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well, the sun is shining, clean white towels are blowing on the line, and I don't feel nearly as bad as I thought I was going to, praise God!
i am blessed. Mind you, I'm still paranoid about every little ache and twinge, but I've managed to keep off a lot of the meds, and just take the minimum. Common sense, so far, is prevailing! Mostly! I am a bit obsessive with the thermometer!
actually feel well enough to try driving to my RT appt later. It will certainly be quicker than transport...
Hello All!
Hope you're all doing OK as you can do being effected by this horrible disease.
I thought it might be helpful to some of you to share what I have experienced so far during having my treatment.
I had my 2nd full day (plugged in from 9am-5.30pm) on Thursday 6th November of R-CHOP chemotherapy. I had asked my lovely nurse if she would pop the injection in my left hand so I could message/eat with my right but struggled so after having both hand battered with a needle had no hands in...
I am due my second follow up
appointment with the RT team this week. Hopefully they will be pleased with the big improvement in my eating and subsequently the improved energy levels. I won't be running and marathons yet but I do feel more up to coping with more day to day tasks and I'm going into work 3 days this week. Not for the whole day, but we'll see how Friday find me
I got in touch with my macmillian nurse on Friday as my original consultant who did my operation said I should...
I'm in an emotional place similar to the one I found myself in when my Dad died: there is this briefest moment of relief when you wake up and there is no emotional pain what so ever... Then those few seconds get destroyed because 'you remember' that life has now changed and the pain comes flooding in.
This is the background...
The last few weeks have been hell. Six weeks ago I was admitted into hospital with severe abdominal pain, they presumed gallstones and I felt like the biggest wimp...
It's been a while since my last post due to a time of reflection needed as to where I am and where I am going. The fantastic news is that I am well on the mend with no sign of the cancer returning, eating well and back at work part time for now. I still have a dry mouth at night which means broken sleep but my saliva glands try their best during the day reducing the need for constant and incessant gargling. Over past month my food intake has improved greatly. From soup and scrambled egg I have...
Nov 1st was the 4th anniversary of my diagnosis. I felt a bit queasy when I realised what the date was, but then I congratulated myself on lasting this long. I'm determined to make the five years at least, even though I'm not disease-free and never will be.
The week of radiotherapy passed very easily. In fact it was a bit like a holiday. I quite enjoy staying at the hotel, there was time to go sightseeing, visit galleries, and indulge in some retail therapy. I bought a slinky leopard print...
Mum lost her second battle a year ago tomorrow, I can't believe it's gone by so fast. I'm dreading tomorrow if I'm honest as I wish she was still her. I'm not working tomorrow but the rest of my family are, yes we are having some fireworks to mark her death and a bonfire which is what she would of wanted.
Most post it's say it gets easier, which yes it does, I think I've been very lucky as it's only this time of year where all the 1st anniversaries are, her birthday in sept...
My other brother made a surprise visit today so we picked Mum up and went for a Sunday lunchtime drink in our favorite pub. The one Rob and I went to quite a lot before the big C happened. I was sat for quite a while before I realized the lady sitting nearby with her son and husband was bald. My thoughts went to cancer immediately and chemotherapy and hair loss, I am really frightened. I knew mum and brother had seen but weren't saying I also knew Rob hadn't seen. I spend time wondering if he will...
