This week is Word Childless week. If I hadn’t found myself in that category, it probably would have passed me by, but I have, and so it is. I’ve read so many Facebook groups, blogs and social media sites sharing the heart-cry of women and men who find themselves excluded from the one group they would desperately have loved to have been part of. To read them and to really understand the outpouring of pain, desperation and isolation is immense. But this year I realise how far I have come.
I’m used to being in a minority group. I have a visible disability. I’m registered blind and I wear hearing aids. I have a Guide Dog. I stand out. I’m vulnerable and I have to ask for help a lot and it’s a daily challenge to do my best to ensure that this isn’t how people see me, nor how I define myself. I am positive, optimistic and independent. I want the young people I work with tosee this and know that whatever the challenges they face, they can overcome them and achieve, if they remain focused and positive.
But being childless- not by choice, is a different matter. It’s rarely a situation people seek to identify with, talk about openly or to ask for support. Whereas with my eyesight I can ask for my needs to be met and often feel empowered to do so, with infertility, it’s unspoken, it’s not talked about and admitting that friend’s being pregnant, attending baby showers, Mothers Day and seeing back to school photos at times all cause a massive ache in my heart to be a mum and can be tough is often just too hard. And it can be a really lonely place.
Yet despite their differences, when I was told four years ago that our dreams of having children were not to be, the lessons I’d learnt twenty years before, when I was diagnosed with a degenerative eye condition which ultimately leads to blindness and deafness came into their own. Having lived with my eye condition for so long, I have learnt a lot. There’s a proverb which says disappointment makes the heart sick. Facing my disappointment and dealing with it was key. With my eyesight, I went through the stages: the shock and numbness, the anger and reasoning and I grieved the career I wanted but couldn’t have, the irony being that midwifery was top of my list. I learnt to accept that the things I had assumed I would be able to do were no longer an option. Instead, a little at a time I planned a future around the my limitations and I learned to appreciate what I do have, and to squeeze every slither of silver lining that I could find out of my life, gratitude being a major key.
Facing Childlessness wasn’t so different. We grieved, devastated at the bottom falling out of our world. Disappointment, a suffocating blanket slowly smothering me. Having gone through years and years of stifling my excitement when I thought I might just might have been pregnant, only to have that hope crushed again and again had left me somewhat fragile. But gradually we started to look at what we could do with our future and we could still be a family, even with just the two of us- and my Guide Dog. We talked about how we can play a role in our friend’s children’s lives, how we could support our friends in their parenting journeys and having the time and opportunities for these special relationships with our honorary nieces and nephews.
To get by, I now practically consider what might be tough. There are films I choose not to watch or events I may skip, or have alternative plans for. This can help, but equally, I value my friendships more than wanting to protect myself from potential pain most of the time. If that means not always being able to partake in a conversation, then so be it – in the same way I sometimes sit smiling at an event that I struggle to see or hear the others I am sitting with, sometimes accepting that talk about children will be inevitable is necessary. One key piece of advice a friend who had walked this road before me gave, was to let things roll off my back and not take offence. Simple advice, but on reflection, that’s how I manage with my eyesight every day. People don’t usually intend to be thoughtless, but it happens, and smiling and getting by is sometimes hard, but it’s the better route in the long run.
For all the people reading this who are facing their futures without children, know that you can get through, that there are others feeling the same way and who have come through the worst of it.
Hope is powerful. It pulls you through devastation and grief and turns you head towards the possibility of the darkest time passing. At my worst, in both these heartbreaking disappointments I struggled to see past the pit I found myself in. Glimpses of light and chinks of silver linings seemed a world away and both times I felt my future was futile and bleak. But my faith in a God who loves me, with or without sight or children, along with a belief that He has a purpose for me which will utilise the abilities He has given me helped immensely. That knowledge, along with the encouragement of a group of friends who helped piece me back together and a husband who is a rock helped keep my perspective on what is important. I still hope for many things. I believe and have witnessed miracles, so God’s healing on both fronts is something I won’t lose hope for, but also I hope for the here and now being better than the lowest points I have known, as well as an eternity with an able body where there are no more tears.
Challenges and disappointments, however big, can powerfully shape us. My life may not be what I expected or even longed for, but it can be more than ok. It can be rich, vibrant and purposeful. At the point I was diagnosed on both fronts, it would have helped to have been told this, which is why I am writing this post. Isolation is excruciating. Feeling that no-one understands and not having others to share with is debilitating. Having hope that these feelings can improve and life can have it’s colour return is so important.
One key thing I have learnt is that to be loved and to be able to love others is paramount. We can do this in whatever circumstances we find ourselves in, if we are open to being honest, vulnerable and to accepting what we have. In a world of social media telling us we will only be happy IF….. we can lose sight of being content with what we have. Being childless does not limit this, neither does being disabled, it just makes it a little harder and challenges us to find a way through, but be reassured,there IS a way.