Carole – Interview 39
Carole was diagnosed with breast cancer 16 years ago. She received a partial mastectomy, radiotherapy and chemotherapy. She also received tamoxifen, which gave her severe side effects and menopausal symptoms. Nowadays, she feels physically and emotionally well.
Carole was diagnosed with breast cancer 16 years ago. She received a partial mastectomy, radiotherapy, chemotherapy and hormone treatment. Carole had originally been on tamoxifen, which was making her feel unwell and experience very severe menopause symptoms, including hot flushes and night sweats. It really affected her life at the time, and she experienced depression due to the side effects of tamoxifen and hormonal problems caused by the original cancer. Someone suggested an alternative tablet which was not oestrogen based which she asked her doctor to prescribe instead, and it really changed her life. She doesn’t think that the radiotherapy or chemotherapy has given her any long-term effects.
She joined a social group of other people with breast cancer, and they used to meet up every fortnight. She found it especially helpful as they were all going through a similar experience, and it was someone in this group who suggested the alternative to tamoxifen.
Nowadays, she feels perfectly healthy and recovered physically and emotionally. She does think that having cancer affected her relationship with her husband, as he was very anxious when she was first diagnosed, and because she was experiencing depression as a result of the tamoxifen treatment. It took some time for them to work their way back to their former relationship.
Carole continued to see her cancer consultant for 10 years, which she feels was an appropriate length of follow up for her. It was a chance to get a physical check and to discuss any worries about the cancer coming back. She thinks that perhaps a yearly checkup at her GP clinic might be helpful for cancer survivors just to make sure everything is ok.
Her message to other people going through cancer is to always ask for help, to not keep things buried, and if you’re not happy with your care to say something about it. Also, she thinks it is important to keep your family involved, and not to be ashamed to have cancer.