We are not alone!!

We had a lovely chat with the super efficient GD today, she's a PROPER old school nurse (so mind out chaps). It would appear that she shares our sense of humour...... lol. (I hasten to add she isn't actually by any means old.) I asked her for directions to the parking control centre, to which she replied:

"It's in the same building as the mortuary, why the burning desire to go there?"

"I'm dead keen to get my concessionary pass." (Boom boom)


Velcade without the saline bag, GD was busy........ painful and went a funny colour. lol

Cycle 1 day 11. At least I think it is.

All this cycle and day stuff is so confusing. We were hoping for a proper day off together next week but guess what....... it's Pamidronate time again. It's bad enough having an illness, but even worse that we never have that elusive "quality time" together. How about the evenings I hear you all cry! Well by the time dinner has been made, eaten and the kitchen rescued from looking like a transport cafe, I'm so tired that all I want to do is sit in front of the tv and chill out. This isn't helped by Mike's nocturnal habits, again due to the mm and the instructions to drink at least 3 litres of water a day, well it has to go somewhere! I love him dearly, but what with plastic water bottles that creak when being poured, the endless coughing (not a chest infection we're informed, well twice actually) and the padding of feet across the landing, I'm just about ready to find a really good sedative to put in his tea!

Being serious though, I'll put up with all that and a ton more. To quote Dai who posts a lot on the Myeloma UK discussion board, "Whatever it takes, for as long as we can."