Hi,
I had a PET scan after my TNBC diagnosis. Its a good thing as it can detect very small tumours. Luckily none were detected but it helped my Oncologist plan my treatment knowing that the cancer hadn't spread. The only bad thing is that they are not covered by Medicare!!! I astually negotiated a cheaper price so it doesn't hurt to try and haggle!
The TNBC.org site in America is a great resource. So is Cancer Council. They can match your mum up with another lady who has had a similar diagnosis and she will offer phone support. This is through their Cancer Connect program. Dial the 131 number and ask for Cancer Connect.
I opted for a bi lateral mastectomy as I had a recurrence. My surgeon had no problem with this. I intended to have reconstruction but not for at least a year afterwards so I could heal and explore my options. I'm glad I did. It gave me time to find the best Plastic Surgeon and the best option for me.
I joined support groups and talked with many women in the same boat as me. It really helps to meet other women who have had BC. Look on this web site and also Cancer Council's for the name of support groups in your area.
You're a good daughter! All the best to your mum.
Diane