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Sandi Parsons, Proud Book Nerd

  • About Sandi
  • Books
  • Contact
  • Teaching Notes
  • Presentations
  • Reviews & Media
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Teaching Notes

 

Pepsi the Problem Puppy

Colouring Pages & Mazes
Teaching Notes

The Mystery of the Sixty-Five Roses

The Mystery of the Sixty Five Roses Crossword

The Mystery of the Sixty Five Roses Wordsleuth

The Mystery of the Sixty Five Roses Promo Flyer About CF

Jeremy Lightbulb Colouring

Jeremy Garden Colouring

 

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Categories

  • Book Craft
  • Christmas Tree Ramblings
  • Cystic Fibrosis
  • Dog Tales
    • Monkey Dog
    • Pepsi Parsons
  • Librarian Lists and Reveiws
  • Library Displays
  • Library Musings
  • My Book Nerd Moments
  • Organ Donation
  • Random Facts & Other Important Things
  • Sandi's Books
    • Pepsi the Problem Puppy
    • The Mystery of the Sixty-Five Roses
    • Writing the Dream

Recent Posts

  • 31 Days of Cystic Fibrosis: Part 3 May 11th – 15th
  • 31 Days of Cystic Fibrosis: Part 2 May 6th – 10th
  • 31 Days of Cystic Fibrosis: Part 1 May 1st – 5th
  • Book Review : I Can Jump Puddles by Alan Marshall
  • Book Review: Westy the Western Swamp Tortoise by Cathy Levett

Social Media

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See more antics from Pepsi Parsons or witness my Book Nerd Moments

31 Days of Cystic Fibrosis. May 21 Setting Off on the Road to Acceptance I went home from hospital with an oxygen concentrator and a referral to the transplant team at Royal Perth. At that moment, an official sleep study hadn’t been done to meet the requirements for state-provided oxygen therapy, so the hospital provided me with a concentrator so I could continue to sleep with supplemental oxygen. Although I had worked hard to maintain my health before, I never worked harder than I did in the second half of 2010. Because with time and effort I had ALWAYS bounced back and this time would be no different. After work I walked around the block, initially taking a stroll with Monkey. Monkey was 16 and her health failing, all too soon I had to walk alone because even my slow pace was too fast for her. I did mini bouts of physio up to six times a day and nebulisers galore, trying to clear the gunk that was clogging my lungs. This extra airway clearance seemed to be working, as my sputum production decreased, but still, my lungs could not breathe. All the while, I continued working, attending clinics at both Charlies and Royal Perth as well as transplant workup appointments. Bonus Fact: The transplant team at Royal Perth (now Fiona Stanley) has the official name of Advanced Lung Disease Clinic. I like to joke that this meant that the team themselves were ‘advanced’ in treating Lung Disease, because the alternative wasn’t worth contemplating. #cysticfibrosis #31daysofcysticfibrosis
A stranger I will never know saved my life seven years ago and made it possible for me to have a future – because her family said “YES” to organ donation. Does your family know your wishes? Have you had the chat? @rejectinglaurenrowe is on a mission (Note: not Jeremy’s kind of mission!) it's her goal to have 1000 people let their loved ones know their wishes to be organ and tissue donors. Anything you sign or tick saying you are an organ and tissue donor does not mean your wishes will be met, as it’s up to your next of kin (loved one) to have the final say. So let them know by… 1. Taking a photo with the #soyouknowsign. - you can download on your device or print at giftedlife.org.au 2. Tag your next of kin and three friends to let them know your wishes and for them to do the same. 3. Post on your social media with #soyouknow and giftedlife.org.au in your description. #cysticfibrosis #organdonation Rather than tagging just 3 people I’m putting the challenge out to everyone following me to do the same 😘

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