What a difference a year makes! Happy 8th Birthday J πŸŽ‚

My boy has now turned 8 and I wanted to mark the occasion by thinking about just how far he’s come in his 8 years on this planet. As well as how much of a challenge it has been for him along the way. He’s a remarkable boy in lots of ways. But hey, I’m sure every child is. J is remarkable because of everything he has achieved in spite of his disability, everything he tries even when it’s so much harder for him and for trying and succeeding despite some people writing him off from the outset.

J is mostly happy; he’s fun-loving, adventurous and full of mischief. He is very determined and he perseveres with things, when even the best of us would have long-since given up. Until recently J would have been classed as ‘non-verbal’ as he could not speak. This didn’t stop him showing us what he wanted though. Yes at times it was difficult to figure out but if he could see we didn’t know, he would simply choose another way to show us and keep on going until we worked it out. It must have been really frustrating for him to have to put up with us, the stupid verbal people who had no real idea about proper communication!

When he was younger we really struggled to make sure everything was right for him. We were finding our feet ourselves and having to engage in fight after fight with various people to get him what he needed or deserved. It was, and still is, exhausting at times.

We knew from fairly early on that J was not meeting his milestones. He didn’t sit up, crawl or copy facial gestures as he should. He didn’t goo or gaa, struggled with rolling over and was sick a lot! The doctors eventually put this down to low muscle tone in his core, amongst other issues. He walked without crawling and kept his little hands balled up into the tightest fists most of the time. When he was around 18 months he was referred to a joint assessment team with a physio, occupational therapist and a speech & language therapist. After a few months a programme was put in place to support his movement and he had visits from the OT and physio to support him.

When he was two I took him to a group for children with disabilities and we focused on movement, stories, songs and other fun ways to get the kids engaged. He attended a pre-three nursery placement to support his needs and it was wonderful, the ladies there just ‘got’ him and he was really loved and cared for.

J used to fall a lot and visited the doctor and hospital many times, once needing surgery under general anaesthetic to fix his torn lip 😒 He’s a resilient little boy though and he always bounced back, it never put him off. His awareness of danger is still not fully developed and we have to constantly on guard to keep him safe.

When it came time for him to go to proper nursery we had a big meeting in his pre-three place. I knew he had issues, but working in education and having seen how nursery provision was set up I was sure he would cope fine with the right support. The nursery he was set to go to, who had never even laid eyes on him, were determined this was not the case. They made it clear that they didn’t want him and the message I got consistently from them was that they were unwilling, rather than unable, to meet his needs. They assumed that because he couldn’t speak he could not do anything. His end of year report reflected how little they knew him or had even tried to understand him. His major achievement for the year being that he could ‘bang a drum with support’! I didn’t even bother to ask them what kind of support you need to give someone to bang a drum.

During that year he was diagnosed with Autism, though we already knew this was the case before we got the official confirmation. After this we applied to send him to a specialist nursery who were more able to meet his needs, not least because they were more willing to try. It was a great year for him and he flourished.

After a fight to get him the most suitable placement he moved on to school. I’m so glad I had that fight. His school is a wonderful place, so positive and full of energy. The children are given so many opportunities and they celebrate success loudly and proudly. It’s a unique place, I have never seen anywhere quite like it. You can feel the energy when you walk in the door. J is happy there and he has come on in leaps and bounds. To begin with he used non-verbal communication; pointing, showing, etc. Then he started using PECS which uses a set of pictures in an exchange process to communicate needs and wants. He has also learned Makaton and can show us many signs (though my own ability limits how much of this I can understand – mostly only what I’ve watched on Mr Tumble!)

As a result of all of these opportunities and down to his own hard work and determination, J can also now use many words in context. Some of these are repeated phrases from his tv programmes or the you tube cartoons he watches (known as echolalia). Others are words he has heard from other people. A lot of what he says is down to his own interests and he often won’t repeat something if you don’t hear it or ask him to tell someone else. Not everything he says is clear, sometimes we still don’t understand, but it’s amazing how far he has come!

His development and all he has achieved are testament to his resilience and capability. He rarely gives up. J is very clever, he knows so much about many things. Since before he went to school he knew numbers beyond 20 and could show you every letter of the alphabet when you asked him to point them out. He knew all of his colours and shapes too. Saying them out loud was not something he was able to do but he knew them and it was really just about finding out how we could help him to show us what he knew.

