as i read MPIP BB and refer to AIM and other melanoma and cancer websites and blogs i got to thinking.
there is no reference material in my docs offices. no pamphlets ,no handouts, no website recomendations , no nothing for resources. This is true of my hospital based infusion clinic nor the big 400 Doc Onc practice I was first referred too.
in the initial stages i had no info and could not really ask any intelligent questions of my docs. It was only after SLNB that i realized i needed more info from other sources.
there is more literature on Weed Eaters at the Home Depot than cancer info in my Onc's office.
I found AIM and MPIP on my own. One onc did get me a photocopay of the NCCM guideline pertaining to my stage of cancer. 1 sheet. From then on it was' 'standard of care' and 'trust us:"