As life has become pretty busy in the last week, Brianna and I
discussed the option of posting our story on a blog to better share with
friends and family. We have decided to start tracking our story so others may
have a chance to see through our eyes. We are currently at the Mayo Clinic in
Rochester, MN and if anyone is wondering, we don't live here and I am not
applying for a job. Brianna is here for medical reasons of which I will explain
shortly. In order to better understand where we are, it is important to know
how we got here.
Where it all began...
In August, Brianna began to show symptoms of what seemed to be a sty
in her left eye. A sty is a red painful lump near the edge of the eyelid that
looks similar to a boil or pimple. Brianna has had a sty before and we knew
that in due time the sty would resolve and all would be well. We waited a week
or so and the sty didn't seem to be getting any better. Knowing we had an
appointment coming up with Brianna's OB-GYN, we decided to wait until then to
seek medical advice. At the doctor’s appointment, the physician thought it appeared
to be a sty but further back in the eyelid and gave Brianna some eye drops to
help her eye heal. We were informed that after a week if things had not gotten
any better to call and let them know. After a week, not only did the eye not
look any better it actually looked as if it was getting worse. We called the doctor’s
office and they said give it a little more time for it to heal. Being a physician’s
son and a health administrator, I was not completely in agreement with that
decision so I scheduled an appointment for Brianna to see an ophthalmologist.
My father agreed that this didn't look like a typical sty and agreed with the
decision. The soonest appointment was about a week and a half away so we had to
wait patiently to see what was going on.
In the meantime, Brianna's eyelid began to shut to where it became
harder and harder for her to open her left eye. By the time we made it to the
ophthalmologist Brianna could hardly open her left eye. The doctor spent a long
time looking at Brianna's eye and examining her face. He ruled out Bell's palsy
and determined that this was a 3rd cranial nerve palsy pupil sparing. What we
had not realized was that Brianna wasn't just having issues opening her eyelid
but she was also not able to move her left eye to the right, up, or down. (Thus
the 3rd cranial nerve palsy). However, the pupil was dilating and working
properly. (Thus pupil sparing). We asked the doctor what could be a possible
cause and he said in a young patient like Brianna, this was not normal and feared
this might have been caused by a brain aneurysm or a tumor. Very emotional, we
left the office with a MRI scheduled for that afternoon. To make things a
little more difficult, Brianna is pregnant and it is not suggested that
pregnant woman be exposed to the contrast used in MRI's. The contrast simply
makes things easier to see for the physicians but an MRI can be completed
without contrast and still be useful. The MRI was on September 22 which was a
Friday afternoon. We waited all weekend hoping for results but they didn't come
in until Monday morning.
We were given the results on Monday and were informed that the
cause could potentially be from demyelination or a low-grade glioma.
Demyelination has to do with the neurons in the nervous system. The neurons
(especially) in the brain have a myelin sheath that is around them. This allows
protection but also allows signals to transmit a lot faster. Demyelination is
typical for someone with Multiple Sclerosis (MS). The other opinion was a
low-grade glioma which would be a small tumor. As we researched both of these,
we felt that her symptoms were more aligned with MS. The ophthalmologist then
determined that Brianna needed to see a Neurologist. He sent the information
and an appointment was scheduled for Thursday October 12.
While we waited patiently for the Neurologist, Brianna seemed to
only be getting worse. She started to have weakness in her right side of the
body. It started with her right foot as it began to drag on the ground as she
walked. This continued as she started to feel weakness in her right hand. She
came close to dropping things often with her right hand and could tell that she
was losing her strength. I then came home one night from work and noticed that
her smile was drooping on the right side of her body. This was very concerning
to me but we had already made the appointment with the Neurologist and thus all
we could do was wait. We met with the Neurologist and she felt that this was
being caused by a low-grade glioma and only a neurosurgeon could determine the
diagnosis. She scheduled the appointment for Friday October 13. We met with the
Neurologist the next day and he felt that it couldn't be a low-grade glioma as
it had progressed too much and didn't follow any of the same symptoms. He felt
that this was more likely an auto immune disorder. Luckily we had taken my
father with us to the appointment and he asked what the Neurosurgeon would do
if it was his wife and he stated that he would be on his way to the Mayo Clinic
where he was trained to get answers. The decision was made that we would like
to be referred to the Mayo Clinic. The Neurosurgeon stated he would start
reaching out to colleagues immediately.
It was a terribly long weekend waiting for what the next steps
would be for Brianna and her treatment. Over the weekend, she fell once and I
could tell that she was becoming even more unstable. I also noticed that she
was having difficulty at times articulating what she was thinking. She and I
discussed the issues she was having and we decided to call the Neurosurgeon
first thing Monday morning to let them know that even over the short span of
the weekend that she had gotten a little worse. I called first thing Monday
morning but was unable to reach anyone so I left a message. I attempted to
focus on work but was worried that no one had gotten back with me. I figured if
I didn't hear anything back from the office following lunch I would call again.
During lunch the office called and stated that they had the Mayo Clinic on the
other line and they were wondering if we could be at an appointment the next
day at 7:30 am. I asked if I could look at plane tickets and was having a hard
time finding tickets that would actually get us there. I luckily found plane
tickets from Dallas, TX to Minneapolis, MN. The plane was leaving at 8:35 pm
that night. I looked at dad and we decided we shouldn't wait. Arrangements were
made for the flight, rental car and hotel as well as leaving Watson with
family. We left College Station at 3:50 pm and got to the Dallas airport at
7:30 pm. We boarded the plane at 8:05 pm and took off at 8:35 pm. We landed in
Minneapolis at 10:50 pm. We got our luggage, got the rental car and began the
last leg of the trip to Rochester. We got to the hotel around 2 AM. We went to
sleep hoping that the Mayo Clinic would be able to give the answers we were
searching for.
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