The last several weeks have been difficult for this writer with MS. It’s normal to run into obstacles while trying to write, but sometimes those obstacles create other more serious obstacles that you may not realize are even there for a while. In my case, I didn’t realize what was happening until I finally did something about the first obstacle.
I mentioned the little 3 day vacation that my wife and I took last month to Glenwood Springs and Aspen, Colorado. That last posting was written on my laptop. It was the last thing accomplished onsaid laptop. My battery ran out of juice and because the charger had died, I couldn’t even charge it. The laptop became a symbol of failure. Every time I looked at it, I wanted to write but knew that I could not. I began to get depressed without realizing that I was. I get some off my inspiration while sitting on my porch and watching people and vehicles pass by. A thought will spring up in my head and I will want to write about it. My first thought is to get my laptop and sit here and write my inspiration. Then, I’d remember, I can’t. Depression was setting in.
I do have a desktop PC (no, I prefer a PC over Mac) and I would come inside to use it. But the depression would come inside with me and all I could think about was how my laptop needed a charger. I spent a lot of time over the next two weeks looking at AC adapters both online and at any store. What I found online was several sites that offered replacements from $5 to $15. However shipping charges were $25 to $30. I could buy one locally for that much, but I couldn;t bring myself to pay that much. There just had to be a better deal.
I didn’t realize it but I was getting caught in this cycle of depression. It must have snuck in during one of the days that I was having trouble with MS. Then a week ago I had an epiphany. Just order it online and get it over with. I looked on a site I had not yet gone to and found one for under $20 with free shipping. I bought it and waited. It arrived on the third day and I was happy.
Suddenly, I felt my spirites lift and I started remembering things I had wanted to tell y’all. Yes I typed y’all. I’m from the south and proud of it.
So, today I felt like writing you guys. I am partly stoked because of the movies I have seen recently. I’ve seen some good movies and I am going to give my thumbs up to these; Hope springs, The Odd Life of Timothy Green, and the most recent one, The Words.
All were very good movies and each may deserve an Oscar nomination for one reason or another. The one that influenced me the most, though, was The Words. It is about a man struggling to become a successful writer. He meets with all the rejection and disappointment we all deal with and even though he chooses to do the wrong thing, somehow I felt the pain he was dealing with.
So, if you are looking for a good movie to go to, I suggest to you any one of these. The stories are great and all actors performed admirably. If you are a writer, like myself, I urge you to go see The Words.
I had planned on today being a day of productive writing, but I am having one of my dizzy dazey MS days it would appear. One of the things I had planned to do today is write this blog. However, my brain doesn’t want me to think today. Still, I am writing. I am hoping this effort will bring me out of this funk and I will be able to make some serious contributions to my upcoming novel. I don’t have a title for it just yet or I would tell you.
This is my biggest malefactor in my being able to write; fighting through the MS. Some days I might as well be a jellyfish. I am not sure what that means but I was hoping that my brain would find a better way of saying that I am having a bad day creatively. I guess, after writing that analogy, this is one of those days. Still I push myself to write.
Hey! Have you heard about the noun, the verb and the adjective that walked into a bar? I haven’t either, and can’t concentrate enough on it to make it a real joke. If any of you would like to take that much and run with it, though, be my guest. Share it with the rest of us. We could always use a good laff.
So, school will be starting up before we know it. I know it because I am married to the world’s greatest teacher. This is her final year to teach. Then she retires and will have to learn to live a life without so much stress. I am proud of her and very happy for her as well. So, in honor of that, I want to share this poem with y’all.
I found it on laughalotpoetry.com. It appears to have been written by Darren Sardelli. I hope you like it, too.
My Dog Ate My Essay
My doggy ate my essay,
he picked up all my mail.
He cleaned my dirty closet
and dusted with his tail.
He straightened out my posters
and swept my wooden floor.
My parents almost fainted when
he fixed my bedroom door.
I did not try to stop him.
He made my windows shine.
My room looked like a palace.
My jackets smelled like pine.
He fluffed up every pillow.
He folded all my clothes.
He even cleaned my fish tank with
a toothbrush and a hose.
I thought it was amazing
to see him use a broom.
I’m glad he ate my essay
on “How to Clean My Room”.
Copyright © 2005 Darren Sardelli
All Rights Reserved
Good afternoon to you all. Today is Tuesday, November 22, 2011, two more days until Thanksgiving day. I guess the normal question this time of year is what am I thankful for? I am thankful for a lot of things, but most important is that I am thankful to Jesus Christ, who is my Lord and Saviour. Because of what He did I am forgiven for my sin and will one day live in His Kingdom. All pain, fear and heartache will be gone forever and love, joy and happiness will prevail. As I observe the direction of the world it has become so apparent to me that we are indeed living in the last days. Either it will all end or we will kill each other off. We are so stupid.
So, I am thankful that my family is blessed with God’s grace and will one day be there where He is. I hope you are all equally blessed. May each of you have a wonderful holiday.
