Today was my last radiation treatment. I said goodbye to all of the lovely radiation therapists, the nurses and the admin girls and was told I could RIP (!) my name off my locker. I told them all that although they were all lovely, I hoped not to see them again.
I am feeling very well, full of energy and very little skin damage compared to what I have been told of some other peoples' experiences.
I am off to Bundanoon to play recorders all weekend and then to Wollongong for a week. The next cancer event will be my appointment on May 14 with Professor Avni Savni in Melbourne.
My experience, my feelings, the way I searched and dealt with breast cancer.
Wednesday, 29 April 2015
Thursday, 16 April 2015
Allandale and good news.
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| Sunset at Rand |
Yesterday Kaye and I went out to the farm where she grew up and which her brother David now runs. There are 3000 acres altogether. It was so interesting to listen to David talking about the scientific way he farms. We had two long lovely walks and collected a boot full of pine cones for our fires. On our way home, we visited the graves of Kaye's Mum and brother and later, her father.Then we did the Corowa op shops (quite successfully) and returned for today's radiation.

The radiation is going well. Yesterday when I had my weekly check up with the radiation oncologist, he was amazed at my only slightly damaged skin. He wanted to know what I was doing. I took pleasure in telling him about the large doses of curcumin I am taking. He immediately searched the medical information online and was surprised to read that there is research to show how good it is for skin problems.
The other good thing is that instead of getting more and more fatigued, as predicted, I am getting more and more energy. So, something is working well.
Saturday, 11 April 2015
All sorts of Things
I have been very busy going to the hospital every day, doing my 1 hour's walking, half hour's meditation and squeezing in some Japanese and Welsh. It has been great to stay with Kaye a couple of times a week to cut down on the travelling somewhat.
The radiation is going ok with only a slight rash so far - 13 treatments to go, so we will see. My biggest upset this week was actually starting to take the dreaded Tamoxifen. I definitely should not have looked at other "users'" blog comments about side effects. The problem is of course, that if I don't take Tamoxifen, I am likely to get the cancer back. If I do, I could get cancer of the uterus and cataracts in my eyes plus numerous other nice things
Keith and I had a bit of a chat about it and "we" decided to try it for a while, at least until I go to see Professor Avni Sali . I am thrilled that I have an appointment with him on the 14th May in Melbourne. This man is the guru of Integrative Medicine, which means holistic. I am tired of the medical oncologist only knowing and dwelling on drugs, the radiation oncologist only knowing and concentrating on radiation and the surgeon only worrying about his surgery. The counsellor and breast care nurses are the only medicos who really care about me.
I have already studied the American Online Integrative Oncologist's information and now I am reading books and watching films suggested by Prof Sali's organisation. It is the same philosophy, thank goodness. It is hard work and every now and then, I get the doubts. I just watched a film about the connection between the mind and the body - lots of professional doctors and researchers advocating for meditation, yoga etc to assist in healing. They talked about "belief" - you have to believe that what you are doing is going to make your life healthier. Moral of the story for me - no more googling and never try to talk to the radiation oncologist about anything except to reply to "Do you have any rash or discomfort?"
On Monday night, in between daily radiation treatments, we are having a night out. The Dederang Picnic Race Club gave us a night at Quest Apartments, dinner and breakfast included. Also, after 13 more treatments, I get to go to a recorder weekend at Bundanoon, have a holiday with my sister Rob and even go to a concert in Sydney. 20 sleeps till I go to Bundanoon! There have to be some rewards for all of this stuff.
Well I have already had some rewards.
Visitors:Karl, Dave, Alison and Molly, Grant and Jan, Irene and Jim, Noellene, Louise, Celia and Jennni and her Mum from CSU, and my lovely recorder friends Suzanne and Rachel.
My constant reward: Keith's loving and patient care.
The radiation is going ok with only a slight rash so far - 13 treatments to go, so we will see. My biggest upset this week was actually starting to take the dreaded Tamoxifen. I definitely should not have looked at other "users'" blog comments about side effects. The problem is of course, that if I don't take Tamoxifen, I am likely to get the cancer back. If I do, I could get cancer of the uterus and cataracts in my eyes plus numerous other nice things
Keith and I had a bit of a chat about it and "we" decided to try it for a while, at least until I go to see Professor Avni Sali . I am thrilled that I have an appointment with him on the 14th May in Melbourne. This man is the guru of Integrative Medicine, which means holistic. I am tired of the medical oncologist only knowing and dwelling on drugs, the radiation oncologist only knowing and concentrating on radiation and the surgeon only worrying about his surgery. The counsellor and breast care nurses are the only medicos who really care about me.I have already studied the American Online Integrative Oncologist's information and now I am reading books and watching films suggested by Prof Sali's organisation. It is the same philosophy, thank goodness. It is hard work and every now and then, I get the doubts. I just watched a film about the connection between the mind and the body - lots of professional doctors and researchers advocating for meditation, yoga etc to assist in healing. They talked about "belief" - you have to believe that what you are doing is going to make your life healthier. Moral of the story for me - no more googling and never try to talk to the radiation oncologist about anything except to reply to "Do you have any rash or discomfort?"
On Monday night, in between daily radiation treatments, we are having a night out. The Dederang Picnic Race Club gave us a night at Quest Apartments, dinner and breakfast included. Also, after 13 more treatments, I get to go to a recorder weekend at Bundanoon, have a holiday with my sister Rob and even go to a concert in Sydney. 20 sleeps till I go to Bundanoon! There have to be some rewards for all of this stuff.
Well I have already had some rewards.
Visitors:Karl, Dave, Alison and Molly, Grant and Jan, Irene and Jim, Noellene, Louise, Celia and Jennni and her Mum from CSU, and my lovely recorder friends Suzanne and Rachel.
My constant reward: Keith's loving and patient care.
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