krisi
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Surgery is ruled out – th8e cancer is placed in such way in the gall ways/liver that surgery is not possible. (very close to big blood veins etc)
Krisi
Hi,
I’m also European – from Denmark. Currently having a pause in my treatment – and enjoying the freedom. In a week I will have my CT scan and getting the feedback the week after.
I have had 18 treatments with Gemcitabine, Oxaliplatine, Xeloda and Panitunumub (I’m a bit confused by the naming of the different treatments, but I hope you recognize the names). When reading the list of possible side effects I have tried them all – but to me they have not been prohibitting me from living my life as a wife and mother of 3 children (1Wauw – what a fantastic description to read. I just logged on to the forum with the objective to write a post about experiences with inoperable cancer and the time that treatment keeps others up and going. I have been told that I will be having chemoterapy for the rest of my life – hopefully with some breaks inbetween. I plan to proof this plan to be wrong!
Reading your story Andy really makes my hopes even bigger. I’m young (37) and have no symptoms at all so I really want to proof the plan to be wrong.
I myself am in the proces of identifying what can help me and boost my body to work better during the chemoterapy. I have some food allergies but I will find a way to solve this.
Thank you again for your encouraging post.
Good luck.Krisi
Glad for your fast responses – now I will try to be active as well, although at this point I think I have more questions than answers….
The antidote that I get is a trial – for CC treatment. It is known for other cancer types. I/we decided to go for the trial as well when my genes fullfilled the requirements.
I go to Vejle for my treatment, but the Onchology department at the hospital in
