Things On My Mind – 1/26/2018

We’re a few weeks into 2018 and the things I’ve done so far are incredible, but it has come at a price and I don’t know if this level of activity is sustainable.

When 2017 started I thought I was ready to crank things up to the next level. I had things I wanted to do, ideas… I wanted to finally take a shot at stand up comedy, play music at different venues, start writing in a regular and organized manner, look for part-time work, and many other things. I still had a pretty good year, but I had to postpone a lot of those goals when some health setbacks occurred. One year later in 2018, I’ve gotten those issues under control and am armed with more knowledge and tools in my arsenal to take that next step forward. I’m almost where I wanted to be last year.

All the things I listed above, I’ve been doing. I’ve been having a lot of new experiences in new places with new people, and with new peo ple comes new opportunities. I have some exciting plans later in the year that have given me that kick in the ass to get to the gym to try and get my body – a body that still spends many hours a day laying in bed in front of a laptop – in better shape. Every day I get up, head to the post office to ship out my latest eBay sales, work on some wild mild music idea (like trying to figure out which genre of music I’m going to play drums over a medley of next), do some cardio and lift weights, meet with friends, and discuss plans.

It’s really taking a toll on my body. For the last few months, I’ve been able to maintain a Mon-Fri schedule, and sleep through the weekends to rest up. At first, I would start getting pretty tired by Friday… then Thursday became difficult too… and now this week, I was already feeling exhausted on Tuesday. The symptoms of exhaustion have been nearly constant, and as soon as things start wearing off around 9pm-11pm I have a couple of choices: take more meds, or drive home before the dizziness gets worse and interferes with doing so safely. There have been a couple occasions so far this year that it gets to the point where extra meds don’t even help and all I can do is lay in bed. This would be fine if I could just sleep it off, but I can’t sleep well until these meds get out of my system.

I didn’t start this blog to bitch about fatigue, you can find that in plenty of other places on the internet. The exhaustion I’ve been feeling is a positive thing, it’s the result of doing so much. I can live with the daily fatigue and there are ways I can distract myself from it. Staying engaged socially helps a lot – I might be tired but I can remain in a good mood if I’m in the right company. My worry though is that I constantly feel like I’m tiptoeing on the edge, that hour I’m just a decision or two away from rendering myself unable to stand up or drive home.

One thing has remained a constant during the last few years… if I have a symptom that’s really bothering me or I’m not happy with the way I’m feeling, I can figure something out if I set my mind to it.

Next week, I’m going hunting for answers.

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Things On My Mind – 1/20/2018

I’m typing up all the thoughts in my head without rereading the post or editing. Enjoy the ride.


People enjoy hearing storing of overcoming life’s obstacles, so I share them when they happen and I have a pretty good one at the moment.

I don’t think I’ve ever enjoyed feeling shitty as much as I did the past 48 hours. I did a lot this week so last night I hit my limit and started having exhaustion symptoms. When this happens I get dizzy, sweaty, nauseous, and have trouble thinking clearly. Standing up is like tipping over an hour glass and I only get 30 seconds on my feet before I start vomiting. I can usually feel this coming – I basically start feeling milder versions of all these symptoms. I can avoid vomiting by heeding the warning and laying down and staying hydrated.

Last night, an exceptional night of music was coming to an end at Rick’s when I started feeling this coming. There was a problem – I was totally out of food at home and needed to go shopping. I decided to try and get it done anyway because I was going to be either equally tired or worse the next day. I had about 10 minutes left of shopping to do when exhaustion moved into its next stage and for a few minutes I thought I was going to puke in one of the aisles. I tried to speed things up and finish. My cloudy mental state led to a couple of unusual purchases, like a boneless frozen turkey (I didn’t see the chicken breasts I was looking for, and it was close enough). I usually use the self-checkout but I looked for one with a cashier so I could lean on something for a few minutes but none were open. I could tell that I was visibly exhausted, and employee noticed because as I approached the open self-checkout station, she saw me and asked “Would you like me to ring you up on aisle #?” It gave me a minute to lean over and get some temporary relief from the discomfort. I sat in the car for a minute to make sure I could drive home, and I did. After laying in bed for a half hour I put the groceries away the only way I could: by sitting on the floor next to whichever drawers I was putting food into at the time, spending 30 seconds here and there on my feet because that’s all I could do. After another short rest, I realized there were some other things I needed to do so I put together an environment of distractions to surround me while getting it done. I threw on a Macho Man Randy Savage documentary and had a chat with my brother, keeping me occupied.

