"OCF Down Under" Platinum Member (300+ posts) Joined: Jul 2009 Posts: 453 | Our introduction with Steve's peg was pretty disastrous to start with but boy are we glad to have it now. It's taken alot of pressure off him, kept him hydrated and eased my mind immensely knowing he is getting everything he needs. A nurse told us that the peg will be Steve's lifeline and I tell you, she was right. Good luck on friday and I will be thinking of you.
Wendy
Wife to Steve 43. DX 5 May 09. T4N2MO SCC tongue, floor of mouth, lymph nodes & jaw bone No surgery Teeth removed 06/07/2009 radiation 13/07/2009 x 7wks chemo 15/07/2009 x 3 Cisplatin last TX 28/08/2009 25/11/2009 PET-lymph node activity. 08/01/2010 CT Scan-ALL CLEAR 03/03/2010-Peg removed 01/2013 left side of Jaw removed and replaced with pectoral flap. 23/12/2020 scan show lesion in tongue 01/2021 SCC stage 3 base of tongue diagnosed 01/03/2021 chemotherapy started.
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