Hi All,
I'm new here and have been busy reading lots of old posts to get ideas and was interested to read here and there of others, like me, who've found that bananas are now for me the demon food. Does anyone know why that is, what is it in bananas that makes them react so badly with my poor ole throat?? I tried a bite of one when I was in my 3rd wk of chemoradiation and it was a steep learning curve of what was to come in terms of my changing palate!
I am keen to enhance my nutrition as at present I'm solely able to have peg overnight feed of a 'lighter' version than the one I originally had when in hospital as that made me vomit and have diarrohea, so the calories are less. As I lately seem to be losing the ability to eat much, I am now also having 3x ensure a day too. One thing I feel I am helping myself with is to take a probiotic but perhaps that's just old habits as I used to be a dead keen juicer and health freak with my diet, all salads and soya etc, but would now gladly eat anything if I could.
Can I just say that I've learnt so much in such a short time over the last few days reading posts here. I soooo wish I'd found this site before I started my treatment, it would have helped me cope so much better than I did going through the treatment. Thanks for all the ideas and sound advice


BOT dx via Pe/CT combined scan Mar2012
Spread to node-removed.
HPV 16 +
Cisplatin x2, RT x30 June & July 2012.
Peg in situ 06 2012 & 1 tooth out.
Visual scope clear Oct 2012
Veggie, never smoked or drink much (polish halo!), no caregiver. Aged 58, Lynne in Scotland