Advocating and Clarifying
Chuck and I both feel like we've been in a whirling tunnel of diagnostic tests, the actual diagnosis, treatment plans, research and questions....so many questions pop up. For those of you that really know me, you know I want to know all the information I can - I am a shoot-it-straight kind of person when it comes to receiving medical info. I like to know the plan, and then I can deal with it better - it's the "knowing" that is best for me and my mental state. Then comes the "why is this the plan?" questions. We keep a book called Chill the Fuck Out Cancer (sorry, not sorry for cussing), and I write the questions that come up for me from my own research, testimony's from other MBC patients, studying symptoms and signs - they are different. SYMPTOMS are things I feel, and SIGNS are things they find (like liver/kidney tests, something on a scan, etc.) I am in a MBC Facebook group with 12,000 (mostly) women that are going through the many twists and ...