Posts Tagged ‘illness symptoms’

Do You Try To Be More Positive?

Friday, January 15th, 2010

Last month, I asked the people in my How to Have a Better Life When You Have a Chronic Illness tips list what their three biggest challenges were and also what the three most important changes they would like to make were. Lots of them said their biggest challenges were their chronic pain and their other illness symptoms, and they said the change they wanted most was to not have those symptoms.

But a significant percentage of those who responded put down being more positive, happier, or more optimistic as either one of their three biggest challenges or as one of the three changes they would like to make. If you’re like them and would like to happier and more optimistic, keep reading, because I’m going to tell you how-and how not-to achieve that goal.

One of the most important things I have learned about becoming more positive and upbeat is that I can’t get there directly. What I mean is that trying to be more positive hasn’t worked well if at all, and whatever increase in happiness I achieve is quickly gone and forgotten when the next setback triggers my fears, or when I experience my next computer problem, etc.

However, if instead of trying to be happier, I give myself lots of compassion for those setbacks and problems, if I use my God-given gifts (and we all have them) to make a positive difference for other people, and if I make the time and take the time to do things I enjoy, the result is that I’m a whole lot happier.

You may be thinking that what I’ve written sounds good, but that your ability to help others and your ability to do the things you enjoy is greatly limited because of your illness. My response is that even if your ability is limited, I recommend that you still give my suggestion a try.

First, give yourself lots of compassion for the symptoms, pain, and limitations you have. Then make as much of a difference for others as you can, and do as much as you can for your own enjoyment. (Brainstorming helps here. When you do, you will probably come up with several ideas of things to do that never occurred to you before.)

If you follow my suggestion in spite of your limitations, you will find that there is what I call a sliding scale for happiness. What I mean is that you will experience as much happiness by doing as much as you are able to as a person without the limitations of a chronic illness will experience following the same suggestions as much as they are able to.

So I encourage you to try my suggestion, and don’t try to be more positive. I wish you much happiness.

Have You Given Your Symptoms Names?

Wednesday, December 16th, 2009

Have you named your illness symptoms? That may sound like an odd question, but there are some very good reasons for giving your symptoms names. One of them is this: when you give one of your symptoms a name, such as Gertrude or Elmer, you separate yourself from it. When you do that, you are much less likely to identify with it, which makes it possible to step back and see ways for dealing with it and managing its effects on your life that you otherwise couldn’t.

Here’s an example of what I mean: if you have a severe migraine, you may say to a friend or to yourself that you’ve been having awful migraine pain. But when you do this, you can easily feel like a victim. If instead, you tell your friend or yourself that “Sylvester” has been acting up and making himself felt, you don’t make it personal, so you are much less likely to feel like a victim.

A related benefit of naming your symptoms is that it allows you to communicate with them. You can write to them and tell them how they’ve affected your life, and you can tell them how you have felt, and continue to feel, with them them. When you do that, you will probably find that you feel a sense of relief and even freedom.

You can also talk to and even have a conversation with “Sherlock” or “Agnes” (or whatever you’ve named your symptoms). When you do, besides telling them how you feel about them, you can ask them if there is anything they want you to know. You can ask them what are the things you do and the situations that make them worse and you can ask them what changes you can make to lessen their severity and minimize their impact on your life.

You can learn about other ideas for living your best possible life when you have a chronic illness in my free report: “How to Have a Chronic Illness Without Letting it Have You.”