The real reason I wasn’t feeling well

September 26, 2017

I have noticed an interesting pattern recently. It goes like this:

  • One evening: Hmm, I don’t feel well. Must be the usual chronic illness stuff.
  • The next day: Wow, I feel really bad. This CI stuff is acting weird.
  • That night: Oh boy, this is not only bad, but also not quite the same as the usual CI stuff.
  • The next day: I’ll just push through. It’s probably a mini flare. Be quiet voice-in-the-back-of-my-head! I don’t want to hear this is something else.
  • That night: Oh crap, I think I’m sick.
  • The next day: Oh boy, I’m DEFINITELY sick!

And that’s what happened this weekend. It took two days of feeling guilty and trying to push through before I realized I was sick. Then I spent an entire day on the couch watching tv, not even trying to do anything “productive,” and I felt so much better afterwards!

It’s hard when you have a chronic illness and have “sick” symptoms on a regular basis. You have to keep living your life, and often, resting wouldn’t help anyway. But sometimes it’s actually a bug, and rest is just what you need. Then it’s important to give yourself that rest.

I’m not back to “normal” yet today, but I feel SO much better. Maybe one day I’ll listen to that voice in the back of my head and realize I’ve got a bug a lot sooner. I haven’t figured that part out yet, but hopefully one day I will.

And in the meantime, I hope you all can give yourselves time to rest and recover when you get a bug. It’s lousy when it happens, but at least, unlike chronic illness, it’s temporary!


Feeling blah

August 30, 2017

This has been an odd summer for me. The thing is, I’m not sure how much of that is because of my chronic illnesses, and how much might be coming from something else.

2016-09-26-15-34-58

For one thing, the weather has been unusually not-too-horrible. I can go outside! On top of that, I seem to be less sensitive to air pressure and humidity than I have been in the last 10 years or so. More ability to go outside! That doesn’t mean I can always go out, but on days that would have caused extreme pain or trouble breathing before, I’m actually doing ok.

On top of that, for the first time since I was 18, I live in an apartment with central air conditioning. This. Is. Awesome!

Because of all of that, I have less fatigue and less pain than in previous summers.

So why do I feel so blah? Why have I been a bit moody? Sure, I still have more pain and more fatigue than at other times of the year, but is that it? I keep thinking it is. I keep thinking that when summer is over, I’ll feel better.

It’s not like me to be so uninterested in certain things. I have been trying to do some part time work, but I’ve barely done anything for my fledgling business all summer. At first that seemed ok. I had worked too hard in the spring and was burned out. So I took a break. The problem is, I still have no desire to go back to it.

The thing that really worries me, though, is that I’m wondering if maybe I shouldn’t get a dog after all. You regular readers know that I’ve been trying to get a dog for more than 2 years, with one problem after another cropping up. And now I wonder if a dog is too much work and too much responsibility for me. And I love dogs, but are they worth it?

It occurred to me that these are symptoms of depression. But I’m not depressed. I’m still very happy. I’m very interested in other things. I have been excited to try some new crochet patterns. Last week I finally picked up a project that I had let go of for over a month, and now I’m excited to work on it again. I’m loving spending time with friends.

So why the hell am I doubting if I should get a dog? Why am I avoiding work?

I think it’s the summer effect. This summer isn’t as bad for me this year, it’s true. But I think it’s affecting my mood anyway. Otherwise, this just makes no sense.

In 3 more weeks I should know.

A lot of people don’t like working. That’s ok. But not wanting to get a dog? If that keeps up, I’ll know something is truly wrong.


When triggers feel absurd

August 18, 2017

Some triggers seem reasonable. If I fall and land with any pressure at all on my hand or wrist, my wrist pain fill flare for days, weeks, or months. If I exercise too much, my pain and fatigue will flare. Some triggers make sense but piss me off: like eating lunch.

Yes, eating lunch is a big trigger if I don’t do it right. As it turns out, eating and digesting food takes a lot more physical energy than I would have every guessed back when I felt healthier.

20120917_181648

If I eat standing up, I’ll feel sick. If I eat too fast, I’ll feel sick. If I eat at the wrong time, I’ll feel sick. If I eat and don’t rest afterward, I’ll feel sick. And “sick” can mean a few different things.

Take Wednesday for example. I had a doctor appointment at 1:40. I needed to leave by 12:40. But I wanted to make a quick stop at the library on the way, so I figured I would leave at 12:25. I usually eat lunch around 1pm, but instead I ate at noon, and I ate quickly. The second I finished eating, I ran out the door. Oops. I ate fast *and* didn’t rest afterwards. The nausea and fatigue set in fast. I was in pain. I felt horrible. But I had to get to that doctor appointment.

I pushed through. I didn’t have the strength to multitask, so I didn’t turn on the audiobook I wanted to listen to. I focused. I managed to drive safely but miserably. I went to the bathroom before I checked in, and a lot of my lunch left my system – not properly digested. Then I asked to wait in an exam room instead of a waiting room. Thankfully, they had a room available and I was able to lay down.

After laying down for a bit I felt much, much better. The nausea was gone, the fatigue was improved. Still, I took it easy the rest of the day. My appetite didn’t come back until the following night.

I know that lunch wasn’t the only problem, just the final trigger. My stress about what’s happening right now (Nazi marches!?!) and the weather (very humid) primed me. It was lunch that set me off.

It pisses me off that I can’t eat an early, quick lunch and then run out the door. But then, I also should have known better. I knew that could be a problem, but I did it anyway.

