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Megan at the Movies: Why I'm Choosing Films in 2024
Wednesday, November 29, 2023
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I Watched the Full Moon Rise and Set Through My Hospital Window
Tuesday, October 3, 2023
I haven't written on this blog since February 2023. It is now October 2023 and I think it's the right time to make a post. Please beware, this story of my current health is a longer one...
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In the beginning of September of this year, I was in a constant state of being overwhelmed. I had started a new job that summer and my classes for school were going to be all in-person for the first time in a year. I also had my podcast that I do all by myself and past guests were asking when their episode was going to be released because I have taken so long to edit. My mental state went in the gutter for a bit but after a routine with work and school was in the works, I felt a little lighter.
After coming out of a time of short lived darkness, I was my happy self again. I drank my coffee each morning, I read a little bit each day, and I constantly laughed (which is my favorite thing to do.)
On Wednesday, September 20th, I had a pain on my lower back. I felt around and there was no bump but the skin was really sore. The next day, a bump did appear. It kept growing and never stopped. It hurt so bad where I couldn't sit without being in horrible pain. On Saturday, the 23rd, I didn't feel great. I was constantly hot when my family was covered in blankets. I didn't sleep well because of my stupid bump.
Then the next day, my parents left for Las Vegas for vacation. I went to Target that Sunday morning to pick up milk and some cute Halloween decor. I kept saying "it's because I didn't have my coffee yet" as an excuse to why I was feeling off that morning. That evening, I was carving pumpkins by myself and my body almost collapsed onto the floor because I was suddenly in so much pain. I laid down on the couch and the pain never subsided. I just KNEW my bump had something to do with it. I texted my mom "I'm going to the immediate care" and as I was sitting in the random doctor's office alone, I was whimpering like a child. The pain was everywhere: my head, my back, my stomach. I apparently had a temp of 99.5 (which I don't believe) and no one asked how I was feeling despite me not being able to hold myself up.
By that point, it was definitely too late.
I felt positive leaving with my packed wound but when I got home, I was dizzy immediately. The time after that went too slow and too fast at once. I was too sick the next day to pick up my newly prescribed antibiotics, so my friend picked them up for me. She brought me a coffee, too, and I almost threw up just looking at it. I hadn't eaten since the morning before and when my friend left, I started convulsing with pain on my downstairs couch. I was shivering but my face kept getting hotter. I yelled out loud a lot (which is maybe a good think my parents weren't there to hear me...) and I couldn't stand. I couldn't walk. I had a searing pain in my gallbladder area.
All in all, I wanted to just respectfully pass away at that point.
It was 2 am when I got wheeled into a room in the Kid's Ward (which I found out had 26 full rooms and only 2 were kids...) and my IV's started. I was delirious from my whole body hurting constantly and the nurse on that floor kept saying "we're admitting you because we're just waiting for your new bloodwork to come back." And that's all they said the first night to me.
I had developed a blood infection, sepsis. It was part of the Staph family. I was given a specific care team full of infectious disease doctors and wound care specialists. The primary doctor I was given told me that my second set of bloodwork also grew a culture but honestly, I was okay, which she stated a lot; It wasn't anything too bad. Even through all that pain, I first believed her that it wasn't anything to worry about.
Then the infectious disease doctor, who couldn't look me in the eye, came in by himself and said "this is really serious."
In the 4 long days of my hospital stay, there were too many people surrounding me. But I was completely and mentally alone. I had 1 friend who wanted to visit but my hair was matted and I wasn't given the all clear to shower. I felt disgusting but with all my insulin shots, my blood clot shots, my antibiotic IVs, and meds galore, I don't think I wanted anyone seeing me like that, even one of my best friends. The days were long and filled with short naps and quick texting. I didn't read my Kindle nor did I watch TV. I was just there, trying to survive a bit.
I was released on Friday, September 29th. I finished a mini packet of goldfish at home (that took me 2 hours to eat, but it was progress!) and as my parents were still on vacation, I still had a this strange gnawing feeling of loneliness that kept creeping up.
Aftercare started that night at 5:30 pm.
I'm 30 years old. This isn't supposed to happen at my age. I never expected a pain like this to happen to me where I wasn't under anesthetics.
I'm currently writing this on my living room couch, where I now reside for the next 2 weeks. I had 1 quick visitor over the weekend and I was over the moon. I have had 2 dinners delivered to my house from my Church family and now that my parents are home, it helps a lot. I love getting "hey how are you" texts from anyone who cares to reach out. My appetite is back but not fully. I like to have little snacks instead of meals. I love cards and now I have 3 "get well cards!"
I am not one to ever relax, but I am trying my best for the first time in my life. I am getting better every day but every hour isn't perfect.
To those who read this post, I'M SORRY IT WAS SO LONG! I even kept out so much and I'm like "wow Megan, calm down."
Too Many Things, So Little Quiet
Tuesday, February 28, 2023
Last night everything came to a head. It wasn't a manic episode or what I call my "breakdowns," it just felt different. There was just so much noise around me and so many people. I couldn't seem to ever be alone and I couldn't rest or relax. I am also very irritable with people recently. I seem to get angry easier and I'm so confused because that's not me. I went to a concert the other night where I was pretty much standing in front row. With the amount of people pushing me and having no space to breathe, I was so afraid I was going to have a panic attack. But I didn't. I just wanted to scream out of anger with these drunk people around me and that's not me.
I looked it up last night why I was going downhill.
I've heard of that phrase before but I always thought it was for people with autism. But ADHD people can suffer from it, too, and I was shocked. It's pretty much sensory overload, when too many things happen at once. I didn't fit some things on the list but I did see myself with some of the checklist.
I want to share some below from my list. Maybe it'll spark some connection between us or maybe it'll show you something new to add to your life!
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1) Smells. Many people with hypersensitivity can't stand strong smells. I, on the other hand, must have smells for some reason. I love candles in general but I have been burning them like crazy now. I think there's a connection of calmness and soothing candles for me. I have to light one when I do school from home and when I go to bed. There's a candle I lit in the living room right now and I'm the only one in the house right now. It's just something I have attached myself to.
2) Leaving the house. I have a rule that after 3 days at home, I have to go somewhere. Whether it be a Starbucks or a library, I have to get out. But with my classes being remote this semester, I stay in my house and I go to work. That's pretty much it. I realized that I've not followed my 3 day rule and it's definitely taking a toll on all of this. I need to start going out during the day when I can, even if it's just getting lunch by myself or sitting by my favorite town dam.
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I have more things I wrote down but I don't want to ramble on here. Reschedule plans that don't fit in your life right now, avoid big crowds when you can, and catch your irritability before it turns into full anger.