I was diagnosed HER2 Positive in June 2011, radical left masectomy Dec.'11. They inserted an infusor port and Herceptin infusions commenced Aug.'11, this week I will have my 80th treatment. Infusions are every three weeks and I am able to attend the hospital on Saturdays - its quieter and suits my schedule. I also take anastrozole daily. I have experienced many side effects and suspect its the anastrozole more than the Herceptin although it is a very strong drug. I have three monthly heart scans and my oncologist recently said that I'll be on Herceptin for as long as my heart tolerates it. Apparently my post-op pathology did not fit any given profile and they made the decision to follow this treatment schedule.
I think the Herceptin impacts on overall energy levels and my nose runs constantly. I kept on working part time until June this year which I managed by 'pushing through' the fatigue. I also learned to say 'no' and put myself first most of the time and to prioritise. I am forever grateful that BCNA fought to have Herceptin placed on the PBS and that I elected to be a public patient - after six years of CT scans, Heart scans, 80 infusions, oncology appointments, two episodes of surgery, I pay for parking - there have been no other expenses and I am very fortunate to live 20mins from the hospital.