I Want More than 5 years Is There a Chance?
Is this reasonable to try to expect? I'm still young, I want to live long enough to see my yougest daugher become sucessful in life or married. I want to be around for my other daughter who has been trying to get pregnant for 2 years, I want to see my grandaughters 8 & 9 go to college. Is this too much to ask? Five years just doesn't seem like such a great thing right now, espeicially coming into the 2nd year post mastectomy. i want to be like Betty White at 88 I am too young to just hope for 5 years or more
Barb
Comments
-
I'm working on year 6, honey.
tl
-
I don't think about it like that. I think every year we are closer to the cure...I will be here for it.
-
I think there's definitely a good chance!
Lane
-
Five years??? Why are you focusing on some crap you might have misunderstood in some magazine or article you read?? If you have a good Onc who knows what he is doing there is no reason, in my opinion, you should not have many more years than that! Now if you are refusing all the treatments and the Aromisans since you are ER+ PR+ then "you" may be cutting your changes for a longer survival. Focus on taking whatever you have to take and do to prolong your life and put your mine on living your life with your family. I don't know where they came up with this 5 years crap but they need to let people know we are in 2011 soon and if they can't do any better for us than 5 years "they" need to find researchers and Oncs who can! Don't program your mine or spirit on this 5 year stuff. Program yourself for MANY more years of survival and fight bc with every weapon you have given to you!
-
Barb...I made it 10 1/2 after initial dx and am over a year post mets dx and have no intention of being a 'statistic' in 2 years...YES - there is a VERY GOOD chance! The 5 year mark is a typical point where if you have not had a recurrence - the odds increase greatly that you may never have one. Live girl!
Hugs to you....LowRider
-
SherriG--I think you nailed it. BCO is a wonderful place but I think it's just a snap-shot of all BC survivors. I bet many if not most, esp once stablized, "move on" "move forward" so you wont hear about them.
Like I said, BCO is a great site, esp for those who have the need. But it's not the big picture of all survivors.
God Bless
-
Someone very close to me was Stage III with many more positive nodes than you have. She had the full boatload of treatments and is alive with no recurrence 14 years out.
-
Also remember that just because the stats say "alive and NED in 5 years" doesn't mean that those people don't go on to live 10+ years. It only means they stopped counting after 5 years not that people stopped living after 5 years.
When I first came here someone said "cancer does not know what stage it is." Seriously is there really that big a difference between your stage IIIA and my stage IIB?
Those stats can drive you crazy.
-
The way it was explained to me by my onc recently, is that the 5 year mark is the one to hopefully get past without a reccurance and then, as lowrider said, the odds greatly increase that you'll never have one.
We are all too young to just hope for 5 years!
I want to see my 14 year old son graduate from high school & find his passion. I want to see my 19 year old continue to find happiness. I want to sit on a porch with my husband in the tiny home we hope to have in the mountains some day and play our guitars until our old fingers are too feeble to press down the strings anymore then I want to just sit there and hold his hand.
I want ...
I keep getting more scared that it is not going to happen, so I understand how you are feeling.
-
Barb....Hugs to you....
Try not to put too much focus on the future or number of years...
Try not to waste your precious moment worrying about what may or may not happen in the future...
I know it's easier said than done but...
What would put smile on your face today?
Talking to your daughters? Lunching with friends? Movies? Shopping?
ENJOY YOUR DAY!!!! Yes it is "one day at a time"...
Thinking of you.
-
Personally I feel 10 years is bullsh*t too. At 49 yo 10 years is nothing. I'm going for 2-3x that amount.
-
They are making progress every day!! I plan on living until I die fighting all the way. Today is a lousy chemo day and I'm really feeling shitty,,,,know what, I'm going to shop online and plan for xmas and the future. Who knows? We could get hit by a bus tomorrow so I'm living in the moment.
Love,
Maureen
-
Thank You all, that's why I come here. It's like therapy... Sherri, sounds like you did awesome raising your kids. Bless you! I think right now I'm going to get busy making Christmas Cookies today
Barb
-
My boyfriend's aunt Evelyn was diagnosed in the late 1960s with Stage III bc. She was in her mid- 40s at the time. She had a mastectomy; no chemo, radiation, or tamoxifen/AIs. She's in her mid-eighties now and is still doing fine.
-
It's more than reasonable to expect to live much longer than 5 years. It's also very difficult at times because BC is such a sneaky disease, but try to focus on the positive, live in the here and now and enjoy your life. I'm 63 and was dx'd with stage 3A just over 2 years ago and am hoping for another 20 years!
-
Barb - just seeing your post.
You must have been having a bad day.......you know that we'll all be here years and years from now looking back on this time and thinking "wow, look how far we've come".
