I have been told numerous times how good I look. I walk without my cane; for the most part, so
I must be much better. My speech has
improved so I must be awesome! Somebody
asked me yesterday how I am and wanted the truth and not the generic “I’m
fine”. She then told me I should share
to show where God has brought me to and where He continues to take me.
1 Peter 2:24 (NIV)
“He
himself bore our sins” in his body on the cross, so that we might die
to sins and live for righteousness; “by his wounds you have been healed.”
Day to day
life after surgery is different for everybody and even if you have an identical
surgery things can be very different.
Here is my day to day life after having a craniotomy for cavernous
malformations:
~ Nausea – I have medications for this,
but there are some days it is horrible.
I am unsure if this has improved because the medication helps so much.
~ Ice pick headaches – off and on I get these headaches that feel like you have
stabbed me in the head with an ice pick and a few seconds later pull it back
out. These headaches are extremely
painful, but thankfully only last a short time.
~ Pressure headaches – these are different than the ice pick; with these it
feels as if something is pressing against my head for an unlimited amount of
time and not as severe as the ice pick. These
headaches can last for a couple of hours or an entire day.
~ Numbness – wow – this one is entertaining.
Around the surgery site it is still numb, but I’m getting some
feeling. At the edges of the numbness it
is very painful. The numb places will
itch, but I can’t feel to scratch, so it drives me crazy.
~ Left side insanity – my left side hurts, is numb, shoots pain, feels weak, and
is sensitive to the wind against my skin, and on and on. This
is the side that had been paralyzed briefly after the surgery.
~ Lump on back of head – it is not a literal lump, but that’s what it feels
like. I feel like I have something huge
attached to the back of my head at the incision site. It bothers me to lean my head against
anything or to lie down at night.
~ Stiffness in arm and leg – My left arm and leg will become completely rigid,
usually in my sleep. The muscles are so
tight that it hurts to the point the pain wakes me up. Sometimes I wake Mike up if I hit him
depending on how I’m laying. I find this
much funnier than he does. Also,
sometimes when I yawn or stretch it will make my arm and leg rigid.
~ Apraxia – this is newly diagnosed – Apraxia is the inability
to execute learned purposeful movements, despite
having the desire and the physical capacity to perform the movements. An example would be: I want to reach out for something, but I can’t
just do that. I have to almost tell my
body step by step – move shoulder, straighten elbow, open hand, etc.
~ Exhaustion – I started to write tired, but that’s not the correct word. They told me in the hospital that I would be
tired and need extra sleep and they were right.
Simple things like taking a shower are exhausting to me and I almost
need a nap from that. Even something
like sitting in church is tiring and requires a nap.
~ Pain in head when laying down – when I lay the back of my head against
anything it hurts. I have to take pain
medicine to sleep at night.
~ Forgetful – Mike added this one. If
I’m forgetful I don’t remember it!!
~ Freakish sound sensitivity – in my right ear my hearing for high pitched
sounds is insane. I heard a sound in
Alabama that people kept saying I could not hear; but it was hurting my
head. Mike could hear it and then somebody
else that had a stroke heard it and asked what that horrible sound is. Maybe the strokes affected our hearing, but
it made me feel better because I know what I heard and now somebody else did
too.
~ Speech / tongue – my tongue is very weak and that is why my speech is messed
up. The right side of my tongue cannot
hold the correct placement for my words to be correct.
~ Balance – My balance is still off and I still have some problems with
dizziness. I do not use my cane all the
time, but I do take my rollator if I know there is a lot of walking. I stumble
now even when standing still.
~ Confusion – when I am in a group with lots of different conversations or background
noise I have a hard time concentrating.
I cannot play computer games and talk on the phone like I use to
either. Anything that requires me to
focus on more than one thing is very difficult.
I will usually stop talking in these situations and just pretend to pay
attention.
~ Weakness in left wrist and ankle – I sleep in a brace that supports my hand
and goes to my elbow and wear a foot brace that supports my foot and goes to
almost my knee. When I take these braces
off I feel very weak. My wrist hurts to
push a buggy (cart) around the store or to lean on it. It is painful to get up and walk without the
brace, but I have been told to not wear it all the time.
~ Missing things – I really hate this the most.
I miss things all the time and it makes me feel so unreliable. I have had to miss things Mike and I really
wanted to do because of any of the above things or a combination of things.
People have
pressured me since 2009 when I was first diagnosed to have surgery. I have said repeatedly the best thing to do
is watch and wait because we don’t know what side effects surgery could cause.
I am very blessed that things are as good as they are for me.
1
Thessalonians 5:16-18 (NLT)
Always be joyful. Never stop praying. Be thankful in all circumstances,
for this is God's will for you who belong to Christ Jesus.
Since I
decided to write this several people have asked me to. I am not whining when I write this or asking
for pity. Our bodies are amazing and the
way we heal is awesome!! God has been
with me through every step of this journey and placed some wonderful people to
help me. Even when I get upset and have
small pity parties I know that God is with me and I start to praise Him again!!
.jpg)
.jpg)