I have Bart and Lyme too, and actually just started taking Rifampin myself. This has happened to me, where my symptoms flare quite strongly. My LLMD says that it is a sign that the medication is working. It sort of agitates the pathogen, causing the symptoms to temporarily worsen.
Two times now, I have spent a week and about 3 weeks respectively, doing the twitching thing. It goes way, although lately I still twitch every once in awhile.
But then there's the good old herx, which could also explain things. It's always a bummer when my symptoms get worse but then I always tell myself at least it means that stuff is getting killed. For me, it's just important not to let my system get too overloaded and toxic, which is why I stopped the Rifampin for a couple days when it got bad.
Cheers,
A.
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The obscure we see eventually. The completely obvious, it seems, takes longer. --- Edward R. Murrow Posts: 923 | From California | Registered: Aug 2005
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NP40
Frequent Contributor (1K+ posts)
Member # 6711
posted
Hey Lalyme, sounds like your herxing so I wouldn't be too alarmed. Pretty normal for lymies to have reactions to the meds, means their working so I'd doubt the MS diagnosis.
Stay out of the sun when on doxy, can get some nasty burns.
Posts: 1632 | From Northern Wisconsin | Registered: Jan 2005
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posted
Yeah, rifampin is insane! Levaquin was great and a breeze. Rifampin if like moving through a blow torch. Than you for your responses.
Posts: 298 | From los angeles | Registered: Mar 2006
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