Here’s my disclaimer. As I sit here putting my thoughts on paper, the television show has not aired which may be a good thing. Or not.
Tomorrow, Suzanne Somers is going to appear on Doctor Oz to discuss the “revolutionary surgery to rebuild her breast.” Let me start by saying I think Suzanne Somers looks absolutely stunning. She is drinking from the fountain of youth and despite some tragic life events, her smile lights up the stage. She has an infectious laugh. I like Suzanne Somers.
However, (you knew there would be a “but”….. ) I hope that people don’t get too caught up in whatever she is going to announce on television. I don’t remember precisely when Suzanne Somers was diagnosed with breast cancer and I did not closely follow her treatment choices. I could do a quick internet detour to speak specifically about that but I would be missing the most important point.
I am an actively involved patient. I’m Inspector Clouseau heading up my own version of The Pink Panther chasing down whatever I could find about my disease, which, fortunately, impressed or more likely, amused my medical team. I was asking my oncologist about testing my tumor “biology” to determine if chemotherapy was necessary way back in 2006. Fortunately for HIM, he knew exactly what I was talking about or he would have been replaced. I can’t know more than my doctor about the newest treatment advances.
The flip side? My doctors, while I expect them to be at the forefront of everything new in breast cancer treatment, cannot and do not know more about my body than I do. I ask questions and I take notice of things in my body. That is just the collateral damage of a cancer diagnosis. You are all nodding in agreement. I know. We get it. Let the doctor tell me if that pain has to potential to be “something,” or more than likely, is “nothing.” I’m not a hypochondriac about this either otherwise I’m fairly certain I would have been asked to find new doctors. Or the more realistic scenario, I would have been treated somewhat dismissively and most definitely would be known as “The Obnoxious Patient.”
Calling the oncologist twelve days in a three week period freaking out about a headache is a very nervous cancer patient (understandably so) or a hypochondriac. My job, however, as my own advocate is to bring (in this example) the headache to the attention of my doctor and to have my concerns addressed promptly, properly and respectfully. I have a right to expect answers or explanations. When I call with the same issue on Monday, Tuesday and Friday in a single week, I earned the obnoxious title and it’s incumbent upon me to consider any suggestions from those doctors about finding ways to manage my anxiety.
Cancer may be a solo journey but it’s a team sport and we are the most important player on the team. Everyone on that team should be kept in the loop with all the nuances specific to your disease and the treatment plan. I can’t think of a WORSE place to seek medical advice than from a celebrity via a television.
Every cancer is different and one person’s magic pill is another’s poison or, perhaps even their lethal injection. I know in my own case, if I were to follow what Suzanne preaches I would be putting myself at risk. I can’t take hormones. There goes my shot at her great sex life and fabulous skin. For me, it’s a big trade off. Am I fueling a rogue cancer cell by following her regiment? The answer is yes. Quite possibly, I am.
My cancer is different. OR, my cancer is NOT different and Suzanne Somers just happens to be lucky. There will always be those who fall on the good side of a statistic. As I already stated, I don’t know the specifics with regard to Suzanne Somers but I do believe the majority of breast cancers are fueled by estrogen. Slathering hormone cream or taking pills is not something I would even entertain. Staying alive and cancer free is far more important than taking a risk because it worked for a celebrity.
I am beginning to see many retweets about the surgery that is going to offer hope to “millions of women.” I can see this reaching a fever pitch by the time Thursday night rolls around. The hype is beginning and it’s only Tuesday afternoon as I type this.
I did a little poking around and this surgical breakthrough is a “cell-assisted lipotransfer” which is in a clinical trial and Suzanne Somers is the FIRST enrollee. The trial is based upon “promising results” of an earlier Japanese study. I will let those lines speak for themselves. I have no doubt the surgery was a success or there would be no appearance on Doctor Oz. I am thrilled for her and I say that with deep sincerity and complete honesty.
I just hope that anyone who is a fellow passenger on this cancer bus realizes they should not be making personal decisions based upon what a celebrity is choosing to do. My cancer is different. Your cancer is different.
Learn everything you possibly can about your own disease. Speak to your doctors. Reach out to reputable websites like Is My Cancer Different. Find breast cancer support communities in the real world or online. Ask questions. See what Dr. Susan Love is saying. She did write the book often referred to as The Bible on breast cancer. Learn how to read statistics rather than parrot a soundbite. Talk to survivors. Gather your information. Make the best decisions for YOU and then, turn on the TV to see the choices made by Suzanne Somers.
I applaud any public figure whose voice will reach millions who is willing to say that all cancers are different and there is no “cookie cutter” treatment. I am really impressed by those who take the time to explain a little about the nature of their disease to help us understand how they came to their decisions. And I have enormous respect for those in the public eye who ask us to respect their privacy when faced with a serious health issue.
It irks me when to hear half a story. It irks me even more when I hear anyone in such a position make statements that aren't exactly accurate (that's another story that's already been told by bloggers far wiser than I am). Tell the whole story or, just announce the diagnosis and ask for privacy. I believe it is incumbent upon anyone with celebrity status to do one or the other. Go public and tell all or go public and say nothing beyond the diagnosis. Once you are on an interview sofa, in my most humble opinion, a person who is reaching many and then is unwilling to say anything but “I refused chemo and look at me,” is doing a disservice. And, quite possibly is advancing some else's disease because there are people in the audience hanging on to their every word.
Her cancer may have been different. Or maybe she was lucky. If it was the latter, is that a chance you are willing to take? I know it’s a chance I won’t take. I’m sticking with the proven science that is medically accepted by the doctors and researchers around the world. I like a holistic approach. I embrace herbs and botanicals as long as I understand what they are doing to my body and how they may negate the benefits of medication that has been proven effective.
Your cancer is different. Treatment should be custom tailored to your unique circumstances. When a breakthrough that provides hope for millions of women is available, it won’t be advertised with headline teasers about a celebrity appearance on a popular TV show. It will be a quiet scientist who publishes a research paper that will hit one of my medical feeds and go viral.
All user-generated information on this site is the opinion of its author only and is not a substitute for medical advice or treatment for any medical conditions. Members and guests are responsible for their own posts and the potential consequences of those posts detailed in our Terms of Service.
Add a Comment2 Comments
Hi AnneMarie,
I agree completely with every point you made. I am currently in remission because I received medically accepted treatment. The rare type of esthesioblastoma puzzled even the best physicians in the field. Every cancer, every patient is different. It seemed as if my physicians were "writing the chapter" on my treatment plan as we went along, it didn't matter. What matters is I am alive.
Thank you so much,
Maryann
December 16, 2011 - 5:29pmThis Comment
Thank YOU, Maryann for taking the time to share your thoughts with me and I especially appreciate that you validated my feelings. Yes, what matters is that you are ALIVE and that you had doctors who found ways to make it work... to attack the cancer.... Remission is a great place to be. Be well & stay well. And again, thanks for commenting.
Happy holidays,
AnneMarie
December 16, 2011 - 5:54pmThis Comment