Having a chronically ill parent: It’s more common than you think.

Do you have a parent with a chronic illness?

Besides the term ‘caregiver’ which has all sorts of connotations, and often doesn’t describe the nuances of our situation, there’s not really a term for us. I like to use the word: ‘Watchers.’ 

Who are we?

We are the children of parents who live with chronic illnesses. That illness may be physical or mental. It may be recognised or diagnosed. It doesn’t matter. What does is that someone we love is suffering. And that hurts.

I was searching for a word that was all-encompassing. I wanted to avoid the label ‘carer’ – which has connotations of being paid and seems constrained to mere physical care of another. Physical care is invaluable and many of us may provide this for our Loved Ones. Yet others of us do not. Nevertheless, our life is mixed up with our loved one’s pain-filled life.

Do you feel helpless or lonely?

It’s easy to find ourselves helpless, and this is painful and even embarrassing. And this is even harder because we didn’t choose to Watch. This is the parent we have – there is no sickness-free version available.

And so we walk beside them, or in front of them, or behind them.

We cannot choose to walk a mile in their shoes, as the common saying goes.

Even that is denied us.

It’s not easy being the “healthy one”

We apparently have the world at our fingertips – and yet we have unique struggles of our own: We watch our parent – but who watches us? We answer the question ‘How are they?’ – but who asks ‘how are you?’ ? As our parent struggles, we suffer vicariously but also personally. There’s nothing easy about Watching.

Am I really a ‘Watcher’?

Do you have a parent? Are they chronically ill? Then you’re a Watcher. It’s not an exclusive club. There’s no entry free, no prize you have to achieve to enter. There’s nothing fancy about it (although, on one level, there actually is). It’s just life for us.

And that’s such a large part of what makes Watching so hard. It can be lonely. Each of us Watch, but we all Watch alone. Have you ever longed for someone to stand by your side, grasp your forearm and say with knowing, quiet voice and full eyes, ‘I get it. I understand.’?

I have.

That is the purpose of this blog.

You see, there are two answers to loneliness:

One is community, the other is God.

Why start a blog for children of chronically ill parents?

Firstly, it’s a journey that never ends – and so encouragement is needed for the everyday. Secondly, It’s a journey that can have distinct beginnings and endings, and so we need help for these times too. Lastly, Watching a chronically ill parent is a journey that, sooner or later (like every journey) will at some point encounter God. This blog is about that as well. I don’t have all the answers. Often I have none.

Nevertheless, I pray that these words will help you ponder your life as they have helped me ponder mine – and that your experience will be the richer for it.

May they provide a feeble sense of community and a less-feebler sense of God. Like C. S. Lewis, I have only,

“… been emboldened to write of it because I notice that a man seldom mentions what he had supposed to be his most idiosyncratic sensations without receiving from at least one (often more) of those present the reply, ‘What! Have you felt that too? I thought I was the only one.'”

~ C. S. Lewis, Surprised by Joy

Welcome my friends and fellow Watchers. Shall we travel the road together? START HERE

After a diagnosis: Why do I feel numb?

There are no safe guards in this life.

Just because someone suffers from lupus, doesn’t mean they can’t get diagnosed with appendicitis.

Last week my mum who has type 1 diabetes and multiple chronic illnesses was diagnosed with pancreatic cancer.

It’s not fair.

And that’s okay. It doesn’t have to be.

I’m going to try not to make this post a mere outpouring of my raw emotions, because that is neither helpful for others, nor in line with the tradition of this blog.

That said, such a diagnosis WILL impact my writing, and it’s not something I can keep quiet about. Partly because it’s real and leaking into every corner of my life, and partly because I hold out the hope that my reflections might help others going through similar trials.

At the moment I’m in the numb stage.
It sort of doesn’t seem real. How can this be happening to my own mum?
Continue reading “After a diagnosis: Why do I feel numb?”

What does society say about sickness (PART 2)?

What does society say about healing, prayer, heaven and sacrificial giving?
Have you been duped?

What do we really think about chronic illness? In the depths of our hearts, in the stillness of our bedrooms… are we really as kind as we think?

Here’s my thoughts on what society is perhaps “really” saying (or thinking!) about chronic illness and care-giving.

If some of these observations seem a bit too harsh, let me reiterate my definitions of “society”:

ONE: secular, not-specifically-Bible-based, thought.

TWO:  individual-focused, 21st century, Western culture (because that’s where I live)

THREE: the ‘natural’ whispers of my heart when it is not focused on Jesus.

You see? If this post is harsh, it is harsh towards myself. If this post is judgemental, I am sitting in the dock as well as on the jury.

Let’s examine ourselves together, and not be afraid of what we might uncover.

This is Part 2 of “What does society say about sickness?”

What society says about prayer

Continue reading “What does society say about sickness (PART 2)?”

What does society say about chronic illness (PART 1)?

We know what the Bible says about sickness, but what does society say?
Perhaps it can provide another answer. Even a better answer.

We learnt that the Bible has some guidelines which can help us formulate an ‘answer’ to sickness.

But we can’t stop there.

I think it is important we look at the flip side.

What does society say about Chronic Illness?

A definition of ‘society’

Now, by ‘society’, I mean secular, not-specifically-Bible-based, thought.

I mean the individual-focused, 21st century, Western culture in which I live.

I mean the ‘natural’ whispers of my heart when it is not focused on Jesus.

can you really define ‘society’ like this?

Wait! If at this point you have an objection, I am with you.

If your objection is: ‘We can unearth what the Bible says about sickness by reading it, but how can we discover what society says? It’s too subjective. There’s no manual.’ then I’m with you also.

There is no book for society. It is made up of so many ideologies and sympathies. ‘Society’ is different in different cultures and countries and times.

How on earth can we hope to pin down in one post the response of ‘society in general’ to chronic illness?

To even consider doing so seems pretentious on the largest scale.

Continue reading “What does society say about chronic illness (PART 1)?”