Wednesday, August 27, 2008

Law of Unintended Consequences



The "law of unintended consequences" (also called the "law of unforeseen consequences") states that any purposeful action will produce some unintended consequences. This maxim is not a scientific law; it is more in line with Murphy's law.


Taken from wikipedia's page on Unintended Consequence.

Wikipedia gives a number of examples of this law, but I like to think of my own. The father who punishes his son for a wrong-doing doesn't expect that his son will turn around and take out his frustration on a younger sibling or by kicking the dog. It happens, it is unintended and it is a direct result of the father's intended action.

There are also good unintended consequences though we tend to look at those occasions as "serendipity", sometimes coincidence. For example, 15 years ago I was laid off from a job in another city. I was being replaced by a computer in 6 months. During that time I had to learn this new system. 3 months after I had left my job, I was able to secure another one (which has evolved into my current position) because I knew this particular computer system. The purposeful action of learning a particular computer system that was replacing me (I could have left at any point after the layoff notice) led me to the unintended consequence of landing another job.

Similarly, what we decide to do with information will have its own unintended consequences. I began this blog for a number of reasons. First, I have a story to tell and continue to be told. Second, I wanted to be a writer when I was a teenager, so this has become an outlet for that desire. Third, while I will not attend self help groups, I consider my fellow MS bloggers my own self help group and I want to contribute as much as I take. Fourth, I read everything I am able to about MS, auto-immune disease in general, and neurology. I need help with the processing of some of this information and have sources I can go to on line for further clarification or for personal stories of drug treatment and what to expect. These are the main reasons I began this blog.

After writing for a couple of months I began to think that maybe someone, somewhere, is going to read something I may have written that will be a starting point for them to unlock the puzzle of MS. If that happens it will be an unintended consequence, but one for which I'll be very happy. Are there MS researchers reading our blogs? Who knows? At least some in the pharmaceutical industry are reading Lisa's blog, so that's a start. And maybe some drug rep who reads Lisa's blog, will read an entry that sparks an idea, that sparks an action, etc.....

S.

6 comments:

Joan said...

Sort of a Six Degrees of Separation idea...
Interesting thoughts!

BRAINCHEESE said...

It's all One big, connected conscience out there... :-)

Linda D. in seattle

Shauna said...

I agree, you two. As I was thinking about this before writing, the 6 degrees thing kept coming to mind. but as you know by now, i think everything's connected.

S.

Blinders Off said...

I am with you about the MS support groups; I prefer my MS bloggers as my support group when I need a pick me up, laugh, or insight on the illness I live with.

From looking at my blog stat site, you can bet a silver dime researchers, pharmaceutical companies, and others are reading blogs of people who talk about their condition and medication.

Shauna said...

Blinders Off,
Good to know I'm not the only one. There is a time and place for any self help group and they are a life saver for some people.

Glad to hear your stat counter is showing interest from the big guys. Hope they come up with something.

S.

LISA EMRICH said...

Connections, connections. Absolutely.

I've found that if you mention a particular drug (product) or the company's name, then they monitoring club come out to read.

It'd be nice to think that they might take a germ of an idea and turn it into a cure or service for us MSers.

Also, MS Bloggers by far are my cup of tea. The 9 or 10 monthly 'newly-diagnosed' meetings I attended at my neurologist's office were very helpful. But I don't know that I'd want to make a habit of those types of groups now.

Online is the way to go.