Wednesday, October 28, 2015

It is 10:53am. I am sitting at the kitchen table. I know I haven’t updated the blog in a while. To put things mildly, this has been a rough couple weeks for me.

While I was going through my cancer treatment, the doctors would always bring in prior cancer patients that they had worked with who all went through and survived the treatment that I was going through. They were there to give hope, provide insight, and answer any questions that I had. I remember speaking to this one gentleman in particular, and he told me that the hardest part of this process was when the treatment was over. He told me for him it was a nightmare. He told me that he was finished with his treatment, he was supposed to be getting better, but he just was not getting better. I thought to myself, “That was really the hardest part?” I am not sure why I doubted that man, because boy he was right.

After the conclusion of my treatment I just sat around and didn’t do anything. I couldn’t do anything even if I wanted to. I could not eat, drink, or talk. As I mentioned earlier, the phlegm in my mouth was unbelievably unbearable. I was constantly drooling and constantly spitting up mucus. I was using 2-3 rolls of paper towels per day to wipe my drool and to spit into. Just think about how many squares are in each roll of paper towels. To go through 2-3 a day was ridiculous. I was literally wiping drool and spitting every 10 seconds for 24 hours a day. And when I say 24 hours, I mean 24 hours. I could not sleep. For one I have this feeding tube in my stomach, which prevents me from sleeping on my stomach. I couldn’t sleep on my back because I would choke on the phlegm that built up in my mouth. So the only thing I could do was try to sleep on my side. So picture me on my side every night literally drooling and spitting into a paper towels while simultaneously trying to sleep. It is horrible. I also found out the hard way that lying on your side for long periods of time really hurts your hips. I mean it really makes them sore. What I did to try to prevent this pain was roll up one of those soft blankets and wrap it around my hips to help ease the pain. It did not work.

Prior to the other day, I left the house like 3 times in the last 3 weeks… all for doctor’s appointments. I was really, really depressed. I am a naturally depressed person anyway since I am prescribed to the depressive realism school of thought (hi Melissa), but the totality of my situation just made things worse. I understood that this was going to be a process. I understood that it was going to take lots of time to get better. That doesn’t mean I had to be happy, or positive, or jovial while going through it. Going through it flat out sucked. There were days upon days where I just sat in the kitchen with my head on the table with my bucket on the floor so I can spit and drool in it. In the middle of the night I would just quit trying to sleep and go sit on the toilet for hours with a spit cup and a roll of paper towels. Minutes felt like hours, hours felt, like, days, etc. etc. Horrible.

Social media and support from others was getting annoying. Let me preface what I am about to say by stating that I truly appreciate everyone who sent me a message or has a genuine concern for me. I really do. I love every one of you who reached out to me. With that being said, I cannot tell you how annoying it is to read and answer the exact same message over and over literally hundreds of times. I can’t tell you how many times I got the message…

“Hey Kyle, just checking in on you. How is the treatment going? It is over right? You getting any better? How are you feeling? I love you, get back to me soon.”

Like I said, I really, really appreciate that message and that concern. I know it is because you care. But when I am feeling like shit, I don’t want to be reminded that I feel like shit, and I don’t want to have to respond by stating that I am feeling like shit. I was tired of talking about cancer. I didn’t want to talk at all. So if you sent me that message and I did not respond… don’t take it personal. I just read it sooooo many times and I was just tired of it.

So after a week of treatment, I had gotten no better. Two weeks after treatment, same thing. Three weeks after treatment, still no significant improvement. If I coughed up enough phlegm, made myself spit, and wiped away some drool… there was a two second window where I could take a very small sip (not even half of a gulp) of water. After the water went down, it would burn my throat and my ears very bad. That was my level of improvement after three weeks. I saw Dr. Nakajima last week and he told me that I am going to turn a corner, and start to come around. When I asked him when, he responded by saying… “Soon.” Let me just say I hate the word soon. If you are coming to my house, tell me what time you are going to be there. Don’t say “soon.” If I am meeting someone somewhere, going to eat, or doing anything else, I need to specifically know when. The word “soon” might as well mean “anytime” or “I don’t know.” I took it for what it was though.

This past weekend I told myself that it was time to kick my depression and try to be more optimistic. Maecee came over and hung out with me. Abby took me for a drive in the country. Even before I was sick we always went for drives in the country. We would drive around for hours… looking at the scenery, old houses, and just enjoy being outside. And the whole time we would be in the car we wouldn’t say a word to each other. I guess it didn’t matter that I could not talk this time.
I noticed this weekend that the phlegm in my mouth started to thin, and it wasn’t as much as before. I could take sips of water for longer periods of time (Like for two seconds instead of one). I was sloooooooowly improving. Even though it hurt I tried to talk, and you can almost understand what I was saying. I was finally turning the corner.

Monday and Tuesday, the phlegm was less and less. It was like there was no improvement for three weeks straight… then all of a sudden for three days straight I saw significant improvements. Same thing goes for my speaking. I could actually be understood (even though I sound crazy), and could have a short conversation. Same goes with the drinking. After a small prep, I could take like three to four gulps of water.

So that is it. I feel like I am turning a corner. Finally! I have a whole bunch of baby food that I bought that I am going to try to start eating on Thursday. Believe me, even though I cannot taste it, I am TIRED of Jevity. I am tired of smelling it. While I appreciate it for keeping me alive, it is time to move on from it! I feel like this is it. I feel like I am close to making some real progress towards normalcy. Once I start eating and have the ability to maintain my weight by mouth, I can have this feeding tube taken out of my stomach. Once I get this tube out I can get some sleep and get back in the gym. If you really knew me before this, you know how important the gym is to me. I wasn’t like a bodybuilder or anything, but I really love going to the gym. It gets my mind right and keeps my body right. I went to the gym 5 days a week every week. It is just something that I loved to do. I cannot wait to get back to that! I cannot wait to build my body back up, and to compete in sports that I love again.

Anyway… that is all for now. If you made it up to this point, thank you. I will update you on my progress soon.

Love,


Kyle

2 comments:

  1. It's really hard for people to understand the process when someone is profoundly unwell, how to interact, how to ask for updates. Express compassion, because unless you've been through this, you can never empathize.

    I always knew silence meant deep effort to keep pushing forward, albeit excruciating and slowly.

    I certainly am grateful for your update. It's great to hear your perspective and candid update. It takes great talent to inspire others during your darkest moments, a skill you possess in abundance.

    Much love and sending fortitude.

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