Hi Sandra,
Have I got it right, the injections are into Sammy's ribs or just normal injections to stop the pain? If it's into the ribs, that sounds really painfull in itself. I would of gone mad to if the doctor told me they couldn't do it, because Sammy must of been worried as we always are when having something new done. I must admit up to now I have been really lucky because my consultant, oncologist, nurses and GP have been great. I will be going to a hospice as an out-patient for my pain control. I am also going for day therapy, it is supposed to be really good. They give you massages, well alkinds of things.
Go today to see my oncologist to see if/when they will be starting my chemo. I haven't slept, feel so tired now. Have had McMillan nurse out to see me, she was really nice. The only thing though is that she stopped my MST and Oramorph for Oxycontin and Oxynorm, also changed my anti sickness tablets to Metoclopramide. Well I can tell you I only started them Friday night and all day Saturday I was awful, really weak, tired, had nausea and severe cramps in my legs and arms. I got out of bed about 2pm and lay on the couch till 6pm and then went back to bed, all I did really was sleep, it was awful.
On Saturday night decided to go back onto MST and I can tell you I felt so much better Sunday. It must of been the medication they changed. Wish they would leave well alone when you are doing ok.
I am going to ask my oncologist today about Tarceva, because I have never heard of it.
Well take care and my love to you and Sammy. Keep intouch and let me know how he is doing.
Best wishes
Jeanette