well to day l was told after having fours chops of chem and two ices and two more bags of the first stuff you have when having the chop before chemo begins with retoxamide ( sorry its chemo brain they say), lots of in and out of hospital and two hickman's line later when the first l must add almost killed me there is light at the end of the tunnel oh yes and two attempt for harvest my stem cell which first lot went bad (say no more,) l have a date to go in for my transplant of stem cells, santa will have to visit me there hoping for maybe a little hair, ha ha who care l am still hear and still kicking and maybe next year my hair. must not be greedy,one thing l have learnt never to be surprise what next just take it has it comes for at the moment treat is a few days with no appointment or blood samples or hospital full stop, still you will all relate to this,today l went for a blood test and a flash of my hickman lines and that was it no way in came the doc and was not happy h aaaaaaaaaaaa until they put a hole in my back yes bone morrow test my husband held my hand felt like a baby but it made him feel good and yes me,the good thing was l never had time to worry surprise worked out well that's over and done with for a while, so you see there is alot they can do and we all live in hope and keep smiling maybe sometimes have a cry,don't like that one mind you need to keep strong for my love ones, l would not say l have got use to all these things we all have to put up with but just decided to go with ha ha haaaaaaaaaaaaa like l have a choice well hope you are doing well and l am enjoying in reading all your journeys with this thing invaded are bodies , thanks for listen to me go on ronnie x x x
FormerMember
Stay with it Ronnie! I'm going to take some of your 'ha ha ha' with me to the hospital tomorrow - sure it'll do the trick!!
Good luck with the transplant, will be keeping you in my thoughts and prayers. Keep on writing and I will keep checking on your blogs. Transplant will be my next line of treatment as well, but hoping and praying that I may get as many years remission that you have had. Though the way I have been feeling lately I am not sure. Anyway chin up and will always be thinking of you.
Wishing it all goes swimmingly! If you have a low moment remember we are all here rooting and waving to you cheering for you and sending positive vibes!! Love Jools x x x x
Ha haaaaaaaaaaaaaa made me laugh, it's just better to laugh at it all then when it kicks you in the teeth you can bite it's foot!
Husband just getting over stem cell transplant - it's all in the myeloma forum instead of a blog - and I hope you don't take too long getting over yours, you can do it for sure for sure.
