With the dismal prediction of living only two to
five years following an ALS diagnosis, plus the high likelihood of needing to
rely on a direct-into-the-stomach feeding tube - - which avoids the need for
teeth altogether - - many ALS patients think, “The dentist? Why
bother?”
And let’s be honest; who amongst us doesn’t secretly wish we
could legitimately excuse ourselves from mandatory visits to the dentist anyway?
My visit to the dentist
But it was a force play when two years after my diagnosis, one
of my fillings fell out and I found myself begrudgingly sitting in the
dentist’s chair.
While arranging for the appointment I thought back to getting
that filling in the first place. It was “back in the day” of having to lean
over and spit into a mini-water fountain next to my chair, staring into a
glaring light above and never managing to open my mouth wide enough for the
dentist’s satisfaction.
Of course, I’m well aware of advances in modern dentistry
since that time, but now with ALS, my anxieties included not wanting to be one
of those high-maintenance patients who require all sorts of
accommodation. And, what if my ALS made things, well, difficult?
Nevertheless, I showed up and nervously stated my needs:
“The chair … not too far back please, as that affects my ability to breathe.
The spray … not too much water at one time please, as I have trouble
swallowing.”
“Not to worry,” my dentist said while slipping a sporty
pair of sunglasses over my eyes. Within seconds a soft rubber gizmo was placed
into my mouth that felt like a mouthpiece for snorkeling. It simultaneously
held my mouth open, held my tongue out of the way, suctioned away any wayward
spray, and amazingly, I was breathing with ease AND relaxing.
“Everything OK?” he asked.
“Uh-huh, “I gurgled.
The process was quick, painless and I have to admit,
anxiety-free!
Halfway through the procedure, a wave of gratitude washed
over me. I felt gratitude and appreciation for having such a skilled and
emphatic dentist.
[The device used to prevent water from entering my throat
is a “dental isolation device”: https://www.zyris.com/products/mouthpieces/]
Fast forward to...
A couple of years later, I began grinding my teeth at night
which affected not only my husband’s sleep – – but was wearing down a few of my
teeth (ack!). So, it was off to the dentist to repair a few teeth and be fitted
for a mouth guard. Again, I worried that not being able to lean back in the
chair (due to breathing
and speaking issues), not being able to tolerate water in my mouth (swallowing
issues) plus, pushing a walker, and wearing
AFOs would lead to a disaster.
Over the next series of appointments, I learned that modern
dentists can accommodate “just about everything.” Mine tilted me back, but a
nifty neck pillow kept my throat upright. A stretchy plastic “shield” (called a
dry shield) protected my throat from water and I held the suction
tube so I could “chase” stray water droplets during the entire procedure.
The result was, that my teeth were repaired, the dentist made me
upper and lower guards to wear at night, and I’ve worn them ever since. The
grinding continues, but safely now.
Things to consider
When dealing with the aftershocks of receiving my ALS diagnosis,
the thought of spending money at the dentist’s office when I didn’t know what my
future held, just didn’t make any sense.
I felt I had much bigger things to worry about than my teeth. But in
addition to maintaining good oral care to reduce the risk for gum disease and
pneumonia (an infection in the lungs caused by bacteria living in the mouth,
nose, and sinuses), the ALS Association recommends getting regular dental check-ups.
Taking good care of my teeth on a daily basis is a priority
in my life living with ALS and I have an arsenal of tools to help me. Such as easy-to-hold flossers, single-tuft-brush,
an electric toothbrush, and disposable flossers for on-the-go needs. Make
dental care a priority in your life too. And don’t fear visiting the dentist;
they have a new normal too and employ advances in technology and can
accommodate all kinds of patient’s needs. It’s all part of learning to live
well with ALS.
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Dagmar Munn ALS and Wellness Blog |
You don’t have to brush all of your teeth - - just the
ones you want to keep
A version of this post first appeared as my column on the ALS News Today website.
I’m going tomorrow and I hope they will help me stand up with the wheelchair. Then transfer to the chair from the walker. I’m very worried about it.
ReplyDeleteThanks, good to know as I was wondering if it was worth it.
ReplyDelete