Angela

Hello Lynne.  This was the first time I'd seen this Oncologist - for a 2nd opinion re the Arimidex.  He seemed thorough and read up various things on his computer.  He's printed me out quite a few pages to read which I'll do shortly.  He read my GP's referral and copy surgeon's report she had enclosed.  Today, I have started on Femara - to see how this goes, though I know Femara has much the same side-effects as Arimidex.  Guess it's a matter of wait and see!  The Onc also gave me a brochure about 'Novartis Oncology Bisphosphonate Access Programme'.  He didn't seem too happy about the Actonel-Combi D medication i take for my bones, opting for this other programme instead perhaps.  It's given by way of infusion and I think it could be yearly.  Doesn't cost anything so long as one is on the programme. I return to see the Onc in four weeks.  I guess by then, I'll know whether the joint pain has increased again.  I wish I didn't have to take it, but the alternative is worse! 

I hope we can keep in touch.  Judi