Neuro Follow Up Discussion - Anxiety Questions

exploringexistence

Well-known member
Yesterday I went for a follow up with my neuro to discuss the EMG and some meds he put me on for my ET. I made sure to ask a lot of questions because as you can see by a number of my posts lately, I am still very anxious.I asked him first that if someone could have a clean EMG and ever have ***. He told me, "No way. No How." He told me that the test rules out a number of NMDs and he read off a bunch of diseases besides *** that I have never even heard of and reassured me I don't have any of them. I also asked if an EMG can be done too soon. He said (as many of you have already told me as well), that if the twitching was being caused by ***, it would immediately show up and that it doesn't matter which side of the body or where that they test. Then I asked him if someone could have an EMG and develop *** like a month later. He told me "No." I also asked how long an EMG is good for, like how long can a person be rest assured they are fine. He didn't say specifics, but he told me, "A good long time." So I said, "Months?" Then he nodded his head. I brought up the under the tongue twitch and he told me it's nothing more to worry about than any other twitch. He said the tongue twitching isn't more indicative of NMD either. I also brought up hotspots, although I didn't use that word and told him I have had an elbow twitch for days. He said that having a twitch that lasts and lasts isn't anything to be concerned about either, if you have normal exams and EMG. Then I told him how I even twitch walking around now in my legs and I mentioned how I was writing and typing and had twitches in my arms and hands mess me up. I told him I jerk sometimes too. So he told me, "It doesn't matter at all. It is all benign." So I said, "Well I heard twitching in tensed muscle is supposed to be bad" and he said, "Poohbah." :LOL: He told me that it isn't true. He told me TONS of people twitch and there is nothing wrong with them. He also told me that a clinical exam is really all that is needed to rule out *** (for those of you who never had an EMG) and that neuros usually only do the EMG to reassure people. I also brought up my continued problems with speaking and I asked if anxiety can really cause slurring and messing up words and he said, "Most definitely. You'd be surprised at what it can cause." He told me that I should rest assure that I am 100% neurologically intact and that the neuro who did the EMG is highly trained and a specialist in reading them, so if something was there, he would have found it. I told him about how Zoloft seemed to make everything worse for me too and he said that my body obviously can't tolerate the drug. Then he told me that he didn't believe any other testing was needed and I need to learn to relax and to come back in a couple months to see how I'm doing. I hope that info might help those of you who are still nervous even after being told you are fine. I have to admit, I did feel a bit better. I went to the grocery store after and my calf was twitching away while I walked and I didn't panic about it. That's already a slight improvement :p I am going to see a psychiatrist next month so hopefully I can get my mind on the road to recovery.Nettie
 
Hi Nettie, sounds like you had a great visit. Wish I could see your neuro. lol.Anyone have a good neuro in Chicago in case I decide to go?Linda
 
I think I made him sound so much nicer in the post lol, but I do think he was getting a bit fed up with me. I can't blame him in a way. He probably thinks I should be completely reassured and yet I am asking him all these questions which prove I'm not.I think you are fine though Linda, and I should have stressed this more in my post, how he said a good clinical exam is really all that is needed to rule out ***. If the twitching was being caused by ***, there would be abnormalities present when the doctor examines you. He said an EMG is considered to be an invasive test and that they just don't go giving them to everyone. They only give it to people when there is reason to believe something is wrong, and when the patient wants it for reassurance.
 
Wow, I just wanted to tell you how helpful to me that post was! This is what I love about these boards, when people come on here and share what their neuro's said, it's almost like getting that reassurance from the doc ourselves! My symptoms sound like yours, and I also have had the tongue twitching, and so that was VERY reassuring to me. The tongue twitching makes me very anxious, and it's a hard one to deal with. So, it was really nice to read that. Did you get the impression that he wasn't concerned about twitching UNDER the tongue, or any tongue twitching at all? Cause mine is not usually under the tongue, it's either pops on the top or sides, and some fluttery feelings on the front tip. I've been concerned lately with symptoms that you describe, such as twitching in my legs as I'm walking, but what really concerns me lately is a feeling of progressive weakness. Although, as I've said before in other posts, I don't know if I would really describe it as weakness, more like stiffness and pain in my joints. I'm having lots of trouble right now in my knees, and my ankles and feet. Also, I feel like I have a slight weakness, or again, more like an achy pain in my right hand on a knuckle. So, you know how everyone on here says don't worry about the twitches as long as you don't have weakness? Well, that's what worries me now, is that I feel like I'm going downhill with my physcial ability to be active. This could be explained by other things, such as getting older, extra weight, but it's just weird timing. I do feel better sometimes when I wear the proper shoes, sometimes I go out of here wearing these slip-on shoes that seem to make my problems worse. Anyway, thanks so much, that was really so reassuring! Thanks for taking the time to post that, it was very helpful!! Val
 
Nettie: I am so glad to hear about your report. It almost made me feel like "I" had been to the neuro :) Many of the things your doc said were reinforcement of what mine have said and it was good to hear again. Thanks for giving us an update. By the way, how was the EMG---was it very painful???Cindy
 
Nettie~~ Again, I can't thank you enough for posting that~~especially right now!! I just posted about a weak hand I've been having, and I'm just in a bad anxiety mode right now, and your post really, really helped!! Like I said before, it's like I just got reassured by a neuro!! I had mentioned on this other post how I stupidly went googling last night about the painful, weak hand and twitching, and found a site in which neuros supposedly give answers. The thing that made me nervous was that this one guy wrote about his wife, saying she had twitching for six months, and then noticed a weakness in her hand, and the neuro answered back that she should get into a clinc sooner rather than later now that she has noticed hand weakness. It's not that my hand is even that weak, there is just something going on with my pointer finger, where it's sort of sore and feels painful when I pick something heavy up. Something I probably wouldn't even make that big of a deal about if it wasn't for waiting for all these other dreaded symptoms of als. Anyway, after reading that last night, I got that thing that I hate, where you are sitting in front of a computer, helpless, you just read something awful, and now feel like crying. I truly just felt like I wanted to burst out crying. I get so tired of the roller coaster, one minute thinking that I might actually be ok, and not have als, and then thinking that it all points to als, and it's becoming more obvious. I feel better today, but still have anxiety about it, and so coming on here really helped, and I just wanted to thank you so much for posting that, and making my night so much better!! Thanks again, I'm going to read what you wrote over and over~~it helps so much. I have to remember NOT to google. I'm usually pretty good about that, but somehow slipped up. Thanks again, Val
 

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