Hi Kathy,

I have read some of your previous posts and, first, I want to tell you that I admire how you are a such great advocate for your husband. I am sure that your suppport, right from diagnosis, has been incredibly valuable to him to him. I, too, am a caregiver, and know how vital that role is to successful treatment.

My husband's diagnosis and treatment was almost 8 years ago. Yes, they got the cancer, but the after effects of radiation seem to be never ending. Your husband will probably continue to need your help and support for a long time, as new after effects manifest themselves.

When Kevin goes to Alaska, will he be in a place where he can get medical help if needed? Much of Alaska is very isolated. Of course, I don't know Kevin's particular situation. It sounds like he is doing well in many ways, and that is great, but he (and you) should feel very comfortable him about going so far from home and from his support team, just a few months after completing this very trying treatment. The treatment he had is not like other kinds of medical treatment where they just fix it and it is over. I am sure that your doctors can help guide you on this.

Best wishes to you and Kevin.



avw
wife/caregiver
SCC base of tongue 2004
teeth extracted (7) 2004 and (6) 2010
Radiation & Cisplatin 2004
PEG tube 7/2004 to 5/2007
ORN 2009
HBOT: 80 total (2009 to 2011)
Mandible resection & titanium implant 12/20/10
Post surg infection 1/1/11
PEG tube again 1/26/11 to 10/2011
Aspiration pneumonia 2/1/11
Pain free since 2011!
Bridge to replace all bottom teeth 2012