So I've had the idea for a while to start blogging. For some reason
when I go to start there is something keeping me from doing it. Maybe
it's the expectation that once I start, I can't stop. Too much pressure.
Maybe I don't want to take the time to do it? I'm not sure. But here I
finally go.
I called this blog my falls and my walls
because I fall. Unfortunately it is a big part of this disease but I
learn so much from those falls. It allows me to see the best in people,
even strangers, as they show me of their kindness. The walls part is
everything that happens in my house that shows me that I have a full and
blessed life.
The purpose for this blog is for
my kids. Hopefully none of them have to live with the struggles that I
do, but the possibility is there. Hopefully, I will be around to tell
them how I dealt with different struggles, but the possibility is there
that I won't. So this is for them. I decided to do it in blog form in
case anyone else is interested in my story. I love, and receive
strength, from reading other people's blogs, especially when they are
enduring trials with strength. So for any of those many people, that I
love, that ever ask me how I'm doing, this is also for you. I will try
as best as I can to be as honest as I can with my feelings. This is not
to draw any sympathy but so that this really may be a help to anyone
else reading this.
Because I've been putting this off
so long, I have a lot of story to catch up on. This post may be
painfully long. Sorry. Maybe I'll split it into two. The fear with that
is that I'll never blog again and only half of my story will be told! It
will be like the recipe book that my mom gave me when I was married.
Most of the recipes are useless. There are ingredients listed but
nothing else. Do you mix them all together? Do you layer them? Do you
cook it? How hot? The name of the dish sounds delicious but that's about
all you get! Anyway, I need to get on with it!
Starting at the beginning:
Growing
up I was aware that something was different with my mom. The first
memory that I have of my mom having Muscular Dystrophy is when I was in
grade four. All of a sudden she was wearing braces on her legs. The only
thing going through my mind at the time was that my Grandpa Steed had
Muscular Dystrophy and that he was always sick. I had no memory of my
Grandpa as a healthy person. This made me extremely fearful for my mom. I
remember crying and telling her that I didn't want her to die. I didn't
want her to be sick like Grandpa. As time passed she slowly got worse,
and I continued to worry, but it became a part of life. There would be
times where something would happen physically to highlight the fact that
her health was deteriorating, and it would bring up those feelings of
fear, but they would pass and life would continue.
I
remember asking my mom how she knew that she had MD? She would say that
when she went to exercise class they would walk on their heels around
the gym and all of the sudden she wasn't able to do it. She couldn't
keep her toes lifted off the ground. She had drop foot. From there I
guess she just knew. My mom is an incredible lady. She endured so much
more than I would ever want to see anyone endure. Some would say my mom
WAS an incredible lady, but even though she has passed away, I know that
she still lives and watches over me. There is so much story that I
could tell of her, and one day I hope to. I do think it's important to
document the past, even though I am terrible at it, but the story that I
am telling here is my story. Undoubtedly her story will intertwine with
mine because she was and is such a huge part of my life. Because I knew
how she first suspected that she had MD I grew up always trying to walk
on my heels, and when I could do it there was a sense of relief.
Time
went on and life was good. I had moved away from home to go to dental
hygiene school in Edmonton. I met Brad and we were married and after a
while we were pregnant. I didn't have a terrible pregnancy but by the
end I was definitely feeling tired, weak, and heavy. But aren't all of
those feelings normal at the end of pregnancy? I'm pretty sure they are.
Olivia was born and the battle of the bulge began. Let me just say that
this was a battle that I'd fought all my life, but I knew I needed to
get the baby weight off. So we bought an exercise bike and I started to
pedal. As I continued working out and losing a bit of the weight, I
noticed that the pedaling wasn't really getting all that much easier. We
lived in a two story starter house with laundry in the basement. The
two flights of stairs that I had to climb to take the laundry upstairs
were also not getting easier. As I would sit on the floor of our living
room changing a diaper or playing with Olivia, getting up was not as
easy as I thought it should be. Fear crept in to the back of my mind. I
would repeatedly try to get up off the floor wondering if it was in my
head. Could I do it without using my hands pushing on my legs? I knew
what my mom had lived with for as long as I remembered and what had
ultimately taken my grandpa's life. I remember standing in my kitchen
and battling in my mind whether or not I should try walking on my heels.
It may sound dumb to place so much emphasis on such a simple task but
it represented the journey that my mom had to take. I hadn't told Brad
anything yet. He's a bit of a worrier and there seemed no point in
making him worry if it was all in my head. So in my kitchen, in our
first house in Leduc, I attempted to walk on my heels. That is where my
journey with this disease began.
You are such an example of patience and faith. Chelsie you are just simply, beautiful.
ReplyDeleteHi, I am your Mom's cousin, on the Hinman side. I would love to follow your blog, but I can't see how.
ReplyDeleteI love that you are blogging!! I love you! You are the best!
ReplyDelete