Today I woke up after a decent amount of sleep hoping it was enough to hold off the fatigue but I got that feeling of impending exhaustion again at 6pm. I had plans with friends at 8pm that I was really looking forward to. I kept my plans, but took some precautions. I got a ride there and back in case I became too dizzy to drive home safely. I made it. I ended up drinking a shitload of water and taking a lot of Adderall. The physical energy it provides is the first effect to wear off after 4-5 hours (the other effects, mental energy and wakefulness last for a good 20h) so I had to keep re-dosing to postpone the crash and it totaled a large (but safe) amount. I had a great time playing music and having laughs with friends. While the feeling of lingering exhaustion never left me, staying engaged socially prevented it from being an obstacle. I eventually did hit that point where I needed to stop, but when it finally happened, we were all sitting on a couch playing a game so I didn’t have to stop doing what we were doing and everybody was heading home a half hour later anyway.

Exhaustion aside, even though by now it’s been a couple years reconnecting with old friends and building a larger social circle than ever before I still don’t take moments like this for granted. Every few hours I at my surroundings and think “Whoa, this is my life now? I have many of the things I wanted all those years?” I don’t mean to harp on it, but it was only a few years ago that it still seemed beyond my reach and in fact many of the things I’ve been doing I couldn’t even imagine.


I have some interesting things on the horizon. Coincidentally, several opportunities to play live music have landed on dates this week and next so music-related brainstorming and preparation what’s currently occupying much of my time.

A couple days ago, I attended an open mic in Providence that featured some of the most unique and talented performers I’ve ever seen. I checked out all the open mics in the area last year to make sure I wasn’t missing out on anything and while I met a lot of nice people, none of them were worth returning to. I guess all the exceptional people have been in Providence all this time. It took place in a small art museum with wooden floors and walls which provided a unique environment with lots of reverb. There were a few dozen people there and each performer got 5 minutes, keeping a quick pace. Get a load of this, I saw:
• Musicians playing a wide variety of instruments (a couple of which I’ve never seen before)
• A guy that played the banjo while singing in an odd Mongolian folk throat style
• A few comedians including a man that was deaf until age 40 cured by a cochlear implant. He looked like Barney Rubble and told a lot of self-deprecating, morbid jokes and was hilarious.
• A female duo named Fanny and Dani, an accordion player and vocalist who sang a medley of songs in French. They were my favorite. Actually, they’re going to get their own paragraph:

When I started taking Baclofen 2-3 years ago, the GABA it flooded my brain with caused me to enjoy music to such a degree that I was nearly moved to tears. The only way I can explain this that will relate to many people is by comparing it to alcohol which also fills you with GABA – if you’ve ever really enjoyed a song after drinking it’s due to a similar thing happening in the brain, it’s why people love to sing and dance after a few drinks. Anyway, I started to really feel music emotionally again for the first time in a while. I began to appreciate many genres that I never did before like classical, ragtime piano, and funk. I explored this new feeling as often as possible, I listened to all the bands I’ve ever loved and all the new bands I had discovered. I don’t enjoy music any less than I did during this time, but I haven’t had that euphoric feeling where my eyes start to water in at least a year. While these two were playing, I got that feeling again and it took a little bit of effort to avoid becoming visibly emotional.

I took a brief video with my cheap phone that I posted on my personal Facebook page:


People have been telling me for my entire life that I’m hilarious and should take a crack at stand up comedy. I always thought about it but considered myself to be more witty as in, I’m good at saying funny things spontaneously to comment on situations that occur in front of me. Creating the situation yourself from scratch in a stand up act is a different entirely. Plus, I don’t even enjoy stand up comedy. Much like TV and movies, when I’m medicated I’m too stimulated to enjoy sitting still focused on a passive activity like that and otherwise I’m too tired too follow it. Regardless, last year I decided that I was going to give it a shot but as 2017 started, it was one of the many goals for that year that sleep apnea derailed.

Although that forced me to wait, I started writing down any thoughts I had that with potential to be turned into jokes. I’ve written many things down since then, but it’s very similar to the way that I used to come up with riffs and jingles but rarely came up with full songs – I ended up writing down a lot of half-jokes, funny observations, and jokes with deliveries that were yet to be determined. While listening to these comedians at the Providence open mic, I was in my head brainstorming and connecting the dots to finish many of these jokes. What I’m getting at is, this open mic experience came along at the perfect time and is the perfect venue to give comedy a shot myself. I’m going to return in a month and try it for the first time.


