I feel like everyone I have talked to with breast cancer has some theory as to why this horrible thing happened to them. You can't help but think "what have I done to cause this?". Any social worker, mine included, will likely tell you that you didn't do anything...this is not your fault! As a patient, that's nice to hear but the increasing number of people getting cancer has to be somebody's fault. It's not just chance that 1 in 8 women will develop breast cancer in their lifetime. Everyone has heard that statistic advertised, especially during breast cancer awareness month in October when you can't seem to escape it. The equally as troubling statistic to me is that 2 out of 5 Canadians (45% of men and 42% of women) are expected to develop cancer during their lifetimes. Not only that but the number of new cancer cases in Canada is expected to rise about 40% in the next 15 years, according to a new report – Canadian Cancer Statistics.
Most of the articles with these statistics usually have a subsequent paragraph saying something like "you can reduce your risk of developing breast cancer with early screening and being aware of the risk factors". Unfortunately a lot of women that get breast cancer, especially young women like me, don't have any risk factors. I have no family history, I am not overweight, I was never exposed to radiation as a child, I drink little to no alcohol...the list goes on. So what the hell caused this?
Genetics - I have been tested for the BRCA 1, 2 and P53 gene mutations. Especially if you are triple negative, this is something to ask your doctor about and the sooner the better as the results take some time (mine took about 2 months). Depending on the results, a different chemo may be prescribed, for example, studies show that BRCA positive women might respond better to platinum chemotherapy drugs like Carboplatin.
The Birth Control Pill - I was on the pill for 10 years and had just stopped it 1 year prior to being diagnosed. Coincidence? I think not. Although drug companies obviously aren't publicizing the fact that the pill is linked to an increased risk of developing breast cancer, there are quite a few studies that have shown this and the International Agency for Research on Cancer has now listed it as a known carcinogen.
http://www.nbcnews.com/id/8759578/ns/health-womens_health/t/hormone-pills-added-list-carcinogens/#.VrFeIVMrJ8c
There are a ton of other things that could have caused my cancer, some I will probably touch on in a later post but for now, I will leave you with this really interesting video of Wendy Mesley who is a Canadian journalist that was diagnosed with breast cancer. It is from 2006 but in it she asks a lot of the same questions I am asking today that we still don't have answers for. There is one part where she says "at what point do you stop looking for the easy answers like 'eat your veggies' and tackle the more complicated issue of all the carcinogens that we are eating and breathing and drinking every day?" I couldn't agree more!
http://www.cbc.ca/marketplace/episodes/archives/chasing-the-cancer-answer
I am 30 years old and was diagnosed with breast cancer, specifically invasive ductal carcinoma. Before my diagnosis, I didn't even know what that meant. Now I have been forced into a reality where I not only know what it means but my doctors appointments and daily thoughts are filled with other previously unfamiliar words like neoadjuvant therapy, metastases, HER2 and triple negative.
I started this blog in hopes that some of the information I share may be helpful to other young women in a similar situation. Rather than posting my day to day experiences, feelings and progress, I plan to share some of the things I have learned along the way. Being dealt this hand in life at 30 years old brings with it some unique issues and questions. Will I ever have kids? How will this affect my relationships with my husband and friends? What is my long term prognosis?
Through this site you may find that my way of dealing with things is a bit different. I want to be educated about my disease and take an active role in my treatment and recovery. I want to understand every part of my pathology report, what it means, and feel confident that my doctors are recommending the best course of action. At each stage in my journey, I have experienced challenges with finding answers to my questions and ensuring that the medical professionals treating me really understand who I am and why my way of dealing with this disease may be unlike other women. My hope is that people will be able to relate to my experiences, learn from them and find some comfort that they are not alone.
I started this blog in hopes that some of the information I share may be helpful to other young women in a similar situation. Rather than posting my day to day experiences, feelings and progress, I plan to share some of the things I have learned along the way. Being dealt this hand in life at 30 years old brings with it some unique issues and questions. Will I ever have kids? How will this affect my relationships with my husband and friends? What is my long term prognosis?
Through this site you may find that my way of dealing with things is a bit different. I want to be educated about my disease and take an active role in my treatment and recovery. I want to understand every part of my pathology report, what it means, and feel confident that my doctors are recommending the best course of action. At each stage in my journey, I have experienced challenges with finding answers to my questions and ensuring that the medical professionals treating me really understand who I am and why my way of dealing with this disease may be unlike other women. My hope is that people will be able to relate to my experiences, learn from them and find some comfort that they are not alone.
No comments:
Post a Comment