Hello to all the beautiful people in this fabulous community.
My wife was diagnosed with CUP June 2018 6 months after we got married.
She was at the recent seminar in the Red Cow last Sat 7th September, thank you to all who gave their time she enjoyed her day and especially the choir at the end, there wasn't a dry eye leaving.
One of the workshops that really has been playing on her mind "Living Life with Metastatic (Secondary) Cancer
You see, my wife Davinia has been diagnosed with such CUP metastatic in her lymph nodes?
We hear all these stats and figures of 5 years etc. ( I tend to stay away from Dr Google). and it all can be really confusing for her.
Over the past 18months, she has been through 47 chemo sessions and 11 radiation sessions,
Recently been told that the Avasten with her Chemo this time round has been good and there has been a significant improvement so she has been given 3 months break from chemo but still continue Avasten every 3 weeks.
The significant improvement in her since her 3 weeks stay in hospital in June has been two-fold, energy levels coming back, being able to be a mother again dropping our sons to school and catching up with friends etc, getting massive compliments of the wigs she wears and able to pull off the different colours lol!!!
Unfortunately, night time is not a good time for her.. Her thoughts run away with her.... I am up with her in the middle of the night most nights when I hear her crying and scared, we even sleep with the light on to try to give her some comfort.
It is confusing for me and can be frustrating when I see her doing so well regarding energy levels and her appetite is back to somewhat normal???
I say to her she should be proud of the battle she is winning and the progress she has made this year...
Gary Kelly Centre in Drogheda has been tremendous support for her as the hospital (Beaumont)
I am trying to be a light of positivity for my wife and our children but can be so hard when she hears the words metastatic which she then implies she doesn't have long left to live???
I hope I can open up a conversation here with both people who are diagnosed and partners who are caring for them.