Another weird nights
sleep, was watching TV at 4.15. John phoned Jane work at 7 and said I needed to visit, she was off
out at 8.15 so I went down early and told her about the tumour and how bad it was, we cried and
laughed together, decided life was shit and had a laugh about other things.
Taking time out sick for now, but I do miss doing the activities in the
home, as my day in there was very busy and I do like that.
9.30 Mo came and Sally woke up, Mo and I went to the mail to take stuff back and buy
stuff for Johns birthday. We then went to John Lewis for coffee, but it was
very noisy . What made my day was seeing a special needs student that I used to
support as a support worker, she shouted across the shop and then came and
hugged me. She knew nothing of the
aggressive brain tumour, that seems to be defining my life at the moment and it
made me feel great, I smiled and smiled
some more. I need some kind of normal.
Mum , popped in and so did Dad and Phil, Julie also popped
in, but by 3.30 everyone had left, just Sophie and I. Sally had gone back to Cardiff. This makes me
feel a bit panicky at times, but this
will be the normal. Emma also phoned up and we arranged a dog walk.
Celia came in after work which I look forward to, felt melt
down coming on, but not completely. We chatted and cried together.
I have gone from
someone who went around at 100 miles an hour to this, sat on a sofa drinking
endless cups of tea with people, 2 weeks seem like 10 years and all my things I
do to combat stress have gone. I miss swimming and pushing the stoke hard , I miss the walking and running. I also miss
the bike.
By the time John came home I was ready for the complete melt
down and I had it!. Why me? I don’t want
to die? I don’t want to leave Sophie and
Sally. I don’t know if I can fight it. I screamed, cried and swore. Luckily
Sophie is deaf and did not hear. There
are no answers and life is not fair, never has been or my sister would not have
died in a riding accident 25 years ago
and Sophie would not have had meningitis that left her deaf and with short term memory problems. Life is
XXXX today and that's the way it staying.
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