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| | Joined: Mar 2011 Posts: 1,024 "OCF Kiwi Down Under" Patient Advocate (1000+ posts) | | "OCF Kiwi Down Under" Patient Advocate (1000+ posts) Joined: Mar 2011 Posts: 1,024 | Amanda, I'm sorry to read this. I know all to well that awful feeling when you are told this news. Please get yourself to a Comprehensive Cancer Centre. These big centerrs have a tumour board and do a team approach to treatment. Research shows that they get better outcomes for their patients. Please also tell your Parents. If you were my 26 year old I would want to know and I would do all I could to help and support you through this. You will most likely need both physical and emotional support to get through this. I am not in the USA, but someone here will tell you which are the CCC's. At least get a second opinion before starting any treatment Thinking of you, Tammy.
Caregiver/advocate to Husband Kris age 59@ diagnosis DX Dec '10 SCC BOT T4aN2bM0 HPV+ve.Cisplatin x3 35 IMRT. PET 6/11 clear. R) level 2-4 neck dissection 8/1/11 to remove residual node - necrotic with NED Feb '12 Ca back.. 3/8/12 total glossectomy/laryngectomy/bilat neck dissection/partial pharyngectomy etc. clear margins. All nodes negative for disease. PEG in. March 2017 - 5 years disease free. Woohoo!
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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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