A relative of mine is getting a PEG tube put in, in a few weeks.
I know they have a disorder of the oesphagus and stomach.
I feel too uncomfortable to ask them what a PEG is?
What will the surgery involve?
How long will it be in for?
What does a PEG look like?
What exactly will he do with it? Vitamise foods? Liquids?
What will it feel like for him? Will it hurt?
Any information is greatly appreciated.
Thanks in advance.
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