Cervico- … what? MS-Related Dizziness and Neck Spasms

Cervico- … what? MS-Related Dizziness and Neck Spasms

You've Got Some Nerves

Multiple sclerosis is so weird. Sometimes I just put up with a strange sensation or painful problem because I do not know how to describe it to the doctor without sounding crazy.

I hope the problems will just go away, and sometimes they do. Maybe I am a little gun-shy from the year prior to my diagnosis, when each symptom I complained about just brought me a new antidepressant.

A couple of years ago, after suffering in silence for many months, I scheduled an appointment with a neurologist. Waiting in the exam room, symptom list in hand, I worried. My new sensation was causing problems, but I did not know how to describe it. The kind (and unusually personable, for a neurologist) doctor greeted me warmly. We covered the usual suspects — fatigue, paresthesia, foot drop. He asked if there was anything else.

“Well, sometimes I get a really weird sensation in my head,” I stammered. He asked questions: Was it painful? No, not really, just very uncomfortable. Where did I feel it? Sort of in my neck and the base of my skull. Could I describe it?  The words finally tumbled out of me, in an awkward rush of pent-up stress.

“This will sound weird, but it feels like a giant hand is grabbing my head and squeezing the back of it. Or like I’m in a pressurized room, and my head is being squished. My neck gets really tight and I get kind of dizzy and sometimes it’s like the floor or the walls tilt. If I’m standing I sort of lose my balance, and if I’m sitting it feels like my head jerks to one side, but I don’t know if it really does.”

Thankfully, the kind doctor did not call for a priest to perform an exorcism. He asked about neck spasms and felt along my shoulders, neck and skull. He gently reminded me that I have lesions in my cervical spine and explained that this was likely a type of vertigo caused by neck spasms and my damaged nervous system. A prescription for Baclofen was sent to the pharmacy.

I have since sought additional ways to minimize this sensation, otherwise known as cervicogenic dizziness.

Good posture

  • Make sure any screen (computer, phone, TV) is at eye level
  • Get up and move around, don’t sit in one position too long
  • Shoulders down and back, sit up straight
  • Pilates lessons have helped with my posture and overall muscle spasms


  • Take this over-enthusiastic stretcher’s advice. G-E-N-T-L-E neck stretches. Less is more!
  • A heat pack can loosen neck muscles
  • Ask a pro for some stretching tips
  • Yoga, under the guidance of an instructor, is useful. I hurt myself if I try to do more than cow-cat at home; Or corpse pose, I am super good at that one!

Professional support

  • Massage therapy is my most effective treatment. However, it is not covered by my insurance for chronic conditions. So…
  • Chiropractic care can be useful. Word of warning: If my neck spasms are too severe, then chiropractic makes it worse. Pre-treatment with something like Baclofen may help.
  • Physical therapists can teach proper stretching techniques
  • Occupational therapists ensure that daily work and living activities do not aggravate neck problems
  • Check with your employer, local Division of Rehabilitation, or National MS Society to request an ergonomic assessment and modifications to your work environment.

Vitamins, Minerals and Supplements – Oh my!

  • Ask a naturopath or nutritionist for dietary and supplement recommendations
  • The National MS Society also has some information on supplements for MS
  • Calcium and magnesium (together!) relieve muscle spasms. I use a powder that dissolves in water for quick absorption.
  • Potassium also works well and is easy to get from bananas, coconut, dark leafy greens, avocadoes, sweet potatoes and other yummy foods.
  • Curcumin supplements seem to help my MS overall, including this dizziness

This is just one of many MS symptoms. When you throw in the other demands of life, it is to be expected that one cannot maintain “best practices” at all times. My recent 10 days of travel made MS management quite challenging. Multiple airplanes, buses, heavy luggage, uncomfortable conference chairs, awkwardly placed presentation screens, and stiff hotel pillows all conspired to invite my cervicogenic dizziness out to play.  I took a little more Baclofen than usual. Thoughts of Botox bounced in my head as I lay in corpse pose on the hotel room floor. Elevators were favored over stairs, or — heaven forbid! — escalators. An unintentional sway or head-shift was just an opportunity to smile broadly at whoever I found myself looking at. Hopefully I passed as either super friendly or tipsy, or maybe both.

Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today, or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to multiple sclerosis.


  1. Colleen Peters says:

    I’ve had MS for twelve years, and though Ihave no lesions on my spine, only on my brain,whenever I’m awake I have issues with my balance, because I feel like I am on a floating dock

    • Judy Lynn says:

      Hi Colleen- I know that some brain lesions can cause balance issues, ‘floating on a dock’, not fun! Do you use anything to help steady yourself?

  2. Corinne K says:

    thank you for the post on cervicogenic dizziness. It describes exactly a new symptom of discomfort/ pain of mine at the back of my skull /neck.

  3. SOFIA TAHIR says:

    Thank you so much for this! I suffer with this but whenever I’ve spoke about it, I just get weird looks like I am a little crazy (which I do feel sometimes!). Sadly, I get severe side effects to all medications but happy that you mentioned the supplements I do take. I just have to take things slow, no rushing around like ‘Flash’ like I used to do!

  4. Ayushi says:

    Wow, this good an article and I’m reading it now. MS happened to mw about 4 years ago, with symptoms reflecting as blurred vision in my left eye once, then 6 months later – some symptom hopped onto my right eye, and then after a year ii found solace in my left eye again.

    Two years after this, I experienced Vertigo. Could literally see the skyscrapers swaying, the tree moving with the wind etc….. Vertigo became my best pal for a while, but without even bidding me adieu, it left soon after.

    Strangely, off late I feel like someone is pinching my left eyebrow, left eye lid, and left side of the head. The pain becomes so unbearable that the only medicine that helps me at that point of time is Crocin. I need to know if it has something related to MS, or am I just assuming too much.

  5. Judy Lynn says:

    Hi Ayushi,
    Thank you for sharing about your fickle vision and vertigo problems. And I’m sorry to hear about your new symptoms- sounds very unpleasant! It wasn’t until I finally explained my strange symptoms to my neurologist that I found some relief from it, in the form of Baclofen. Your healthcare provider is the best starting place as you try to determine if this is related to your MS.
    Good luck!

  6. Yoni says:

    Hello My name is Yoni. I’ve had MS for 5 years now. I had neck spasms before but I felt it on thesideof the neck. I couldn’t move my neck it would hurt so much. Baclofen relieved the muscle.

  7. Debasis says:

    Spasms are too irritating. But the most pinning is neck spasm pain indeed. I read you and found very informative. Keep on prevailing such caring posts.

  8. Rachel B says:

    Hi I came across this post in my search for some answers. I was diagnosed 12 years ago with RRMS, the first few years were very rough with a lot of different symptoms, ranging from spassms and tingling, numbness and fatigue, but thank God I have been in fantastic health for the last 5, up until about 6 months ago where I woke up one morning not able to move my head and neck, like a severe creek. My head felt like it was on a stretchie string and could only look down or around so far. It disappeared after two weeks and has appeared back up two or three times since, each time for a minimum of a week or so, I’m wondering if anyone has these type of symptoms too or am I going crazy!
    I have no health care coverage as it’s way to pricey here so I have not been to a neurologist since I moved to this country 6 years ago, any tips or advise from anyone on this forum would be greatly appreciated. Thanks in advance?

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