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Archive for the ‘family’ Category

(Reluctantly) Reentering the Cancer World

Posted in Boston, Cancer, connections, family, Fundraising, hair, recovery, work, tagged , , , , , , , , , , , , , on September 17, 2013| Leave a Comment »

Sometimes I forget. It’s actually getting so that I think about cancer less and less. By this I mean it only pops in my mind a few times a day rather than every few minutes, but still. It’s progress. But in the last week or so there have been more and more reminders:

  • Before the walk and trip, I had an appointment with Dr. H. Luckily, my tissues have relaxed and we are finally able to schedule the implant surgery! It’s looking like December. I am so looking forward to not being rock hard and feeling like a freak any more…
  • A dear friend of mine, who has been so supportive and encouraging through my journey, had a double mastectomy. Rest up and feel better, Jillian!
  • And multiple friends had family members or friends die of cancer. Every day I am so thankful mine was caught so early, and that there are treatments for my type. I know I am so blessed…

And it’s because I am so thankful that I want to do all I can to support others in their cancer journey. While most of the time I’d like to erase it from my mind and pretend it never happened, any time retelling my experience or even just supporting things like walks, can help someone else, count me in! And the month of pink is quickly approaching – in fact, events are starting this month:

  • This Thursday, Sept. 19, 7 p.m. is the Bright Pink Experiential Outreach – Enjoy light bites at  Joe’s American Bar and Grill, Newbury St., Boston, while connecting with other Bright Pink women in your community to discuss mutual experiences. This event is open specifically to high-risk individuals. If you have any questions or to RSVP contact Community@BeBrightPink.org.
  • Sunday, Sept. 29, 9 a.m. is Komen Race for the Cure 5k Walk/Run  in South Boston. It is so much fun – so much pink! 🙂 I’m excited not to be bald for the walk this year! 🙂 Oh – and for a couple more days there is a half off deal for registration on Living Social.
  • Sunday Sept. 29, Nashua, NH, Harley-Davidson Second Annual Save Second Base Ride for Breast Cancer. No, I’m not riding in this but encourage anyone with a bike to do it! Info: http://www.nashuahd.com
  • Thursday, Oct. 3, 7 p.m., Revere Hotel, Boston: Runway for Recovery, a fashion show, silent auction and raffle to benefit families who have lost mothers to breast cancer. I’ll be volunteering with some friends from Genzyme, but you should attend and enjoy the evening!
  • Sunday, Oct. 6, 8 a.m., Hatch Shell, Boston: Making Strides Against Breast Cancer Walk I’m really looking forward to doing this walk for the first time – the American Cancer Society helps so many people every day, and certainly helped make my experience better…
  • Sunday, Oct. 6, 11 a.m., Worcester Run Like an Antelope: The 2nd Annual Memorial 5K and 1-Mile Fun Walk in Memory of Megan Proceeds go to Metastatic Breast Cancer Research conducted at UMASS Medical School. I am hoping to make it over to this after the walk, if at all possible!
  • Sunday, October 13, 10:15 a.m., Providence, RI – Gloria Gemma Foundation Pink Pump Palooza, 5K Run/Walk and 10K Run – join Alicia and me on the Pink Pumps for a Cure Team or sponsor us! And hey, it starts and ends at Providence Place, so you can get some good shopping in after…
  • Friday, Oct. 18, 8 a.m., Lucca Boston: Breast Cancer in Young Women Forum for Patients and Survivors (A great day, no matter where you are in your cancer journey – and I will be speaking on the patient panel! And Dr. H will be talking at this event, too, so if you need a fabulous reconstruction surgeon…)
  • Saturday, Oct. 19, 4 p.m. Nashua Harley-Davidson Fashion Show and Live Auction – this is organized and run by my friend Robin and it’s one of my FAVORITE events of the year – so much fun! Fun Harley-Davidson Pink Fashion Show, live auction, huge raffle, great BBQ – and I think I’ll even be getting my first tattoo (a survivors ribbon) at the event. Who wouldn’t want to go witness that? LOL!

I’ll try to keep the event list on the right as up-to-date as possible, but never hesitate to e-mail me if you have any questions. Hope you can join us for some (or all) of these great events. Hey, if we have to be in the world of cancer, at least we can be there together, support each other, learn from each other, make each other laugh and smile – and wear pink! 😉

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Flashback

Posted in Boston, Cancer, chemotherapy, family, Fundraising, prayer, recovery, tagged , , , , , , , , , , , on August 18, 2013| 2 Comments »

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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What a Difference a Year Makes

Posted in Boston, Cancer, chemotherapy, family, hair, Planning, radiation, recovery, tagged , , , , , , , , , on July 1, 2013| 2 Comments »

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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