Yep, you read that correctly, I had back surgery 7.5 weeks
ago; and it was all because I sent to see my PT for an IT Band issue.
In my last couple of blogs you know that I was going to a PT
for an IT Band issue, and things were going fine. Craig was giving me more and more exercises
to correct the strength in my legs to get them to track correctly. My left leg went laterally at the knee, and
my right leg went medially at the knee, both causing IT Band pain. He was also working on changing the way my
posture was when I was running. The
lower back takes a lot of pounding when you run, so the idea is to strengthen
it by pushing it out, and getting rid of the “sway” in your lower back. I was to use my core to do that, and round my
shoulders while running to help that happen.
I was given several core exercises from the day I walked into his
office, some of them incorporated a balloon.
This would also relieve the tension on my IT Bands at the pelvis – everything
is connected.
Shortly after I started PT, I started getting a tingling
feeling in my feet, and sometimes it went up the back of my calves. I thought it was a temporary issue, and I
didn’t think much about it; but it started to happen more and more, and started
to go up my legs even more. When I sat
down, it went away. I told Craig about
it, and he wasn’t too concern because it was mild, and it was relieved when I
sat down. So, he added in more exercises
to help this. But, it still got
worse. Some days I was fine, other days
I wasn’t. So, in addition of the worry
of my IT Bands giving me problems while I was running, I started to worry about
the tingling, which moved on into numbness.
Then I started worrying it would happen when I was running, which it
did, and then had to take time out on runs to sit down and let it go away. It was very stressful. It occurred more when I was walking them
running, this was because you typically lean forward when you run, so it
provided relieve in that position. I continued to go see Craig every week, my
It Band issue was doing much better, but the tinging, numbness, and piriformis
issue got worse. And I got more and more
scared to run, but I kept running; but I was running scared. Craig suggested I take two weeks off of
running, and during that time I started to feel different. What I mean by different, is I felt worse.
Well, these two weeks were hard, it became harder and
harder, more and more painful to run. My
low back and across the hips became very painful, and I became very frustrated
and cried a lot. I was struggling, a
lot. I continued to run races we had
signed up for, but I was running scared.
The last ERS race in Louisville I ended up getting an early start and
did slow running and walking to finish it.
I wanted to finish out the series.
Yes, it was painful, but I did it.
It continued to get worse. When I
went to see Craig again, he suggested it was time to go see a Sports Medicine
doctor. I made an appointment.
At this same time, I was told that my mother was getting
worse, more work for the Staff at Collinwood, couldn’t transfer, was not
toileting herself, and more and more combative.
I was told I had to get her into the Hospice program or move her to a
full-care facility. What a mess. I was worried and stressed about that, I
didn’t want to move her, and my legs were more and more painful. The mornings were the worse, and I finally
was just walking, and then stopping to sit, then walking. Running was out of the question, I had also
stopped working out at the gym by this time.
I just couldn’t do it anymore, even on my good days.
I went to see the Sports medicine doctor in an afternoon
that I had been dealing with issues with Mom.
When I got there, my BP was so high, he wouldn’t see me and sent me to
Urgent Care. I normally have very normal
blood pressure. I went to urgent care,
they started me on medication to lower my BP.
I kept telling everyone that it was stress (Mom and my numbness issue),
and the pain. At Urgent Care they took
Lumbar Radiographs. The radiographs
showed a congenital narrowing of the spine on L4L5. I was hoping they would give me something for
my anxiety, but they did not, but the next day I went to see another doctor,
because I was urged to by the Hospice people.
I was stressed and I had high anxiety.
In the meantime, because of what the radiographs showed, an MRI was
scheduled. My Mom passed away, and two
days after that I had an MRI. The same
day as my MRI, the Sports Medicine doctor called me and wanted to see me right
away. Friday afternoon, when he was
usually off. Dr. Abrahamson went over my
MRI. I had a severe stenosis of the
spine at L4L5 and my disc was damaged; most of this was congenital. There was too much movement front to back in
that joint as well, so I was referred to a neurosurgeon, who I saw the next
week.
