Oh thankyou for your replies, now I know what a Pack is, completely different from my daughters treatment. Maybe because we live in the country, every 3 weeks my daughter will fly to the city and have it induced into her vein. This is a day procedure then she will take 6 tablets (don't recall their names)a day for two weeks then will have a week off.
She seems to be coping pretty well except for the tiredness, metalic tastes and unable to touch, drink or eat anything cold. Unfortunatly they can't cut the damaged area of my daughters liver out because there's too many spots, the doctor says they can only try and contol it.
Yes Customline our daughter stays with her 23 year old daughter for a few days in the city (she lives there)and she drives her to and fro to the hospital. I stay at home to help look after her other two school age children as she is a single Mum, they don't have their Dad.
My daughter will have her 1st scan since the commencement of the Chemo treatment next week..so we all have our fingers, legs and eyes crossed (Lol)the tumor has shrunk. Our daughter wants us all to stay strong and we are not allowed to think anything but positive and we are not allowed to shed any tears! She is so strong about it all, we are all so very proud of her.
Your also very young Carole, does your medical team think you have inherited the cancer, they seem to think our daughter has. I hope and pray all your treatments goes well for you Carole and the same goes for you Customline.
I just wish I could just wave my magic wand and everyone will be cleared of this horrible nasty cancer.
Pam