Mammoversaries // Cancerversaries
Comments
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Thank you, EastCoast and Michelle, for your good wishes. It’s so true that this diagnosis makes you take a good look at your life and what’s important. Throughout this process I’ve turned my focus to my tiny grandson (he’ll be 2 next month) and my burning desire to see him grow up. The right thing for me to do has been to throw everything I can at this disease so I can do that. I didn’t need chemo but I had my radiation and now I’m taking my daily pill. I’ve made a commitment to go to a fitness class every day - no weight loss but I’m much stronger than I used to be.
BTW, I’m from the East Coast (Massachusetts) originally and my daughter is right now on her way back to the Midwest from Colorado, where she had been living for the past five years. I can’t wait to visit her in Oshkosh, Wisconsin, next month!
I haven’t been as active on this forum for quite a while as I’ve been busy with work but I do keep up on my Favorite Topics. The wise women here truly helped me through this entire experience!
MJ
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I was diagnosed with BC August 17, 2017. However, Friday, October 5th was the first anniversary of my BMX. I had been obtaining annual mammograms since
age 35. My mother had been diagnosed with BC at age 40. Her sister was also BC
survivor. All my prior screens had been clear expect for last year. After the
call back, ultrasound, and biopsy, it was confirmed, Stage 1. I was to have a
lumpectomy with radiation. However, BS requested an MRI and a second primary
tumor was found. I elected to have both breasts removed with reconstruction.
Genetic testing was negative for the BC genes. I recovered from my surgeries
and have long since returned to work and to my life as best as possible.
However, as I write today, I am sad. Sad about the extreme surgical treatment,
sad about the not knowing if it’s really over, sad when thinking about my young
daughter and what the future may hold. But I am glad I’m here to tell my story
and I am glad for this community. This is my first post, but I have received
much help and comfort from this site over the last year. Thanks.
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I understand Mia. The only thing that lessened the worry for me was the passage of time. I like to think that there’ll be medical breakthroughs for our daughters. For now I try to make the most of every day. That’s all we’re promised. Gentle hug to you.
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Thanks for the encouragement!
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I would actually have to dig through my appointment calendar to figure out when I had my mammogram or biopsy, and it was just this year! I guess I don't have the emotional markers for these kind of things. I do remember the surgery and re-excision dates, but only because they're easy ones: 7-11 and 8-8. Maybe because I had a different cancer ten years ago, I did my (mild) freaking out then, so this time my reaction was, "oh, okay, what's the next step?" And even with another cancer surgery last month, my reaction was the same, although the actual surgery scared me a little because it was a deep internal one. But I don't remember the diagnosis date without checking. It was all just things that had to be done, and get them over with. But then, it took me about 20 years to remember my hubby's birthday, so maybe I'm just bad at dates! 😈
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Mia, welcome to Breastcancer.org. Thank you for sharing your experience. Please visit my other thread, Uplifting and Lively Messages on the Hormonal forum. We discuss day to day living, hobbies, tips for moving forward after the active phase of treatment Looking forward to hearing from you.
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Three years down today. Hopefullymany more to go!
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LimnoGal, that is fantastic news! Thanks for sharing with us here
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congrats limnogal!
Farmerlucy, i agree with your post. Most seem to say that the passage of time helps. I also hope that there are breakthroughs for our daughters.
I had my BMX a year ago today. So I guess I can say 1 year NED. I came home on valentines day which was also my sons birthday. Some dates we just remember.
Going back to make the most of each day..this sounds a little silly but I will share anyway. I use my cell phone calendar for appts/events and the events are color coded. It's just an easier visual for me to keep me on track. Work hours in blue, appts in red etc. There sure was alot of red last year..anything related to BC was in red. Mammo, biopsy, surgery, chemo, labs, iron infusion, post op appts, scans etc. Everything. What a visual to see how this disease takes over your life. Yellow is my favorite color. So over the last few months I decided to add more 'yellow' while I can. Appreciate how I'm feeling today and enjoy time with loved ones. Dinner with family/ friends, yoga, occasional massage, vacation, cooking class etc..things that make me happy. When there is less yellow I make an effort to add some. I guess doing this keeps my spirits up and reminds me of what's important.
Wishing everyone many, many years of good health and "yellow" in your lives. Deb
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Congrats! My cancerversary will be easy for me to remember. I had my mastectomy on my birthday 2016😄🎂 So 3 years down for me as of Jan. When I had my surgery, the whole surgical team, Dr's, nurses, tech's, all sang Happy Birthday to me, as I was roiled into surgery😂.God bless'em!
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Congrats on everyone doing so well!!! It is strange how this diagnosis changes your life forever. I do not take every day for granted, and appreciate the smallest of gestures. Some non bc persons complain about where they live, what they have, who they date, yada yada yada. If they had to face their worst fears and come out the other side, they would live their lives more fully.
So, to each and every day well lived........
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Two years ago today I got the results of my biopsy. My surgeon was on vacation so his office faxed the results to my primary care physician’s office. He misread the results a bit - only saw the DCIS, not the IDC. I asked for and got a copy of the report and dissected it when I got home. It was a whirlwind after that - I saw my surgeon the day he got back (March 23), had my lumpectomy on March 31. I’m doing fine now - have. Been on anastrozole since July 2017 with minor SEs. Scheduled for my six-month mammo next month. It never stops!
MJ
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