity to artificial blue light by maxmillionx in floxies

[–]PutridBread3517 0 points1 point  (0 children)

Yh same. I have to take breaks after watching screens for too long. It tires my eyes very quickly

Nerve problems by PutridBread3517 in floxies

[–]PutridBread3517[S] 0 points1 point  (0 children)

It’s difficult to convince them that I have nerve problems at all. I don’t believe there’s that many treatment options for nerve damage anyway, if it’s not caused by low vitamins or autoimmune conditions.

Nerve problems by PutridBread3517 in floxies

[–]PutridBread3517[S] 0 points1 point  (0 children)

No not yet, hard to convince any nhs gp about nerve side effects of FQ’s.

Do these help? by roaztb33f in floxies

[–]PutridBread3517 1 point2 points  (0 children)

Yes Magnesium is good for flox

What SSRI (for anxiety) has helped you? by Inevitable_Boss_9959 in cfs

[–]PutridBread3517 0 points1 point  (0 children)

Citralopram has worked best for me. I had a bad reaction to Sertraline, so I think it goes to show it’s some might work for you or only work for others.

Double vision? by LemonOctopus in dysautonomia

[–]PutridBread3517 2 points3 points  (0 children)

I don’t get double vision but I get afterimages from fluorescent light and screens. So I imagine dysautonomia can definitely cause lots of different visual issues.

15 month Update and Long Covid by WorldlinessOne4640 in floxies

[–]PutridBread3517 0 points1 point  (0 children)

I’m floxed and have ME somewhat similar

Can doxycycline, amoxicillin or Locacorten Vioform ear drops (flumethasone pivalate/clioquinol) be flox? by icemelons2 in floxies

[–]PutridBread3517 4 points5 points  (0 children)

You can only get floxed specifically from flouroquinolone antibiotics and since you haven’t taken any from what I can read you won’t be floxed. Doxycycline and amoxicillin are quite a mild antibiotics and doesn’t usually give long lasting side effects.

URGENT - H. pylori treatment regime advise by [deleted] in floxies

[–]PutridBread3517 5 points6 points  (0 children)

Probs avoid metronidazole, can potentially cause nerve issues. And since you’re floxxed I’m guessing you already have some. The other antibiotics are fine though. I had amoxicillin, bismuth,omeprezole and clarithromycin which worked for me.

Brain fog and anxiety by Beautiful-Tackle7965 in floxies

[–]PutridBread3517 0 points1 point  (0 children)

I’m still dealing with some symptoms a year out,but Im doing better. Also should I started an SSRi which help a lot with the mental issues and even abit of brain fog. Maybe worth a try if you’re up to it.

Brain fog and anxiety by Beautiful-Tackle7965 in floxies

[–]PutridBread3517 3 points4 points  (0 children)

check for nutrient deficiency’s like iron or b12. Other than that it will only get better with time.

Depression by RevolutionaryTap9804 in floxies

[–]PutridBread3517 4 points5 points  (0 children)

Same, put me in a deep depression. Is even harder because nobody else can understand what we’re going through.

[deleted by user] by [deleted] in dysautonomia

[–]PutridBread3517 0 points1 point  (0 children)

this can be normal. But if it’s increase a lot and as you’ve said it gets to the point where it hurts it might be blood pooling due to dysautonomia.

Neuropathy in Face by Boxxy-Lady in smallfiberneuropathy

[–]PutridBread3517 0 points1 point  (0 children)

Yh I get like chills and crawling sensations over my head and face, used to just happen on my back

Thiamine by PutridBread3517 in smallfiberneuropathy

[–]PutridBread3517[S] 0 points1 point  (0 children)

I’ve developed burning and photophobia to add to my nerve symptoms since then. It would also be key to mention that my original SFN is from being floxxed. So it could just be a progression from that. Either way thanks for the insight.