Hi, thanks so much to all the recent support I received in this corner of Mumsnet, I am so grateful.
About a month ago my mum’s 2 week old diagnosis of myeloma (and about 8-10 years) changed to an additional diagnosis of plasma cell leukaemia and a year at the most.
They live 300 km away, and have been in one the strictest lockdown areas in the U.K, so we hadn’t seen them for months. I went up at Easter, and she was really unwell; I managed to get her on the local hospice’s books, organised getting a stair lift in, a cleaner, a respite carer for my dad, various other bits and bobs. By the time I left at the end of the hols, she was much brighter, pain much better managed - out of bed, going for drives, talking to friends on the phone.
But I am a F/T primary teacher and I have had to come back down to my husband and 3 kids as term starts again on Monday.
The petty thing eating me up at the moment: I am struggling with how often to go up to see them. The district nurse said ‘ooh, ask if work will let you go early and you can pop up every weekend’. I have a lovely Headteacher but I don’t know how he’s going to feel about me ‘leaving early’ every Friday, and ‘popping up’ on the train involves an hour across London, 2 hours to Manchester and an hour to their small town.
I just don’t know what to do. Term time was already intense (it’s my NQT year), I don’t know how I can go up north and back every weekend. Every other weekend? Every 3rd weekend? Go up Friday and come back Saturday night, so I see my kids? If it was a month, I could just stay up there - but I can’t stay up there for a year...
I just don’t know what to do? Mum and dad were expats all their life, and used to see their family once a year; my brother and his family live in Dubai.
My dad is very understanding; my mum did not work after having kids, and I think doesn’t understand that I can’t move in 24/7. I feel so guilty and trapped in a hamster wheel of not knowing what to do.
Has anyone else had a similar experience? What did you do?