My Visit to the Speech Therapist - A discussion of swallowing problems.
I want to share what transpired at my first visit with the speech therapist
in hopes that it might help others who are experiencing swallowing problems
or difficulties with speech. She wanted to focus on my swallowing problems
first and offer some recommendations on how to compensate. I told her that
sometimes, after I had taken a drink, I would choke and spray it all over.
I also told that I find myself actually thinking about swallowing, which
had been all involuntary before. She said this wasn't too uncommon.
Evidentially, because of HD slowing down my response times to almost
everything, my epiglottis is no exception. This is the little flap that
covers the larynx during eating or drinking so that everything you swallow
goes down your esophagus.
I'm actually having to swallow several times
because it doesn't feel like everything has gone down okay, or that it's
delayed. She stated the correct way to swallow when I'm having problems is
to take a small bite, or drink, and then tilt my head forward until my chin
rests on my chest. I tried this a few times and I was surprised how easily
everything went down. She said this was because, in bending my head
forward, I caused my epiglottis to partially close over my larynx using
gravity. With it already partially closed, when my brain gave it the signal
to start closing because a swallow was coming up, it was already over
half-way there to begin with, thus compensating for the slow response to the
signal it was getting.
She also recommended drinking all liquids through a
flexible straw in order to keep my head level or tilted forward, instead of
thrown back like when you take a normal drink of something. Some of her
recommendations were common sense, but none-the-less, needed reinforcement,
like cutting everything I eat into small pieces. She told me I needed to
keep all distractions to a minimum while eating to avoid choking. I told
her she's never been to my house- it would be easier to count the number of
times a day when there weren't any distractions, rather than when there
were, especially with six kids still home and a granddaughter next door
who's always playing here! She stated that as the swallowing gets harder,
it would be easier to eat alone, without any distraction such as the TV,
etc. I told her that that would be hard.
She then recommended that if I
wanted to continue eating with the family, that either I start before they
sit down to eat so that I would be almost finished, or come in to eat when
they're almost finished so that I can still feel like I'm a part of them! I
liked that idea! Although my swallowing problems are still intermittent,
it's been real scary when I've tried to swallow and haven't been able to.
She said that if this happens again then she would suspect that the muscles
in my esophagus weren't synchronized any more because of the HD. She said
that I could request an esophagram to verify this, once it starts getting
worse.
I told her that I had already had a modified barium swallow test
done a while back that didn't show anything wrong, at least at that
particular time. Two separate things she said. The modified barium swallow
test shows how well you are swallowing and the esophagram measures how well
the esophagus is expanding and contracting in rhythm to move liquid or food
down. I recalled hearing weird bubbly sounds in the back of my mouth at
times for the last couple of years. I could never figure out what it was.
She said that it was a sign, once again, of the epiglottis not closing
during normal swallowing and some of the liquid making a "bubbling" or
almost "hissing" sound around the opening of the larynx. I was glad to
finally find out what was causing that weird sound. All-in-all the visit
was very informative.
This Tuesday we work on some more swallowing
strategies and will hopefully move on to my intermittent slurring stuttering
and choppy pronunciation problems. All of these are exasperated while under
stress but normally, they're pretty good. If anyone has any questions
please ask.
Provided by Phillip J. Hardt, E-mail: phardt1@HOME.COM
Answers to this question can be found through these links:
- Eating and swallowing difficulties (includes Heimlich Maneuver)
- Published by the Huntington's Disease Association, London.
- Eating and Swallowing
- Published by the Kansas University Medical Center.