As I’m writing this it’s 6:40AM. It’s not uncommon for me to stay awake this late into the morning when I’m planning on resting on the following day. Tomorrow I won’t have the ability to accomplish the things important to me now and in fact they won’t even be important any more, I’ll be too tired to care. I stay up late to cling to every additional minute that I can keep this momentum before slowing to a crawl and eventually starting again on Monday. The other reason I do this is so I can easily fall asleep without Temazepam. I didn’t have Temazepam in my arsenal until recently, and it’s no coincidence that I haven’t had to deal with any sleepless nights recently. Seroquel works partially in the opposite way that Adderall does – it blocks dopamine, which along with norepinephrine floods your brain when you take Adderall. That sounds like Seroquel would make for the perfect drug to get some sleep on these days and while it is indeed pretty good, it isn’t enough to work reliably. During the many years that I took Seroquel to sleep (along with Trazadone, a gentler sedative) I just accepted that insomnia was a part of my life, something that occurred at least monthly, sometimes weekly.

Here’s the problem (which I mentioned earlier). Adderall has three stimulating effects that help me function: physical energy, mental clarity, and wakefulness. The physical energy wears off after 4-5 hours, but the other effects last about 20 hours. See the problem? The rest of the world is going to keep living on their 24-hour clock without caring if I slept or not. If the day was 30-something hours long this health puzzle might be half as difficult, but in order to live a 24-hour day I have to do this constant push-and-pull with my energy level. I wake up tired and I go to bed wide awake every day. This led to a built of guilt for many years before I really understood how these meds worked and realized that expecting to sleep the way most people do was unrealistic. Once I understood this, I gained the freedom to do one of two things: I could explain it to people that expected me to go to bed at a decent hour and make them understand too, or if that didn’t work I could disregard their criticism because I couldn’t meet their demands even if I wanted to. You can’t go to bed early with amphetamines in your system, only later.

The original point I was leading towards but got away from is that the other reason why I stay up so late on my last day before a couple days of rest is that by waiting so long after my last dose of Adderall, Seroquel puts me to sleep reliably.


Perhaps I’ll write more of these “Things On My Mind” posts in the future. There are always things on my mind, but today’s situation was perfect for spontaneously writing out all of my thoughts. I’m very stimulated and the gears are turning in my head yet I’m too exhausted to do much else, and I had a very eventful week full of new memories and ideas.

Now if you’ll excuse me, I need to sleep for a couple of days.

The Importance of Environment

Think about the way your dentist’s office smells. When that smell is in the air, how does it affect you? Do you start to feel anxious or uncomfortable like you Would rather be anywhere else? Does it trigger memories of previous appointments, maybe that one time when the dentist poked the wrong spot and stabbed you in the gums?

Our environments have a much stronger influence on our feelings and behaviors than we often realize. Even when we’re consciously aware of some of a particular environment’s effects, there are others at play that we don’t realize. Personally, if I’m trying to accomplish something, the worst place I can be is the spot I wake up in every day: my bedroom.

I’m very comfortable in my bedroom. I have a large bed with plenty of room for both my 6’1″ 200lb body and my laptop. Distractions are few and far between living on a quiet street surrounded by trees which muffle most sounds emanating from the nearby highway. Inside the house is equally quiet, as I live with my quiet, predictable parents. To get even more comfortable with my surroundings, I recently covered my plain white walls with images that excite and inspire me:

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I’ll write about my walls in this blog at some point, but for now you can read more in this Reddit post.

However, laying in bed in front of my laptop is the way I spent most of my time during my worst years. After spending so many years feeling like crap wasting time on my laptop while laying in bed, I’m now conditioned to do exactly that: feel like crap and waste time on my laptop whenever I’m laying in bed. I browse Reddit, check Facebook, and search YouTube. The only productive thing I regularly do while laying in bed is my daily moneymaking routine which usually consists of an hour’s worth of whichever marketing jobs are available for the day, earning me a few bucks.

It’s hard enough dragging my ass out of bed on days when I feel relatively fine, but if I’m behind on sleep or otherwise dealing with additional fatigue it can be a real challenge. I started becoming aware of the fact that I subconsciously look for any excuse to stay in bed a little longer, fooling myself into thinking I’m being productive. For example, I have a set of tools I developed to complete those aforementioned marketing jobs more quickly and efficiently – I’ve made buttons to copy-and-paste email addresses and social media links, take pictures of the screen, etc. If I think of a way to improve that program by adding a new feature or improving an existing one, I can stay in bed for another hour while I write some code.

