“I’m Feeling Totally Empowered”
Meeting an oncologist seems so daunting. Yet we were so excited to meet her. We knew it would be a long appointment. We heard she was thorough and with one appointment before us we ended up waiting a good 90 minutes. We had had many discussions this week. I think we were both nervous. All I knew is that I didn’t want my wife to have to go through chemotherapy. It is such a toxic solution. On my way back from the restroom I heard the fellow tell her colleagues, “they’re a nice couple and will be very receptive to options”. We had met her a few weekends before when we were having drainage leaks on a weekend and she patched her up.
After the wait, we filled out more forms and met the fellow, the resident, and the pre-med student who crammed in the room with us. You’d think that meeting a fairly well-known oncologist you’d think of a big oak desk surrounded by books. Well this wasn’t Marcus Welby. We pused into a tiny 8 x 10 room and the wait was finally over. She told us the Oncotype number. An 11, which means an11 percent chance of recurrence. Tamoxifen hormonal therapy would put that number at 7%. Chemotherapy would not be recommended! A smile hit our faces.
Then the information hit us like stats on a Wall St. ticker tape. 25% of all cancers are undetectable on mammograms, tamoxifen is sometimes not metabolized by women, soy is not necessarily recommended product as tests are being done to check its relation to breast cancer, ……..it hit like a dumptruck of information being thrown on my head and my hand got cramps writing everything down. Fortunately the pre-med student was typing notes away as the oncologist spoke. Thorough and reasonable in her presentation, the oncologist laid out the basic plan for us and then gave us alternative trials with names of drugs and tests that i could not even begin to spell. We’ll have to peruse these options before our next meeting, or we could just email her our decision.
She did turn to me and ask me at one point how I was doing and what questions I had and thanksed me for attending this session and being supportive of my wife and others. This woman knew everything. I told her I was concerned because my wife, some aunts and both of my daughter’s grandmothers had breast cancer. She took notes and then told me I needed to be tested as well to see if I carried the gene that could possibly be passed to my daughter. I gulped. Wow. Sure i will get tested. When my wife goes to get tested for the Braca gene, so will I.
The only time I felt uncomfortable was when they started talking about the side effects of tamoxifen and the other therapies: Tiredness, osteocrenosis of the jaw, menapausal symptoms, loss of libido, hot flashes…sitting in a small room with 5 women, all I could do was look at the tips of my shoes. I cracked a small joke and everyone laughed. They were uncomfortable too.
Three hours after we entered the clinic, we walked out hand in hand and I could recognize a little skip in my wife’s step. “Are you okay?” I asked. She smiled and said, “I finally feel like I’m in control. I feel empowered”. It was not the answer I thought I’d get, but I definitely could understand her thinking.
We’ve still got a bit of a way to go, but this is a move in the right direction and quite possibly the beginning of the end of this chapter. As we sat at home we discussed how surreal this all felt. Cancer? No chemotherapy? No Hair loss? It just seems like we’ve been groomed to think hair loss, cancer and chemo go together. Well, maybe this is just part of the new age of medicine.
It sure works for me.
Hello. I read your blog post and was moved. It’s difficult walking through this with a loved one. My Mom was diagnosed with Stage III lung cancer six weeks ago and I’ve been the one in the family who’s been doing all the research for her – to help her make her decisions.
She decided not to do chemo either. They said the tumor was too close to her heart to do surgery and Mom didn’t feel comfortable doing radiation.
She went to a Naturopathic MD who specializes in treating cancer, instead, and she’s had good results so far. They are giving her high doses of Vitamin C intravenously – with other things in the bag that help her too. She goes three times a week. One of the ladies she sees in the IV room every time she goes was just diagnosed as being in remission from breast cancer after four months of the Vitamin C IVs. She also has had several lymph nodes removed too because they had metastacized.
Anyway, Mom has stopped coughing up blood since she started the treatments, so we’re thrilled about that. She also changed to a vegan diet and we’re doing fresh juices every day for her too. We’ve addeed a bunch of supplements like maitake and shitake mushrooms, and a few other things too.
I found a very interesting series of videos on YouTube yesterday (which is the reason I was commenting on your blog). They are from a persentation by a Dr. McLaughlin, who was a Professor of Pharmacognacy (someone who researches medicines derived from plants) at Perdue for 28 years. His life work was studying out the Paw Paw plant and it’s effect on cancer. If you go to YouTube and search for “Paw Paw & Cancer: From Discovery to Trials” you can see this very informative series. It’s like 9 parts. But, the information is very good and he’s certainly someone with a lot of credibility, in my opinion.
I don’t know if you’re open to complementary medicine, but if you are, this might be a good one to consider – since it seems so thoroughly researched.
Anyway, blessings to you and your wife. It sounds like you’ve found a really great doctor who will help find your wife’s pathway to recovery.
Tracey
Thanks Tracey, I have forwarded the videos to my wife. I think my wife is pretty set with the bisphosphonates for now as her main trial as she wants to help the clinic she is working with. Very interesting stuff.
Good luck to you and your mother.