So my oh has vascular dementia, after various tests at the hospital they have now diagnosed myeloma as well. We are now on the rounds of chemo. Hospital every week using hospital transport who are brilliant but it takes a whole exhausting day. Add this to the bathroom problems and the wet beds every day, the piles of washing and there doesn’t seem to be much fun in our life anymore. We seem to eat soup, ice cream,and other soft food every day. At least I have discovered a soup maker that makes soup in about 20 minutes.
The only blessing is that oh doesn’t remember the trips to hospital so he isn’t too much trouble to get there.
But my life is just one round of work, when oh sleeps I do work to catch up.i try to wake him at night to go to the toilet, two or three times, anything to get a dry bed.
I really don’t know how much more I can take. I feel better having a moan. I’m not the saint friends think I am, I shout at him, lose my patience and cry by myself in the bathroom.
The only blessing is that oh doesn’t remember the trips to hospital so he isn’t too much trouble to get there.
But my life is just one round of work, when oh sleeps I do work to catch up.i try to wake him at night to go to the toilet, two or three times, anything to get a dry bed.
I really don’t know how much more I can take. I feel better having a moan. I’m not the saint friends think I am, I shout at him, lose my patience and cry by myself in the bathroom.