My solution to the problem of my room is simple: get the hell out of it. Not only do I bring my laptop somewhere else, but I have a separate user account that I log into while using my laptop out in the world. This account looks like a fresh install so there are few desktop icons and no programs that start automatically to minimize distractions. I originally created this account to use when I do the Rick’s Music World open mic livestream each week. I wanted peace of mind knowing that I could leave my laptop unattended without my personal files being accessible. Over time, I realized that this account is also a great way to separate myself from my routine.

The library down the street has free WiFi and quiet rooms that can used for up to two hours per day. I’ve yet to explore any other options, but there are plenty: libraries in surrounding towns, restaurants like McDonald’s, Dunkin’ Donuts, local cafés, etc.

The only way I was able to write this blog entry was by getting myself out of my unproductive environment.

Introduction

Welcome to Shaking Off The Chains!

My name is Adam, and many of you reading this are already familiar with me. If not, check out the “About Me” page I wrote last year.

The goal of this blog for the time being is to have all the things I write about ME/CFS in one place. Over the past couple of years, my writing has been all over the place: Facebook posts, direct messages to friends, Reddit posts, verbal rants, etc. I’ve written in this blog a few times but I’ve never kept up with it consistently. Over time I gradually started to receive a lot of messages, usually on Reddit, from people that found something I wrote and identified with it. Many of these people are where I was a few years ago and want to get to where I’m at now.


Over time this blog will evolve to include new features to become modernized. I need to add all the usual stuff like social media charms and an e-mail list. Right now though, I just need to make this public and get moving with it.

To provide context for some of the things I’ll be writing about, I’ll explain my life.

At the moment, I’m active about 4-5 days per week. By active I mean I’m up and out of bed, dressed, and can function both physically and mentally. I have enough energy to get through the day, socialize, and achieve my goals. I’m limited to 4-5 days because of the way these meds work: Adderall gives me physical energy and mental clarity but like all stimulants, tolerance builds fast and if I took it every day it would stop working in no time. The other issue is that a powerful stimulant requires a powerful sedative at the end of the day, and if I took Temazepam every day it would also stop working and worse, I would have to go through benzodiazepine withdrawal to get off of it. That doesn’t sound too fun.

I made a lot of progress in 2017. First, I improved my sleep apnea symptoms through weight loss. This was a big obstacle, making it impossible to be active for more than a couple days in a row due to the lack of sleep. Although these symptoms have significantly improved, some still persist. Next, I identified the cause and treatment of the severe nausea and vomiting that I developed in the middle of the year. I suspected it to be related to the motor tics and tensing of muscles that can occur due to stimulant use, it was wrenching my gut.

2017 also brought an achievement I believed to be impossible: I received my first paycheck! I’ve been able to do a lot of fun things over the past couple of years, but working in any capacity remained an impossible dream. It’s easy to do things here and there when I can plan ahead and ensure I’ve had enough rest but work requires predictable, consistent good health for the vast majority of days in the week. Since my early 20s, I’ve visited college career centers, disability services, and had several appointments with Mass Rehab which lead nowhere. The work I found wasn’t the result of official aid but from the social circle and connections I had built up.

Again, it was only four years ago that I could barely get out of bed, had been years since I spoke to any of my friends, and I found no enjoyment in life. I hope you enjoy following along my journey and find the experience informative and entertaining.


Soon I will change the main categories you see up top to something like this:

  • Commentary: I’ll give my take on whatever topic is on my mind to give you a look at the world through my eyes.
  • Treatments: I’m always reading about or experimenting with different treatments. I like to talk about my experiences and the things I’m learning and I’ll do so here (instead of random outbursts of “so guys, I’ve been reading about fluromodafinil…” at social gatherings).
  • The Healthcare System: Quite often, finding the best treatment is the easy part – the challenge is navigating the healthcare system and acquiring it. The organizations meant to be on your side often become barriers. Between the FDA, DEA, doctors, insurance companies, and the pharmacy, there’s always a challenge and I’m still learning.
  • Blog: My daily life, less formal writing and rants about whatever happens to be on my mind.

Feel free to reach out to me via email at adamsotcblog@gmail.com until I set up more convenient contact methods.