-
9 years in feb here...my friend is working on 11 years....stage 3c.
-
We all have those days-when it hits us and we get sooo scared---- Such a blessing we can come here and express our fears and have all these amazing women lift us up so we can go on!
With that said of course you can live more then 5 years. Rigt now your NO stage-you have NO cancer-and your free to live your life... Find a way to just live and be happy with the here and now. Noone knows what is going to happen in 5 years left alone 5 weeks. At some point you have to let go and move forward. Let go and live:)
-
I guess I'm one of the women that you want to hear from. I was Stage IIIB because my tumor was attached to the skin. I went to a new OB/GYN because we had moved. He did a biopsy which came out negative. 18 months and 3 mammograms later,I had dense breast from HRT, my nipple began to bleed from the biopsy sight. I was diagnosed in February 2002. I had a double mastectomy, 4 A/C and 4 Taxotere treatments and am still dancing with NED. I was on Arimidex for 5 years and am now 3 years into a clinical trial where I might be getting Femara or I might be getting a placebo. So it has actually been 10 1/2 years since I went to the doctor with a newly retracted nipple. It's great to be here!
-
Barb..not sure what you mean by 5 years!!! I was never told an expectancy.....I am coming up on 5 years from Dx in feb 2011...I want to live old as long as I have a good QOL....bc or not bc...QOL is the key thing....and I don't have plans on dying anytime soon.....
-
I am 7 1/2 years out from stage III ovarian cancer; was told I had a 50% chance of being alive in 3 years. I have every reason to believe that I will be just as successful with the BC.
There are many success stories out there.
-
I had a similar diagnosis to you Shanagirl - IDC 7.5cm, 1/11 nodes, ER/PR+, Her2 neg, Grade 1. I'm in my 8th year post-BC with no further problems. I was diagnosed on my 41st birthday. I want to make 90, at least! At the time of diagnosis, I thought I'd be lucky to make 50, but only one and a half years to go and I'll be half a century old....
I have read many other *success* stories. There's no reason to suppose that you won't be one too.
Mel
-
I think I know why I've had this fear on my mind. Last January I had my first anual mammo after the surgeries and treatments. I must be very triggered this time of year which brings up a lot for me. I found my lump in Dec 2008 diagnosed a few weeks later in Jan 2009 followed by unilateral mastectomy on left side and immediate reconstruction with free tram. The nightmare began at this time of year and now I'm constantly thinking about the mammo in January. I hate the thought of having to still go for this, especially knowing the micro calcs are there. I guess I'm just expecting the other shoe to drop.
Barb
-
^ Yup.
I think that (worry) will always be with us.
-
Barb- I understand your fears coming to the surface this time of year. Holidays bring a lot of issues up and for you this time of year reminds you of what you were doing the year you were diagnosed.
I can tell you that on January 22nd it will be 5 years for me and so far so good. I had 6 pos. nodes, grade 3 and extracapsular extension. I also felt that anxiety around the January date since my followup tests were all during that month. I finally decided to change that and made my mammo for December. This way it's out of the way. I think the lead up to the checkups take a big toll on many of us.
-
hey, Shanna.. plan ahead.. for next yr. get your testing done a lit bit earlier, to miss the dreaded anniversarry mark.. or go wild.. if all is well, get them done after the holidays. i rearranged my testing till my GD was born last yr. Dec. 28th. am changing to 1st of 2o11; to not mess up the holidays. i plan on being here, doing the best i can with QOL..thats' imp to me, but on the MS side.. the BC side is always a little scared, but i know i'll keep fighting, if, and when, if i have to. i have a friend 12 yrs out, with mets just about everywhere... and she has a good QOL. goes to chemo for 6 wks. off 2 mos, then does chemo again, they rotate the drugs on her. she's an inspiration; and she lives a pretty full life. more than i do, with MS. so, don't even Think that way.. we all ahve our scared days, our days wehen we worry, but when we live our lives as fully as we can, thats' the key.. IMHO... 3jays
-
3jayasmom - Tell me more about your friend....I could use some inspiration.
-
My sister was stage 3 and she is working on her fifth year now......It was 4 years this past August for her and she is doing fabulously!........Remember, we are not statistics!........We are human and not one of us has an expiration date stamped on the bottom of our feet!.........
-
Don't worry about numbers, and remember these are just basic statistics. As someone with BC and working in medical research, numbers change. My sister is 5 year survivor and I have two maternal aunts that are 30 and 35 year BC survivors. Live each day as full as possible and don't stress the little stuff. We are all survivors in this war!!
Cheryl
-
I agree with everyone else. Don't focus on the numbers. Enjoy your life.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team