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The Faces and Stories of MdDS

Darilyn Rice's MdDS STORY
 June 2011        

     It was August of 2010 when my husband and I and three other couples set sail on a weeklong cruise out of Long Beach for the Mexican Riviera.  I had been on several cruises before, one of which was even longer and required international travel, and although I'd had a long history of getting motion sick in the car and on boats, I'd never had trouble on the large cruise ships before. This sailing was no different. The weather was nice, the seas cooperative. I had no motion sickness and no migraine headaches while on board. We had a delightful trip with our friends and many memories and photos to last a lifetime.

     Getting off the ship however was another matter. Walking to the car, I did not have my "land legs." I shrugged it off and got through the day unpacking and making a trip to Costco with my husband. Over the next several days, the sensation of being on the boat continued but I didn't panic,I'm a Registered Nurse, and just felt it was somehow related to my inner ear and it would go away on its own. I continued my daily routines and worked my part time schedule in the allergy office and tried to push through the feeling of rocking, swaying and bobbing. Then suddenly I had more migraines than usual, ear pressure, brain fog, fatigue, and nausea. Admittedly, it was time to see the doctor. It had now been three weeks.

     The family physician gave me the once over. She couldn't find anything major wrong with me. That was a relief. Also believing it was related to my inner ear, she referred me to the ear specialist. I didn't rush right over to see him since again, I just felt this would go away on its own. I made an appointment for two weeks out believing I would end up cancelling it when my condition improved. By sheer coincidence, the day before my appointment with the specialist, there was an article in the LA Times Travel Section on Mal de Debarquement Syndrome. It was like someone had sent up a flare! That day, I probably received a dozen phone calls or e-mails from friends asking if I'd seen it. I took it with me to the specialist the next day but really, it was unnecessary because I was one of the lucky ones who made an appointment with a physician who was already familiar with the condition. The good news and the bad news was that yes, I surely had it and no, there was no cure. I waited another two weeks and went back for VNG testing and then had a follow-up consultation with a neurologist to confirm the diagnosis.

     I was offered a variety of treatment options but for many reasons opted to ride out the wave mostly on my own. I have other medical conditions which complicated the issue. The ENT had not had good results with vestibular therapy with other patients and it sometimes made it worse and I did not want to risk that since I was still somewhat functional. I had tried many of the medications before for my other condition and knew that I was very sensitive to them so avoided taking most of them. I did get a prescription for xanax to have on hand because I had a new symptom of anxiety that I had never really had before this. It was an internal vibration that would start up and get worse until I wanted to jump out of my body.

     The affect on my life may not be as great as it has been for others. Because of my other heath conditions, I had already reduced my work schedule to part time, and I had already learned to pace my lifestyle to accommodate my household chores and my social life. This helped me tremendously in terms of coping with the devastating effects of this syndrome. But still, while it lasted, it greatly affected my work, my home life and my social life. For instance, during the holidays last year, I couldn't do any shopping and we either declined party invitations or ended up leaving parties early due to noise. Doesn't sound like a big thing but after a bit, you do start to feel isolated and the depression sets in.

     For me, it turns out, the depression may have been what saved me. During this same time period, my mother was quite ill, I ended up going for counseling and then I was put on a low dose of zoloft for depression. This medication usually takes about 2 weeks to kick in for depression. However, within 3-5 days of starting it, my MdDS symptoms started to improve. From there, I went right into remission.

     I can't say for sure whether it was coincidence or not but personally, I am leaning toward the notion that the zoloft sent me into remission. Every person is different. We all have different chemical make ups and shortages. I believe I run a tad low on serotonin and perhaps that little boost up did the trick. That's my story and I'm sticking to it.

Darilyn Rice
June, 2011

      
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Last modified on June 4, 2011