Landlubber: My Symptoms

Mal de Debarquement Syndrome is truly an invisible illness.  If you didn’t know me well, you wouldn’t know anything was wrong with me. My symptoms are all in my brain, so they aren’t outwardly noticeable.  In the past 4 months, I’ve recovered enough that I can do most of my usual daily activities. It is amazing to me that I can look completely normal on the outside, while my perception of my surroundings is so different from reality.  The best way to help others understand is to describe what I’ve learned about my “new self” on this maiden voyage.

How I Rock:

I feel rocking motions constantly, although some days it can be very subtle.  For the first month and a half, I mostly swayed back and forth. Occasionally I would bob up and down. In mid-September (about 2 months into MdDS), I started to rock back to front and slightly up and to the right.  

In early October, I started to feel other motions that didn’t feel like a boat.  This was hard to get used to at first and pretty disorienting, since I was starting to adapt to the boat feelings.  The new motion sensations, described by my perception of them, include the sensations of:

  • being pushed on from the left while walking
  • walking or sitting on a people mover
  • one foot falling through the floor when walking or standing (mostly standing)
  • walking on uneven ground or up/down imaginary hills or mounds
  • being pulled from different directions

Now, in November, these sensations all intermix and change throughout the day (like a real boat ride).  Sometimes they are subtle and sometimes they are strong (read on to find out why). 

Is this dock moving? Nope, it’s just me!

How I Walk:

I appear to walk normally even though it never feels like I am. On my bad days I bump into the edges of furniture, objects, people, etc. I rock in all of the ways I listed above while walking.  On bad days I also will touch walls or railings, not because I need to, just because it makes me feel more comfortable. I have come to learn that I am stable while walking, I just don’t feel stable.  

Why I Rock Harder Sometimes:

There are some things I have identified that pretty consistently increase my boat and motion sensations.  These include:

  • Strong emotions (positive or negative)
  • Running and other forms of high intensity exercise
  • Stress
  • Lack of sleep or tiredness
  • Weather (rainy or snowy days, change in temperature)
  • Menstrual cycle changes
  • Enclosed spaces (the shower, hallways, stairwells, small rooms)
  • Caffeine

Some things increase the rocking sensations and/or cause nausea (a motion sick or seasick feeling) and migraines. These are:

  • Fluorescent lights
  • Blinking or moving lights (especially when contrasted with darkness)
  • Some blue or colored lights
  • Lights from tech devices and amount of time spent on tech devices
  • Scrolling on a tech device
  • Tracking objects or people in motion with my eyes (especially things that are close up)

I have been sensitive to the fluorescent lights since this started, although it took me a while to figure out that it was a trigger.  In the past 2 months, I feel like my sensitivity to moving or blinking lights has gotten much worse. I get immediately nauseous when seeing them, and if they last long enough they will trigger a migraine.  Extended exposure to these lights also causes fatigue again.

When the motion feelings or migraines get bad, the only thing that helps is rest.  I let myself sleep a lot on the weekends, so I usually feel best on Saturday mornings through Monday.  Most of my symptom triggers are present at work and are unavoidable to a degree (fluorescent lights, stress, lack of sleep, emotions).  So as the work week goes on, I get worse each day unless I get a lot of sleep or quality time away from symptom triggers in the evening.

How I Feel When Actually in Motion:

When I am actually in passive motion (floating, riding on a scooter, on a swing) or in a vehicle (plane, train, boat, etc.), I feel almost normal.  I can drive during the day without issues. When the car stops at red lights, the rocking starts back up and then goes away again when in motion.  I don’t feel safe driving at night. All lights have bright halos that hurt my eyes. The contrast between the dark sky and the brights lights moving, especially car blinkers, make me nauseous and give me migraines. On a boat or floating in a pool, I feel fabulous and like my old self. Unfortunately, these things could worsen symptoms long term.

November 11 2018 006
I feel almost normal on a kayak. I actually feel better for hours afterwards.

Migraines and Headaches:

For the first month without a break, I had a dull headache in my forehead.  It goes away sometimes now, but is triggered by the same things that trigger motion sensations.  I get pains now in different sides of my head, sharp and dull.  Now lights and screen time are my most frequent migraine triggers.

