5 years since my diagnosis...
I used to lurke on this forum when I was first diagnosed. I was always saddened by the fact that there were no postings from longer term HER2 survivors. I wondered if they existed? So here I am...Jan 11, 2012 marks 5 years since my diagnosis at age 36. We do exist! Well wishes to all the survivors out there!
Comments
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Thank you for this! I just found out mine is HER2 pos...you encourage me!
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I, too, am a 5 year survivor..her2 positve!
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Thanks for these posts metoodf and talbrig13! Love seeing them. My oncologist keeps talking about how one day, 30 years from now, we'll be chatting about our favorite topic: photography. I'm looking forward to that day!
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Thanks for posting. Its always great to see
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I'm also a 6 year 9 months survivor
Yes we exist
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Congratulations to all of you!
I plan on being a 35-40 year survivor. I've already past 1 year and counting.
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I'm 5 years out now- looking forward to the next 5, 10, 15 etc.
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Fantastic, thanks for sharing that with us, we all need to hear good stories every now and then. Hope to see your 6,7,8,9,10........anniversarys here too!
Dawn
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great news!! keep on counting!! cheers to all of us!
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Awesome news metoodf, talbrig13 and sheila888! Thanks to all of you for posting! Her2 success stories are so great!
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Woo hoo! We are loving all of your posts! Congrats to you all!
--Your Mods
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Hi metoodf
Wonderful news! Thank you for spreading such optimism as we her 2 girls need it! I must confess to being a bit twitchy about the lack of posts for long term Her 2 ladies (especially those who are node positive) Perhaps I haven't been searching enough. I had one pos node when dx in Feb 2011 and have been worried about it every since.
Thanks again for such good news
Liz
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Congrats on your 5 Years and many many more. I was Stage 4 from the get go and 6 years & 4 months out and plan on celebrating many more as well. Cheers!
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Congratulations. It's been 6 years 8 mos since I was dxed with Stage IIIC!!
that was then, this is now NED and happy as a clam.
See you all in the old timers club!
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I go for my 5 year CT/PET scan and tests next month. They will be for my 5 year anniversary since finishing chemo (4 years herceptin). My oncologist says we will be partying when they come back all clear as my chance of recurrence will be somewhere around 1 - 2% after this.
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I'm 3 years 3 months past starting chemo and expecting many more years.
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These posts are so inspiring! Thanks for sharing.
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Hi
I was diagnosed 8 years ago, stage 2b, ER+/PR+, HER2+ with 2 positive nodes. I had chemo, no radiation, and have been on Tamoxifen and am almost done with Aromasin. I didn't even receive Herceptin since it was only used to treat metastatic disease at that time, and I'm still here!
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Wow - I see lots of familiar names on here - bluedasher, Ikc, Sassa, orange - hi and congratulations to you all! So many great stories on this thread. Tomorrow marks 4 years since my diagnosis - and I want to be part of Linda's old-timer's club too.
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Hi to all of you familiar faces, I will be 4 years in April...Hi SUE good to see you and Jackie too!
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wow CurlyGirly. I'm so excited for you. Keep on counting!
MMM5 4 years… whoo hoo to you too
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Thank you metoodf, talbrig13 sheila888 and 4everhopeful for sharing.
You certainly given me hope!!!!
Long may NED continue, for all of us xox
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I'm almost 3-1/2 years out. I was node positive. Had a small local recurrence 2 years ago, but resumed Herceptin and added Tykerb for a year....now I'm doing just fine. Very curly hair, but just fine! Hi to all the familiar names I see in this thread.....glad to "see" you.
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I'll be four years since diagnosis in May. Still scary, but getting easier
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I'll also be four years out in May, and so far, so good.
I think we may not see posts from many long-time Her-2 positive survivors because they're out there, busy living their lives.
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Thanks for the positive posts. I am going through chemo right now but someday I hope to be able to post on here to give that same hope back to others.
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my2boys, I'm glad you posted. I saw some of your posts when you had the recurrence and I've been wondering how you are doing. Congrats on getting through this a second time.
Regarding hair, I guess I'm kind of odd. Most people post about their hair coming back curlier than it had been pre-chemo. I've got chemo-straight rather than the more common chemo-curls. My pre-chemo hair was naturally curly. Post chemo, it is quite straight - the kind of hair that I wanted in high school in the 60s. But now I miss having curly hair that can be cut short and create a hair style with just a quick brushing.
It's a small thing and seems petty to complain about especially when I once wanted straight hair so much, but sometimes when I look in the mirror, it just doesn't look like me after over 50 years of curly hair.
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2 year anniversary of my diagnosis was January 8th. Feeling fantastic - a little tired, but who isn't after all of this?! God is good!:)
Love,
Brandi
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Hi there Blue!!! Glad you're good.
)
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I very rarely come on to the forum because I'm busy with my life. I just calculated and was amazed to note that I am almost 8 years since diagnosis with Stage II, 2.5 cm, Grade 3, ER+HER2+++, 0/3 nodes. I had mastectomy, chemo (ACT), and Herceptin for a year. Even my 5 years of Arimidex is ancient history.
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