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I am still trying to get the hang of this site. I am not always sure how to get where I want when I want. I am not always responding to wonderful friends in a timely fashion...if at all. Seems I stumble upon pages more often than actually knowing where I want to go and then just click a button and get there. Seems I have to search around a bit to find the pages and buttons. I am not sure if it is just me, the chemo brain or what...
I am also not sure why I need to know how many times we post...is...
Well....it was my 50th birthday last week...the day i had my 2nd cycle of chemo...id had a lovely nite out the nite before with the girls from work n my day at hospital was nice to..gettin a cake off the chemo ward n generally being made a fuss of...all in all i had a really good birthday...the chemo took its toll after a day or 2 n i was wiped out.
My son n his wife asked if i wanted to go for a quiet drink..just to the local pub...for an hour or so...just to get out the house...so i sed yeah....
Saturday, October 3rd 2009
Andrew had a fairly good night. He was in and out of pain and in and out of sleep. He wakes up mainly to push that pain button.
7:45am Dr Karnes arrives and shakes Andrew's hand, "hello partner". He
spent 15 mins telling us about the operation - he is very pleased with
the outcome and said that Andrew is a star patient. Yesterday, he gave
me a box with the gallstones in it - there are over 50 of them and
quite large. No wander Andrew suffered with them but in a way...
Tuesday 29th September
Well an hour or so after my last blog, I left a message for the consultant just in case the 4am pain bit hadn't filtered through. He rang straight back and after the usual questions, said he thought it would be a good idea to come in. "Ok,when?" says I "Now" says he - "we need to make sure it's not a pulmonary embolism." "Sh*t" says OH. "I'm not rushing!" say I. So we threw my still unpacked bag back in the car and headed...
Today has been one of the even worse variety. I need to talk to Robert and he's not here. Friends and family visit but they don't understand. Robert was the person who knew me inside out, knew all my faults and still loved me.
I don't think I'll ever have that again and that breaks my heart.
Its taken me ages to get onto this site !!! My lovely paul lost his fight on 20th Sep. We held his funeral yesterday. I'm so sad and very lost
We were told to arrive at St Mary's Hospital, Mayo Clinic, at 5:45am. We arrive at 5:30am. It's still dark outside and slightly drizzly. By 6:10am we are in a side room and Andrew is being prepared for surgery. Gown, white stockings, and non-slip slipper socks. People come and go, blood pressure, breathing 'toys' to be used post op to prevent pneumonia. Andrew and I talk about what's ahead. We both know that we are here in America because the doctor here gave us the best option of having a neo bladder...
As I write this, my darling is asleep on the sofa. Have spent a lot of time watching him sleep this last week - he caught me doing it the other day and told me it freaked him out!
Not sure how I'm feeling at the moment - tired for sure. Have bought an airbed so we can sleep in the same room still, but at the moment he needs space and room to get comfortable in the double bed.
'We' got discharged from hospital on Tuesday, following an appointment with the head honcho at the oncology unit. It...
Hi all,
I had a sentinal node biopsy which led to them finding cancer in one of the three nodes they took out. a week ago I had an auxiliary node clearance and the fluid build-up was painful and whilst shopping it found it's way out as a fountain which I mopped up with some tissues from my bag. I went into the breast clinic the next day and they syringed more off (Thursday 1st Oct). It then started to fill again overnight and I went in again.
My thoughts are that as this seroma fluid...
This is strange territory for me ,but thank-you for the welcome back on my return visit .will get there but it probally will take longer for me to find everything.
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