Muscle/joint problems?

Anyone else not have any muscle/joint problems as one of their symptoms with Lyme Disease? It seems like an awful lot do but I've never had issues. Most of my symptoms are neurological with poor balance being at the top of the list.

I have muscle and joint pain/stiffness. The muscles aren't as bad anymore, but the joints still are.

I have neuro issues, too.

Yah, it sucks being me on some days, too!

I've had it for 16 1/2 yrs, lots of muscle pain but now some joints are starting to hurt but off and on.

It's a weird disease, I also started with the dizziness about 4-5 yrs ago but seems like weather highs and lows is more of a cause for my dizziness. Nots of raining days these past few weeks and really having a lot of dizziness and finally today no storms and I haven't been dizzy.

They came later, at least for me. For two or three years, nothing but the occasional pop, clicking of the joints, and one area in the joint/tissue of my right elbow that'd get sore, from time to time. I wrote it off, as I had another ailment during my early, early teens that's known to effect the bones and stuff.

Other than that, all neurological - very slow, gradual onset, until like 2011. Then, the burning, the aching.. muscles, joints, bones, etc. Fun stuff. I haven't been getting it as much. Good thing, but don't know if it's actually a GOOD thing (healimg vs symptoms alternating), but.. yeah.

*shrugs*

Glad you've been seeing some small gains. Hope there's more for ya in the near future.