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You are here: Home / Symptoms / Muscle Spasms vs Muscle Twitches

Muscle Spasms vs Muscle Twitches

Last Updated: July 26, 2010

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

So evidently what I’ve been referring to as muscle spams are actually muscle twitches. After doing a little research last night I realized that what the medical community refers to as muscle spasms are the same thing as cramps. I thought they were two different things.

I do occasionally get muscle spams (aka cramps) but it’s pretty rare since I upped my Magnesium intake. However, the twitching has continued. It’s still primarily on my left side, my entire left side, but mostly in my arm, neck and shoulder.

 

Is it a muscle spasm or a muscle twitch? What's the difference via Counting My SpoonsWhat I read online describes muscle twitches as:

A muscle twitch or fasciculation is uncontrolled fine movement of a small segment of a larger muscle that can be seen under the skin.

Here’s the problem. What I have is not a small segment of a muscle, but seems to be the entire muscle (at times). Sometimes you can see it under the skin, but most of the time I just feel it. In a way it feels as if my muscle or nerve is a rubber-band stretched as far as it can go, and then someone pulls on it. I get that initial “ding” of the rubber-band going back followed by the reverb down the muscle or nerve. Sometimes it makes my arm or leg jerk or shake.

Whatever the case it’s tiring. In the last few weeks it’s been so bad that I could barely hold a book in my hand and read it without it just becoming downright painful. Having any weight in my left hand seems to increase the “twitches”, even a weight as small as my Ipod.

Muscle relaxers help to calm things down at night, but I can’t take them during the day or they knock me out. Not that that would really be a problem lately since for the last few weeks I’ve barely done anything during the day except watch tv or listen to music, because various symptoms have been that bad.

These twitches or spasms, or whatever they are, have been bad enough lately to make me feel like there has to be something else here. It’s getting worse. Is this really Fibro? Yet, every other test has come back clean. It’s frustrating and I feel like I’m wasting away, mind and body. It’s funny, the pain I could deal with and work through, it’s all the other little things that put me to a stop. It’s the fatigue, the twitching, the feeling almost paralyzed when I wake up in the morning.

I guess thinking about it, it all makes some sense. Fibro is a nerve disorder. My nerves are sending random signals out to my left side (for some reason) and those random signals cause twitches. Instead of just one random twitch like a normal person might have, my nerves are firing over and over again causing twitches at such a frequent rate and so scattered that you can’t really see it or feel it in just one place. Instead, it becomes like my entire side is twitching.

At least now I have the terminology correct and that will help me when I talk to my Dr again. When I told him I was having spasms he kept telling me to stretch. I couldn’t figure out why all the stretching I was doing and my “spasms” kept getting worse. Maybe he’ll have some new advice when I tell him it’s twitching.

Related Posts:

  • Talking With Your Doctor About Pain
  • The Chronic Pain Scale: Communicating Your Chronic Pain
  • Fibromyalgia Nerve Pain – there might be more to it than you think.
  • 3 Things that Affect Our Communication with Doctors

 

8 Comments Filed Under: Symptoms Tagged With: magnesium, muscle spasms, muscle twitching, nerve pain, stretching

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. lovie Horton says

    August 26, 2012 at 12:52 am

    i just found out i have fibro.

    Reply
    • Julie Ryan says

      August 26, 2012 at 11:43 pm

      So sorry to hear that Lovie.

      Reply
  2. Rachel Runyan says

    August 13, 2012 at 12:11 pm

    I know this is an older post, but I was wondering if they ever got your larger twitches stopped or figured out what they were. I’m having to go in patient at a hospital today for a couple days to make sure they are not part of my seizure disorder (neither I or the doctor think so). I’ve had them for at least as long as you. I’ve been diagnosed with Extreme Fibromyalgia plus many co-diagnosis that it would make your head spin. I can’t help but think that something has been missed.

    Reply
    • Julie says

      August 13, 2012 at 7:44 pm

      The twitches (at least for me) were just part of the Fibro. When it gets REALLY bad they are one of my worst symptoms. Gabapentin and a muscle relaxer (I take 8mg of tizanidine) seem to keep them in check. When I try to cut the Gabapentin I notice the twitches trying to return.

      Also, physical therapy helped a lot with the twitches (mainly by way of kinesiology taping and massage). Check out this post for more on the taping: http://fibrokitty.blogspot.com/2010/06/muscle-spasms-taping.html

      Reply
  3. Missy Schranz says

    July 29, 2010 at 5:15 am

    I take Neurontin, a pretty hefty dose, too. 800mg three times a day. It does help, to a certain degree, especially for the “hot, electric” nerve pain. It hasn’t helped me with the twitches, though, I’m sorry to report. But you may be different! :0) I hope it works out for you. I’m praying for you!

    Reply
  4. Julie says

    July 27, 2010 at 8:31 pm

    I went to the Dr today and he said the twitching is part of the nerve pain. He started me on Neurontin, so hopefully that will help.

    Reply
  5. Missy Schranz says

    July 26, 2010 at 2:37 pm

    I have exactly the same thing! Except in my case, I will be sitting and typing and all of a sudden, my body will jerk. My WHOLE body! Or sometimes if I’m holding a fork or book or whatever, my hand will jerk for no reason whatsoever. I think it’s a fibro thing. I’ve heard it described enough from others with fibromyalgia. Whatever it derives from, I wish it would go back to hence it came from!!!!
    Hope you feel better,
    Missy
    PS….stop in and visit my blog at:
    http://missyschranz.blogspot.com

    Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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