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Posts Tagged ‘doctors’

This week I pretended I don’t have cancer. It was much like the first six months of being 16 and pregnant when I simply pretended I wasn’t pregnant (yes, really, six months for those of you who don’t know the story). You’d think I’d learn that ignoring something doesn’t make it go away. (And in that case I thank God every day he didn’t go away!) Well, this time it was just a week and there’s nothing I can do about it anyway, so why not ignore it?

It was an easy week to do it. It was my first week since finding the lump that I didn’t have even one doctor’s appointment! Work was crazy busy as usual so I was able to stay busy with that. And, even more distracting, a couple of my loved ones had serious issues of their own that I was distracted by and wanted to help in any way I could. I so prefer to focus on others than on me.

I am a fixer. I try everything I can to help solve everyone’s problems and just want to help make everyone happy. But I know I can only do so much. There are some things I can’t fix – both for others and myself. And some people don’t need my help or want me to fix things for them. Sometimes you just need to give them space to do their own thing and be confident they know you’re there if they need or want you. And there are some things only prayers, well wishes and positive vibes will help. These are all things I have to remind myself when I see those close to me in pain.

It was back to reality yesterday as I realized what day it was: exactly one month from when I found the first lump. I can’t believe it’s only been a month – it seems like a lifetime. Only two weeks until surgery, and so much to do before then. I expect to hear the results of the genetic test early this week, have an appointment with my GP for a vaccine and some other tests one day, and my pre-op another. Makes it a little harder to pretend it’s not happening…

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So it took me a little while to get past the fact that I hate all the options: frankly, they all suck. But since I have to (as Pete says) ‘choose life’ I have to pick one. And the doctors really weren’t much help. Well, at first it seemed pretty clear: mastectomy would be the best choice. Least chance for it to return, possibility of no radiation or chemo, best chance for a somewhat normal looking breast. Longer surgery and recovery process, more painful – but I can deal with that.

So last Tuesday, as we made our rounds, by the time we got to the reconstructive plastic surgeon, I was pretty convinced it was the right move. We waited over two hours to see him and then got about 10 minutes of his time (after the video), in which he threw me a curve ball: basically said that he could never make a breast as good as a real breast and that if it was him he’d do everything he could to save his real one and to try the lumpectomy first. What?!?!

I don’t know about you, but I wanted a really confident – cocky even – plastic surgeon who would tell me how beautiful I would be when this was all over and that I wouldn’t miss it at all. Ha! Not even close. So it pissed me off and I just wanted to forget the whole thing. Then I remembered that is not one of the options. Which pissed me off even more.

So I calmed down a bit on Wednesday, and on Thursday called my breast surgeon asking for a referral to a different reconstructive plastic surgeon. She was shocked. “But Dr. H is the best! We’ve never gotten one complaint about him and he’s the very best at breast reconstruction.” She assured me that she’d get another referral for me, but also asked if she could talk to Dr. H’s admin about it, as she was sure he’d want to talk to me again. I agreed, conceding everyone has a bad day.

Long story short, he called and we spoke for about 45 minutes. He was genuinely sorry we got off on the wrong foot, but he also wanted to be clear that he cannot perform miracles and only God can make a real breast. This will not be the same and I shouldn’t expect it to be. I probably won’t have any feeling in it. And while he will do a lift on the other side (should I be lucky and not have the gene and have to do a double), they won’t look the same. Yes, this sucks, but it’s also better than having one that is much smaller than the other from the radiation and also has a huge chunk taken out of it – nothing normal about that either!

I realize I’m being vain. That I shouldn’t worry about how it will look and only be concerned with my health. I’m sorry but I can’t help it – I plan to live and thrive after this and I want to be happy with myself too, and hopefully be able to stand looking at myself. I guess we’ll have to see about that part.

Anyway, after our talk I agreed to see him again – and that appointment was today. Tara joined me this time. He was very similar to before – all business and straight to the point, but I got it this time. We talked through the procedure, which will be the tissue expander option. Basically after the breast surgeon removes my breast, he’ll start to put me back together, inserting the tissue expander (like a balloon). Then over a couple of months I’ll go in periodically for saline injections. Once the skin has stretched enough, I’ll have another surgery to put the implant in. And then a few months later will be nipple reconstruction. And the lift on the other side so they somewhat match. Yes, a long road – let’s hope the lymph nodes are clean so we don’t have to add chemo or radiation!

So I am now scheduled for a double mastectomy on April 30. We scheduled for worst case scenario because it’s easier to take the time off and just do one if the gene test comes back negative than it would be to add the time. It’s so late in the month because I asked what was the latest I could safely push it off to because I need some time to get my head around it all, and to get things in order at home and work (although everyone is so supportive and has assured me all will be fine and not to worry about it).

I feel better this way. I have time, I can get things in order, I have a plan and know, for the most part, what’s going to happen. I know, I know, the best laid plans… but you can’t blame a girl for trying, right?

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Another perspective

To help me on this strange new journey I’ve been forced to take, my good friend Vicky took the time to share her own cancer story. I am sure you will be as inspired by her and her family’s strength and courage. She was just 19 and was giving birth to her baby when the cancer was discovered. Read more here: http://mycrazylife37.wordpress.com/2012/04/02/reflection

I am still in awe, and so thankful you are here today, Vicky! xoxo

 

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