A Reminder To Myself To Always Challenge My Limits

The last time I tried to be active for three days in a row (by active I mean waking up at a decent hour, taking stimulants so I can function, and leaving the house), it didn’t go so well. After the first day, I went to bed hoping to rest up and recharge, but I didn’t get as much sleep as I needed. I was hoping that I could catch up when I went to sleep after the second day, but instead I woke up after only three hours of sleep. After tossing and turning for an hour, I recognized that I was definitely not going to be falling asleep again so I started my day.

I can handle one night of insufficient sleep, but any subsequent nights leave me in very rough shape. Lack of sleep amplifies all of my symptoms: brain fog thickens, every muscle of my body aches, nausea increases, and an overall feeling of severe discomfort comes over me. This is precisely what happened the last time I tried to be active for three days in a row. Making matters worse, the third day was a Thursday. That evening, I went to the open mic at Rick’s Music World like I do every Thursday to run the Facebook livestream and see all of my friends there. Usually, socializing with everybody and playing music can take my mind off of my aches and pains while I’m there, but on this particular occasion there was nothing I could do to distract from the discomfort. I knew that I looked as miserable as I felt, which really had people worried because everybody at Rick’s is used to seeing my at my best when I’m there. This unpleasant time was the worst yet of several bad experiences I had attempting to stay active for more than two days within the past few months at that point. Much like touching a hot stove, we as humans learn to avoid things that hurt us. During the last couple of months, I made sure to get lots of sleep and rest between my active days. I’ve mostly been getting as much as I can get done one day, resting the next, and repeating, with a few double-headers here and there.

Although it’s human nature to avoid things that have caused us pain in the past (and those who are constantly sick learn to do this even more than the average person), one of the most important things I’ve learned over the past couple of years is that I constantly need to be challenging my limits. Sometimes our situation changes but we don’t realize it because we’re still playing by the old rules. I have lots of memories of certain scenarios causing me pain and discomfort: things like travelling, standing up in the same spot for long periods like at concerts, and car trips causing nausea and muscle stiffness. These memories caused me to avoid a lot of things for a while. After getting myself a bit better, I’ve tried to overwrite those bad memories with good ones and I’ve achieved that in many situations.

I reflected on the changes that I’ve made over the past couple of months and figured that I was due to give a three day streak another try… and guess what? It was a success. I’m writing this at the end of day three. Yesterday was a little rough, but I still accomplished what I set out to do. I wanted to go to some thrift stores and look for some things that I could flip for a profit on eBay. I called up my friend Laurel to see if she wanted to come with me, thinking that socializing might help distract me from my aches, and I was right, it worked. I went to bed last night hoping that I would not wake up after three hours as it happened last time, and I fully expected my body to demand many hours of sleep. I was pretty sure I was going to wake up at 5pm. To my amazement, I woke up at 2pm feeling totally rested and ready to face the day!

This experience just reinforced everything I already knew in the first place. Any time I suspect my situation has changed even just a little bit, I need to re-evaluate my limits and see if I can push the barricade around me a little bit more. I got a lot accomplished during these three days, and I hope I can repeat this experience soon.

I considered using this post to explain the pros and cons of keeping momentum for several days in a row like this, but that’s a post for another time.

What Sick People Are Sick of Hearing (You’re Probably Guilty of It)

I want to talk about something most people don’t think about and it’s something most people are guilty of without realizing it. If you know anyone who is sick – either chronically or temporarily – it’s something you’ll want to read.

I still stick around in some online chats related to the game I used to play/moderate and have developed and maintained friendships from people around the world. I began talking to one girl shortly before she was diagnosed with cancer. She’s a young girl in her early 20s, and it sucks to have to go through something like that especially when you’re young. She knows my health situation and that I find all health and illness topics interesting, so I told her to keep me up to date with the experience. We spoke off and on, she told me about all the shitty things she had to deal with – physical discomfort and the mental challenges that go along with some of the procedures… the cancer’s effect, the drug side-effects, uncomfortable preparation for exams and operations, etc. After talking for several weeks she thanked me. She told me that she spoke to many people about her situation, friends and family, but talking to me was so refreshing. It’s not because of something I did, but rather something I didn’t do: I didn’t tell her “You’re so strong, you’ll get through this!” “Keep fighting, we’re all behind you!” or anything like that. I listened and replied in a very matter-of-fact manner about the realities of dealing with such a thing: it sucks. I didn’t insist the future was bright, because when you’re going through such an ordeal you’re concerned with the here and now. She told me that my reaction was so refreshing because everyone just kept telling her to get through it and fight hard. On top of her existing pain and discomfort, comments like this also made her feel like she was letting people down by not being stronger throughout the ordeal. I explained to her that I reacted this way because I had gone through the same thing myself many times over for as long as I’ve been sick. When you’re sick or otherwise uncomfortable or in pain, people feel like they need to do something about it. In my experience, that means that they do one of two things: The worst of the two is they’ll offer stupid advice, suggesting you try something that either would have no effect or something that you’ve obviously tried when the problem first started. To give an example of each, one person suggested I try chicken soup to cure my ME/CFS symptoms, and another suggested that I try getting more rest. The other less ridiculous reaction people have is to offer verbal support: things like “You can do it! We all believe in you! You’re so strong, you can beat this!” Unless you’re the only person they’ve ever spoken to, they’ve heard this dozens of times already ad nauseum.

