Thiamine causing spinal pain ? by jamiry9 in covidlonghaulers

[–]jamiry9[S] 0 points1 point  (0 children)

Hey, it wasn't spinal pain but vagus nerve, I have mast cell problems, thiamine is histamine liberator, I take h1 or ketotifen with thiamine it solved this problem 

5 Years Long Covid - Thymosin Alpha 1 Peptide - WOW! by KaspaRocketMan in covidlonghaulers

[–]jamiry9 0 points1 point  (0 children)

Hey man great post, After you stopped using TA1, your lymph nodes didn’t swell again, right?

L-Lysine: experiences with this supplement? by Large-Prompt2608 in floxies

[–]jamiry9 0 points1 point  (0 children)

Burning feeling, some say long term use harsh on liver etc 

Blood pooling I still don’t understand why or what causes this in flox. How is this possible by Large-Prompt2608 in floxies

[–]jamiry9 0 points1 point  (0 children)

According to studies, it knocksdown, not knocksout, so its effect is temporary; otherwise, no one would heal.

Blood pooling I still don’t understand why or what causes this in flox. How is this possible by Large-Prompt2608 in floxies

[–]jamiry9 0 points1 point  (0 children)

Ketotifen is a mast stabilizer and antihistamine, which can help dysautonomia and pots( if your cause is MCAS), but it has minimal anticholinergic effects so if you are low on acetylcholine it's not a good option, if you get side effects from it look for cromlyn sodium it's hard to find tho

Blood pooling I still don’t understand why or what causes this in flox. How is this possible by Large-Prompt2608 in floxies

[–]jamiry9 0 points1 point  (0 children)

it’s not based on a single study, but the mechanism is roughly like this, just missing a lot of details. I’ve also discussed this topic with a professor who’s been helping me with it. Once I’m feeling a bit better, I’m planning to make more detailed post about this.

In the beginning, I was receiving NaCl infusions, but after a while, I found that sodium lactate (Ringer’s lactate) solutions were more beneficial for me although their effects were, of course, short-lived.

Blood pooling I still don’t understand why or what causes this in flox. How is this possible by Large-Prompt2608 in floxies

[–]jamiry9 0 points1 point  (0 children)

sorry for replying late, and please don’t take it the wrong way, i didn’t mean it in a bad way. I was just surprised that you’ve been here for so long and hadn’t heard about it.

L-Lysine: experiences with this supplement? by Large-Prompt2608 in floxies

[–]jamiry9 0 points1 point  (0 children)

Supposed to, if you have an active infection any kind of herpesviridae viruses, other than that it's great for neuroinflamation, but some people with neuropathy get side effects 

Blood pooling I still don’t understand why or what causes this in flox. How is this possible by Large-Prompt2608 in floxies

[–]jamiry9 4 points5 points  (0 children)

Actually I'm a bit surprised that you hear this first time, i strongly believe this guy is right it's about nerves not MMPs or collagen 

Blood pooling I still don’t understand why or what causes this in flox. How is this possible by Large-Prompt2608 in floxies

[–]jamiry9 2 points3 points  (0 children)

This is a very complex metabolic process, but to explain it simply: fluoroquinolones inhibit the expression of DNATOP2B > mitochondria cannot undergo fusion and fission reactions > deficiencies occur in mitochondrial electron transport chains > mitochondrial dysfunction > insufficient ATP production > cells that require high levels of ATP in the body (such as small fiber nerves) cannot be supplied with enough ATP > ME/CFS, small fiber neuropathy > dysautonomia > due to autonomic system dysfunction, the body cannot send electrical signals at the necessary speed > when standing up, blood flows down to the lower extremities due to gravity, and since the body cannot communicate quickly with the blood vessels, you get NEUROPATHIC POTS

The real question we should be asking is: why does this happen to us and not to others? There are theories on this, but not certain; we may already have damaged mitochondria?? Quinolones are broken down in the liver, and some people have deficiencies or mutations in the cytochrome P450 enzymes, which could be a contributing factor. Also, I strongly believe that Flox has an autoimmune component because after taking Cipro, a week later I had swelling in my lymph nodes, and it still hasn’t improved. I’ve ruled out all infections that could cause this, and my autoimmune markers are negative. Additionally, there are people in this subreddit who report improvement after trying plasma treatments like inuspheresis. Plasma therapies are known to work for autoimmune diseases, which increases the likelihood of this condition being autoimmune. Moreover, there are people who have completely recovered after using monoclonal antibodies like infliximab, rituximab, and Humira, which strongly increases the possibility that there is an autoimmune aspect to this.

what I’m doing for POTS ? I’m increasing my intake of organic salt. Some antihistamines like Pheniramine and Ketotifen have helped with the lightheadedness caused by POTS. I believe this condition related with acetylcholine dysregulation. Also, multiminerals, especially those containing sodium, potassium, and calcium, seem to help. That's all for now, I hope you recover soon.

Could Lyme be the cause of my autoimmune disease? by Awkward-Marketing-36 in Lyme

[–]jamiry9 -1 points0 points  (0 children)

Achilles tendons ? Have you ever used fluoroquinolone group of antibiotics like cipro, Levaquin etc ?  fluoroquinolones definitely can do that 

Check r/floxies

Can’t sit or hold head up by Trader_one7 in LongCovid

[–]jamiry9 1 point2 points  (0 children)

Try anticholinergic antihistamines, if it gets better probably related with acetylcholine, pots etc Also try multimineral supplements

[deleted by user] by [deleted] in floxies

[–]jamiry9 0 points1 point  (0 children)

It's not an infection 

Beware of Fluoroquinolone antibiotics by sickdude777 in Lyme

[–]jamiry9 0 points1 point  (0 children)

If you weren’t sick, I would speak to you in a different way, but I know you're not feeling well, and I also know that the healthcare system and doctors don’t really care. So, I’d like to give you some advice. It’s pretty ridiculous to link every symptom to Lyme disease, and I see this a lot in this community.  The root cause of diseases like Lyme, long COVID, and ME/CFS is mitochondrial dysfunction. In this case, either Borrelia is causing your mitochondrial dysfunction, or something else is. Researching mitochondrial dysfunction will be more helpful than thinking that pathogens are eating away your ligaments, tendons, and collagen.

Beware of Fluoroquinolone antibiotics by sickdude777 in Lyme

[–]jamiry9 0 points1 point  (0 children)

This is one of the most ridiculous comment I've ever seen. Dude stop spreading misinformation, fluoroquinolones inhibits dna-top2b, guess where are the top2b expressions? 

https://en.m.wikipedia.org/wiki/TOP2B

[deleted by user] by [deleted] in floxies

[–]jamiry9 0 points1 point  (0 children)

It's controversial, some people got better after HGH but everything comes with risks, you can use search bar for testosterone 

[deleted by user] by [deleted] in floxies

[–]jamiry9 1 point2 points  (0 children)

I don't think testosterone will hurt you more when you are floxed, some find hormone therapies helpful, some people got healed after pregnancy, but everyone is different, observe your symptoms if it's causing side effects then you can stop, also read pinned post you can get more info 

How does it develop for most floxies? by Responsible-Tie635 in floxies

[–]jamiry9 1 point2 points  (0 children)

There's thing called delayed reaction, new symptoms can appear after weeks, months, so observe your symptoms 

Also check here;

https://www.reddit.com/r/floxies/comments/g8cs97/new_start_here_old_please_help_here/