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.
Hi Muse,
best thing to do is chat to the staff- most of the people having pelvic radiotherapy will be having similar effects. I met a lot of men having treatment for prostate cancer while undergoing my treatments. Imodium is good and there are ways that they can advise you to take it depending on your symptoms and when they are at there worst. There are also other medications that they can give you which really help too. They can also give you a can't wait toilet card which helps with the anxiety of having to access toilets quickly.
Bland foods but keep eating regularly even if a small amount and lots to drink. Limit fibre and caffeine I was told. I found I became quite weak quite quickly so its good to talk to them at the first sign of trouble.
Not too much longer now
Jane
