Posts Tagged ‘Depression’

Wanted: Pain Whisperer

Friday, October 4th, 2013

Whisper-in-ear

I had an interesting appointment with my rheumatologist recently.

I have a standing lab order at LabCorp; my doctor renews it every six months. (I get blood drawn every six weeks.) Several months ago, at the beginning of a new six-month period, I noticed that the lab technician only drew three vials. (Usually it’s six or so.) So I asked, and it turns out that my doctor dropped several tests on my most recent lab order. Right now the only tests being done are the CBC and two liver tests (ALT and AST). The ones that have been dropped include things like sed rate and CRP. So, as I understand it, I’m mainly being checked for damage from medications – not for any of the markers that indicate inflammation or give an idea of disease activity.

So at my last appointment, I asked my doctor about this. He said that he doesn’t find the blood numbers particularly meaningful, and that he believes that patient reports are a far more important indicator of disease activity. (He does have me fill out a detailed questionnaire every time I come in, and he always does a joint exam.) “You are your own best sed rate,” he told me.

“But I’m not always sure that I really know how the disease is doing,” I said.

He smiled at me. “Oh, I think you do.”

I have my doubts about this. On the one hand, I think it’s great that he really listens to his patients. I know that it’s a very bad thing when the opposite occurs. (Kelly at Rheumatoid Arthritis Warrior has written about this a lot.) But I also hear other RA patients talking about things like the Vectra DA test. I also know that disease activity can continue when symptoms are quiet – I’ve even heard stories of people who thought that they were in remission while serious damage was happening underneath their level of awareness.

There’s another problem with this, too. I have always had trouble interpreting my own pain. I’ve never been athletic, and when people talk about the difference between “pain” from injury and the good “soreness” from exercise, I have no idea what they mean. Even long before the RA diagnosis, I always had trouble with this distinction. Once the RA came along, it got even more complicated for me – is this a flare? Muscle pain or joint pain? Is it the exercise or the RA? Is it caused by stress or depression? Sometimes, especially if I haven’t gotten enough sleep, everything seems to hurt, even though a joint exam and bloodwork show no problem. Other times, I have such a high pain threshold that I don’t even notice it. I once walked around for two weeks on a sprained ankle with no idea, simply because I had gotten so numbed to RA pain that the injury didn’t even register.

Do any of you have this kind of “pain-deafness,” or am I unusually out of touch with my body? I wish I had a Pain Whisperer – someone who could tell me, “This is from the RA.” “This is normal muscle soreness from exercise.” “This is because you hurt yourself.” Someone who would always be right, who wouldn’t miss anything. (I’m thinking back to the many alternative-medicine practitioners who got it wrong during the months before my RA diagnosis.)

In the meantime, I don’t know what to make of this change to my lab work. I’m suspicious because of the timing. I’ve noticed a lot of changes (almost all negative) in the way my insurance handles things since the new year. Right now my Remicade infusion has been delayed because of one of these insurance changes (a subject for another post). So I have to wonder – is this an economic decision? An insurance decision? Or is this how my doctor really feels?

Now I wish I had a Medical Practice Whisperer.

Edit: I just read this post over at Pollyanna Penguin’s blog – seems I’m not the only one with this issue! And I was also reminded of this 2009 post at Carla’s Corner – funnily enough, I see that I commented on it at the time! Guess this is a long-standing issue for me!

Where Have I Been?

Sunday, August 25th, 2013

Another one of my long radio silences. This one is harder for me to write about. Wren sometimes calls RA the rheuma-dragon, and I’ve been looking for a good name for the beast who’s been visiting me lately. I think I’m going to go with Depression Zombie.

Depression and RA seem to go together a lot of the time. Several other bloggers I admire have written about it, and I’ve appreciated every word. But when it comes time for me to write about it, I get stuck. For me, one of the symptoms of depression is deep shame about being depressed. When I’m not depressed, or when it’s happening to somebody else, I understand that it’s a medical condition like any other, and that you can’t just will yourself out of it. But when I’m in it, I can’t see this. Somehow it’s my fault, or means that I’m weak, or… well, the self-attacking thoughts go on and on.

While the Depression Zombie had its bony fingers in my brain, I happened to read this post by The Bloggess, and it is an exact description of what I was feeling. I love The Bloggess – she is awesome – and although she’s not really an RA blogger, she does have RA. And what she said about depression really resonated with me, especially this part:

When I’m in a depression I want to write about it, but I usually can’t. I’m too overwhelmed and paralyzed and exhausted. I end up writing 100 angsty drafts that never see daylight and I convince myself that no one cares.

Anyway, I hope Jenny (The Bloggess) won’t mind me borrowing her words. I just can’t seem to find them myself, and hers are pretty much a perfect description of what’s been keeping me away from my blog. Please read her whole post, especially if you are dealing with depression too.

