He
basically blew me off. (of course, there was that less than stellar review I wrote on the questionnaire they sent me after my first visit) We looked at the CT scan images of my nasal
passages and he pointed out how constricted the left side is and how
I don't breathe out of the left nostril because of this constriction
which is why I breathe through my mouth and most people would have
got that corrected. old news All this is damage from when I
was 3 and broke my nose and my parents never saw fit to have it
corrected later and then as an adult with no insurance and living and
raising a family on an artist's income it was out of the question as
long as it wasn't life threatening and it hasn't been life
threatening. I am aware that my breath through one nostril is
restricted, I take care to sleep with my nose and mouth not smooshed
into the pillow, I don't like stuff around my face, I try to keep my
nasal passages clear within reason. For the record, I can
breathe out of my left nostril and only breathe through my mouth when I'm stopped up. It's not
like what happens is a slow asphyxiation. When it happens it's sudden, one minute
I'm fine and the next I can't breathe or just barely.
So
he does the camera down the throat thing which didn't hurt (the
attendant put numbing solution soaked cords in my nostrils first) and shows
me my vocal chords and has me make noise and I see them constrict and
he pointed the camera into my nasal passages. All looks good and right in there, no obvious
malformations down there.
Then
he kept pointing out this thing in the image of the CT scan in my
nasal passage on the left adding to the constriction from the broken
nose...a skin sac full of air. It was very clearly there (hmmm, I
wonder if that's why the left side seems full so much more often) so
a malformation there in that most people don't have this but I was
born like this he says, born with it, that it shows up in about 15% of
people. I'm like...OK, so this is something I've lived my
whole life with and I'm not really sure what he's saying or
recommending, it doesn't seem to be a problem that demands to be
fixed to me unless it is or will get worse for which he didn't
really have an answer. So yeah, OK, but what about the problem I'm
here for, the whole suffocation/choking thing. Perhaps I should get
a second opinion, he said, because he could not see anything wrong,
perhaps another doctor would be able to see something he wasn't able to, and
he was done. What a colossal waste of time and money. I got more
attention and useful information from the speech therapist that
helped administer the barium swallow test than from this doctor.
So
no. I'll not be going through this again just to find out what I
already know, that it's just one of many swallowing disorders that
you learn to manage among the many weird things that affect and
afflict the ever diverse physical form of a human body, unless
something extreme happens.
Maybe I am choking, or rather, aspirating and not suffocating, only instead of one big thing blocking my airway, it's small droplets (saliva or liquid) that take some effort to expel. Who knows. The only answer is the same...mindfulness. Mindfulness when I eat and drink so I may be a pretty dull dinner companion from here on out, just saying.
Maybe I am choking, or rather, aspirating and not suffocating, only instead of one big thing blocking my airway, it's small droplets (saliva or liquid) that take some effort to expel. Who knows. The only answer is the same...mindfulness. Mindfulness when I eat and drink so I may be a pretty dull dinner companion from here on out, just saying.
But,
y'all, I kept my promise and went to the doctor about it.