So to you; my beautiful, clever, funny, loving, adventurous, mischievous, amazing eight year old; happy birthday! Enjoy celebrating and being the centre of attention. Be sure to get everyone to sing the song over and over again and keep getting the candle re-lit to blow it out. Make everyone clap and cheer, enjoying the big smile it puts on your face and the joy that shines out in your eyes and your flapping hands from the excitement. It’s your day and you’ve earned that right. You’ve come so far and learned so much. You’ve grown into a wonderful boy who brings lots of happiness to us and you have taught us so much in your life. You’ve taught me to be grateful, to celebrate the little things, to keep going when things are hard and to never underestimate people. Most of all you have shown me that I can also be a strong and determined person when I need to be, that I do have that little bit more fight in me even when I think I’ve used it all up and that I can achieve things others might doubt of me if I just go ahead and do it anyway!

I have so much to thank you for and all of this is only the tip of the iceberg. You have helped me to become the person I am, the mum I am, the teacher I am and to keep on pushing through the hard times. For someone so young, you have shown so many people so many things. I often worry about your future and who will be around to take care of you when we are not. It keeps me awake at times. Then I see how far you’ve come already and it renews my hope. I hope you will continue to flourish, you will continue to find that joy in the little things, you will be able to keep that happy innocence and that one day you will show the world just how much you can do!

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Memories, Milestones and Moderate Tantrums – Happy 3rd Birthday Baby Girl!

My baby girl turns three today. I know people say time flies but I can’t really believe she has reached this milestone already. From tomorrow she will be, in her own words, a big nursery girl. She often tells me that she’s a big girl now, usually when she wants something she knows she’s not allowed because she’s still just a little bit too little!

I’m not sure I’m ready for this. In lots of ways I can believe she’s a big three year old. She’s so very capable, can do lots of things by herself, her speech is just amazing for her age and she certainly knows her own mind. There are times when she knows her own mind just a little bit too well!

In many ways she has been the easiest of my three to get to this point. She has taken most things in her stride and made it clear when it’s not quite time for certain things to happen (like giving up her dummy or staying put in her own room without half a dozen bedtime stories and at least a hundred songs!) However, she’s also been so quick to walk everywhere and give up her buggy – she’s certainly little miss independent when it comes to getting around.

She’s always in the thick of things. My girl has a brilliant imagination, an amazing sense of adventure and an insatiable thirst for knowledge. She has attitude and a joie de vivre that would put many adults to shame and she just generally gets on with things. My boys didn’t know what had hit them, as she’s definitely the boss. She has her daddy wrapped around her little finger and knows how to get her grandad to do just exactly what she wants, without him even realising he’s been conned into it!

My baby is most definitely a force to be reckoned with. She throws herself at everything and has boundless energy. At times I don’t know how she is still standing at the end of the day. She could teach us a thing or two about determination and fun.

On the other hand she’s still so young. She still needs a little reassurance from time to time, needs a hand to hold and a kiss or a cuddle to make things right again when the world takes her by surprise. My girl has such a cheeky smile and always knows just the right look to give to get you to forgive her or make you laugh when you need it. She wears her heart on her sleeve and you always know just exactly how she feels about things. Her face gives it all away. If she’s happy it beams from her beautiful eyes and gorgeous smile and when she’s sad that little pout would just melt you.

I know I’m biased, she’s my baby after all. She is also my saving grace. She keeps me sane. That little face can light up the room and help even the most rotten days feel so much better. There are times when she just knows I need a smile, a kiss or a cuddle. She’s a whirlwind but she’s my girl, my friend and my partner in crime. At times I don’t want her to grow up, I want her to be my baby and always need me to look after her. I want to hold that little hand and see that lovely smile, wipe away those tears and sing that ‘one more song’. These moments don’t last very long and at times we miss how beautiful they are, as we are caught up in the busy throes of life.

I already see the things she doesn’t need me to do for her any more and my heart breaks a little, but I know there are many more adventures to come. We have a lot to do and learn together. She may not need me to zip up her coat or help her put on her shoes, but there will be many different ways she will. I will always be there to hold that hand, calm that fear and wipe away those tears. I hope that as she grows she knows how much I love and appreciate her, how she has helped me so much already and I hope that we will always be best friends and partners in crime.

