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The Faces and Stories of MdDS

BILL SMITH'S MdDS STORY

Thought I would send you this note just for your records.  A little history first.  I am one of the "blessed" one's who got mdds and it went away.  I got it the first time on a 40' yacht I spent a week on in Alaska.  It lasted about a week or so.  Then about 3 years later I went to Alaska again and spent another week on a like yacht.  When I got off that time it lasted for 3-4 months and slowly decreased to just afternoons and evenings and finally was went away, at least that is the time frame as I remember it.  I never went to a doctor.  That was many years ago, at least 15 and maybe more.

I knew it had something to do with the water and being on it constantly and overnight.  I never got it when out on a boat on a lake or floating for hours down a river. 

I told several people about it and they said, oh take this or that before and during and you won't have that "motion sickness".  But it was not motion sickness and I knew that.  Anyway, I had the opportunity to go on another one of those trips about 2 years ago and I was worried about having the same problem again, (something, as you know, I would not wish on anyone) so I got on the internet to find out what to take to stop it. 

And that is when I found the mdds site and realized that is what I had.  I joined, but have not been active, so I wanted to share this with you.  Of course I did not go on the trip.

This past winter I had a horrible sinus infection.  It lasted about 4 weeks from start to finish and I was on antibiotics for two weeks.  And guess what, I had the same symptoms after the sinus infection. 

I went to the mdds site and saw that "upper respiratory" (I am recalling this from memory and maybe it said sinus) infections have been known to reinstate symptoms.

They lasted about a month, were full time some days and part time others and then gradually went away.

That's it.  Got your email and read it today and decided I would share this with you.  If you wish to put it somewhere on the site you have my permission. 

Hopefully someday they will find a cure.  I hope the lady working on it comes up with something.  It certainly is a horrible thing to suffer from.  I feel so very lucky that mine went away all three times.

William H. "Bill" Smith

Cody, Wyoming

June 22, 2010

      
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This site is designed for those suffering from MdDS (Mal de Debarquement Syndrome) and the health care professionals who treat them.  If you have been diagnosed or suspect that you have MdDS or Disembarkment Syndrome, sign up for a free membership at our support site and review or search the thousands of messages from those who suffer from MdDS. Here, you will find caring people who understand what it is like to live with this rare balance disorder; members are from all over the world. Please join us to share and learn from others.

The MdDS Balance Disorder Foundation is an all-volunteer 501(c)(3) nonprofit PA foundation dedicated to promoting awareness of Mal de Debarquement Syndrome and seeking treatments and a cure for people suffering from this disorder.

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Last modified on June 21,  2010