Hello Ladies
Well, it was indeed a brutal week, what with Monday, Wed, Thurs, Fri - Radiotherapy, Tuesday - Brachy and Wenesday - Last Chemo!!
The brachytherapy was quite intense, but actually fine. I had a spinal block. I was asked to sit sideways on on a trolley and then they raised the trolley quite high and put a stool under my feet. They sprayed my back with (very) cold water and at some stage, I had a cannula inserted but can't quite remember when that happpened. I then had to form what I can only describe as a "foetal" position so that they could inject an anasthetic into my spine - that was painless - and then ask you to lay down and they monitor all the way how numb you are and how far it has reached. I believe they administer the painkiller through the cannula but please correct me if I'm wrong. I was then taken through to the theatre and didn't feel anything other than a twitch in my leg as they worked away. They constantly check your blood pressure and your vitals are constantly monitored. The nurses and team were fantastic, and the anesthetist stays with you constantly making sure you're not in pain and talking to you. The team explained everything that was happening and were so gentle and attentive I cannot fault them in any way. When you are finished there, they take you for a CT and MRI and then back to the recovery room where you can eat and have a drink. The worst part for me was that I felt very frightened and overwhelmed when I couldn't feel the lower half of my bod at all. Felt totally out of control but that was only for the beginning. I soon got accustomed to it. Approximately 2 hours later I was taken down for the brachy which lasted 10 minutes and then they took out the packing and the rods and mercifully I didn't feel a thing as I was still numb. When you can walk, go for a wee, then they will let you go but you must have someone with you, or they will take you and somebody must be with you overnight. If that is my experience for the next two as well, it is perfectly do-able. I did have some bleeding and soreness overnight and into the following day but it wasn't unbearable. This was the procedure at my hospital. The Oncologist comes around to see you before you go down to the theatre and told me before I was taken down for the brachy that I had had an excellent response to the treatment and from the pre-brachy MRI, at this point they can see no cancer!!! It feels almost as if I dreamed that - hardly dare to believe it!!! That makes everything so worthwhile and it really is worth fighting for ladies. I am sending healing thoughts and wishes to all of us and I hope this brings strength to all that follow xxx
This is fantastic to read, Julie! What an absolutely inspirational post for everyone coming up to brachy! Well done you little trooper! This is such great news! So happy for you. xx
Thank you so much Sarah, I hardly dare believe it and have to keep pinching myself! I know I still have a long road ahead but gosh, it is made so much easier in the knowledge that it is working! You have an extra large slice of lemon drizzle or carrot cake and enjoy for me too!! Hugs to you xxx
Thank you so much Jen! It just makes everything easier and so worth while no matter how tough the going gets. I hope you are keeping well. We have all been through so much and some so much more than others on this road to recovery and long may it continue for us all. Have a lovely weekend Jen xxx
Hi snowbird, so pleased that the brachytherapy wasn't as bad as you had imagined.
That's a very different experience to the one I had. I was given a general anesthetic and the brachy rods were inserted, then a CT to confirm correct position. I then had to spend 14-16 hours in a lead lined room while the therapy was delivered every hour. It was a very long process. There was no GA for the removal of the rods, just some pain relief. The nurse was only allowed in the room to check on me during a ten minute window each hour. I had this procedure twice, one week after the other and - the first was the week following my external radiotherapy ending. I actually managed to sleep during a lot of this time, eating was tricky as lying almost flat.
Interesting to hear how it's delivered in different areas.
Wx
Hi Welly
My understanding is that it depends on the equipment the hospital has, as to how they carry it out. My plan was for much the same as you had- admission on the Tuesday, CT scan, GA for rod insertion, then lying flat on my back in the room with periodic visits from nurses while the pulse doses of radiotherapy were delivered. Scheduled if I recall to be around 18 hours. Then rod removal with gas and air if required, and discharged on the Thursday. I had no idea how I’d cope not being able to move, but in the event didn’t get the treatment at all. I was scheduled for a single long treatment.
I understand that it’s also different if you have had a hysterectomy and have no womb. Sounds a lot more straight forward! I was treated at a specialist cancer hospital-cancer is all they deal with- but it amazed me that in this day and age we have to go through something that seems so barbaric almost.
Sarah xx
Hi Welly and thanks...As you say it really is fascinating how different areas use different methods and the method I have does seem to be the least common. I suppose they all have their advantages and disadvantages but will be very happy when it's finished and I can concentrate on recovery. Have a good week xxx
Morning Julie
Number 2 will soon be out of the way and done, then you can start to recover from your treatment. Nearly all done, so hope this last brachy goes as smoothly as it can for you. Big hugs, ready for the final push!
Sarah xxx
Hi Sarah,
Quick question. So my eyesight is bad and I'm wondering if you(or anyone) know if I would be entitled to free eye care? I'm in UK and currently on benefits due to treatment. Whilst working I was unable to afford the luxury of sight tests etc lol. Any advice welcome.
Thanks Angela xx
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007