Hi,
I was diagnosed with triple positive, stage 2 grade 3 breast cancer a couple of years ago. I had a WLE and therapeutic mamoplasty, chemo, radio, herceptin and am taking aromatose inhibitors. At the time I mentioned a history of ovarian cancer in my family but it wasn’t really taken up. I’ve asked more than once about genetic testing over the past couple of years. Anyway my oncologist agreed a few months back and I got my results back a couple of weeks ago. I have the PALB2 mutation. I am so glad I continue to push and ask for this test.
I am waiting for my genetics appointment in a few weeks time but I’ve had no other information or support.
I just wanted to ask what other people’s experiences of the process was and what to expect from here. Do I ring my breast care nurses next week and ask for a chat or is it just best to wait for my genetics appointment? What happens at the genetics appointment. Will they refer me for preventative surgery if deemed appropriate? Any experiences or advice welcome.
Thanks in advance xx
Hi @walkies,
I’m so sorry you haven’t had a reply to your post. Hopefully my reply gives it a boost and that someone shares their experience with you soon.
I’m so sorry to hear everything you’ve been through - and that you’re waiting for more information on what it means to have the PALB2 mutation.
Please know that your can ask our nurses your question on the Latest Ask our Nurses your questions topics - Breast Cancer Now forum section, or you can give them a ring on our free helpline, on 0808 800 600. They’re very friendly and knowledgeable, and so it might be helpful to talk this through with them.
We have the following blog on our website about someone who has the PALB2 mutation that you might find helpful to read: I struggled to find support for my PALB2 gene mutation | Breast Cancer Now
We also have this information Genetic testing for altered breast cancer genes | Breast Cancer Now
If you search ‘PALB2’ using the search function on the forum (top left corner) you’ll be able to find other’s talking about having this gene, and you might find it useful to reach out to them.
Hoping you get the answers you need soon,
Alice 