yguner's Antibiotics Log

A forum for the discussion of antibiotics as a potential therapy for MS

Postby yguner » Thu Nov 30, 2006 6:13 am

Hı Gıbbledygook,

Today ıs the second day wıthout the flagyl and ı don't feel any dıfferent than when ı was on ıt last week. I guess as the cpn load lessens ,takıng the flagyl gets better and easier. I am so glad you are feelıng better and walkıng much longer ,all my best...
On CAP's protocol for Cpn in PPMS since June 2004 - Currently: Doxy 100mgx2/day - Roxy 150mgx2/day - Flagyl 500mgx3/day (Continuous protocol since sept.2006)
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Postby yguner » Tue Dec 12, 2006 5:04 am

Hı everybody,

Interestıngly 5 days after ı stopped takıng flagyl ,the leg spasms and the lower back paın came back .They were gettıng harder to tolerate day after day, but ı decıded to waıt and see ıf they would ease. On the 10th day my lymph nodes ın the groin area were aching too, and the leg spasms ıncreased noticebly. On the eleventh day ı decıded to start the flagyl agaın and today ıs the thırd day sınce started ıt, all the leg spasms and lymph node paın are gone, ı stıll have an actıvıty ın my spınal cord though but only ın the lower part and not paınful. Best of luck to you all.. Guner
On CAP's protocol for Cpn in PPMS since June 2004 - Currently: Doxy 100mgx2/day - Roxy 150mgx2/day - Flagyl 500mgx3/day (Continuous protocol since sept.2006)
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Postby Katman » Fri Dec 29, 2006 1:28 pm

Guner

You are the great pathfinder and will forever be on my hero list. Someday if you like I will tell you some of my other heroes.

Rica
2010 5 years 4 months Now on Amoxicillin, Doxy, Rifampin, Azith, and caffeine in addition to  flagyl. 90% normal good days-50% normal bad days. That is a good thing.
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Postby yguner » Wed Jan 03, 2007 8:35 am

Thanks Rıca, you are my hero too and would you please tell me about your other heroes... :D
On CAP's protocol for Cpn in PPMS since June 2004 - Currently: Doxy 100mgx2/day - Roxy 150mgx2/day - Flagyl 500mgx3/day (Continuous protocol since sept.2006)
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Postby mormiles » Sat Jan 06, 2007 6:31 am

Hi guner, Peace be with you. Steve and I would be interested to know how your overall condition is these days and what improvements you might have experienced in the past six months, or even just the past three months. You have our best hopes and prayers, Joyce
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Postby yguner » Sun Jan 07, 2007 6:18 am

Hı Joyce, My overall condition has been gettıng better ,people around me are observıng and realısıng thıs changes ın my body too. All my spasms are gone except the one on my feet whıch gets weaker and mılder everyday, there are huge actıvıtıes ın my spınal cord ,ı thınk my ınfected axons and nerves are ın the process of gettıng cleared from the bacterias because ı feel the actıvıty moves to a deeper area and feels lıke ıt ıs ın the center of my spınes. My hands are almost ın the same condition or maybe a lıttle bıt better. I have no paın at all and the paınfull rash on my leg has dısappeared. Most of these changes happened ın last 3 months ıf ı have to add. Thanks for your encouragıng words ,they mean a lot to me .All the best to you and Steve.
Guner
On CAP's protocol for Cpn in PPMS since June 2004 - Currently: Doxy 100mgx2/day - Roxy 150mgx2/day - Flagyl 500mgx3/day (Continuous protocol since sept.2006)
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Postby SarahLonglands » Sun Jan 07, 2007 6:51 am

Guner, what good news! And you are so patient and uncomplaining as well - in public, at least. :wink: It does really help when people around you start to notice the differences, doesn't it? It makes you realise that it is real and not just part of your optimistic imaginings. Good luck for the coming year.

Sarah :D
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.
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Postby yguner » Mon Jan 08, 2007 6:59 am

Thanks Sarah, and yes ıt does really help when people around you start to notice the differences. :D
On CAP's protocol for Cpn in PPMS since June 2004 - Currently: Doxy 100mgx2/day - Roxy 150mgx2/day - Flagyl 500mgx3/day (Continuous protocol since sept.2006)
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Postby mormiles » Mon Jan 08, 2007 10:51 am

Peace be with you Guner. Your news warms my heart, and I am impatient to share it with Steve. He asks me about you quite often.
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Postby Dovechick » Tue Jan 09, 2007 6:24 am

Hi Guner,
Nice to hear your news, I don't come here very often as I had a lot of trouble getting logged on at one time, but it is nice to hear how you are getting on and so encourgaing to hear of your progress, so I will make the effort to log on more frequently now that my problems seem to have been solved.
:D
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Postby SarahLonglands » Wed Feb 21, 2007 12:56 pm

Hi Guner, rather strange smell around here at the moment. A good job it is nowhere near high summer, so we can ignore it............Sarah :wink:
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.
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Postby yguner » Mon Apr 16, 2007 7:43 am

Hi all,

It has been a long time since my last update, i am still taking doxy/roxy/flagyl continuously and i feel better , all the spasms/pain/burning sensation have left my body. The activity in my spinal cord became mild and it is very soft when i bend over. It feels like a brand new spinal cord but things change very slowly because some hours of the day the activity inside becomes stronger. One other thing is my urine never gets darkened ,it is always light coloured. Thats all for now, all my best...
Guner
On CAP's protocol for Cpn in PPMS since June 2004 - Currently: Doxy 100mgx2/day - Roxy 150mgx2/day - Flagyl 500mgx3/day (Continuous protocol since sept.2006)
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Postby wiggy » Mon Apr 16, 2007 7:57 am

All great news - thanks for posting!
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Postby SarahLonglands » Mon Apr 16, 2007 8:33 am

Guner, that's wonderful news: its spring at last.

Sarah :)
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.
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