5 year survivors, post your screen name here!
Comments
-
5 Years from diagnosis ~ Stage 2 IDC
-
congrats Alice
-
CONGRATS to all of you!!! Nothing like getting a jolt of true inspiration on this thread! What a joy to hear from all of you!
-
Congratulations on five years JustmeAlicia:)
Happy birthday Sandie! Hope you enjoy the movie - sounds way too scary for me!
x x
-
Ladies
I am six years out today-- after lumpectomy, chemo and radiation-- 5 years of hormonals--- feeling great---and really don't think of bc that much--- I get an annual mammogram and an MRI every other year---- healthy, happy- healthy kids and h, good job--- it all did work out---- I think of myself as someone who "had" cancer, but does not have it any more. I consider myself cured. If you are at the beginning or slogging through the middle of treatment, I want you to know it does come to an end. Life will go on--other things will happen and cancer will recede.
I was dx with papillary thyroid cancer this summer and ironically, having had bc really helped me cope with that dx--- thankfully very curable but still scary---- so, the experience was worth something. Having bc also made me a much greater medical advocate for myself and my family and a critical thinker about how much treatment/searching/surveillance is appropriate for me. I question everything now and do not agree quickly and really try to pick medical professionals who are good at what they do and are also compassionate.
Hang in there--- it does get better.
-
Hey Alicia!
-
nice to see some faces i havnt seen in a while
Congrats to all
I think I'm in shock that I made it....It was a ruff ride.
-
Hola - I passed the five year mark on Oct 19! I'm doing great, and am thankful for every day!!
-
Congratulations lovetosail. May the wind forever be in your sails:)
x x
-
Many congrats to Love2sail and momof2kids on your five and six year milestones, we are delighted for you both.
Big hugs to you both, from the mods
-
TODAY IS FIVE YEARS FROM MY LAST RADIATION & MY 1ST FEMARA PILL. TODAY IS MY LAST VISIT TO MY ONCOLOGIST & MY LAST FEMARA PILL!!!! I AM SOOOOOOOOOOOOOOOOOO HAPPY!
-
Happy Dance for you Eph3_12!
-
Joining in that happy dance for Eph3_12!!! Congrats!!!!
-
I was first diagnosed in 2005.
-
Keep it going Adnerb 9 years, Wow!
-
Five years for me as of April. I live with intention and love. I also live with the feeling that I am always about two steps in front of a runaway bus...maybe one of the legacies of stage 3.
Thanks beyond words, BCO community, for tons of important information and for being faithful companions through many sleepless nights! -
Congratulations on your anniversaries Eph, Adnerb and Octobergirl:)
Iago - Looking forward to congratulating your five years next year!
Octobergirl - I love that you "live with intention and love" and also feeling you're two steps in front of a runaway bus. May I borrow that? I'll return it to you in, oh let's say another 15 years?
-
5 Years out for me too! I've made so many friends on BC.ORG! My BC was pretty easy, compared to losing my hearing from a small stroke causing my hearing loss... But THEN stumbling and falling on my hip and breaking my Femur, was worse yet!
It's best to stay up-right, and living life to the fullest every day.... Thanks BC.ORG, for all of my friends!
-
CHevyBoy! More happy dance!
Thanks songbird68. You will get there too. I can't believe it's been over 4 years for me already)
-
ChevyBoy what fantastic news! I am grooving with Iago - she's got some pretty good moves & helping me out with the steps
x x
-
Morning gals! How fun to see you "here!" Congratulations to US!
-
Morning ChevyBoy:)
I get so much inspiration from you longtimers!
Thank you
x x
-
Great to hear these 5 years + survivor stories. Hope you all have many more happy years of NED. Really hope I will get to post in 5 years time. I am 7 months and 1 day since the diagnosis and my feet haven't touch the floor with 2 lots of surgeries and 6 rounds of chemo. Had another WLE and ANC last Tuesday (11th Nov), pleased to say there's been very little pain and I have full movement in my arm with no sign of the dreaded lymphodeoma (touching wood several times now).
Got my follow-up appointment on 26 th November and really hope this is the end of the surgery so I can move onto radiotherapy then 10 years of tamoxifen. 2014 has truly been the most horrible year ever and I just hope that the future will be better and cancer-free!
-
Sandie, one of these days, like me.... and the others on here, you will look back and wonder how you really DiD it! Sometimes we have a more simpler DX, but we are still afraid.... Then each day that goes by, seems a little bit easier....
And it's alright to be mad, or cry.... we all do that sometimes... but these threads will give you more strength... so just remember.... we are all here for you.
And Thank You Songbird! That was really sweet! Stay warm friends!
-
Thanks for sharing your stories!
Awesome Octobergirl!
-
Hi Chevyboy
Thanks for the kind words. Nearly a week on from the op, the drain is out and keeping up with the exercises. I feel so well and that's hard to get my head round. I feel like I am cured of this even though there are no guarantees of this. Hope I will be here to post in five years time....:)
-
Yes! You will be here Sandi! I know it's hard to believe, and I know there are no guarantees, but we just do what we can, and hope for the best, and keep a positive attitude. It helps a lot. If you aren't really "into" what your Doc's are saying, write it all down.... your questions, and their answers.
I just had my 5 year mammogram, and I'm good to go! I had a much easier time, than a lot of my friends on here, but I'm still here and hanging on to them all!
Glad you had chemo.... It's like re-assurance! You rock girl!
-
Hi Chevyboy
Finished chemo 6 weeks ago
was told I probably didn't need chemo but were given it as 'insurance'. Not on hormonal treatment yet but will be starting the tamoxifen in just over a week's time. All of this journey has been terrifying and in the midst of it all I have felt physically well. Its so surreal.
Glad you had your 5 year mammogram and everything is fine. Here's to more years of NED for all of us xx
-
Got my results back, the further breast tissue taken and the 8 lymph nodes removed showed no cancer cells. I am officially cancer-free or NED
all being well will be posting in 4yrs 5mths on this thread
-
Sandie I hope your still dancing since your post on FB. Life is better with you (in it)!
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