posted
I cant seem to find this info anywhere.Is Rocephin the best for penetrating?Thanks,Joe
Posts: 308 | From new bedford,Ma. | Registered: Dec 2004
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posted
yes....Been on iv clinda alone and in combo with zith tinidazole and mino at different times since feb. Still continuing the journey, and making improvements.
posted
Wow ,great to get some info on this,thanks all.Out of 4 years of orals I felt the best on cipro until it ate my tendons,wonder if it was penetrating the brain.I think Im going to push for Rocephin and just be nervous about my gallbladder.
Posts: 308 | From new bedford,Ma. | Registered: Dec 2004
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Pocono Lyme
Frequent Contributor (1K+ posts)
Member # 5939
posted
Dear Joe,
Out of all the orals I've taken, Cipro is giving me the best results so far, which to me indicates Bartonella since Cipro doesn't work on Lyme.
Cipro is used in cultures to suppress everything else from growing so the Lyme bacteria will grow.
I may be looking at IV Roc. also, but plan on continuing treatment for Bart. as causes CNS symptoms also. Will be in touch. Maybe Rifampin would be an alternative to Cipro.
Posts: 1445 | From Poconos, PA | Registered: Jul 2004
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posted
Thanks Pocono,I did rifampin for about three months but the cipro was better for me,to bad I had the tendon problems.How long have you been on cipro?
Posts: 308 | From new bedford,Ma. | Registered: Dec 2004
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Mathias
Frequent Contributor (1K+ posts)
Member # 5298
posted
Florquinlones in general have good BBB penetration, hence all of the CNS warnings and side effects.
Posts: 1250 | From New Jersey | Registered: Feb 2004
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Pocono Lyme
Frequent Contributor (1K+ posts)
Member # 5939
posted
Joe,
Just got back from LLMD appt.. After two months on Cipro, going to stop for IV Rocephin. If the symptoms return, that cleared with Cipro, I can restart it.
I guess I'll probably be joining that choleycystectomy club. I've had pain in that area for quite a while now, so if it's gallbladder issues, I'm sure the Rocephin will let me know.
I get the impression, you are ready for IV too as these neuro symptoms are the absolute worst.
Posts: 1445 | From Poconos, PA | Registered: Jul 2004
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posted
Ive been needing IV for 3 years now but getting treatment for this disease is a crime.The neuro stuff is horrible and my own brain tortures me,it all could have been avoided if the CDC and local docs did there job.
Posts: 308 | From new bedford,Ma. | Registered: Dec 2004
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