It begs the question:
Get Involved Search Breastcancer. More people than ever before are choosing to get genetic testing. Inherited gene mutations that raise the risk of breast cancer are actually relatively rare in the general population. Your doctor or genetic counselor may recommend that you get tested if you have a higher-than-average risk of carrying a mutation linked to breast cancer.
Many people who undergo genetic testing find it to be helpful or even empowering. If you test positive for certain gene mutations and have never had breast cancer, you can take steps to reduce your risk.
For example, you may opt to have protective surgery or make lifestyle choices such as exercising regularly and eating a diet that is low in processed foods and sugars.
If you test positive and develop breast cancer, your doctor will work with you to figure out how the gene mutation might affect your treatment decisions and how to reduce the risk of a new, second breast cancer or ovarian cancer. Genetic testing also has drawbacks.
For some people, an abnormal test result can trigger anxiety, depression, or anger. You might worry about your children or other relatives who also may have inherited the mutation.
Here, members of Breastcancer. Testing Negative After a Breast Cancer Diagnosis "When I was 64 years old, my annual mammogram revealed an anomaly, which when biopsied led to a diagnosis of invasive ductal carcinoma IDC.
After my lumpectomy, both my surgeon and medical oncologist recommended genetic testing based on my diagnosis even though I was postmenopausal and my ethnicity. I am Ashkenazi Jewish on both sides. There is absolutely no history of breast, gynecologic, pancreatic, or colon cancer on either side of my family, as far back as a century.
My medical oncologist issued the necessary written authorization for the genetic testing. Therefore, my treatment plan remains unchanged. Knowledge is power, either way it turns out. I tested positive for a BRCA2 mutation.
If I had tested negative, I would have opted for radiation and enhanced screening. This prophylactic surgery decision was easy for me as I already had all my kids and as I am now in menopause there is no chance of having any more kids.
It kind of kills me a little when I think about it too much. But just because a person may be positive does not mean that they will get cancer, just an increased risk a mantra I tell myself, it sorta helps.
Also, knowing that I have a gene mutation has helped me steer my treatment to hopefully prevent a future cancer from forming. They will explain what the findings can mean and can really prepare you for whatever comes up.
I received genetic testing due to age and family history, and I tested positive for a CHEK2 mutation. My docs know little about the mutation, and neither does anyone else, as far as I can tell. If so little is known about these rare mutations, why are you telling me about them?
My CHEK2 support group is full of people getting prophylactic bilateral mastectomies. Is there really just cause for it? It all feels very reckless to me, though I know for others it offers peace of mind.
This is just my experience. My mother was diagnosed with ductal carcinoma in situ DCIS at age Sometime after that, she tested positive for a BRCA2 mutation. That seemed like a lot of cancer in a small number of people.
I decided to get genetic testing because I wanted to know if cancer was stalking me.
I also have a variant of unknown significance in the gene STK I had a prophylactic bilateral salpingo-oophorectomy and a prophylactic bilateral mastectomy with reconstruction. I feel that I had surgery before my breasts had a chance to turn cancerous.
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