What the Hell Happened to Amy Anyway – Circle Back and Follow Up
For
those of you who are confused as to my current status or for those of you who
are new to my blog and have no idea what is going on or for those of you who
just like to read what I write – this is for you!
In
my line of business we use a lot of buzz words like “circle back,” “follow up,”
“touch base” and even the ever popular “under a bus.” If you have ever seen me do stand up, I have
come up with funny and some what accurate definitions for this corporate
jargon. (If you have not seen me do
stand up – look for me hitting the stage again in a couple of months – I promise!) At the risk of over using these buzz words
outside of the workplace and at the risk of “overusing” quotation marks where
quotation marks are “not needed,” I wanted to take a moment to “circle back”
with you all on a few things and provide a “status update” as to where I was,
where I am and where I would like to be with my condition.
Some
of you have seen me around town – doing things like drinking and driving – separately
of course, not at the same time and are unclear as to how I can be fresh off of
surgery, not showering or wearing pants and yet playing beer pong or dancing at
a Dave Matthews Band concert.
The
facts are these:
These posts were written not as they were happening, but shortly thereafter. Many of them at the same time and I am just
now posting them – one a day until I catch up with myself.
I
expect to be posting in “real time” in the next few weeks – probably not every
day, but close to it.
Once
I catch up with myself, I will be posting not only on my recovery and the
challenges I am facing moving to the next step, but getting to the good stuff
as well – Writing letters (see the first few posts I did if you want to know
what the letters are about), maybe some movie reviews and some new comedy type
material – like how I annoy and scare my neighbors – complete with photos.
I
started writing posts as they were happening when I returned to work on July 1,
2009. So those posts will be a little
more “fresh” since they were written as they happened. When I post them, I will include a “Written
on” date.
Here
is a quick timeline for you:
End
of Feb 2009 – I got a headache. Like, a
really really bad headache and they were happening daily. It was around this time I realized that these
headaches were not normal and I set up an appointment with my doctor.
March
16, 2009 – Met with my doctor who seemed unconcerned with my headaches but
ordered blood tests and an MRI.
March
23, 2009 – First time I realized MRIs are like giant techno music
machines. First time I ever removed the
piercing I have in that little piece of my ear that protects the hole.
March
30, 2009 – Doctor tells me the MRI and blood tests are all normal. To which I said, “Great! But I am not normal.” Doctor diagnosis’s me with migraines.
For
the next 2 weeks, I start to get worse.
Headaches are worse and the pain has moved to my upper shoulders and
back. Ringing in my ears starts. My vision graying out when I stand or bend
over gets worse.
April
10, 2009 – Meet with my eye doctor and go over symptoms. He immediately diagnosis’s me with pseudotumor
cerebri (also known as intracranial hypertension).
At
this point, I can still see pretty well, though my vision field test shows
blind spots in my peripheral vision.
April
13, 2009 – Meet with neurologist who orders a second MRI and a spinal tap.
April
14, 2009 – Second MRI completed. Had to
refrain from bringing glow sticks and a pacifier with me.
April
16, 2009 – First spinal tap. First time
I saw my brain fluid.
April
18, 2009 – I now have blurry and double vision and decided to stop
driving. Amanda becomes my chauffer.
April
20, 2009 – Neurologist calls me back and concurs with diagnosis of pseudotumor
cerebri and prescribes a medication for me.
I explain my vision issues and the doctor tells me to take the pills and
that I’ll be fine.
Noon
April 22, 2009 – I go home early from work because I do not feel well – bad reaction
to the drugs. Last day of work – unbeknownst
to me – for 10 weeks.
April
23, 2009 – Admitted to the ER because I could not keep anything “down” (that’s
the nice of way saying I was puking my brains out for 24 hours straight).
April
24, 2009 – Released from the hospital.
Told the doctors my vision was worse, they told me to keep taking the
pills.
That
weekend my vision got even worse, to the point where all I could see were
shapes and light and dark.
April
28, 2009 – Go back to the eye doctor who tells me I need to go directly to the
hospital for surgery to relieve pressure that is being put on my brain and my
optic nerves – causing my “blindness.”
April
29, 2009 – I have surgery. A shunt is
placed in my lower back at the base of my spine. The shunt drains fluid from my brain, down my
spine, around my side and deposits the fluid into my abdomen. I have 3 incisions from the surgery and about
40 staples.
I
am now in the hospital where I throw up on a nurse, am convinced my roommate is
trying to kill me, don’t like the food and am doped up on all sorts of drugs.
May
2, 2009 – I am released from the hospital and head home.
At
this point the headaches are pretty much gone, so is the ringing in my ears and
my vision is already starting to improve.
May
4, 2009 – First follow up with eye doctors – miraculous improvement.
May
8, 2009 – I have my staples removed by something that actually looks like a
staple remover – weird.
Over
the next few weeks I am at home recovering.
My days are spent either in bed or laying on the couch. I am going to see at least one of my three
doctors about once a week. I am on all
sorts of drugs and eating very little.
Friends and family are visiting with me and I am relearning how to live
a normal life. All of this will come up
in future posts.
July
1, 2009 – I return to work after being gone for 10 weeks. I have 25000 emails. I erase all but 3 of them.
My
eye sight is better, but not 100% recovered.
I still have blind spots in my peripheral vision and some dark spots,
but it is manageable.
July
16, 2009 – I am given the all clear to start driving again. My eye doctor informs me that the swelling of
my optics is completely gone and he expects my sight to continue to get better –
though slowly – over the next 9 months.
Today
– July 30, 2009 – Things are good. I am
getting back into the routine of life. I
am going out – without freaking out – I am working and even working out again, and
of course I am back to some of my old hijinx.
Physically I feel really good, though I have some aches and pains here
and there. My vision is still recovering,
though everyday I think it is getting better and better. Or I am just getting used to it.
My
recovery – of my eyes especially – is going to be long. I need to be patient and I need to focus on
getting myself physically healthy – which will help my condition overall as
well as my vision.
So
there you have it – there is my “status update” for you. Feel free to “follow up” with me in person if
you want to discuss it any further. Otherwise,
I will continue to post something daily and eventually we’ll all be at the same
place in time.
In
the meantime, thanks for reading and be sure to keep reading. I will try and keep things light and airy and
funny.
And look for a new site design coming soon! Yay improvements!





1. One of my many English pet peeves is people who don't know what quotation marks are for. Quick rule of thumb: Say the sentence out loud and use the hand gesture in place of quotes. Then ask yourself, Do I look or sound like an idiot?
2. "I return to work after being gone for 10 weeks. I have 25000 emails." 10 weeks. 50 days. 500 emails a day. No comment.
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I'm amazed by the human body and your experience has blown my mind. My curious mind wants to know...did the shunt make you have to pee more frequently for a period of time?
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Megan - I have never been pregnant but I imagine I pee more than pregnant lady because of the shunt. Couple that with drinking and lately I spend more time in bar bathrooms than I would like to admit.
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