Tuesday, January 13, 2015
7-Months post-SLAD/R Surgery
It’s been 7 months since my SLAD/R surgery; I’ve been a slacker with updating this blog.
My voice is not perfect but it is so much better than it had been. There is no doubt about it, when I am tired,
my voice is horrible and when I do not sleep well, I pay for it with a raspy
sounding voice the next day.
I still use my voice amplifier when teaching, I get tired
and after 2-3 hours of lecture and talking, honestly, without the voice
amplifier, my voice is soft and weak. So
with the voice amplifier I am able to talk softer and my voice is projected
farther into the room. I do not use this
unit at home or anywhere other than in the classroom.
I also do not use a straw anymore because I need it, though
I do use it because I prefer drinking fluids this way. I can gulp down a glass of water just fine
and choking is not a problem.
My husband told me the other day that I have to get rid of
the giant container of “Thick It” I have in the pantry. I am not sure why I kept it. I got about 40 individual packets from the
hospital and I doubt I used anything from the extra large container I
bought, I did not mind the taste of the
stuff when I “had to” drink it, as it tasted like cereal, but now the thought
of using it is certainly disgusting!
I have thought about my trek with Spasmodic Dysphonia over
the years, I did not wake up one morning and decide to have the SLAD/R
surgery. In the 20+ years after diagnosis,
I tried many alternative things. I tried
herbs, essential oils, vitamins, acupuncture, acupressure, vegetarian
lifestyle, juicing, wheat grass, eliminating foods (food allergies), T3
(Thyroid) doses, see alternative care doctors, and I am sure there are many
other things here that I am not listing.
While these things may have helped me be healthier, they did not
eliminate the SD! Through the years I
used Botox and was so glad when I heard about the SLAD/R surgery, for me I felt
as though it was an answer to my prayers!
Each of us have a different road to get here. When I read about the surgery, then started
looking at the quality of my life as it was, it was just a no brainer, I was
going to do what it would take to get this surgery.
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