I sit here in my living room, lights off and just staring at the walls. I hear traffic go by every now and then but I keep my blinds closed, so I can’t see what is going on outside. I am sure that it is just everyday stuff; people going to and from the lake or just passing through to get to the other side of town. All in all this is a nice quiet neighborhood. I like sitting here without the distractions that can interfere with my train of thought. I like being alone with my thoughts. Our dogs like it too. No TV blaring, the only sound I hear is of the dogs playing and my space heater that warms my feet.
I think about family and my writing. My wife is my hero. If not for her, I would be dead already. For some strange reason she loves me and I feel it every day. I love her with my entire soul. Just yesterday, I was experiencing some of the effects of MS. I was nearly a zombie, but new enough that I needed to clean the kitchen and get to cooking dinner. I was very slow, though in my mind I couldn’t tell it. I could only concentrate on one thing at a time. By that I mean, washing one dish at a time not recognizing the many dishes that were in the sink. Each dish was an adventure in itself. I was weak, physically and mentally. If not for the cabinet to lean on I would have fallen. My wife, having just come home from her day at work, recognized my condition very quickly and came and made me sit down while she did it all. A few hours later I began to feel better. Today there are some residual effects but at least I am able to cope.
I think about calling my mom but then I am reminded that Thursday is Thanksgiving and I should wait and do it then. There may be other family members at my mom’s house then and I can talk with them too. So, I’ll wait.
Looking at the blinds of my front window I can see the pattern of sunlight highlighting a portion of the blinds and that tells me that the sun is out and is a beautiful day here. The weather people say it is going to be nice for Thanksgiving. I hope you all have a wonderful day and enjoy the presence of family. God Bless you all.
It’s early this Saturday morning. Our puppy, Jiggy, always wakes me to let me know he needs to go out so that he can potty. So, I get up and let him and his best friend Esther, our other dog, go out to do their business. I usually let them stay out a bit to give them time to “git er done” and to play outside. While they do that I normally go back to bed for more sleep.
Today, Jiggy woke me earlier than normal for the same reasons and I did my usual deed. They, though, started barking their fool heads off. Concerned that the neighbors would like to sleep in this morning, I crawled back out of bed to let them back in the house. I didn’t feed them yet but I did give them a dog biscuit and put them back in their kennels.
It was nice for a while, maybe 5 minutes and then Jiggy let me know that he wasn’t happy in the kennel this morning and would not let me or my wife sleep until I let him out of the kennel to play with Esther.
While I lay there I started thinking on how my life has changed since MS has reared it’s ugly head. I know that I am a little harder to live with now. God bless my wife because she is the one who is catching my mood swings and all the other things that make me think I am an asshole. Well, I do feel that way. A positive outlook is what has always made me a nice guy, but here lately it would seem that positivity only comes by every so often.
Stress, at any level is something that will take me over the edge quickly. By that I mean, the need to make a decision on something as simple as whether or not to wear a blue t-shirt or a grey one today. Throw in a third option and I feel like my brain has left me in the middle of a raging sea without even a life vest to keep me afloat. I get so confused as to which way to swim or how to swim that I feel panicked and I can’t do anything. I can feel the stress growing inside of me and sometimes I feel like I am having trouble breathing. Mostly it feels like my brain is trying to figure things out but that feels like it has been sealed up like a mummy and can’t move. It’s like their is no room for my brain to open its file drawers, much less actually retrieve a file and lay it out on a table to see what is there. There is no room for anything. I can’t even get to my files! I am a computer whose hard drive has reached capacity and can’t do anything.
They say that MS is an unpredictable disease and it affects everyone differently. Oh, there’s also not a cure. For me, it seems that strangling my brain is going to be my lot. There is medication that will help slow the process of the disease, but I can’t afford it and my insurance won’t cover it. Thank God that I have excellent health insurance. Imagine where I would be if I couldn’t pay ungodly amounts of money to my insurance company every month. Wow! I would probably buy that medicine and maybe live a normal life! But this is America and that ain’t the way it works.
In America nothing works. It’s like an air conditioner on a hot day that has a short in the circuitry and it only comes on for a minute and then shuts off for a few more hot and muggy days. Well, why don’t I fix it? It’s because I don’t have the money to pay for a repair man and I don’t know anything about electronics.
The United States Congress is like that. This country is broken and no body wants to fix it. Instead of fixing it like a responsible human would, our Congress is more concerned with how they are going to line their pockets. It doesn’t matter which side of the aisle they sit on. It’s all the same country and it is in dire need of being fixed. But these people, our Congressmen aren’t concerned with the good of the country. They are more loyal to lobbyists than they are to the citizens of this country. They are going to carry on this childish bickering until its too late and this becomes a world wide crisis. Just make a decision. Isn’t that what we hired them to do? The U.S. Congress is impotent.
So, I’m caught up in this boat with all of you. I feel most of the time like I am a little drunk and it’s not because of alcohol. It’s because of the MS. I need to fix it but can’t. I need to get the medicine that will slow it’s progression, but I can’t. Did I mention that my wife is also having to suffer through my impotence because of MS? I really have the best wife in all the world. I feel like I can’t make a decision on what to do. I feel like a U.S. Congressman.