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Archive for the ‘Cancer’ Category

The other night I was at a family party, laughing and eating and chatting away with everyone, when another guest arrived. She walked slowly, tentatively as if it hurt to move. She wore a heavy coat even though it’s August because she gets chilled so easily. And her face was pale, with sunken eyes. I heard one of her relatives whispering about her having just taken a Compazine to try to calm the nausea. 

A feeling of nausea suddenly rushed over me – it brought me right back to one year ago. Getting poked repeatedly to try to find a decent vein for the IV before we gave up and had the port put in. Feeling sick on the way to the hospital just because I knew what was coming. Sitting in the big comfy infusion chair, wrapped in heated blankets. Trying to smile and laugh as my family and friends tried to distract me and keep my spirits up, as the poison rushed through my veins. Feeling loopy on the ride home – and then sick for days.

I am so lucky. That was a short period in time for me – and every day it gets buried further in my past and becomes a smaller percentage of my overall life. This woman – as so many others – is not so lucky. It’s too late, they explained to me after she left. They’ve done all they can but it’s spread so much there’s nothing else they can do, except try to keep her comfortable. My heart ached for her and her family. And my mind raced, repeatedly thanking God for letting me find that lump when I did, and for being able to stop the cancer in its tracks.

I am scared all the time. I, like many survivors I know, see Tamoxifen as my wonder drug. As long as I’m on it, it will ward off the recurrence. I should be safe. But what then? There is no telling. A lot can happen in a few years – particularly in research and development. Maybe by then they will be able to not only detect earlier, but prevent – and cure. So I have hope.

It all takes money, though. This is why I’m doing the Jimmy Fund Boston Marathon Walk on Sunday, September 8. I want to do everything I can to stop this monster of a disease. Please join our team – Team Inspire Boston – and walk with us, or sponsor me. You can walk 3 miles, 5 miles, 13.1 miles or the full marathon: 26.2 miles. No matter what you decide – to walk or sponsor us (and no amount is too small – every cent counts!) – you will be helping to kick cancer and helping people like me (and maybe you) live a longer, happier life. Thank you.

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Wandering the North End tonight, we discovered that a Pinkberry – my favorite yogurt place – just opened on Hanover St., diagonal from Mike’s Pastry. Not being able to resist, we joined the line.

When it was my turn, I asked to try cherry, since it’s one flavor I haven’t sampled. As I tasted it, the girl behind the counter kept looking and smiling at me. ‘I just love your curls,’ she finally said. That, of course, caused a huge stupid grin to appear on my face. ‘Thank you so much!’ I exclaimed.

My perma-grin lasted as we got our treats and headed out the door. I turned to Chris and asked, ‘Do you think she knows I had cancer? That she knows I was bald and this is new hair and she’s just being nice?’

‘No,’ he assured me. ‘How could she tell? She just likes your hair. It’s beautiful. No one can tell.’

And that just made my night. Maybe my week. So the next time you see a stranger – or someone you know, doesn’t matter – and you like their hair or their shoes or their dog or their super polite children, tell them. Smile and say it. I bet you’ll make their day.

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One year ago today I shaved my head. So many other things were happening – I was moving, I had just started chemo, my relationship was ending, I fell and fractured my arm and bruised my knee – and then my hair started to fall out, so I shaved it. I remember the day so well; thinking about it makes me feel like I’m reliving it. (It all really hurt, some mentally and some physically, so I’m not going to spend much time thinking about it or rehashing it here.) But then in other ways, it feels like it was a lifetime ago. Sometimes I’m amazed at all that happened in the span of a year!

Last night, I took a break from unpacking (yep, I moved again!) and Tina and I went to see Tim McGraw at the Comcast Center. And of course he sang Live Like You Were Dying. Just as last year when I saw him perform it live at Gillette, it wrecked me. As I listened to the words (and cried my eyes out), I thought. Have I lived like I was dying? I know that was my original intention, but what have I really done in this past year? The first thing that jumped in my head was “survived.” I have survived the year. I fought through the year. I struggled to remain some semblance of normalcy through the 24 weeks of chemo and six weeks of radiation. I bought any beauty product that I thought might make me look more normal while bald. I tried to keep everything going even when I felt like just going to sleep.

I didn’t go sky diving. I haven’t been mountain climbing or bull riding since my road trip in 2010. I’ve tried to stay close to my friends and family, but I haven’t seen or talked to them nearly as much as I would like or feel I should. In fact, my life has seemingly resumed its normal chaos, pace and craziness. Maybe that’s not a good thing. Maybe it’s time to change that.

The problem is, there simply is not enough time in any day, not enough days in a week, not enough… well, you get it. There are so many things I want to do and never, ever enough time to do it. So maybe what that song means is not just that I have to rush to do all the things I want to do (in case I die tomorrow), but to take the time to do the things that really matter. To spend what precious time you do have wisely. I need to think about that. And I will. But for right now I am happy and thankful. Happy and thankful to have hair again, to be settling into my new apartment, to have a job I love, and family and friends who mean the world to me. And that I don’t have to go through chemo this summer and remember to put lotion or a hat on my bald head!

Tim2013

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