Finally I am home, after 20+ doses of IV antibiotics, many more IV flushes, umpteen doses of oral antibiotics, 1 trip to the operating theatre, 1 Hickman line removal, 1 ECG, 1 chest X-ray, 1 CT scan, 4 different cannulas, many blood tests, blood pressure, temperature and sats checks, swabs, blood cultures, codeine, paracetam'ol, oramorph, several Gluten Free meals (thankfully!), dozens of cups of green tea, lots of gf supplies along with their visitors and not surprisingly very little sleep.
The staff looking after me were lovely and kind and of course overworked. Sometimes I had to wait a long time for drugs or someone to stop the IV pump from bleeping or didn't get a cup of tea. Although unlike some people who have secondary cancers and are having to raise huge amounts of money to go for available treatments abroad, as the NHS can't offer them anything else, I am getting my treatment and tests and am thankful for this.
I am desperately hoping this week's chemo isn't delayed but we will have to see. I go to clinic on Monday and I'm sur I can convince them! I will have to have it through a cannula in my hand now the line has been removed. My infection markers are going down thankfully and counts are good so here's hoping!!!
Thanks once again for all the ongoing support, cards, gifts, messages, visits, food and childcare it is VERY much appreciated as always :-)