The neurosurgeon went over my MRI with me and gave me three
options 1) injections, 2) cut ligaments in my back, and 3) L4L5 back
surgery. He also wanted more
radiographs. I had the radiographs that
day, and they showed that my back was not stable, with 7mm movement front to
back. Surgery was the only option. Surgery was then scheduled for December 30th
at 8am.
On surgery day I had to be at the hospital at 6:30am (on a
Saturday) for pre-op, and I was taken into surgery about 8:15am. I was really nervous, but I knew I wanted to
be better. When I woke up, I knew I was “better”,
but I was in pain from surgery. I spent
2 nights in the hospital getting used to everything I needed to do, had two PT
sessions, and practiced walking without a walker. My restrictions are No Lifting, No bending,
and No twisting. Basically, I am not
allowed to do anything. I can’t do any
housework, barnwork, or anything. I also
cannot take a shower alone, flush the toilet, dress, get in and out of bed – or
anything without help. It was then I
knew that is was going to be a really long recovery, both mentally and
physically.
Now that it is 7.5 weeks since I had had surgery, I can tell
you it hasn’t been easy. I didn’t need
much pain medications after about 10 days, and at that point only took them at
night (Tramadol and Flexril). Everything
was hard to do, it still is, only it’s more frustrating than ever. Tying shoes, putting on pants, getting in and
out of bed, etc. The worst has been sleeping.
I have some nerve issues at night in my right quad, which feel like “pins
and needles”, goes numb, and I getting stabbing pains that keep me awake or
wake me up at night. Tonight I am trying
a bed wedge to keep my upper body elevated.
Just trying things that other have had success with after this surgery.
I started walking after the 3rd week post
surgery, and today was my 32nd walk on the Dreadmill since
surgery. I am up to 3 miles at this
point. I don’t like the dreadmill, but I
am so thankful I have it. I need an
outlet, and I can’t go outside when the weather is bed or there is ice or
snow. I am a fall hazard. I cannot fall. I have been on three walks on the cement bike
paths in town while Tom goes running.
Last week had some really nice weather, and it was great to get
outside. The surgeon and the PA said I
could walk as much as I want, and “I would know when I have done too much”. This has happened a few times, mostly the
days that I had company. There is one or
two days a week that I am so down and hate how I am and how I feel. Today is one of those days, I am having extra
pain, and the last two days I just feel like crying.
The great news is that I have none of my previous
symptoms. I can walk without pain, the
buzzing numbness and pain is gone. I am
so grateful and thankful. It just been
frustrating, and I hate feeling this way.
I just have to keep moving forward.
I am stuck at home, but get out for movies, CSU Women’s Basketball
games, and shopping once a week. Today
was my first haircut since before surgery.
I have to wait until March 26th for my 3 month Post-Op check
up with radiographs. At that time I will
find out if there is enough healing for me to start running again. It is frustrating not knowing how the healing
is going, especially on the bad days, like today. It’s frustrating not getting good sleep, but
it is common with the surgery. It’s frustrating gaining weight and feeling fat.
I read, do puzzles, color, and journal.
I have a new journal: Dragon Tree Dreambook and planner. Ebeth suggested I get it. It has been really good for me. I am also
doing my own little Bible Study and looking up all the times “donkey” is
mentioned in the Bible. So, I walk every
day, extending my distance each day. I
journal, color, read and build puzzles – and watch the Olympics. I have to learn how to be STILL, be strong,
don’t quit. It’s going to be a long
process.
|
Morning of surgery, driving to MCR |
|
The afternoon after surgery |
|
My MRI |
|
My incision with staples |
|
Post-surgery radiographs |
|
Post-surgery radiographs |
|
Incision after staples removed - 2 weeks after SX |
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