We arrived at 3.15 at the hospital to be told there was no one of that name expected and no bed. After some debate the nurses found out we should be there but no notes no letter or anything about Malcolm had arrived on the ward. So we sat in the waiting room. 2 hours later a registrar a lovely Chinese doctor came and told us all about the operation. It will start about 10,30 tomorrow after the doctors have their weekly chat and will last 10 hours. So I will not see Malcolm on Friday at all as he will be kept asleep until Saturday. Also blood was needed to be taken to cross match 4 units for the op so that had to be done tonight. ( 9.30 . no blood taken yet) Why could that have not been done in out patients? At 6.30 we came home and had a lot to eat and drink as we were starving. We then returned to the ward at 8.00 and a bed was ready for him. We parted with many tears and prayers. Continue reading »
Laughter is indeed the best medicine. Both Malcolm andI have a terrible sense of humour. We laugh a lot and play jokes on each other a lot. His losing his hair we turned into a joke and now he seems quite comfortable with no hair or the little fuzz on top. We are also experiencing many joys from family and friends showing so much care and thought for us. Continue reading »
Being given the news that your husband has a life threatening illness was not new to me. 40 years ago when my 2 eldest sons were 2 and 1 Malcolm was involved in a very serious road acciddent. He was left with no unbroken ribs and a mangled right leg and paralysed gut. He had a 50/50 chance of surviving. So I had to stay calm for the chilldren and prepare for my life as a widow. Continue reading »
Soon we go to Christies for Malcolm’s 3rd infusion and hopefully the last 3 weeks of chemo. Many people have been asking me how i amcoping and want to hear my blog as well so I have summoned up energy from heat exhaustion and here goes. You asked for it. Continue reading »