A Christmas gift to you, dear Readers

What. A. Year. It’s my prayer that you are all able to take some time over the holidays to reflect, grieve and rejoice over 2020. I am planning on doing so soon. But for now, let’s all take a deep breath, and celebrate!

I promised some exciting news before I left on my Sabbatical-Which-Didn’t-Happen. Now it’s time to deliver… and what better time than Christmas? My heart longs for my exciting news to be a gift to you all, dear readers and fellow Watchers. It has certainly been a gift to me. A gift of God’s kindness, a demonstration of his faithfulness.

For a while this year I wasn’t sure I’d even have this gift to offer you, so uncertain was life with COVID and other circumstances. But because of God’s goodness and generosity, I can – and so I pray you will join me in celebration.

Two Sisters and a Brain Tumour: My Christmas gift

What is this mysterious gift, I hear you ask? 

It’s this: Next year in August, my memoir, Two Sisters and a Brain Tumour will be published by Elephant House Press!

It is the story of my sister and I, the tumour which changed our lives, and the God who saved them. In 2015 my younger sister was diagnosed with a brain tumour, and my life was irretrievably altered. We went on a tumultuous journey together, and this is the story of that journey – the tears, the laughter, the crazy, quirky things which happen when you’re in hospital for 3 months, and the many kindnesses of friends, family, and strangers alike!

If you’re anything like me, you find ‘hospital stories’ rather depressing, and sometimes dry! I give you my word, I’ve done my best to make sure this story is anything but that. Rather than coming up with a list of ‘lessons learnt’ Two Sisters and a Brain Tumour is simply me opening up the window of our lives for three months, and inviting you along on the journey. 

I’ll be sharing snippets of the memoir on the blog up until publication, so here’s three little snippets from the first chapter as an early Christmas gift!

(mock cover)

Excerpts from Two Sisters and a Brain Tumour

A beginning

           You can read an x-ray and tell someone they’ve broken their wrist.

You can glance at a CT and tell someone they may have kidney stones.

You can’t study an MRI and tell someone they have a brain tumour.

Even if it’s true.

I haven’t quite finished my final year of radiography, but I still know this much.

**

A phone call

          ‘Jasmine had her MRI today. You know, the one the doctor -’

‘I know.’

‘Anyway, they gave us the printed out scan right then! All the pictures. Is that normal?’

I shrug out of habit. ‘I don’t know. So there’s no report yet?’

‘No just the pictures, and Emily, I think she has something.’

‘Has something? Has what?’ A brain? Unexpected, certainly, but hardly worth a phone call. I crane my neck. Or a missed bus.

‘I don’t know, I can’t read it properly. I just looked at the brain and there’s something there, and I thought you’d be able to read it. When are you home?’

**

A reassurance

               The back of the graffitied bus shelter rubs against the high wall of Rookwood Cemetery. It’s the largest burial ground in the southern hemisphere, according to Wikipedia. Ironic, really. A Health Science University campus, dedicated to saving lives, across the street from an overgrown, sprawling reminder of death.

Annoying little sisters don’t have ‘things in their brains’. The MRI will be normal.

I relax on the metal bench. It can’t possibly be otherwise…

*end excerpt*

Want to read more? For updates and more snippets throughout the year, add your email below. 

Join the journey:



Don’t worry, I won’t be flooding your inbox. Neither of us have time for that!

New monthly posts will begin again next year, and for now here are some of my reflections on Christmas, the New Year, and holidays in the context of chronic illness:

Christmas + Travel
New Year

May you have a refreshing and blessed Christmas. Thank you for Watching, and for joining me on the journey.

PS: Enjoyed the post above? Get the next one delivered straight to you! Sign up for email notifications  

I’m also on Facebook, Pinterest, Instagram & Twitter! Meet me there for more interesting reads, resources and community.

My husband has chronic inflammatory disease (Katie’s story)

“There are people willing to be with you during the dark times.” May this interview be an encouragement that there are others out there too, struggling to love and seeking to give, all the while figuring out what it looks like to do exactly that.

It’s time… for the first interview with another watcher!

The blog series Another Watcher’s Story is a compilation of interviews with other people just like us who are in a relationship with someone suffering from a chronic illness: mental or physical. They may or may not be in an ‘official’ caregiving role, but they have a unique tale to tell.

The purpose of this blog is to remind us that we are not alone.

So without further ado, let me introduce Katie, a wife whose spouse struggles with chronic inflammatory disease (and also the founder of a wonderful ministry: Broken and Mended!)

My husband has chronic inflammatory disease

1. How does your husband’s illness impact his life? 

He is always in pain to some extent. It limits his ability to join in some family activities, but not too many. 

2. What has been the hardest part of Watching them?

The way it has taken so much of his energy and focus away from other things. He is using it for the glory of God and so I am proud of him. He is, however, focused on things many people in the 40’s do not have to even think about. 

3. How has this impacted you?

I have had to adjust my expectations. We are still working out how this affects our relationship and our family. 

katie's story inflammatory disease chronic www.calledtowatch.com #caregiver #struggle #chronicillness #writer #hope #chronic #faith #watching #spoonie

4. What have you learnt as a result of this relationship?

To be more supportive. To realize that he has limitations and I have to respect those. 

5. How has God been present in this relationship?

Every step of the way. We both acknowledge His hand is how we found out about his disease. We believe he has lead David to start the Broken and Mended ministry. 

6. Have you seen any fruits or purpose for their suffering so far?

We see how he and I can relate to others who are suffering. 

7. What does Jesus mean to you? What aspect of his character has impacted you the most?

Jesus is my rock. I can not imagine going through any of life’s difficulties without him. I know that he understands each hurt and disappointment. I trust him with my future and know he will bring any good possible from this situation. 

8. What’s the best piece of advice or encouragement someone has given you? How have they shown they love you?

Early on we had friends who would help out with the kids in order for me to be with David for doctor appointments and surgeries. It is wonderful to have a network around you to help manage life that cannot stop when you need it to. 

9.   What piece of encouragement would you give someone in a similar situation to your own? 

There are people willing to be with you during the dark times. You do not have to pretend that you are okay with what you are facing. Lean on God for strength.

THANKS Katie!

// Are you a Watcher? If so I’d love to hear from you. Please don’t think your story isn’t exciting enough, or your loved one’s affliction not devastating enough! There are no wrong answers! Contact me at gloryafterwards@gmail.com to be part of this series (you can remain anonymous!)

PS: Enjoyed the post above? Get the next one delivered straight to you! Sign up for email notifications  

I’m also on Facebook, Pinterest, Instagram & Twitter! Meet me there for more interesting reads, resources and community.

My Daughter has Chronic Fatigue (Helen’s Story)

“The journey is slow, and it consists of tiny steps.” May this interview be an encouragement that there are others out there too, struggling to love and seeking to give, all the while figuring out what it looks like to do exactly that.

It’s time… for the first interview with another watcher!

The blog series Another Watcher’s Story is a compilation of interviews with other people just like us who are in a relationship with someone suffering from a chronic illness: mental or physical. They may or may not be in an ‘official’ caregiving role, but they have a unique tale to tell.

The purpose of this blog is to remind us that we are not alone.

So without further ado, let me introduce Helen, the mother of a daughter who suffers from Chronic Fatigue Syndrome.
Continue reading “My Daughter has Chronic Fatigue (Helen’s Story)”