This is a dedicated thread specifically for those who have had, are having, will be having or are considering the option of external radiotherapy or internal radiotherapy (brachytherapy). The idea for the thread has been approved by the Macmillan Community Team and the aim is for it to be a safe space where members can ask questions and share concerns and experiences.
I would respectfully ask that the chat is kept on topic to things specific to radiotherapy.
My own situation is that, pre-hysterectomy I was a probable grade 1 stage 1a, and was not likely to need adjuvant therapy. But my post op histology disappointingly revealed a few unexpected cells on my cervix, so I was restaged to a 2, meaning I was offered external radiotherapy x 25, and internal radiotherapy (brachytherapy) x 2. I’ve had my planning CT and am due to start radio on 11/4. I wanted to start this thread so that others facing radio can ask questions and seek support more easily than in an ordinary thread.
So please do feel free to post and tell us about your situation, ask questions, seek support and share tips/advice etc! I will also probably use this thread to post diary updates once my treatment has started.
Well done Love to Walk. I was told that as I lived less than an hour from my hospital I could do the enema at home. So it is worth asking, however once you get used to it, it isn't too bad and becomes part of the routine. I was told to use them for the first 10 days only. Good luck with your treatment
Glad it went ok for you
