9 months on Arimidex
I' 54, and after bi-lateral mastectomies in May 2015 I started on Arimidex in June 2015. I've had what seems to be massive side affects (to me anyway). The first thing I noticed was utter depression, I couldn't even get out of the house and cried for no reason. I went on anti depressants to counteract that, and it's working, thank goodness. In the meantime the nausea and a metallic taste in my mouth that makes food and drink taste awful started to creep in. Hot flushes a plenty to the point of absolute despare. Then the joint aches started. Firstly in my hips, knees and ankles. Now I have severe joint pain just about everywhere, every morning is difficult to get the joints moving. Once out of bed and moving it gets better and is OK as long as I keep moving. Cancer council offer yoga classes and I started through them. I now continue with the yoga twice a week. Try to walk every day and attempt to stay positive. Fish oil and glucosamine are a daily ritual, along with anti nausea medication and antiinflamitories for the joint pain.
i'm now seeing a clinical psychologist just to help me to accept this as 'the new me, post Breast Cancer'. Yes... I have the all clear and to stay that way I refuse to give in to the side affects and need to find a way to live with it. I'm a positive person by nature and I know i'll get through this sometimes we just need to accept that we need help along the way.
For those on Arimidex and suffering, hang in there it has to better than a metastatic cancer down the track. I wish you all well!!!