HALT

Saturday, March 16th, 2013

Halt

There’s an acronym used in self-help and recovery circles – I think it originated with Alcoholics Anonymous. When you find yourself feeling low, you’re supposed to assess yourself to see if you are feeling Hungry, Angry, Lonely, or Tired – H.A.L.T. Any one of this four states can weaken resistance and put people in a vulnerable position.

I’m lucky enough not to have issues with addiction, but I think H.A.L.T. is a useful tool for pretty much anyone. I know that when I let any of those states get too far, and especially if I’m experiencing all four at once (which has been happening a lot lately), I sometimes make decisions that are counterproductive, even self-destructive. I deal with Hungry by grabbing huge handfuls of M&Ms. I turn being Angry inward and end up with migraines. When I’m feeling really Lonely, I isolate myself. And, of course, when I am Tired is when I most resist going to bed on time, much like a toddler. The relationship isn’t always linear, either – being Lonely or Tired can also get me reaching for the M&Ms. When I am feeling all four, I generally make poor self-care decisions – I don’t eat, sleep, or play well, and my mood gets pretty bleak.

I feel the need to add one important variable to this list: Sick. (Also In Pain, but “HALTS” sounds better than “HALTIP”!) When I am sick or in pain, good decisions become really hard for me. My plans and goals fly out the window. I feel helpless and out-of-control. Also, I develop a strange blind spot – I don’t realize at all that being sick or in pain is the reason for my emotional state. I came face-to-face with this yesterday – it was the day after my Remicade infusion, and I woke up feeling amazing. (This doesn’t always happen.) Birds were singing. Colors were brighter. It was like this.

I used to have all kinds of systems in place for times when I wasn’t doing well. I used to take methotrexate once a week, and because I knew in advance that I would be feeling terrible that day, I had a whole routine set to go. But my RA has actually been doing pretty well for awhile now, and even though this is a great thing, it means I get thrown for a loop more easily when things aren’t good.

It’s not just my own Sick that gets me down. I have a five-year-old son, and he’s been bringing all kinds of germs home from preschool. It seems like one or the other of us has been constantly sick for months. We just seem to pass the bugs back and forth, even though I know that’s not how it works. And when my son is sick, I end up home alone with him, day after day, getting run-down and exhausted. Not to mention that thanks to Remicade and the immunosuppression, and his normal five-year-old tendency to need lots of cuddles when he’s not feeling well, I almost always end up sick too. (That’s a topic for a whole other post – probably my next one.)

I’m struggling with how to make H.A.L.T. work under these circumstances. The idea is that you recognize how you’re feeling and take action to meet the need. It’s clear (although not always easy to do) that you need to eat if you’re hungry, sleep if you’re tired, etc. Anger and loneliness are a little bit trickier, but there are still proactive things you can do to address them.

So what do you do when you’re sick, or your kid is sick, and it’s relentless and constant and it’s depleting you in all of the other four areas too? What do you do when the pain isn’t responding to meds? How do you take care of yourself and protect yourself from coping mechanisms that aren’t helpful in the long run?

This question isn’t philosophical – I know people will want to respond by talking about faith or religion or positive thinking. I’m not discounting those things – it’s just not what I’m asking. I mean, what are some practical things I can actually DO in these situations? What are some things I can do other than reaching for the M&Ms or withdrawing into myself? How do you make yourself do the things that you know are healthy?

I really want to know. It’s clear that I need some new tools.

Appreciation

Thursday, May 5th, 2011

I recently learned that my blog has been named as one of  “40 Excellent Blogs for Arthritis Support” by NursingDegree.net. This has really made me think. It’s also given me the kick in the pants I think I needed to start writing again.

The list is divided into blogs of two types. The first are called “Informational Resources.” Many of my favorites are included in this list, and I really value what these people do. Sometimes I feel guilty that my blog isn’t more like these – I feel that I should be doing more to help others with RA.

But then I look at the second part of the list, called “Living With Arthritis.” This is the category to which my blog belongs. And there, again, are so many blogs I love to read. And I remember how many times someone has written to me to tell me that my blog puts into words (or sometimes music) the very things they think and feel. Some have shown my blog to their partners, family, or friends, and said, “This is what I’ve been trying to say – this is what it’s like for me.” And that, I realize, is of value.

I have been hiding out because things have been hard lately, and I’ve been pretty depressed. I guess I haven’t wanted to put that out there; so many people in our community work hard to stay positive, and I admire them. I also tend to go silent when things are wrong, even with my real-life friends. (This is something that started with the RA – oddly, I used to share everything before.) But, unfortunately, sometimes depression is part of the deal with chronic illness, and if I want to be honest about my experiences, I have to include it. There are some things I still don’t want to write about because they are too personal, but there are plenty of other things I could share. Some are good, some are bad, but they are all part of the deal with RA.

So I will try to do better. I’m so grateful to those of you who continue to read my words and come back even when I’ve been silent for awhile. I’ve been silent across the board – not participating in RA bulletin boards, not commenting on other people’s blogs. I want you to know, too, that if you’re on the list of blogs on my homepage, I still read you whenever you post. I’ll try to be better about commenting – it’s nice to know that people are out there!