Fatigue:

When I first returned from my trip, I was sleeping up to 16 hours per day.  I was lucky to be off work for three weeks in August following my trip. I could usually muster up enough energy to go for a walk or attend a social gathering, but if I did too many things in a day, I would get exhausted for the next few days and need more sleep or rest.  As I started getting better, I would go to work for 8 hours, but spend the entire night “recovering” from work. This was really difficult. As the weeks went on, the fatigue reduced little-by-little.  I’m at the point now where I can sleep mostly normal amounts and do most normal activities. About three weeks ago, after a long weekend off of work, I had the first day where I did some cleaning, laundry, and ran errands all in one day.  It was an amazing feeling! I felt like my old self. I have been able to go back to most normal activities since this reduction in fatigue, as long as I avoid my triggers.

Boat Brain:

One of the most difficult aspects of my MdDS to explain is something called “brain fog.” I still have the intelligence and abilities that I had before MdDS, but I’m more forgetful and have difficulty making decisions or figuring things out if I’m not rested.  It reminds me of trying to think with a really bad hangover or after going a few nights without sleep. Tasks that require a lot of working memory are more difficult (like doing math in my head or figuring out directions with a map). Until recently, I would need long breaks after thinking creatively or working on new ideas or plans.  In the first two weeks after returning from my trip, I had significant word-finding issues. This was very strange for me because I’m a speech-language pathologist, and I teach strategies for word-finding issues for my job. Most of the time I’d have to go to sleep before I could think of the word or name that I was trying to come up with.  This went away completely after the first couple of weeks. The reduction in this “brain fog” has been the biggest and best improvement I have made since the symptoms began. I would not have been able to write this blog before the “brain fog” lifted. I was lucky to get through the mental activities required for a workday, and then came home mentally exhausted.  

Waves of Emotion:

When I first started having these symptoms, it was extremely scary.  I had no idea how I was going to continue to live my life. For a while, I was taking things moment by moment, counting down the hours until I could go back to sleep, hoping to wake up normal again.  Before I had a diagnosis, I was worried I was dying of a brain tumor or some strange disease. This caused a lot of crying and panicking. I’m always feeling the motion, so it is hard to stop thinking about it.  I’ve had to miss out on things that I never would have said no to before I was sick, making me feel very sad. Before I found the MdDS Facebook community, I felt very alone, experiencing a reality that no one else could understand. Before the fog and fatigue lifted, I had many days where I was pushing myself just to step out of bed in the morning or do simple chores. Before I figured out my triggers, I felt completely out of control and what I would be capable of doing on any given day seemed unpredictable.  

Changes in your sensory system and not understanding your body anymore causes anxiety.  

Realizing that you are different and that you might never be the same again causes depression. 

I am very, very, very lucky to have supportive loved ones who have tried to understand my new perception of the world, which has helped me get through the tough days.  My recent improvements have made me feel very hopeful and happier. After sharing this blog, it has been easier to talk to people about it, which has lifted a huge weight off of my mind.  This section has been hard to write, I am crying and rocking hard right now! It is all worth it if someone else can read this and feel less alone.

Other Weird Things:

There are lots of other strange, subtle symptoms that I experience.   

  • I get tinnitus (a ringing in my ears) in short bursts throughout the day.  
  • Noises bother me more than they had before.
  • Sometimes patterns (on clothing, carpets, wallpaper, etc.) look very strange, almost 3D.  This is especially disconcerting when walking on patterned carpet. 
  • When I was first figuring out my equilibrium, I had horrible jaw, neck, and shoulder tension.  It returns when my symptoms are high for a long period of time.
  • As my fatigue has recently reduced, I’ve had difficulty sleeping through the night. I’ll usually wake up for a few hours each night and can’t fall back asleep.
  • Navigating crowds feels really difficult and stressful, even though now with experience I’ve realized I’m able to do it. It looks like people or things are coming at me in places like the grocery store.
  • My vestibular system is overly reliant on my vision for input, so when I close my eyes I lose track of where I am. That’s when I am actually unsteady, not just feeling it. I’ve fallen when my eyes are closed. It makes me really nauseous to close my eyes while standing or moving.

Overall, every day is a different mix of sensations.  Most are now predictable, but there are always changes and surprises. 

In my next post, I will explain in more detail some of the things that have made me feel better and helped me manage my symptoms, like connecting with other people who have MdDS, special glasses, and changes in routines.

I’m also planning to write posts about working with MdDS and some more upbeat posts about positive changes that MdDS has caused in my life. I am still planning to keep writing about my experience even if I go into remission.  

