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View Full Version : How long have I go left? "I can’t go on. I’ll go on.”


kk1
01-26-2014, 10:21 AM
Next week will mark 5 years of continuous NED and and a month shy of 10 years living with metastatic disease to the liver...the article this morning in the NY times really struck a chord with me. "I can’t go on. I’ll go on.” Well written and uplifting.

http://www.nytimes.com/2014/01/25/opinion/sunday/how-long-have-i-got-left.html?_r=0

sassy
01-26-2014, 12:52 PM
Thanks for this article.

One point we especially should all remember is that new developments are taking place in treatment continually.

My prognosis changed in the first 3 months of being diagnosed because of the release of Herceptin. Statistically at diagnosis, I should have recurred within two years, and not lived to five.

I'M ALMOST NINE YEARS OUT AND NO RECURRANCE! Because of new developments in treatment.

Statistics change......

BonnieR
01-26-2014, 02:30 PM
Thank you for posting this!
Keep the faith!

suzan w
01-26-2014, 09:20 PM
Thank you for this kk! As more and more time passes I realize even more how lucky I am to have been diagnosed when I was and to have been able to get the treatment that I got. The survival statistics laid out for me at my first oncologist appointment in June 2005 were grim. Within a few months everything statistically had changed. Bottom line...never say never!!

Pamelamary
01-26-2014, 10:49 PM
Thanks kk - both the article and your own story are uplifting
Best wishes.... Pam

'lizbeth
01-27-2014, 01:19 AM
Wow. That is amazing. He should truly write that book.

The targeted therapies are a god send, and now we have 2! and a ADC. I am lucky being diagnosed right after Herceptin was approved for primary breast cancer.

sarah
01-27-2014, 05:56 AM
very good.

Jackie07
01-27-2014, 02:58 PM
That reminds me of Stephen Jay Gould's famous treaty: http://cancerguide.org/median_not_msg.html

Mtngrl
01-29-2014, 07:56 PM
Thanks for posting this article. The moderator of my in-person support group sent it around. "I can't go on. I'll go on." I sent it around to immediate family.

It's also great to hear from someone five years NED after brain mets. I'll keep your drug regimen in mind.

KDR
01-30-2014, 02:26 PM
This is wonderful news! You are truly an inspiration to us all! Do you continue to be on Herceptin? And, if I may ask, where are you treated?
Thanks,
Karen

Barbara H.
01-30-2014, 04:00 PM
It will be ten years in May that I was diagnosed with with a 3cm brain met as will as mets in other areas. I was originally diagnosed in 1998. I am currently NED. Tykerb (4 pills in the morning) and Herceptin every 3 weeks. I have continued to teach in an elementary school through out my treatment. I will turn 66 in April and have made the decision to retire in June.
I do believed that their are multiple forms of all breast cancers, and that my type of cancer responded. Fortunately, new information from research is providing more hope.
Kind regards,
Barbara H.

KDR
01-30-2014, 04:02 PM
Barbara, you too! Amazing!
Karen

KsGal
02-02-2014, 05:26 AM
Thank you for sharing that. You are very inspiring.
Jody