OP "OCF Down Under" Platinum Member (300+ posts) Joined: Jul 2009 Posts: 453 | I agree Ray. I look at it, not with bad memories but as something that has helped us to fight this disease. Without it where would we be. But then again it's not mine although in some sense it has a very strong effect on my life as well. I suppose everyone's different and that's their right but I don't hate it.
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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