Please note that every person with MdDS has a different variation and severity of symptoms, which may or may not include those I mentioned.  I was lucky to have full health before this indefinite boat ride began, which has made it easier for me to continue to function. I am also very lucky to now have enough energy and stamina to be writing this blog.  Many people with MdDS can’t work, walk normally, or complete everyday tasks. My heart goes out to my fellow MdDS warriors who are struggling with these symptoms and many more! To my MdDS crew, how do my symptoms compare to yours? I’m sure there are some things I left out, anything important I forgot to mention?

11 thoughts on “Landlubber: My Symptoms

  1. Just read your story, but I have to read it again and again. I am always wondering how people with MdDS can walk without a support like a cane, I loose my balance and am afraid to fall. Maybe it is also my age of 77 and my 2 hip replacements. But moving around is a real problem for me, Do you have European background. We share the same name Brunner, I am Austrian but living in the Netherlands. Veronica von Brunner

    Liked by 1 person

    1. Hi Veronica! Yeah some days I am amazed that I still walk normally! I’ve been lucky, but I can see how that could happen. I think my symptoms are milder than a lot of people. That is so cool we are both Brunner’s! My husband is of German ancestry and we live in Wisconsin which has a lot of German influence. Thanks for reading. Wishing you wellness! ❤️❤️❤️

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  2. Overwhelmed here with emotions!
    To have validation that yes indeed it is not just all in my head, really it is, all in our head, (not meant as a joke.)
    Your description is spot on, a few minor variants in my own life, but so much the same.
    As for myself, pre MdDs, I was runner, I believe I went go through the stages of grieving, adapting to a new way of life, but grieving for the way ‘things used to be’. Much like you, determined not to let MdDs control me, I ran a half marathon 1 year & 1 month after the onset on MdDs.
    Yes, life is different without landlegs, But we continue pushing forward, together! Hoping for better understanding of this life changing condition and maybe someday a cure!
    Thank you for your blog, I am grateful!

    Liked by 1 person

    1. Wow Dana!! That is so amazing about your marathon. I am hoping to run a 5K before the year is over but right now running is too much of a trigger! You are very inspiring!!! Thank you for the kind words and reminder that we are in this together! ❤️

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  3. I’m so glad I stumbled upon this. I’ve had MdDS for a little over 6 months now. Your descriptions are very similar to mine. Everything from the beginning to how your symptoms changed and the triggers that make it worse. I took 6 weeks of short disability after being diagnosed so I could rest because I could hardly even move from my couch or bed. I totally understand the feeling of the uncertainty of not knowing if you’ll ever be the same way as you were before. I’m grateful that I have friends and family and coworkers that understand however at this point they all think I should be back to ‘normal’ and can’t believe that I still tell them I feel the motion sensations. Just makes me feel a little better to know that I am not the only person going through those exact feelings and emotions and just trying to be a warrior every day. I will look forward to your future posts. Thanks.

    Liked by 1 person

    1. Thanks, Shirley!!! That is such a good point about everyone thinking we should be normal or better. I get asked all the time if I’m better, and I wish I could say yes, but I’m still always feeling in motion. It is so comforting to know that you can relate and understand. I hope we both get better together, too!

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  4. It’s so comforting to find this blog and realise I’m not the only one going through this. After struggling with “vestibular” symptoms and trying to find answers, after 3 years I got my diagnosis of MdDS. Mine started spontaneously (I didn’t even enjoy a cruising holiday to get this!) – just out of the blue!
    I can relate to most of your triggers. A few for me is sometimes when I’m scrolling through a computer screen or reading – words just jump around a lot and then that gets me swaying again. Or watching TV with most shows now opting for that jumpy filming – hard to explain but the constant movement of the camera just brings on another symptom. Even washing up – looking down into the water has me again swaying and rocking.
    I’ve been wanting to share my own story of this for so long as i’ve come to a stage in my life where it has affected my work life and my independence and I was hoping to find support from others in the same position. So I have started a blog of my own – really just to get my words out on paper – I find it quite cathartic.

    Liked by 1 person

    1. Hi Jane! Writing for me has been cathartic as well. I’d love to read your blog. I was very lucky to get diagnosed 2 months in, but the months before were so scary – I can’t imagine 3 years. I think I know what you mean about certain shows. It’s worse for me with reality TV or before or after commercials for sporting events when they shows crowds or cars moving in high speed. Thanks for reading. Wishing you wellness and stillness!

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      1. Thanks for sharing the link! It is helpful to read your story and recognize some parallels. Ugh when they asked if you just had depression that KILLS me!!! I know it’s hard for people to understand, but what we are feeling is very far from mental – it’s very, very physical even if they can’t see it! Good for you for holding strong on that point!

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