Still, I feel good about one thing: instead of pushing through and trying to “brave it out,” I asked to lie down. And it made ALL the difference.

Learning to ask for what I need has been invaluable. I don’t always do it, but when I do, I feel good about it. Now I just need to find ways to eat lunch before a doctor appointment that don’t have such terrible results. (And yes, eating after the appointment would have been just as bad – I have a very narrow window to work with.)


Feeling moody from pain

July 19, 2017

There’s an emotion toll to chronic pain that’s easy to miss if you have only ever experienced short term pain.

A banged finger will heal soon enough. A sprained ankle will cause frustration. Even a broken bone rarely leads to anything permanent, and so you just wait it out. But the chronicness of chronic pain means that you need to handle it long term, and that comes with a lot of emotions.

Over the years I have had many feelings about my pain. Working through them has helped me to deal with my feels now, and yet, I still struggle.

I have new pain. Just 2 short months ago my thumbs weren’t even on my radar. I used them without thought. Now, everything hurts. I cringe when I realize I have to go to the bathroom, because I know I will feel extreme pain when I pull down my shorts. Picking up a plate is difficult and painful. I wonder how long it will be before I break and drop something not from clumsiness, but because of the pain or weakness. [Side note: I say my thumbs hurt throughout this post, but more specifically, it is the joint that connects each thumb to my hand. Thankfully the rest of each thumb is ok…. for now. Since every movement affects that joint, I can’t use my thumbs without feeling the pain, though.]

I’m scared. This pain could be permanent. I might literally have it every day for the rest of my life. Or it could go away. Or it could go away and then come back at random times. There’s no way to know.

I’m frustrated. When I feel horrible, I spend some time on the couch watching tv and crocheting. That makes me feel better. But I was in too much pain to crochet. I always fidget, always need to keep my hands busy and my fingers moving. But now any type of fidgeting I do is painful, because I use my thumbs, or I use other fingers and that pulls at the muscles that connect to the thumbs. What on earth will I do if I can’t crochet or fidget? I can’t even begin to imagine.

I’m sad. So very sad. Because I know that my thumbs will probably never be the same. And because I know there are other joints in my body that I am taking for granted now in the same way I took my thumbs for granted two months ago. I want to appreciate everything now, while I can. I even want to appreciate my thumbs because I know all too well, from 26 years of joint pain, that things will probably get even worse and that I will look back on this time and wonder with amazement at how I didn’t realize how good I really had it, despite the pain.

I’m overwhelmed. My head swirls. Did the onset of summer cause this or exacerbate it? If so, maybe things will be better in the fall? The increased dose of my anti-inflammatory supplement, from 1/day to 4/day, hasn’t helped. I really hoped it would. When I started with 1/day last year it changed everything and made me feel so much better, but it seems no match for my pain-filled thumb joints. Or maybe it’s disease progression, and I need to go back to taking Plaquenil. I don’t want to, for many reasons, but I can’t deny that it has helped a lot in the past. I’m in so much pain that I almost want to try it now, but should I wait to see if things get better in the fall? Then again, what if they get worse? What if waiting just leads to more damage and makes it impossible to halt things? No one can make these decisions but me. I could see my doctors, but would they say anything I don’t already know? Besides, I just saw my rheumatologist a couple months ago and I have another appointment to see her in a month. It seems silly to move that up so soon. We can discuss it all then. But when every day is such a struggle, a month feels very far away.

I feel trapped. I feel trapped in my body, which is so filled with pain. And I feel trapped in my apartment, because the evil humid air outside makes my symptoms worse. I know that even a walk to my car will increase my pain and fatigue and will bring on nausea and diarrhea. I can’t go out there. But I need to move, to be distracted, to do something.

I feel cut off. Texting has slowly become a primary form of communication amongst my friends and the new person I’m dating. But texting is far too painful. I dictate messages into my phone, but I find that frustrating. And even just navigating to my messenger app is painful. I can do it, but it hurts. I am SO GRATEFUL that typing on my laptop isn’t too painful yet. But what happens when it is? I lived through that 20 years ago, but computers weren’t as vital for communication then.

Yesterday my neighbor stopped by for a visit with her puppy. I hadn’t left the apartment all day, thanks to the weather and my pain. Even just opening the door and feeling that wall of thick, muggy air for a few seconds wasn’t good. Having a visitor felt so good! And the puppy was a darling! Petting him hurt, but it was worth it. They left all too soon. I wish there was a visiting puppy program for the sick.

I am so fortunate. I have a lovely home, a caring family, wonderful friends, and enough food and medicine. But the emotions still engulf me at times.

Unfortunately, my mother called last night at the wrong time. When we started speaking everything was fine. But during the call the pain became worse, and by the end, I was moody and bitchy. I was too busy talking to her and feeling sad and frustrated and overwhelmed to take a step back and recognize and work through my feelings of sadness and frustration and overwhelm. So I took it out on her.

And my mom, being the amazing woman that she is, listened, expressed sympathy, and never blamed me for acting like a selfish child. She has chronic pain too, though it’s less disabling, and I think she understood.

Halfway through writing this post, my mom called. She said that she wanted to do something for me and I could not say no. She is going to come to my apartment one day and clean it for me. I can’t clean it myself, and the cleaners I hired didn’t work out, so I have been feeling stuck. She wants to do this to help me.

I have so many negative emotions right now. This thumb pain is upsetting to me in ways I haven’t been able to express to myself yet, much less write down here. But having my mom in my corner definitely helps. Even if sometimes I still get bitchy. After all, I’m only human. And I’m scared.