Thank you for this you inspired me because I'm crying at the moment worried i might have as my mom has it and am going crazy thinking about it I can't even look at my breast it's been days now and i feel pain in my breast but hopefully I don't have it
I am 52 yoa. My risk assessment number from the cancer center was 58% based upon my own personal history, extremely dense breast tissue , still have a menstrual cycle and not in menopause. I have had multiple biopsies with ADH, Benign Hyperplasia and the microcalcifications that keep appearing in both breasts. I have been progressing since 2014 with the changes throughout each breast. We feel this is possibly related to the hormonal changes that are taking place in the body. My mother had stage IV cancer two separate times and two separate cancers. I went through genetic counseling because I have multiple cancers of the same cancers on each side of my family. I was BRCA negative but have VUS mutation that they do not know enough about yet. My doctor ordered both the genetic testing and an MRI before ever cutting on me. I did have an allergic reaction to the MRI contrast dye, which left me with a headache for over three weeks that never abated even with tylenol. I was also very foggy and could not think clearly. While this is highly unusual, I knew that taking the monitoring route would not work for me. I have 5 close relatives who had BC (3 on one side with 1 metastizing and passing from BC; 2 on other side) 3 of the family members were between 50-54 years old, one uterine cancer, strong history of multiple colon cancers, melanomas and many others that seem to keep passing down to each generation. After seeking out three opinions, my family and I have decided to proceed with prophylactic nipple sparing mastectomies and reconstruction. It was not an easy decision but one that was well thought out and researched over the last 10 months. I appreciate your very informative videos. While I am nervous about the actual surgery, I can see that it will be the right decision for my little, active family as I was blessed to have a precious boy at 43 years of age. Thank you again for sharing your wisdom.
Thank you for a great advice I been diagnosed with early stage dcis high grade breast cancer waiting to have surgery DONT know which one yet will find out on the 7 November 2023
When I told my parents I want to get the brca testing he says be careful what you ask for because it might cause issues in the future of them not wanting to treat you because they'll say oh you have the gene mutation we're not going to cover you he said like when people smoke they have to pay higher insurance. Is that something I have to be concerned with if I get this testing
It is upsetting to me that not even one doctor told me to get tested for this chain until I was almost 60. Especially since I am a 99% Ashkenazi Jew, and had so many other risk factors for the gene. I believe that it should be illegal For gynecologist and Mammogram imaging centers to NOT at least, hand a flyer or a brochure to patients about the gene and/or testing for it- from either their gynecologist-and CERTAINLY from their breast cancer mammogram center. I will not go into my own personal story-any more than to say that I tested on DNA tests as being 99% Ashkenazi Jewish. The other one percent was low probability that I was anything else. EVERY ONE of my doctors knew about this, and so did my mammogram center. It makes me so angry that so many gynecologists and mammogram centers still do not offer any way to inform their patients about the BRCA test. It could be as simple as simply handing a patient a flyer or a brochure, and the medical practitioners can get even these brochures for free from organizations. Again, it should be illegal that this is not done Studies have shown that if patients test positive for the BRCA gene, they are more likely to get tested on a regular basis, so the test saves lives. They get tested earlier, and that saves lives. For ANY gynecologist or mammogram center or imaging center that does mammograms not even offer that information to patients, by SIMPLY handing them a flyer about the BRCA gene when they leave their appointment, or Simply mailing it to their Patience is CRIMINAL Gynecologists and mammogram imaging centers sure as HELL know how to get hold of you, when they want to get your money to pay them your co-pay.
Just the reason why we created the Breast Cancer School for Patients. www.breastcancercourse.org It is so important to learn everything you need to know about breast cancer "during" your treatment, not "afterwards".
Breast Cancer School for Patients At the time I wrote the comment here, I was going to thank you for this service here, your videos,and I’m shocked there are More viewers. Sorry for the typos, dealing with an emergency. What you are doing is hugely important, got a run
Thank you for the feedback. Make sure you visit the complete Breast Cancer School for Patients. Same video lessons, but organized in the order of topics you will experience them. www.breastcancercourse.org/
First of all a big thank you. I just been diagnosed with DCIS, medium grade, I am 45 years old and 2 tumors in right breast,6 mm distance from each other, small breast and has been offered lumpectomy followed by radiotherapy, history of breast cancer from my mom and not been qualified for Braca mutation test and aldo refused to have mastectomy as they already discussed in MDT me and decided by other dr. Is anythings I can do...?! Do I really don't qualify?
How do you get breast cancer with no family of any form of cancer and both of my genetic test came back that I have no form of any cancer genes. The kaufman cancer center in bel air, md keeps telling me that I have breast cancer. I'm trying to understand how I got breast cancer.
I think patients not wanting to be tested, especially if it is preventative testing, as in they don't have cancer, but have family history etc, should be left alone. There is a push for people to do testing. The right to not know needs to be protected and promoted more
Are you kidding me? I didn’t even know that genetics testing was a thing until I kept prying it out of my nurse practitioner! I wish this procedure was more well known, it could certainly help those of us in the dark
Ms. KM. I saw your question and recognized that your question was not answered. Is that correct? Did you seek consultation about the BRCA variant? In essence, the variant itself does NOT mean an increased risk. However, it also means that there is not enough information as to what the variant means since there is limited information. This happens sometimes in women of color and or latin populations. The important aspect of this is to determine if there is strong family history of breast or ovarian cancer for example, or even pancreas or prostate cancer. If those in your family were tested and the variant was identified, then that is a RED FLAG and needs to be reviewed by genetic counselor and a medical/surgical oncologist. At the present time, there is international research examining these variants and to see the incidence in some of the countries in Africa, particularly Ghana or Nigeria. Wishing you good health, Dr. Hill (surgical oncologist)
Thank you for the feedback. Make sure you visit the complete Breast Cancer School for Patients. Same video lessons, but organized in the order of topics you will experience them. www.breastcancercourse.org/
