« A solution in search of a problem? | Main | New Favorite Recipes »

Excuse me while I go on a rant...

Can I just say, I HATE THE STATE OF HEALTHCARE in this nation. Contintent. World.

Whatever.

Now, before you start jumping down my throat about the upcoming rant, I offer the following caveats:
a) I know that healthcare in other countries is probably not any better than that in the US. Different yes, but probably no better or worse.
b) I have not done any research to back up my claims. So if I get something wrong? 1) not surprising and 2) I don't care. (For the moment, at any rate.)
c) I might use some nasty words.... You've been forwarned.

The phone rang midmorning today and on the other end of the line was a representative of my State Farm insurance agent calling to tell me that, surprise! They hadn't yet managed to sell me any life insurance! I knew this, already, and had made the decision, consciously, not to purchase any, so I wasn't sure why she thought calling me was a good idea, but I listened patiently while she went through her spiel.

When she was through, I politely told her that, at the moment, I had life insurance and accidental death & dismemberment (that word gives me the willies...) through my employer but thank you anyway. Oh, and by the way, what are their long-term care policies like?

Well, she told me cheerfully, we can sell you one of those!

And then, knowing full well that she couldn't sell me one, I mentioned my MS and asked if she could still sell me one. Well, she'd have to check on that, she said. So we hung up and I forgot about the conversation entirely. She called me back later this afternoon with the news that, Oops! Sorry, no can do!

Now, let me just say: this came as ZERO surprise. I was pretty sure she'd come back with that answer. But I was not prepared for the wave of anger that washed over me after I hung up the phone.

Not anger at her, of course - I'm sure she would have sold me anything I wanted to buy if she could have. No, it was anger at the whole fucking system that makes it so that the people who freaking need it the most cannot get coverage of any kind. I understand the way things work - the better health you're in, the less likely the insurance company is to have to pay out a bunch of money to care for you, and the happier they are to take your yearly premiums. I get that.

My frustration with it should be obvious: IT'S JUST NOT FAIR. (And yeah, I know. Life's not fair.) I understand the thinking behind it, but what just seems completely wrong is that there are no affordable, useful options for the people who are NOT in perfect health. This is the way it is with life insurance, health insurance, long-term care insurance, every kind of insurance that might help people feel more secure about having a permanent disease.

And what's even worse is that the people with these life-long, incurable illnesses typically are spending much more money on healthcare anyway, and yet they're charged MORE than the 100% healthy person. It's no freaking wonder that healthcare costs so much: the people who need it the most can't get covered and if they can, they must pay through the nose for subpar coverage that basically covers you for acute problems.

It just isn't fair right, and it seems to me that something ought to be done about it. The problem is, I don't know what can be done about it. But I do know this: I'm going to start looking into how I can help change things. Because somebody's got to.

GARRRRRRRRRGHHHHHHHHHHHHHHHHHHH!!!!!!!!!!!

Comments

We need to put it at the TOP of the agenda when it comes to who we vote for. I'm tired of politicians who can vote to fund a war but can't vote to fund healthcare.

XO,
ACJ

And just to throw some "gas" on your burning fire...you CAN'T donate blood again...ever...for the rest of your life!

I'll bet if somebody was bleeding out and needed a quart, they wouldn't really CARE if I had MS or not!

Linda D. fanning your fire in Seattle

You go girl, change the system!

US or Canada, the issues with insurance are the same here. I'm not leaving my current job because I know the minute I do, I will never be able to have LTD coverage again. I'm "pre-existing" now. So nice to be labelled isn't it. So, I'm stuck. I know I'll have another attack at some point with my disease, so I need the coverage, but maybe I would like a different job. And round and round we go.


"I could have me a million more friends, and all I'd have to lose is my point of view."

~John Prine

My Multiple Sclerosis Diagnosis

On June 23, 2006, I was diagnosed with Multiple Sclerosis. Among other topics, this blog is devoted to my ongoing experience with the disease.

Pharmaceuticals

Shortly after my MS diagnosis, I began taking Avonex. Although I managed to mitigate the "flu-like" side effects, for the most part, the drug unfortunately seemed to exacerbate my clinical depression.

So, on July 19, 2007 I switched to Copaxone.The Copaxone worked quite well for a couple months - except for some minor issues with injection-site reactions - and I felt much better.

Unfortunately, the Copaxone also exacerbated my depression. So I met with my psychiatrist to find a mix of anti-depressants that would counteract the debilitating depression I experienced. After spending most of December 2007 in a complete funk and - some days - being totally unable to leave the house, I finally stopped taking the Copaxone on my own. I immediately began to feel better and with some help from my primary care doc - who discovered I also had a mild case of hypothyroidism - I started to feel like myself again.

On May 16, 2008, I had my first infusion of Tysabri. With the exception of some anxiety issues, I've had no trouble with it so far. Still, it's early and the jury is still out... stay tuned for ongoing updates!

MS Blogs & Websites

Portland and Northwest-area MS Resources

MS Resources



Subscribe!





Search

Creative Commons License
This weblog is licensed under a Creative Commons License.
Powered by
Movable Type 3.2

Powered by FeedBurner