From time to time I felt a little tired over the Christmas period but I can’t necessarily blame that on the chemotherapy. After all, we were catering for eleven people, although with a lot of much-appreciated help and support from our guests.
Once again, the only real side-effect I have suffered since the last chemo session has been some occasional indigestion. Or maybe I ate too much Christmas pudding!
I think I have been incredibly lucky so far; even my hair loss seems to have slowed down a bit. I only wear my wig or perhaps one of my trendy hats on important outings. Around the house I still have enough (thin) hair to get by.
Today I had my third chemo session which was uneventful apart from the discovery of a stray suture following the insertion of the Port-a-Cath (it should have been dissolvable, but it wasn’t).
While chatting to my nurse, Lily, I asked how long her shift was and was shocked to find out that they all have to work 12 hour shifts with just 30 minutes’ break. They all work so hard and are so dedicated.
I decided to have the “cold cap” treatment again to try and save my remaining hair.
Just before the treatment started I was visited by my Consultant Clinical Oncologist who examined me and said I am doing very well, which was encouraging.
Everything took rather longer to finish this time because many of the medical staff were still away enjoying their Christmas break; however, we were home by 17:00, a total of 7 1/2 hours.
If my hair should go much beyond its current sad state, not bothering with the “cold cap” for future sessions would save several hours each time.
Next Friday, 4th January I am due to have a further ultrasound-guided mammogram and then on Monday 7th a follow-up review with the Consultant Surgical Oncologist. I will post again after that.
Thank you, as always, for all your moral and practical support. Have a great New Year’s celebration!