Halloween Holiday Spirit
Call it tradition. Call it writer’s block. Call it laziness, boredom or the result of today’s brain fog. But here is one of my most popular blogs, just in time for Halloween!
Get ready for your own horror movie marathon and I would love it if you answer the question at the end.
Happy Halloween my friends!
It is the afternoon and I am shuffling around my house, trying to focus. I have my lists; all the MS helpful tip books suggest lists.
There’s the to-do-this-week list.
There’s the to-do-before-Christmas list and the things-I-should-try-to-do-in-general list.
There is, of course, the things-I-should-try-not-to-forget list.
But the lists and lists were not helping me focus. Oh, I know, the dishes need to be done. I will feel better when I have finished that.
So I start with the dishes and realize I might have more motivation if I had music going. I dry my hands and head to the stereo.
But then I see my computer and try to remember if I responded to that important email I received this morning. Yes, I see now that I did but there are some more emails to read. I get overwhelmed with the amount of junk emails and chain emails coursing through my web account and give up, deciding to play FreeCell instead.
What is up with us MS’er’s and FreeCell? Every MS’er I know is addicted to FreeCell.
My meds are giving me an awful taste in my mouth so I get up to brush my teeth and drink some water. I see that I barely started the dishes and dunk my hands in the soapy dishpan yet again. And three plates and five minutes later the 8ozs of H2O has gone right through me and I am off to the bathroom.
How on earth am I supposed to drink eight more glasses today? I might as well move into my bathroom.
The fog in my brain continues. The only thing I can focus on is my lack of ability to focus. I am forever existing in this fog-like state.
Perhaps because Halloween has just passed I think of the movie The Fog. Figures. Leave it to me to equate my multiple sclerosis to a horror movie.
But is The Fog the right horror movie? I am wandering around lost in my own little world and not feeling quite right- almost zombie like.
Yes, zombies, zombies are a good description. I am an MS zombie for sure. I will likely stay like this until I fall asleep where I will be alive but dead to the world for at least ten hours. Then it hits- it is not The Fog but Night of the Living Dead.
Somehow thinking of my MS in terms of horror movies brings me comfort as I try to remember what it is I was supposed to be doing. Night of the Living Dead, that is definitely the horror movie for sure.
Or is it? Sometimes I just want to scream. Actually, I just want to scream a lot. Maybe my MS really is Scream? I have always been a Neve Cambell fan. But does the movie Scream completely reflect all that my MS is to me?
It likely depends on what my MS is doing on any given day. Often, it makes me think I am going crazy. I think of the classic line in Psycho, “she just goes a little mad sometimes. We all go a little mad sometimes.”
I remember all the hysterical mood swings and weird symptoms I experienced before I knew I had the disease. I remember hundreds of times of being convinced I was getting the flu due to the insane body aches, only to have them disappear, believing myself to be a hypochondriac. I remember the all the people in the world around me being totally off kilter but acting as though I was the one who was screwed up. Like when I had to go to my drycleaner’s several times in one week insisting that they had given me the wrong pants.
“Yes, they fit. Yes, they are the same color. Yes, they have the same fashion label and size label. But these pants have cuffs at the bottom hems. My pants don’t have cuffs. Yes, of course I would know if they were my pants or not. I will keep them as I need black work pants but one day soon someone is going to come in and say they have the wrong pants and I am telling you, I have theirs and they have mine. Feel free to call me when that happens and I will exchange them.”
My drycleaner and I had this little diatribe over and over. Funny how the other customer never realized she had the wrong pants. Yes, Psycho is the movie. That is the one that most describes my MS.
And it is appropriate and personal as when I was a teenager I had actually waited on Anthony Perkins at a candy store only ten days after seeing Psycho for the first time. My friend Heather worked at the store too and she was too freaked out to wait on him so it was left up to me. I gave him a whole extra ½ lb of penuche fudge so he wouldn’t bring out his knife and start swinging.
Yes, Psycho feels right.
Bathroom again, but first I stop to remove the pebble in my sock. But there is no pebble. What is that annoying feeling?
And that one, the sudden sharp, jab in my left arm?
And that one, the squeezing and releasing of my abdomen as if my stomach were in a vise?
And here are those weird ear noises again- has my body been taken over by aliens? That’s it, Invasion of the Body Snatchers. That is definitely the horror movie that best describes my MS! It all makes sense now- aliens have taken over and turned me into a screaming, psychotic zombie living in a deep fog.
Finally, having this serious question answered and finishing up likely my tenth trip to the bathroom, I try again to remember what I was supposed to be doing. Oh right, the dishes.
I shuffle back and plunge my hands into the now cold water. As I do so I feel awkward and completely out of sorts. I am tired and clumsy and blinking from the glare of the setting sun.
Funny how images of The Creature from the Black Lagoon begin to cloud my foggy, psychotic brain.
If your MS was a horror movie which horror movie would it be???????
Completely engulfed by The Blob!
Great one Susan- I can see/feel that!
TV show “Criminal Minds” episode “God Complex” where the bad doctor cuts off people’s lower legs and then attaches the lower leg of another person.
Eeeeewww- never seen that one but it does seem fitting doesn’t it?
I don’t have MS but I do have to do list which seem to take forever getting crossed off. Sometimes I feel like Carrie just trying to do my best to fit into the world doing everything the way your supposed to but always getting dumped on, other times I feel like the guy from Christine when I seem to have no control over what is going on. I get so overwhelmed and exhausted I usually look like a zombie from night of the living dead.
Great suggestions friend! And since you are the horror movie junkie I consider your opinion as expert!
“Abby something.”
“Abby who?”
“Abby…Normal.”
That’s me- Abby Normal brain.
That’s a great one Joe/Abby- thank you!
I was told to get out of the place I was living. My landlord had had a breakdown when she told me that. Her and her daughter kept stealing things of mine and from stores so I was glad to be out of there. Anyway, I moved into my new place and could swear I have the wrong black sweater. I insisted mine was more of a bolero type as I suffer from heat exhaustion and don’t want a big heavy one. Not that this one is. I’m still confused by this sweater and kept saying my old landlord took mine and gave me hers which would be impossible for her to wear as she several sizes bigger than me. Her daughter wears only T-shirts and sweatshirts and it’s definitely not her ‘speed’. I’ve been in this apartment since the end of March and I still feel guilty wearing that sweater. I’m baffled by this and never thought to associate it with my primary progressive ms. I do suffer brain fog and extreme exhaustion, so maybe that’s it? Oh and I only drive really local and hate being on the interstates. I stay to the outside lanes when I drive because the middle lane is more stressful. And yes I don’t drive if the ability to is affected. I’m just blessed we have Paratransit buses here in town that pick me up right at my house and they’re quite affordable, so I use that a lot to get around to save my energy for more important things. Here in Naples Florida we have snowbirds from October/November through anywhere from March to May adding to the traffic so the bus is a blessing for trips to the store and my doctors. Sad isn’t it that we have to have doctors and not a doctor? You said it’s expo be disabled and it sure is!!!
Thank you so much for reaching out and sharing Susan- I really appreciate it! Good to know I’m not the only one with the weird clothes issue. I blame the cognitive factor and fatigue that come from MS. I like to make sure the MS best gets all the blame!!! Wishing you a healthy and feel good start to the New Year my friend- my very best to you.