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    If you have popped over here from my facebook page could you please add comments in the blog rather than on the link on facebook itself. I dont want to worry YD unnecessarily Thanks. You can now use your facebook log in so you dont need to enter extra details if you like
  • All about Gertrude

    Gertrude is the name we decided to call my cancerous breast hence the title of this blog. Although I had to keep my breast through chemo and radiation due to the nature of IBC - once it 'blew up' it no longer looked like my breast and I couldn't wait to get rid of it. Calling it Gertrude was a way of seperating it from myself. This main page is where I write about the general goings on that relate to Gertrude, there is another page that are more a diary of treatments etc This blog is a public blog so although I am being very honest about my battle with Gertrude I have "changed names to protect the innocent" - because everyone can see it if you write comments on the blog pages please use the same abbreviations for other family member or friends that I do. Please feel free to ask questions if you want clarification because then other people who might have been wondering the same thing can read your question and our answers.
  • Abbreviations

    OH- Other Half (Hubby), OD- Oldest Daughter, MD- Middle Daugher, YD- Youngest Daughter, SB- soulja boi MD's fiance in the army (now ex fiance), OD's R OD's partner, BS- Breast surgeon whose initials just happen to be BS as well, BC- our GP (family doctor), Dr H- my medical oncologist, all other friends family etc will be referred to as initials etc
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  • SUSAN’S ARMY

    No Princess Alone button

January

I’ve been a bit missing in action on the blog front in January.

I have struggled to find balance.

I have been either too tired or too busy to write any blog updates.

The new chemo (Adriamycin) and pain medication has  been affecting me a lot more than the last two chemos, (vinorelbine and xeloda – oh not to forget the top up of herceptin) that I have had over the past two years, have and I have struggled finding a ‘new normal’, a new equilibrium where I can do the things I need and want to do without wearing myself out too much.

What have I been doing?

my column of our calendar for the last few weeks

 

I spent a day and a half in Christchurch for K’s Funeral, meeting up with CR and CM and spending the night with nieceB and nephew S and his lovely fiance J.

I have carried on with the ‘Cancer Wellfit’ programme.  My trainer was away for 3 weeks over Christmas but I kept up with the cardio part of the exercises on a Tuesday and a Thursday,  while this made me tired it also I think  conversely gave me a little more energy or ability to deal with being busy.

I have helped OD find her wedding dress and bridesmaid dresses

I have had blood tests every Wednesday and Chemo every Thursday.

I have spent a few moments catching up with friends.

I have indulged myself by having High tea at the Langham and Yum cha

high tea

I have helped C our French daughter acclimitise and helped her sort out her uni enrollment

I spent time with N (another exchange student) that was in New Zealand for a month. (and bought beads for my bead bracelets to commemorate their visits)

I have been to the beach once or twice

beautiful day at the beach

I have had a bone scan which required me to be in Auckland most of last Wednesday.

I have had a nap most afternoons.

and when I haven’t had a nap I have gone to bed early.

That has been my January 2012 up to now.

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