When I told my friend, Ingrid, that I had written a novel, she laughed. “So, working full time and bringing up two children’s not enough for you, then? You needed something else to do after you’d finished tea, put the kids to bed and done the washing up?” I know. Sounds like a recipe for burn-out. But it’s not impossible, and I know I’m not the first mother with ambitions to be a successful writer (or vice versa!) without giving up her day job…
Though, for me, that’s not the half of it. My oldest son, who I shall refer to as “J” was born both intellectually and physically disabled. He is a beautiful, complicated, funny boy who needs an awful lot of help. (Not to mention that I have found myself typing with only half a keyboard on my laptop of late – one of J’s less endearing habits being to pick off the keys, chew them, then deposit them in the toy box).
The truth of the matter is that “Swimming Upstream” has been a slow burner. I wrote the first draft 17 years ago and only around 3 or 4 years ago did I start breathing it back into life. Fortunately, the last 3 or 4 years have been relatively uneventful, emotionally, leaving me the mental space to write as and when I can find the time. The 5 years prior to that, however, were probably the most difficult of my life and writing was the last thing on my mind.
J’s birth was complicated, but no more so than many, and for the first 9 months we were blissfully unaware that anything was wrong. I noticed that he seemed to be slow to do things that other children were doing – he wasn’t sitting up or reaching out for toys, for instance – but the Health Visitor reassured me that some children just take their time. At 9 months of age J had a fit and we rushed him to hospital. The fit lasted a long time – a good 10 minutes – and even when it stopped he was listless and still, his eyes blank, and I thought he was going to die. I remember holding him in my arms in the front of the car as my husband drove the short distance to the hospital and pleading, “Wake up, J, wake up. Look at Mummy” over and over again. The next day he was diagnosed with epilepsy and Global Developmental Delay (GDD). We were told that his problems were “significant”. When we asked if he would ever walk or talk, the doctors couldn’t say.

For a long time it was hard to come to terms with, for both me and my husband, especially when seeing other children of the same age who were crawling, walking, running, talking, riding bikes – all the things that our J was supposed to be doing too. After our second child was born it was like having two babies at the same time, only one was bigger than the other and on a practical level this caused all sorts of difficulties. We bought a double buggy, for instance, which was impossible to manoeuvre and would only turn in one direction. J cried a lot of the time – whether from pain or frustration or general autistic distress at the everyday events his brain couldn’t cope with – we didn’t know. I remember crying, too – at work, on buses, at random and unpredictable moments, usually when talking about my children. In hindsight, I realise that I was suffering from post-natal depression. And all of this was compounded by some hurtful and unpleasant behaviour towards me from some members of my family at a time when I needed their support the most. Those events zapped my energy for months and even years afterwards.
J is now 10 and he still can’t talk, but he can walk, unsteadily, in the way that a toddler does. He has limited understanding and is mentally somewhere between the age of a baby and a toddler. He has never been officially diagnosed with autism but I am certain he is on the spectrum. As a family we now laugh at the funny things he does, such as walking into a room and turning the lights off while we are all sitting in it, then walking straight back out again. It may sound crazy but when he does something like that (or picking the keys off the laptop!) for the first time, we are delighted. It’s yet something else that he has learned to do. “Clever boy, J,” says his little brother. “Well done sweetheart. Mum, Dad, look what J just did?”

They say that in times of trouble you find out who your friends are, and I can categorically vouch for that. Talking was the key for me. Without my dear friends, Tracey and Clare and some wonderful women on Mumsnet (www.mumsnet.com), I honestly don’t know how I would have got through. Life is still hard at times. It’s never going to be easy, because J will always be dependent on us. He will never leave home, marry, get a job or have children. But it doesn’t stop me and my husband feeling happy and positive about the future.
There is a lot of comfort to be had in coming through hard times and knowing you can survive. I know so many fantastic people who are in the same position – or worse – who are not only surviving, but living truly amazing lives. And if they can take the worst thing that has ever happened to them and turn it into something positive … then, can’t we all?


Hello Ruth,
I found this post very moving and salute your courage and energy. Inspiring! (I can’t imagine writing a book with young children around, let alone with a full time job and one child needing the intensive care J needs.) I’m very much looking forward to reading Swimming Upstream. And to reading more posts! I’d love to read more stories about specifics of how you manage your life from day-to-day, what (and who!) helps and what doesn’t, where you find space to regenerate, your triumphs and disasters. Lovely to read that Mumsnet helps.
Hi Marian. Thanks so much for the comment. I think it’s feedback like that – the support and encouragement of others – that has kept me going when things have been really tough. I can specifically remember times when the words of a stranger on Mumsnet lifted me out of a fog and inspired me to see things in a more positive light. And there are definitely more posts coming soon along the lines you mentioned!
Ruth,
I honestly cried when read it.Such a moving story,probably because it’s real… I do admire your strength, both mental and physical! As a new mother I can barely manage my life now,can’t even imagine how you do it all! I can’t wait to read the book,always wanted to write one myself,maybe yours will inspire me;) Will follow your blog to learn more about your life as its extraordinary!
Love,
Anna
Hi Anna. Thanks so much – I am glad my blog post meant something to you. Being a new mum is hard, whatever your child’s abilities. More posts coming very soon… xx
Hi Ruth, it was a pleasure in getting to know ‘J’ & his brother, I have some lovely memories of taking ‘J’ swimming, it took a while for him to enjoy it, but when I stopped seeing you all he thoughly enjoyed it!! I hope things are going well for you all, thanks for the updates.
Thanks Helen. You were a huge support to us at a very difficult time … x
You’re amazing, lovely lady. I am in total awe of you and this post brought tears to my eyes. You’ve got yourself a rather special family there. Can’t believe you’ve managed to write a novel too – respect!
Maja x
Hi Ruth,
I’ve just finished reading you book that Helen lent me. It was a great read and story throughout I really enjoyed it. Keep up the good work and best of luck with it. Really hope it works out for you. You deserve it as it sounds you really work hard for everything.
Sharron Roberts.
Thank you Sharron, and I’m glad you enjoyed Swimming Upstream!
Thank you for sending me the link to your blog. I was unaware of my sons disability for 4years. This post made me shed a tear, my son is just about to turn 10. Reading your story is a reminder of how far ive come with my son, Samuel. Xxx
Hi Ruth I think were incredible to write a book with young children about. I also admire the way you help raise awareness of J . I think sometimes you just know that a child is on the spectrum without the offical diagnosis. I am pleased you have found solace online . I know my online friends help me get through some very tough times xx
Thanks Wendy. To be honest, all the assessments we had for J were hell on earth. He cried all the way through, and I made a decision not to put either of us through any more. He’s getting the help he needs and a further diagnosis won’t change anything.