Too Much Trouble

So, I decided to look into reconstruction again. First I called the Breast Center. They won't give me an appointment till I get all my paperwork in. I filled out a health history and sent it in. Then they wanted all the medical reports. Seems strange to me that they don't request them themselves, but OK. I had to call to get a few I was missing.

Then the financial lady called. She ran my insurance. I have a 2500 deductible for out of network, and then it pays 50%, The total cost of the three phases of this surgery is over 100K. Now I am no math whiz, so she told me that my share of the first phase would be 30K.

She did say they have financial aid, and payment plans, and don't worry we'll get you set up.

Meanwhile, when I called my surgeon's office to request a report, the person I talked to told me about another plastic surgeon who IS in network, and does this procedure, and works with my surgeon (who would do the mastectomy). So we're looking at $55 copay vs 30-30K, less whatever "financial aid" is available and plus finance charges, what to do, what to do.

I called the network guy to set up a consult. After 30 minutes shuffled around on hold, I decided to let my doctors office do it for me today. She also got shuffled around on hold, was able to give them my insurance info but finally was told that the ONE person who makes the appointments for 10 doctors in 4 different towns was, and I quote, "BUSY".

(Ya THINK????!?!??!?!)

So now I get to wait for a phone call, it's been 3 hours already and of course I can't leave my phone in case I miss it. Hooray!

Also the local office only sees people on Friday. I happen to be busy for the next few Fridays. I can do it THIS Friday, but next I will be doing GS day camp, the next I will be at college orientation for #2, the one after that would be OK, then the next is Cub Scout Day camp which I am directing and it's my big week.

Then it will be July. I wanted to actually HAVE the surgery in July, so that I would be recovered in time to take my kid to college in September and work in the concession stand and all the stuff I want to do. It's not going to be convenient, any later than July.

I'm not saying I want to forget it, but I wonder. I wonder if it's really worth all this trouble when what I really want to do is just LIVE. Do I really need it? I don't want to wait till next year because then it will cost an extra $2500, but do I really want to worry about that amount of money when the alternative was 30-50K?

Seriously, I just want to get on with my life!! I am so tired of all the BS and hoops. I just want to live my life. WHy is that so complicated.

Raising Awareness

We're all painfully aware of breast cancer - me, because I have it; my friends, because I have it; the world, because pink has taken it over. Even before I was diagnosed the pinkness bothered me. Where is the awareness for other things? I will do my part to try to spread some.


MELANOMA


It has really started to bother me when I hear people talking about tanning. I admit to being a sun worshiper when I was younger. I had dark olive skin back then, which is hard to believe now. My skin has changed and I am more fair. Back then, I would take a long time to get a burn. It would be red and painful for the evening and turn to tan by the next day. It was pretty painless for me so I really never wore sunscreen. In fact, the "thing" to use back then was a product by Hawaiian Tropic - the dark bottle of oil that had NO sun protection at all! Man, did that stuff smell awesome. It's what the cool beach bunnies wore! If I didn't have enough money for the oil, I would use plain baby oil. Hard to believe now! Can you even still buy that no-SPF oil?? OMG, you can! I would think there would at least be a warning on the page, but there isn't!

When my kids were little they were just coming out with things like SPF swim shirts. I would watch the kids in those and scoff in my head. Now I'm not so sure. I would always put on a plain T-shirt if I was getting too much sun, and it seemed to help. Sun shirts are really out of my financial reach, especially since it sounds like they have to be replaced often. Here is an article on the topic.

And now, here is a video made by real people (not actors) to increase awareness of melanoma. It's what they wish they had known at 16...realistically, I can't imagine listening to something like this at age 16. Heeding it, I mean. Aren't we all above this stuff? But that's why it's so important to spread the message. Now that it's spring, I can't tell you how many people my age - 48 - are posting about going tanning, whether at the beach or the tanning bed. Tanning beds are NOT safer than the sun. If anyone says anything, they do what I would have done - scoff. Cancer? That's what happens to OTHER people. Please watch this video, and consider sharing it on your own Facebook page. It is a powerful video and a powerful message, made by the very people who thought it would only happen to somebody else.



Now the obvious answer seems to be - SUNSCREEN. But not so fast - there are issues with that, too. Read this article and see. There is a place on that link where you can type in your own sunscreen and see how it rates.

I have a friend who buys special sunscreen for $65 a gallon, but it isn't perfect, either. it needs to be re-applied often and stays white on the skin. Not too likely a teenager will be willing to do either of those.

I think the better answer - as with anything - is balance. Find a sunscreen on that list that is lower risk, and USE IT whenever you are in the sun.

One thing I noted for myself is the danger of sprays (when inhaled). We usually buy spray because it at least seems easier (even though it really isn't). I will now stop buying sprays. Lotion is easier, and it also won't bother anyone sitting nearby.

We can not avoid all dangers. Life itself is the only risk factor that is common in all death and disease! But we can continue to do the things we love, and be smarter doing them.

Giving Blood

Over the years I have given blood. Not really all that often. There was often some medical thing keeping my blood from being desirable, like anemia and thyroid medication. But I gave it when I could. I just found out that I will not be able to donate blood ever again. I may or may not be able to donate my organs - something I feel very strongly about doing - it will depend on which organ and how long it's been since chemo and some other things. But that's OK. Because now, according to the article, there is a great way for all you guys who say "I wish I lived closer so I could help" to help. Go donate your own blood! It said you could do it in my name, I don't know if that was literal or figurative and what the point would be. Just donate blood, and think of me when you do. Edit: on further searching it looks like maybe I will be able to. http://www.kantrowitz.com/cancerpoints/donatingblood.html But it will still be at least 5 years till I can, so still, go donate! :)