Update on Cass Treatment
23 December 2025As we come to the end of WEEK 5 of my cancer treatment, this week has been a little more challenging than I anticipated. I transitioned from my NG feeding tube to needing a PEG procedure, as the NG was irritating my throat and causing significant reflux. The PEG hasn’t been easy, but I no longer have reflux or the constant urge to vomit, which has been a relief. With the PEG, my feeds and medications now go directly into my stomach.
My port is still very tender and painful, especially when I move or cough. My throat is extremely raw, with ulcers throughout, so sips of water or flat lemonade are about all I can manage right now.
The radiation has also started to make my jaw a little stiff, but I’ve been given exercises to help manage this and keep things moving. I’m still receiving IV fluids to help keep me hydrated and supported.
Even though I’ve been incredibly exhausted and often nodding off, having David has made hospital life a little more bearable and far less depressing. I was also lucky to have visits from Raewyn and Gareth, and of course Uncle Mike I’ve really enjoyed his company over the last few weeks. Their support and presence have meant more than they
Also I just want to say thank you to those that have donated and shared my Givealittle page, we are so grateful for the generosity that many of you have shown, thankyou once again🙏