Muscle twitches all over

Hey fellow Lymies!

I've only had a two week round of antibiotics for my treatment so far-had some BM issues so the Dr stopped it until it returned to normal (which I think will likely start up next week for two more weeks). For the past ten days I've been having muscle twitches all over and almost like charlie horse cramping in my calves (but not a true one because I had the full blown ones before). I currently take 250 mg of Chelated Magnesium as well as getting mag from my multi vitamin (not sure how much). So I'm wondering for anyone else who has had this symptom what'd you do to help? This is sad but I was at work the other day and a guy was tapping a phone wire (random I know) on my shoulder and I didn't even react I thought it was a muscle twitch. He said uh, Anne you in there? I wanted to say oh if you only knew the inside of my body right now... haha

I take a special magnesium salt pill and liquid vitamin B12. You can't get either at the store because they are specialities of my herbalist and naturopath. But, between the two supplements my twitching has pretty much stopped.

i get twitches, i take LDN, hasn't helped twitching.
I take at least 1000 mgs of mag chelate a day...

I'm not sure what my potassium is like but B12 gives me heart palps unfortunately. The b12 was giving me a good boost of energy but the palps freaked me out so I quit taking it.

I had an appointment with my neurologist today and she was in there for about 4 minutes asked if anything had changed, had me do a "follow my finger, stick your tongue out, close your arms hold your arms out" test and then said alright we will just go ahead and repeat the MRI of the brain. I swear it was almost like she was pissed I was coming to see her while I'm being treated for Lyme. The thing for me is, she scared me when I went to her originally saying she thought it may be early MS so that's why I decided to keep my six month follow up to see what the MRI says. Oh Dr's!