Yes I would love to know what the word is out there with us triple+s, I always got the impression that the HER2+ sort of "trumped" the ER/PR+... and I'm going on 8 years out. If anyone has,, as Sydneybased ask - clairfication "what the current robust evidence says" about triple+ recurrence, I'm sure many of us would like to know.
Two years for me!
my MO is fairly confident that I have a 15% chance of reoccurence. He did add that once I'm 2 years out the chance if reoccurence gets even lower
So I would suggest that we not focus on it because we can't change anything. I'm trying to do this as best I can
2 and a half here.
Maybe there are no real milestones but it sure feels like one! LOL
I am Stage IV (right from the start). However, I have been NED now since June 2008!!
Great to hear about such milestones! I'm working on it!!!! :-)
I think there are too many variables for a doctor to give %'s.
I feel good and loving life even with the chemo treatment. I feel good about my medical team and thrilled that I've connected with all of you! Here is to leach day and making the most of it!
You are all my inspiration!!
I had my 2 year check-up last week. So far, so good. I too try to focus on factors I can control rather than those I can't although I've been in an exercise rut lately. Life showed up. I'm on a business trip today and I had time to go exercise but I didn't find the heart / steam to push on and do it today. Tomorrow is another day.
Just dropped by to say that I am 5 1/2 years out and never felt better. My hair never came back to its original thickness. Super see through thin. So I got extentions and they look great.. Hang in there and love every moment as it a great blessing.
great to hear about good health!! We are super heroes and survivors!!!!!!!
My general impression is that Her2+ has a shorter term window of recurrence risk, 2-3 years, but the longer term risk continues with the ER/PR+ aspect. There is not a point in which risk disappears - it is always there.
there is a risk with living. We can get hit by a truck, we can be in the wrong place at the wrong time, we can be diagnosed with something else, plane crashes, car crashes, train derailments, crime. Who knows. There is always risk.
What are the risks? When will they show themselves? There are also women with more than 1 tumour which are totally different. One might be triple positive, the other not.
If we knew all if the risks out there would anyone leave their homes?
I am triple positive. Today I feel fine. I don't know anything about tomorrow. Let's celebrate our achievements and we all have so many and try to forget about what might be
Live for today with the hope of a healthy rewarding tomorrow
According to CancerMath the risk starts dropping slightly each and every year after 2 years. I will take it!
Rita and those who post- thank you for inspiring those of us still in the trenches who are so scared. Bless us all.
Just reading these posts gives me enormous hope. I was recently diagnosed w/BC (HER2+) and my first MO & RO appointment is coming up in June to learn about what treatment is best for me. God bless and continue with many more years of negative results!
Hugs to all
I will be 3 years out in August
Just had a clean bone scan (for some rib pain) so as far as I know still NED
hang in there newbies...it does get better!
such great news! Awesome milestones! Here's looking at 10, 20 and more NED years!!
I get to scared sometimes! I have a good cry then go back to living. My mother is 91 and dad passed at 87 so hoping that I'll keep rocking for many years to come. I will be 51 this summer so would really like lots of good quality years ahead of me
live from credit valley hospital. Round 2!!! One more round of FEC then on to taxotere and herceptin. Rock n roll!! So far so good. Hoping for minimal SEs although felt strange while being infused.
Can't wait until the chair days are over!!!
Have a great day all!!
Keep going footballnut! I'm so glad this gives you hope. Next Friday I will be celerating the end of ALL my treatment's one year anniversary. I had my last Herceptin on 6/13/13! I plan to rreally celebrate this one as a year out from treatment is a HUGE deal to me!
I am 2.5 years out from diagnosis and in July I will also be 1 year out from all of my treatment. I had scans recently as part of a clinical trial I am in and just received word yesterday that they were all clear!
Wow, Sduch1 our situations have a lot of similarities. Next week will mark one year since I completed Herceptin. Fantastic news on your scans!!! Thanks for letting is know. I see you had some damn scary chemo too - particularly the big A. I worry when I see all the things linked to it that aw to impact aurovi. But I keep a good attitude anyway.
this wed is my final round of FEC. That will make 3 rounds. In early July I start taxotere and herceptin for 3 rounds then herceptin for the year with tamoxifen starting in the fall. Anyone have this cocktail?
If so how were ur SEs?
I'm loving the positivity of this thread. I'm nearing the one year point of my diagnosis, a year ago today I had that dreadful suspicious ultrasound. I'm sure that I'll be posting in December 2015 saying that I have been cancer free for two years. I consider myself being cancer free as of when I had my surgery where I had a pCR.
Footballnut - I had/have the same treatment as you. I found the side effects worst on FEC but I had severe fatigue and some nausea. I had a different fatigue on taxotere, I was tired but could not sleep. It wasn't as bad as the FEC though. I also had bone and body aches that were well managed with Advil and Tylenol. As for Herceptin, I just really have a runy nose and sometimes feel like I'm coming down with a cold the day I get a treatment. I started tamoxifen over two months ago and the side effects are minimal for me. I have some of the side effects listed but I'm not sure if I can fully blame it on the pill, there are other things that are happening in my life right now that could cause these things too. Hopefully your side effects are not too bad.
Just found this thread. Not sure I should be here because I'm way paset 2 years. This August 31st will be 2 x 2 NED. Yup that's 4 years, Large tumor, premenopausal, stage IIB.
It gets better as time goes on. It takes time for your body to heal from all the treatment too. Hang in there.
oncearunner tx for sharing!
Lago good to see you here!!!!
yeah Lago. So happy to hear about your 4 years. I'm having a horrible day today crying about my lymphedema and generally feeling hopeless. Yesterday was one year since I completed Herceptin so trying to be grateful. No one I know cares how I feel anymore. They just want me to shut up.
Mariasnow just sent you a PM
Thanks to all those who reached out to me. I'm trying to keep my chin up. I truly, truly hate lymphedema but I know my case could be MUCH MUCH worse than it is so I will count my blessings. I feel so much older than I did 3 years ago when I was skinny, fit, tan, had long blonde hair, could wear high heels, had great boobs, nice toned arms, ran half marathons without a care, etc. Being this menopausal old broad has seriously messed me up. So for today I will stick with being grateful for being NED and try to just keep going! My sister is undergoing a scare with some suspicious scarring so we are awaiting results for her. I just found this out today - which made snap out of my pity party a bit.
And another one reporting in as cancer-free. Just got results of complete blood count. All normal.
Good luck to those of you going through it now.
It does pass.
Alice, thanks for the info. It gives us all a lot of hope.
Maria, I saw a woman at the doctor's office yesterday and she is doing accupunture for her lymphedema. You may want to ask your doctor about that. It might be a clinical trial that your doctor may be able to check into. Good luck and hope you are feeling better!