Hi,
I’m new to the forum. I have been wondering lately if I would meet the criteria for brca testing.
My Mum contracted BC in her late 60s. She passed in 2005 after it had metasised to her brain, lung and bowel.
She did however have a lumpectomy in 2000 and was told that they had got all the lymph nodes affected.
I have a half sister in Australia who is on my father’s side, and no siblings. My sister had the test in Australia and was negative. Mum had two brothers who passed of other causes and my NaNa passed with a heart condition. So it appears that my Mum is the only relation who has contracted anything.
There has been much in the news about brca lately, so it has set me thinking that I may need testing.
Would you know if I am at risk or should I consult my GP?
Thanks
Goldiewing
Hi Goldiewing,
If you have a concern then speak to your GP and see whether you meet the criteria.
The way it was explained to me was if you have 2 blood relations within the last 2 generations to develop cancer under the age of 60 then there is a chance there may be a genetic mutation that is worth investigating.
Over the age of 60 tends to be more likely environmental, age related or just one of those in-explicable things.
To give you an example my familial history is my Maternal Grandmother had BC in her 40's, she was one of 7 sisters, all but 1 had various cancers throughour their lives. My Nan never had a recurrance and eventually passed from Parkinsons in her 70's.
My Mum had cervical cancer in her late 30's (unlikely to be BRCA related) and had a full hysterctomy. We think this may have been a positive as it may have delayed any BC until later in life, there are some medical studies that suggest this can help with confirmed BRCA mutations. She then had BC at the age of 59. The tumour was inoperable initially but chemo worked and she then had a mastectomy and radio and was given the all clear. She continued with Herceptin treatment for 5 years.
We were then recommended to be referred to see a genetic counsellor during a check up by her oncologist because of the familial history. We later discovered Mum carried the BRCA2 mutation that must have passed through the Maternal line. I also inherited it, my brother did not and neither had my Aunt (Mum's sister). Which goes to show the 50/50 chances of inheriting the mutation.
Sadly after being advised to stop Herceptin at the 5 year all clear, my Mum was found to have secondary BC in the form of a Brain Tumour. It had returned in the worst possible place and advanced because they did not offer her a full body scan to ensure she was completely free of cancer cells in every part of her body. Without Herceptin in her system it advanced aggressively and we lost her 7 years ago in 2014.
I would like to say the chances of you having a BRCA mutation are unlikely, but I am not a medical professional, so if you are in the least bit concerned then see your GP. I think your Mum having BC in her 60's is still a concern, so as her daughter the least they can offer you is more frequent screenings to give you some piece of mind.
Hope this helps you.
Warm Regards,
Anne
Hi Goldiewing, i lost my sister to bc 2 yrs ago aged 43, I wondered if it was genetic but I wasn’t sure, when I spoke to her consultant she asked me to complete a family tree, it was only then when I could see the ages of a couple of family members having cancer young, I was able to be referred to genetics through my gp. I have tested positive for Brca 1, good luck, all you can do at this stage is go to your gp
Hi Anne, Thank you for your reply. Yes, I have been hesitant for a while, and my Mum was a similar story. She was on Tamoxifen and was due for her 5 year all clear in the October but passed in August 2005. Again, she was not given a body scan to see if the BC had spread, which it had. I will speak to my GP when I can get an appointment and go from there.
Thanks again
Goldiewing
Hi Previvor and thank you for your reply. Sorry to learn of the loss of your sister. I have gone through my family tree, and my Mum is the only one who had any cancer that I can determine. I think I will consult my GP when I can get an appointment.
Thanks for the advice and take care.
Goldiewing
Hi GoldieWing,
I was diagnosed with LCIS in 2013, the same year we lost my mum to ovarian cancer. I lost my sister last month to beast cancer that spread to her lungs snd liver. We were checked but are negative for the BRCA gene but due to the number of cases of other associated cancers in the wider family (prostate and bowel) were put on annual mammogram screening. We were told that even though we weren’t positive there could be other as yet unknown genes at play.
it is helpful to speak to a genetic counsellor as they will assess your risk and even if not BRCA positive may offer screening to give you some reassurance.
Best wishes,
Lisa
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2024 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007