I think I have been expecting too much, I just so want to feel better and able to at least get up and walk around the garden. I must just listen to my body that needs to rest after the trauma it has been through. From what I have heard and read I am probably a third of the way there. By day 90 I should be able to do much more and hopefully I won’t feel so nauseous. So patient I must be .
Yesterday my day was cheered up by a visit from a friend and fellow myeloma sufferer. It was good to be reassured that all I was experiencing was very normal and as expected. Jet is a great inspiration to me as she takes life with both hands and gets the most out of every day. But she also rests when her body tells her to . It was great to be reassured that I will feel stronger and be able to do so much more in a few months time.
So most of my days are pretty slow. If I have a bath that’s me done in for. Although at the moment I am enjoying some long soaks with the help of Epson salts, thanks to Jo and Lorna.
It is good to get visitors so if you are infection free and fancy popping around for a cuppa, you will be most welcome.
On Thursday we are back down to the hospital which will be a good chance to get my latest blood results and check everything is going in the right direction. Fingers crossed all will be well.
Today my daughter and grandson will be popping in , it’s just a shame that I can’t get up and play with Elliot but that time will come and he is very good and seems to understand,
Have a good day and thank you for your continuous words of support, I know I am not alone and I will get through this time.