Often when somebody talks about the issues they’re having they just want somebody to listen and understand the things they’re going through. Personally, when I bring up the fact that one or many of my symptoms are really bothering me, all I want is for somebody to know that it sucks. That’s all I need. The pain or discomfort will pass, I already know what I can do (if anything) to help, but for now I just want someone to understand what I’m going through.

Sometimes I feel obligated to let people know that I’m not feeling well because I can tell that the discomfort is affecting my behavior. It hasn’t happened as much in recent years, but especially during my teens when my illness was just starting to take off I would frequently have people misread my body language. People would ask me why I was mad or sad when in fact I was just feeling sick. After so many years of this, I learned to explain myself before there was a chance for people to make any assumptions.

If you’re reading this and have been guilty of the things I mentioned in this post, don’t worry about it, most people are. You don’t need to apologize to anybody or even feel bad about it. It’s just one of those things most people haven’t realized or ever thought about. Just keep it in mind for the future and you’ve done your part.

Insomnia and Music

As I write this, I am sitting on a stool in front of my laptop at Rick’s Music World. I’m here every Thursday night to perform at and livestream the open mic. Anyone who knows me on even a casual level has heard about this place and probably seen some videos of my performances. It was here that some of the greatest moments of my last few years took place, including my incredible Halloween feature, which happened during the months that I got away from writing in this blog. I’ll need to write about that and fill in the blanks sometime.

Right now, I have other things on my mind. Sometimes my symptoms start causing a chain-reaction and really kicking my ass, and this is one of those times. I’ve fallen way behind on sleep, which is increasing my fatigue and brain fog. It also makes my Adderall tics worse, and the stiff muscles are causing that burning pain in my shoulders. For some reason, the past few months, when I get that burning shoulder pain it eventually causes nausea… so yeah, I’m pretty uncomfortable right now, but the symptom that caused this chain reaction was insomnia. If I could fix that, all the other symptoms would improve. Well, tomorrow I hopefully start dealing with that.

I finally had a sleep study done a couple of months ago to confirm the obvious: sleep apnea. Every night I sleep for 2-4 hours and then wake up. If I took Adderall during that day, there’s still enough floating around in my brain stimulating it that as soon as I’m awake, my brain is all “We’re awake again? Great! What are we doing? Let’s work on that project we started yesterday or start another one! Let’s go!” so I can’t get back to sleep. I can afford a 2-4 hour sleep night here and there, and actually I like having one from time to time. When you’re blasting your brain with amphetamines, missing one night of sleep isn’t a big deal and during these 40-hour bursts, I get a lot accomplished. The problem starts occurring on days 3, 4, etc… I become a zombie that can’t think or move or get anything productive accomplished.

Tomorrow I pick up a CPAP machine, which basically makes sure you keep breathing through the night to prevent waking up. The company is named Enos, which is funny to me not only because of wrestler Mike Enos, bus also because it rhymes with penis. I’m easily amused after falling way behind on sleep I suppose.

Anyway, I’ve heard mixed comments about CPAP machines. Some people tell me that their sleep improved from day one and it was the answer to all of their problems. Others tell me that it eventually helped, but it took up to a year. Others say they still can’t sleep at all. My hopes are high, but the one thing I know for sure is that my sleep can’t possibly get any worse.

The two symptoms I took aim at overcoming this year were sleep and pain. I’ve got my pain somewhat under control, now sleep is the biggest enemy. There are so many things I want to get accomplished that aren’t possible when I don’t sleep.

Fixing insomnia is one of the final pieces of the puzzle. I’m getting very close to finally figuring it all out.