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Vital Info


MIchelle (michelle67)


April 1, 2011


near Philly, Pennsylvania


February 28, 1967


Cancer Survivor

Cancer Info


Breast Cancer


Infiltrating Ductal Carcinoma & Ductal Carcinoma In Situ


November 30, 2010


Stage 1


02


Grade 3


Negative


Negative


No


No


Re-excision Surgery, Lymph Node Removal, Lumpectomy


Cyclophosphamide (Cytoxan)


That it makes my kids afraid for me. How it altered me and my life forever. The fact that I'll always be looking over my shoulder for it.


To make the most of every moment with my 2 young daughters. That I deserve to be happy every day.


Don't be afraid to laugh with me. I am still the same person, but my perspective has been altered.


No


Rena Rowan Breast Center at University of Pennsylvania, Philadelphia


Hydrate during chemo, with water and Gatorade.


Stats


Posts: 29
Photos: 5
Events: 6
My Supporters: 61
I Support: 79
Comments: 338
Views: 17825
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MIchelle's Cancer Blog

New year, new opportunity

Nearly a month into 2012 and this is my first BFAC post of the new year. I’ve been checking in often but have been unable to update because I’ve been so busy – and I’m happy to say not busy with cancer (fingers crossed).

I’m working a lot (maybe too much) writing for various newspapers and magazines, and recently volunteered for a breast cancer organization (not the pink ribbon one!). I helped beta-test some new website and app software that it is readying to help patients learn about their illness, treatment options, etc. and connect with each other. Basically, I was a random user testing to see how well people can use this new technology to access cancer info and other patients, much like we do here on BFAC.

Through this process, I talked with the great folks who work for it, and we chatted about how I’ve been changed by my experience; how my 20 years as a journalist shaped my behavior as a cancer patient; and the emotional fallout after treatment ends. I’m still grappling with this, and am surprised by what a roller coaster ride it can be. They were very understanding and interested, which was nice.

Long story short: I’ve been asked to write a blog for them, detailing the post-treatment phase, which they recognize has been under-reported, under-emphasized, and generally downplayed across the board. Stuff like the side/after-effects, the PTSD, the loss of support, the insanely horrible things people (hopefully unintentionally) say to us, & the fact that sometimes cancer offers gifts that seem incredible, unexpected and so unlikely.

I’m excited to be able to do this, because it gives me a way to try to give back, to help other people, even if it is just my personal story. I’m grateful and nervous and excited all at once.

I also take this as a sign that I am finding the path I’ve hoped to find ever since cancer sent me into a tailspin. All through chemo and rads I realized I was in the right profession because, even as docs and techs were sticking me and scaring me with stats and making me wait for my results, I kept thinking “people should know this stuff!” or “how is this not out there? why do we not know about this kind of cancer, this insurance issue, this lack of medication?”

I wanted to write about it, to get it out there, to help – and now I hope to have a chance to do that. The added bonus is that writing helps me too.

I’m not looking for praise, just wanted to tell my BFAC family about it because I hope you’ll be able to appreciate and understand. It strikes me that this is a way to tell all the stories that cancer makes—the way you were walking down one road in life and suddenly, without warning, you were put on a totally different, alien road – without a map or GPS - and asked to find your way…to an unknown destination.

I’m no scientist, doctor, or nurse. I can’t knit hats for chemo patients. I sure don’t have a lot of money to donate. Words are my skill to give back, my calling (and more than once I have wondered why couldn’t I have been good at math?!).

I’ve built a career with words, but now it is more than just reporting or informing, its also about compassion, support, education, humanity.

Actually, this may be the most important writing assignment I’ve ever been given, and I can’t wait to get started.

3 people like this.

Good Luck, it beats the hell out of sitting around worrying about cancer. Be Happy.

Michelle, I’m glad you’ve found your niche. : ) And you’re right..so much more information needs to be available. I was handed a folder of info about breast cancer from my one doc, and that was it. It wasn’t very helpful to be honest. Most of my info came from the internet. The “after” is important…I know I still have feelings in my head that non-survivors don’t have…and no one understands those thoughts. except my fellow survivors. it’d have been nice to read something and be like “oh YES…that’s ME…that’s how I feel!”

I’m so happy for you…you’ve made it through! I hope I can read your work someday!

Congrats!

What a lovely invitation for you to go blogging, MIchelle.
Don’t you get the feeling you’re exactly where you’re supposed to be, doing exactly what you’re supposed to be doing? ...That’s how I feel about being a BFAC blogger.

We certainly do need more descriptive “Users Manual”s for all the Active Duty and Veteran cancer warriors. Sure we may get chapter outlines, but we’re left to fill in all the detail on our own. And we never know when there’s going to be a pop quiz. ...Gasp, what if we fail? Is that even possible?
Sounds like you’re going to have a wonderful new project to love. A new cancer warrior quest, in full radiant MIchelle armor.
Hugs to you, Nicole

That is such great news Michelle and I wish you the best. I have always enjoyed your writing here on this site. I hope you continue to find your way and happiness in this new year.

Congrats! That’s so cool! I agree with you entirely about what cancer patients experience after treatment. I was told all the possible side-effects of a transplant, but my docs said some of them were done by companies to keep themselves from being sued in case some were to occur. I love how once something awful is experienced, the “victim” helps others who may experience it! I know you are going to love what you do now, so again, congrats! And have a great New Year! :D

Congratulations and good luck. I hope this gets to a lot of people. I cannot express how much this site has helped me and if your blog does even a fraction of that it will be a huge success.

