Hi Clayton I perhaps have a longer history as carer than you and I am sorry for your wife to pass away from cancer. I still insist cancer not bc once bc becomes a secondary it is not longer bc (for statistical reference and purposes only). men that choose to be carers face two strong barriers.
If one takes interest on the subject often people in the role of carers are perceived as putting up obstacles on the way to the medical profession. Too many questions, buts and ifs, expectations and life expectations and prognosis privy to treating doctors etd. I was there too arguing with oncologist about the variations, drugs, radiation therapies cycles you name it.
On the other hand many women perceived bc as women's only concern perhaps a natural barrier I do not know why is that I can't answer that question/problem myself.naturally they seem to find more empathy with other women rather than men. As I was repeatedly told is a woman thing and many prefer to keep it that way. Others do not even bother to join sites like this they prefer to suffer in silence and within family cultural circuits of their own mainly ethnics
Personally it has been a fourteen years battle with a four time cancers each one worst that the one before yet my wife proved to be very tough to break down and wittle away into oblivion even when she has been in palliative care hands twice before.
Now my wife in the good care of a professor who is not even clear in his own mind of the kind of operation the other professor has done to keep my wife alive so she is in the lap of God to decide for the rest of her life.
I do not know what state you are from but if in Vic I'll join you in the project if you accept me. I love your courage and initiative I hope you'll get support and funding for this venture.