As patients and caregivers, we have more sources of medical information available to us than ever before. When making decisions about treatments or support what source(s) do you rely most on? Did you feel confident about the information you were receiving? Do you feel you were provided enough information to make a decision or did you need to search for more information yourself? Is it possible to have to much information? Has the way you approached medical decisions changed over time? What advice would you have for others just starting this journey?
How do you make medical decisions? - Melanoma Wellness...
How do you make medical decisions?
I reply on my Medical Oncologist to lead my care, but I have on occasion sought second opinions from other Oncologists, one time even at a different hospital. I also am fortunate to have a fantastic family doctor who is a strong advocate for me and has taken the time to research items she wasn't familiar with. It's unfortunate but true, we, as patients (and caregivers) have to be very strong advocates for ourselves and ask as many questions as needed until we are clear on our options or the things that are being told to us. Keep a journal of questions and answers from appointments, take a friend or family member to every appointment if you can, and don't be afraid to use the resources offered to you. It takes a village. xo
Its so refreshing to hear you speak so fondly of your GP. I love to hear the positive side that there are engaged GP’s out there 💖