thanks so much for coming back .. Im newly diagnosed and for once this made me cry for good reasons ... hope
Bless You XXXXXXXXXXXXXXXXX
Well, 11 years on has become 13 years on. I posted last year being 12 years on, but this thread seemed to be more popular. I hope this thread will bring courage to those who are new to this game, there is light at the end of the tunnel. I'll be back again next year and I hope all you reading this post will be too.
All the best to you all, lots of hugs
$PS A special hello, to Marcelle and GeriF and Hope
Hello Lorelie, Lovely to hear from you, I do hope you are doing well and enjoying life. I write every year and wrote in 2015 too. I will come back in October to celebrate my 13 years of living with bc in the back ground. I don't think any of the girls use our thread now. I have kept up with some of them and most are doing well, although unfortunatly 3 now have mets.
I don't know how the forums work now-a-days, but I certainly send you a hug back.
This may be a link to the old thread:
you may not remember me but I was part of your group for a while until life became overwhelming. But I am still here too...yeah! Doing well also as regards the cancer "thing" so given my "triple negative diagnosis" I am grateful. I am hiping that that "triple neg" thing has moved on...not so sure, though I know that there are more specific markers and more is being lerned all the time...thank goodness. So glad to hear you are doing well. Not sure why your message dated 2014 only just arrived in my inbox?!!
Hope that anyone who sees this gains power from the fact that we are doing well xx Good luck!
p.s. you may know me as "Hope" had major problems with the BCC site which has resulted in a new identity but means I have lost communication with others sadly.
Thank you so much for taking the time to post this posiive message. It does help. I am 2 years past diagnosis, 18 months into hormone therapy and still have wobbly days.so your words re very welcome!
It's October, so here I am back to the forums, to let you know I am still alive and very much kicking. I hope I can give hope to those who are new to the horrible frightening journey of tests, diagnosis, waiting, and treatment.
I don't come here very often, because my life is full of plenty of other stuff these days, thank goodness. But when I was diagnosed in 2003, I desparetly wanted to hear about people who had survived. When I was diagnosed in 2010 for the 2nd time, I met some wonderful people on these forums, and we are still in contact, and meet up several times a year inspite of our busy lives. You will get support, understanding, infomation and so much more on the forums.
Take care of yourselves and let others take care of you too.
All the best