On the drive home from the bar, I began to panic. I called another friend and blurted out the news to her. She immediately pulled up Paget’s Disease on the internet and began to read to me. I recognized some of the same information my dermatologist had shared: it is rare, the treatment is surgery, it can be DCIS (ductal cancer in situ) or there can be an invasive cancer in the breast, it is usually confined to one breast, one surgery involves removing the nipple and aureola, another is a modified radical mastectomy, sentinal nodes are removed to check the lymph nodes, sometimes there is follow up radiation, no mention of chemotherapy. The information from WebMD and the Mayo Clinic was almost identical.
Once I told her I would have to go to the state capital, to the medical center there, she immediately volunteered to accompany me. I accepted, with gratitude; I did not want to face a surgeon alone. I have had a great deal of experience with major medical centers because my son, as a child, was frequently ill. There was never a clear diagnosis as to why and I learned that the physicians who can just say, “I don’t know.” are rare. I also learned that if you questioned doctors and their decisions on how to proceed, you were quickly labeled difficult, in denial, or unrealistic. Most suggestions about alternative medicine or healers were dismissed or ignored. I’m older now, more self confident, and more willing to state my questions and needs and expect to be treated with both courtesy and respect.
When my son was ill, I usually faced it on my own, not asking for help. Now my heart is open and I am willing to ask for help and be grateful for all that is offered. I am well blessed with friends. As soon as I get home I plan to call two friends who are breast cancer survivors and ask to hear their stories and solicit their advice. I know I don’t have to do this alone.