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#14300 06-20-2003 06:14 PM | Joined: Jun 2003 Posts: 8 Member | | Member
Joined: Jun 2003 Posts: 8 | The chemotherapy was for the breast cancer. My oncologist said there was no chemo available for the ACC.
At nearly 6 months from the end of radiation treatment, eating is still difficult. I live primarily on Smoothees, ice cream and Boost. My taste buds have improved, but things still don't taste right. I also have no saliva, as all the remaining salivary glands were killed by radiation.
At this point I figure I'm a member of the "in crowd." These days it seems everyone carries a water bottle everywhere they go, as I do also.
Stage III Adenoid Cystic Carcinoma, submandibular salivary gland. Diagnosed 10/02. Neutron radiation completed 12/24/02. Stage III breast cancer 3/03. Mastectomy, 4/03. ACC Mets to lungs 9/03.
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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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