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#58932 09-25-2006 12:24 AM | Joined: Apr 2004 Posts: 837 "Above & Beyond" Member (300+ posts) | | "Above & Beyond" Member (300+ posts) Joined: Apr 2004 Posts: 837 | Michelle,
I had most of the same problems that you describe (although I guess in my case they showed up earlier -- about halfway through radiation, and continuing on for many weeks after the end of my treatment). It doesn't surprise me that she's feeling the effects of nerve damage -- that happens with major mouth surgery and radiation. I had several areas that were numb for awhile, and then when the nerves started to regenerate, there were lots of strange pains and other sensations that would crop up suddenly.
It's also not surprising that she still has to force herself to eat. The effects often linger for months afterward (I know they did for me) and while mealtime was a tedious chore, I knew it was absolutely essential to my recovery.
Cathy
Tongue SCC (T2M0N0), poorly differentiated, diagnosed 3/89, partial glossectomy and neck dissection 4/89, radiation from early June to late August 1989
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This is another custom island. This one could be used for ads. This spot is one of the best places for ads on your site to be placed. This can be enabled/disabled on a per forum basis.
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