Thanks for the info, airkitty, So strange that the PEG route was exactly what my brother had done today in Ca. They also had to change his PEG. I am hoping & praying this will work. I appreciate all the people on this forum who so generously give of their knowledge & experience. You all have been through so much yet still give back to others. I am awed every time I visit this forum with the courage & grace that is displayed. Thank you.
Sister to Randy (47, nonsmoker) Base of tongue, scc, stage IV, lymph node involvement Dx Nov 2009, started rad/ chemotherapy 12/09,PEG tube Finished 02/10
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