Chronic Illness, Marriage & Parenting (Pinterest)

There are many topics which fall under the chronic illness umbrella which I am simply not qualified to write about – or others can write about better.
One of these is what chronic illness looks like within a marriage and/or while parenting.

I’ve spent the past year collating resources on the Called to Watch Pinterest account which I thought may be helpful for myself and others. It’s time to do a few reviews so you know what’s there!

Enter….

Pinterest review: Chronic illness, marriage and relationships

(Includes 65+ pins to articles on the topic!)
Continue reading “Chronic Illness, Marriage & Parenting (Pinterest)”

Help! I’m jealous of their chronic illness!

Imagine this. Or perhaps you don’t have to…

Your Loved One has lived with their chronic illness for ten years. There’s been highs and lows, but you’re just beginning to understand what life looks like for them and also for you.

Then a close friend receives a diagnosis. They’re sick. Chronically sick… perhaps with the same illness as your loved One, perhaps a slightly different one.

Everyone is dismayed and shocked. They surround the newly-diagnosed one with gifts of love and support. Maybe they look at you, and assume you too will visit and offer your help. After all, you and your Loved One are ‘old hands’.

Perhaps someone nudges you and quips that maybe the past suffering of your Loved One was preparation for loving this person – that all that agony was raising you up for “such a time as this.”

You know you should help. You know you should love. But instead you feel… jealous.
Continue reading “Help! I’m jealous of their chronic illness!”

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)”

How to write about Chronic Illness (Watchers, we are not Biographers)

Are you ever tempted to sit down and try and order the pieces of your life?

As you love and care for your sick Loved Ones, do you ever wish you could straighten your hardships out into a coherent narrative, one with a tidy moral and neat conclusion?

Do you feel that if only you had a polished version of your life, it would be a enough to redeem your suffering, because then it would have a purpose?

In short, do you ever neglect your role as a Watcher in order to become ‘Biographer’?

This is what it looks like:

You are often on the look-out for a purpose or a theme behind your Loved One’s suffering, or in day to day occurrences

You have a yearning desire to put each new experience into words so that others can learn

You are tempted to dismiss parts of life which don’t lend themselves to ‘story’

You are drawn to those areas of life which seems just a little bit more dramatic, heroic or exciting

You feel that your life and experiences are wasted if nobody reads about it and learns

I’m going to switch to ‘we’ now, because this is something I am guilty of at times…

Continue reading “How to write about Chronic Illness (Watchers, we are not Biographers)”

2017 taught me that my timing is not always right (and that’s ok!)

They say you never stop learning. Though sometimes it’s hard to pinpoint exactly what you’re learning while you’re learning it!

Often I come away from a season in my life with the sense that I’ve just learned something: that my character has been shaped, that my knowledge has grown… but am unable to put into words exactly what.

That’s why I Iove reflection. Over the last few months there’s been an increasing pressure on my soul because I learnt something in 2017 that is important, and I don’t want it to dissipate as the calendar flips over.

Instead I want to cradle this truth close  as I march out into 2018. So here’s my attempt to put it down in letters on a white screen, so that the lesson might be worth the learning.

2017 taught me that my timing is not always right

2017 was full of projects…

Read more here

this post is published in its entirety on my personal blog, but I felt it was helpful for us over here too!

//What about you? What did 2017 teach your heart?

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

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

Chronic Illness won’t let me celebrate the New Year 2018

As the old year ends and the New Year begins, society gears up to welcome in a new period of life. Parties and fireworks are often external signs of our joy and anticipation of a fresh start.

Many of us begin to make New Years resolutions… but the problem is these simply may not be applicable for you or your loved one suffering from a chronic illness.

With chronic illness, the most common resolutions may seem:

Unachievable (because you have limited energy):

Learn a new skill or language
Organise your life

Ridiculous (If only you had these problems):

Get a better work/life balance
Only party 1x per week

Heart-breaking (if only you could!):

Be the healthiest you possible
Achieve your dreams

Continue reading “Chronic Illness won’t let me celebrate the New Year 2018”

Twenty-Seventeen – your favourite posts

Only a few days left of twenty-seventeen! I hope you all had a lovely, rest-filled, Hope-filled Christmas.

For those of you who didn’t, I pray you were able to cling onto the hope that one day Christmas will conquer chronic illness.

It’s time for some stats! Out of the 54 posts published this year, let me share which ones you liked the most, and then I have a huge favour to ask you…

(These do not include the introductory – But what is Watching? and the About Me pages, both of which were very popular.)

So, without further ado –
Continue reading “Twenty-Seventeen – your favourite posts”

Why my blog will never go viral (reflecting on 2017 as a Watcher)

What I’ve learnt from blogging about chronic illness on Called to Watch

At the moment, even as I’m preparing to look forward to Christmas, 2018, and the future – I’m also looking back.

This is what I’ve learnt:

1. I have everything to gain and nothing to lose

Blogging over the past year has taught me that Watching is a ‘thing’. By this, I mean, loving someone with a chronic illness is a state of being worth talking about. It’s a relationship worth sharing.

It’s actually an important part of who I am – just as it’s a crucial element to who a lot of people are!
Continue reading “Why my blog will never go viral (reflecting on 2017 as a Watcher)”

Traveling, chronic illness and character preparation

If you share a life with someone who struggles from a chronic illness, travelling can be difficult, exhausting and even terrifying.

As we progress further into December, many of us are preparing to go on holidays.

Recently I went away, and beforehand I did some preparation. Not the ‘buy insurance’, ‘print your papers’, ‘get the correct address’ sort of preparation, which unfortunately I was rather sadly lacking in (thank you Long-Suffering Friend!) – but character preparation.

What’s that, you ask?

It’s the type of preparation that I’ve discovered is essential for me to ‘get the most’ out of a holiday – as a human, friend, Watcher and Christian.

While this was one of the few times I travelled without my loved ones who struggle with chronic illness, many of the ways I prepared were born out of  holidays I’ve taken with them in the past.

These 5 ways are (in my mind!) applicable whether you’re travelling with chronically ill friends or by yourself, and even whether you’re going overseas or simply staying at home and taking some time out.

However, because they’re not specifically about chronic illness, I’ve published them on my other blog.

Here’s a taster image! Read the post here!

travelling as a christian www.gloryafterwards.wordpress.com #travel #christmas #hope #prepare #life
PS. I took this photo while I was away!

// I’d love to hear your thoughts! Do you agree, disagree? How do you prepare for holidays?

HAPPY CHRISTMAS!!

Christmas is coming up, and I want to thank you for following my blog. When you sign up you’ll receive 3 downloadable and printable cards suitable for someone with a chronic illness – and anyone in need of some love!

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

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

Christmas & Chronic Illness… friends or enemies?

Chronic illness or Christmas? Which would you prefer?
I know which one I’d choose. But too often we don’t have a choice – and this is very evident during the holiday season.

Over Christmas we often spend more time with family, and for many of us, that means spending more time with Chronic Illness.

Chronic Illness doesn’t go on holidays over Christmas…

While the shops and the media try to convince us that by November 1 we have entered into a ‘new world’ of perfectly laid tables, wrapped gifts and dizzying heights of tinsel – most of us know that’s not quite true.

Nothing’s really changed.

Certainly not our loved one’s health struggles.

The rest of the country may be feeling care-free and relaxed – but often our Loved One’s have more cares than ever before. Continue reading “Christmas & Chronic Illness… friends or enemies?”