Hi, I am a sudden carer for my brother Jason who has been diagnosed with advanced small cell lung cancer with extensive brain mets. The change in our life has all happened so fast! One thing I have yet to get a handle on is how the care from home to hospice actually works. I am connected in with the local palliative community nurses - so it is something I plan to ask about in some detail - but I was wondering if others might have some advice and insight. Thank you.
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