Cipro Update @ 3 years (Adverse reaction to Fluoroquinolones)

[@donblade5405]

THank you Jimmy for this update.. ANd i read all the comments... My family member is experiencing everything in all the commends and what Jimmy has said.. I can ramble on and on.. we all gotta pace ourselves and do those little steps like Jimmy said...... We did goto California to seee that DOCTOR who was on the show.. was not worth the money for us.. We are 2 years into it.. very stressful.. anexity..etc.. etc..

[@donblade5405]

@CrispyCruiser complicated question..this is the website regenerativemedicinela.com/ .. they do a few things, but mostly infusions via IV of peptides.. did not work cost about 1500 a day- maybe 15k for about what they consider FULL TREATMENT.. Some of the treatments make u feel good and so do not but its all temporary we woudl NOT do it again.... THey have video of well people jumping around and stuff but many of us know thats not how it works. Large % get better very slowly- and it takes time and just as important you find out the triggers than can reflox

[@professorbutters]

Yeah, something about that doctor set off my alarm bells. I just got floxed and don’t know how bad it will get, but I started feeling problems last Sunday and I’m already supplementing with magnesium. Wish I could take Advil, but I hear it makes it worse. I have to inhale corticosteroids or I can’t breathe. Still, I figure that staying positive can’t hurt.

[@donblade5405]

@@professorbutters I am very sorry. Yes please watch medications that can reflox u. Wishing u the best

[@Rachelllllll2024]

Good on you. Thank you for sharing your experience. I wish you a full recovery.

[@phonies]

God bless you Jimmy! Honestly seeing your you after so long, keeps me driving no matter how bad the pain is. I guess this a test for all of us in patience and Humility and in that respect you are definitely winning the battle. I believe one day you will make a full recovery.!

[@sturmanaskie]

You’re looking well man. Glad to hear you’re getting better. How’s the neuropathy going? I’m 2 years out now... getting better but still have the nerve issues around my calves and forearms a bit. Much better tho. Some bad days where I get really fatigued but that’s it

[@Myworldmymind908]

Did you ever suffer breathing issues from it ?

[@jimmyhacksaws3300]

I don't think so. Anxiety can mess with breathing?

[@Myworldmymind908]

@@jimmyhacksaws3300 I've been having a breathing issue with it now . I'm 7 months out . Left with numb and heavy legs and get this breathing issue from time to time . Been to cardiologist and had multiple tests done on the heart they say my heart is fine . As of anxiety .. could be . But this feeling is really annoying . Almost feels like shallow breathing or as if airways are going numb . Been to the hospital plenty of times for it all to be told over & over there's nothing wrong

[@Myworldmymind908]

@CrispyCruiser I will definitely give it a shot. Never had this til after Cipro . What are you going through now if you don't mind me asking ?

[@Myworldmymind908]

@CrispyCruiser sorry to hear of your issues . This Cipro shit really sucks . As of myself I've been dealing with numbing and heaviness in both of my legs , balance issues at times and a breathing issue that comes and goes. I've been fortunate to not have any pain through all of this. But the numbing and heaviness makes it very difficult to walk at times . Especially when climbing steps .

[@Myworldmymind908]

@CrispyCruiser Only supplements I've been on is Rainbow Light Multivitamin one a day Vitamin D3 with K2 10,000 iu daily Calm & Relax supplement every night which is a mixture of Magnesium and Ashwaganda The only thing I felt helped me significantly but it didn't really last long was a Myer's cocktail IV infusion at a Holgistic doctor. It lasted about a week til it wore off. Felt pretty normal that whole week when I got the Myer's