• Pages

  • comments

    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
  • Enter your email address to follow this blog and receive notifications of new posts by email.

    Join 60 other followers

  • visitors


    No Princess Alone button

I’m not that sick really!?!

It’s been great being out of hospital this week, only trouble is trying to convince people that even though I have been in hospital for the best part of the month that I am not that sick really.  Its just the necessity of needing IV antibiotics because of the doses needed to budge the infection in the tunnel left by the portacath tube that insured my prolonged stay in hospital.  I was not feeling actually sick at all – just had pain at the site of the infection.  I am on antibiotic tablets (augmentin) til next Monday.  The Drs on the ward checked the site on Tuesday and are pleased with its progress but will check it again on Friday.  The PICC line is staying in until we are sure that the infection is not recurring after the antibiotic tablets are finished.    Radiation nurses are flushing the PICC line each day when I am there. 

Radiation is such a piece of cake,  compared to chemo.  I am still having after-effects from chemo, its part of the reason I am having so much trouble with this infection.  My hands and feet are still suffering side effects although the water retention in my feet has dissipated.  The soles of my feet is very cracked still and I still have residual numbness in my toes and in my index fingers and middle fingers of each hand, they’re are still not quite right. And my fingernails is still recovering I may lose some of them.

On the good news front my hair has started growing back.  I need to get it trimmed before a wedding we have got next week.  I have also lost most of my chemo induced weight gain.  So I am feeling great about that!!

Previous Post
Leave a comment

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

%d bloggers like this: