I had two phone calls I had to make. That's done and I'm headed back to bed. Pain is rising every minute that I'm up.
This is the story of my life with Fibromyalgia, Chronic Myofascial Pain, Chronic Fatigue Syndrome, Peripheral Neuropathy and Lymphedema. Every day is a challenge. Join me as I meet each challenge head on.
Friday, December 9, 2011
Thursday, December 8, 2011
Checking In
Woody in his napping spot at the end of our bed |
Isn't that a cute face. |
Right now I'm hurting so bad that I'm headed to my chair to prop my feet up. Mr. Supportive is in charge of supper so I'm waiting to see what comes out of the kitchen. He's a much better cook than I am and I'm not ashamed to admit it. LOL
I've got some new things going on that I'll start sharing with you tomorrow. Be sure to check back here soon.
Wednesday, December 7, 2011
Monday, December 5, 2011
It's Raining...Again
Today was a busy day.
Mr. Supportive had an appointment to set up surgery to have his cataract
removed. Since he was having his eyes dilated,
I was the designated driver. Considering
how much I hate driving in Memphis traffic and it being dark and raining cats
and dogs, I’m not sure how good of an idea that was. We did make it to the next doctor’s
appointment in one piece but he assured me that he really could drive when we
left. I guess I scared him pretty
bad. LOL
My degenerated cervical disks keep me from being able to
turn my head to look behind me in traffic.
I can tell if anyone is right beside me but have to depend on my side
mirrors to check if it’s ok to move over.
That’s the main reason I don’t drive any more than I have to and I stay
off I-240 as much as I can. Add the big
time construction going on, the rain and my neck and it was touch and go. Did I mention that I need new glasses too???
After his appointment we had a few minutes at home and then
we were off to see my pain management doctor.
After the three of us talked, Dr. D is changing some of my medicine
around. I have to tell you that it
scares me to mess with what is working but I’m beginning to feeling like an
airhead. I think we’ve finally gotten
ahead of the pain and now it’s time to back off some. At least that’s what I’m hoping.
Surprisingly with the cold rainy weather, my pain has gone back down into the “normal”
level four
or five. I’m almost afraid to say that out loud for fear of it going back
up. It probably will go back up some
this time tomorrow night. I take my
mother-in-law to the eye doctor tomorrow.
She suffers from Macular Degeneration so about every 6 weeks she gets a
shot in her eye in an effort to keep what little vision she has. The first time I walked into the room and she
had the q-tip with lidocane on it poking out of her eye, I just about freaked
out. Gave me the willies! She said that it really doesn’t hurt at
all. I still can’t watch the doctor give
her the shot.
Her mobility is an issue these days but she’s almost 85. The sad thing is that up until about 6 months
ago, she got around better than I do. We
call ourselves the cripple leading the blind.
The distance between the door to the building and the doctor’s office is
not good for either of us. I got a great
deal on a light weight transfer chair ($25 at Goodwill!) that we use in cases
like this. Unfortunately, it only holds
one person at a time. Out of respect for
her age, I’ll be pushing her. That means
that my lower back will go crazy by the time our day is over. It’s not from pushing her, it’s from the
walk. It gives me fits even walking
around at home more than usual.
I grabbed that wheelchair the day I saw it because walking
any distance does me in. There are so
many places (like doctor’s offices) that even with handicap parking, I may as
well be running a marathon instead of walking in an office building. My lower back hurts horribly and my legs turn
to mush. I suspect the lower back pain
is from my degenerated lumbar disks and the mushy legs are from the Fibro and
Neuropathy with a little Lymphedema thrown in.
So that’s how my Monday went and the plans for Tuesday. How’s your day going?
Nasal pillows |
Full face mask |
Ayr doesn't pay me to recommend their product, I just like it! |
Adrianne, I asked Mr. Supportive what problems he remembered
when he first got his CPAP. He said the
hardest thing for him was waking up with his nose sore. We are using the nasal pillows instead of the
full face mask. I had the full face mask
for several years and it was hard for me to get use to it because I’m claustrophobic. Since I was so exhausted from not sleeping
well, I would crash almost as soon as I put it on. That took care of the claustrophobia and I
figured out a way to lie on my stomach with my head off the side of the bed. Now I sleep on my sides and it’s fine. I recommend using
Subscribe to:
Posts (Atom)