Well, Pat and all, I think many people post when THEY are ready to. I was a "lurker" for quite awhile once I did post I very swiftly was overwhelmed with very well meaning information that I was at too tender a stage in this journey to assimilate. As a result I withdrew. While I know now how very important this information is to receive it did just simply blow me away and away from this site. I didn't immediately go to another site, far from it, just stopped surfing the net to recoupe my senses. I don't need to tell any of you about how this miserable b**tard cancer BC takes over all of your life when you are diagnosed and that was what happened to Jim and me. I can't tell any of you what exactly except information I was seeking but I did feel it was as will all things in life...presentation that terrified me. I always say presentation is so important whether a fine meal or a discussion about BC. I do know so many people who post here are very knowledgable about BC and the "best" ways to get what needs to be done accomplished but I do think sometimes it is so aggressive that it may simply take people aback. When first diagnosed...folks are very nervous, scared, overwhelmed and frankly since so little is available due to the lack of info out there about BC they simply need someone to direct them, tell them what's what and offer them a shoulder to lean on. I know how important and urgent it is to get help as soon as possible, from the best facility with the very best surgeons etc but that's just how I saw it initially. I was scared away. I finally did send private message to Mike and he helped me get back on the "horse" of this forum. Hopefully almost a year out from my first postings, I can and do offer new comers information, support and defer them to others who have been at this alot longer than I have. Hopefully the above doesn't offend anyone it isn't meant to...I am just telling you how I felt at a time that I believed that my husband would be dead within months...that's what the surgeon had told us! Not a good time in our lives. As I always write now..."we are choosing to LIVE with BC and not DIE with BC". Thanks to all of you over the past year, Mike, Pat, George, MotoMike and Cynthia you have helped us out so much!