If I could write about one aspect that many people might not immediately jump to, it would be how to explain the idea that if you do not have cancer, to some degree you do not fully understand what it is like for those who do. I never was much for that type of idea, saying “you don’t get it unless you are me” type of things, but when I got diagnosed I started to understand. That does not mean your support system cannot be sympathetic and helpful, but people here would write things that just showed how they “got it” on a fundamental, subtle level. Trying to explain this to my wife was not easy, and despite my best efforts may have been a bit insulting. Maybe you, as a career writer, can expand on such subtle, hard to understand concepts and help both the fighters and their supporters understand how hard this is.

I hope your assignment is helpful to you as well as others. I look forward to reading some of it if you can share.
Cheers

Congrats on finding your new direction. If I can ever get healthy enough to work again I can only hope to be so lucky.

TJ

OD@aT

Good for you! This seems perfect for you!
I blog a bit on the Caringbridge website. I am amazed what comes out sometimes. I did not even know I felt that way about cancer and when you start writing deep feelings JUST come out! I would never say those things out loud, so in short my little knowledge on blogging has led me to share feeling that I would not have otherwise done and lets others know what is going on with my treatment without sending out constant emails. Good Luck!

Hi Michelle,
I just wanted to see what you are up to. A LOT! Good for you. I have more to say but am tired as I’ve read others’ stories and blogs (is that redundant?)
I will try to catch up later this week to discuss your writings. :O
Prayers and hugs (and KUDOS)
Carol

Brilliant news. I think it helps to make sense of it all when you can use your experience to help someone else. Good luck for the check-up xx

So happy to hear you are back doing what you love and what you are so good at…crazy as it might sound but the “goodness” of your tango with cancer is what you can write about….a nurse once told me that a healthy mind will find good out of a horrible situation or event. You sure are seem to have made that leap and yo are so right information is lacking and sites like these help spread the word.

Totally off the topic, my girlfriend brought over the new Gary Newman and it is excellent….I also bought tickets to go see English Beat in April. Who knew they’d still be touring.

Well, like someone posted below, be happy!

Love, love, love it! I think it’s a perfect assignment for you. I know you will do very well. I am fortunate to have been asked to write a little and now I too, feel a sort of obligation to my community to raise awareness whenever I can. I just received another offer to do an interview for a cancer research website, so I’m excited to get started. I hope you’ll post a link so we can see what you are writing, I really love to read your posts.
Champagne time!
xoxo

This is for You!

I guess holidays make everyone think of the past, those special days gone by, and those of us who’ve gone through cancer can look back with longing, gratitude, such a mix of emotions.

Today is Christmas Eve and last year on this day, I was facing my first-ever Christmas with cancer. Everything was so upside-down. I put on a brave face for my loved ones, especially my daughters who were only 10 and 6 at the time, but my moments alone were dark, scary and included a lot of tears. I remember my hands shook at times & I’d never seen myself react like that for any reason. My reactions confused even me. It was disconcerting to say the least.

This year I feel so much stronger, smarter, more peaceful even as I deal with the fallout that comes when treatment ends. I resolve to take time off from worry, to not let cancer ruin this Christmas – not just for my kids or husband or mother, but for ME. I’m going to enjoy it despite stupid cancer.

I am also compelled to post this update because I must write about how valued, how important, how amazing the people on this site are – all of you!

I didn’t find BFAC until I was halfway through chemo, back in April of this year, but I have found an understanding and compassion that could come from nowhere else. At times I take strength from your words, your prayers, your personal triumphs. I worry about you, think of you, send wishes and healing in your directions. I breathe sighs of relief when good news is announced, I wish I could really hug you, I want so badly to kick some ass on your behalfs at times. ;)

To each one of you I say Happy Holidays! I am so glad you’re here.

Bill Curry, Texas Jeff like this.
8 people sent you a hug.

And we are all thankful that you are here with and for us. Have a Merry Christmas—you and all your important loved ones. It’s very good revenge against stupid cancer.

You deserve a giant, smooshy- cheek kiss for that! (where’s that button?)
xoxo

What an amazing post. You said everything…much more eloquently than I could. I am also so thankful for this site. Last year, I was recovering from my last chemo…..this year so much better! Hugs.

Well said and so true. Even though it’s online this site and people on it has been such a great support for me. So happy holiday’s to you and your family as well.

MIchelle, What a wonderful gift your post is! You’ve fought hard to make this year for you, not stupid cancer.
Thank you for sharing this for all the awesome cancer warriors on this BFAC site. I’m thankful everyday that I found this space, even though it wasn’t until after I’d completed treatments.
Like you I wish I could actually hug bloggers; so I imagine that I am, every time I click the “Hug” button. And I love Debbie’s idea of a smooshy kiss-on-the-cheek button! ...I’m clicking that one right now.
Holiday Hugs to you and your family, Nicole

Yes stupid cancer

You are a strong lady, MIchelle!

Michelle,
As this being my first year going through cancer at Chrismas with 3 children, I can totally relate to your post. I can thank you for your support to me as well as everyone on BFAC. This is an amazing site and you have said it all. Happy New Year!

Thanks for your post. I am currently in the place you were last year – and have had all of those same emotions. Knowing that you are much more peaceful and happy in your 2nd year – gives me hope and comfort that things will look brighter once done with treatment.

Thanks for this Michelle!

I hope this Christmas was much less stressful than last year. Wishing you health and happiness in 2012! Take care.







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