So, to my beautiful baby girl, happy third birthday. Welcome officially to being a ‘big girl’. Just remember that even big girls are allowed to need their mum sometimes and I will always be here when you do! πŸ˜˜πŸ’ž

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Would you change things if you had the chance?

Is it possible to grieve for a child who is alive? To wonder and miss the life you thought they would have but can’t?

I see a lot of posts saying that people wouldn’t change their child and that autism is part of who they are. They say that given the chance, they would have their child exactly as they are. I admire these people and I really wish I could share their sense of peace with the status quo or their wish to keep things as they are. If I’m honest, if I could take away J’s autism I would.

Is it wrong to think of and be sad for the person you thought your child would or could become? For the potential that will never be realised and the future that is so drastically different from the one you envisioned when thinking of having children? Is it awful to wish it could have been different and that events had taken a different turn? These thoughts have me very conflicted. On one hand I know I am lucky. Lucky to have him and to know him, to see all that he achieves in spite of his difficulties, to see how hard he tries and how much he perseveres. On the other hand I look back at his birth and the issues surrounding it that I hold responsible for the issues he now has. I wish that none of that had happened and that he could be living a ‘normal’ life, free from the burden put upon him by his disabilities. A life like his brother and sister can have, albeit restricted for now by the need to support J as we do.

I know I’m lucky he lived through it and survived to come out the other side of his birth and post birth experiences. Someone once said to me that if he had died we would have grieved and moved on from it but this way we are trapped in a constant grief for what could have been, always wondering if things could have been different. I was horrified by this thought. Of course I would never have wished the alternative. He’s a miracle and amazes me every day. I couldn’t and wouldn’t want to imagine a life without him. He’s taught me so much and I still tell myself that it all happens for a reason, though sometimes I find it hard to understand that reason.

I often find myself worrying about what the future holds for J and how he will cope or be looked after when we are no longer around. I worry about how people will treat him out in the big bad world and how he will deal with this. I wonder if he will ever be able to have a job or to live by himself. If he will ever meet someone and fall I love. If he can’t will he know what he’s missing out on and how will this affect him?

I love J so much, I love who he is and his personality. I love his little quirks and that way he smiles at me when he’s up to no good and hoping I will either not notice or just let him away with it! I can’t actually imagine him being any other way than he is.

Why then do I have these other thoughts? The ones where I wish he didn’t have he start in life that he did? The ones where he doesn’t have a global developmental delay or autism or speech difficulties? I read often on the subject of autism awareness and acceptance and many people very eloquently advocate for acceptance of people just as they are. They say they wouldn’t change their children even if they could. I am all for this and believe that we should all accept people as they are. I am an advocate of being kind, always. I fight for my child and his needs and his rights. I find out what’s good, what’s needed and I seek to get it for him. I accept J as he is, for the person he is and I love him unconditionally for it. Does this mean I can’t wish he didn’t have his difficulties?

If I’m completely honest I would take away his autism if I could. Not for me or for anyone else out there but for J and the potential he’s missing out on, for his future and the opportunities he could have, for his present and the difficulties he faces and for his past and the struggles he’s had to overcome. I would take it all away in a second because I’m his mum and it’s my job to make his passage through this life as easy and good as it can be. It’s my job to look after him and give him the best opportunities and chances I can. If I had he chance to change all of that for him then of course I would. It doesn’t mean I love him any less as he is, it doesn’t mean I don’t accept him for who he is and love his little personality. It means I’m able to accept my son as he is, to love and support him in the life he currently has but that given the chance to take away his struggles I would do it in a heartbeat. Why then do I feel so guilty for the thoughts of the life that could have been?

I suppose then that in answer to my question I would mostly like to change the start to life J had. I would like him to be less frustrated by being able to communicate his needs. I would like him to not be overwhelmed by the world around him at times and to know how to cope with his worries in a less stressful way for him.

I wouldn’t want to change his loving, smiling, fun and caring personality. I wouldn’t want to change how much he loves me and how often he shows me this. I wouldn’t want to take away his innocence in how he sees things and the wonder he gets from even the littlest of things at times. I sometimes wish I could see the world through his eyes and capture the raw joy in what he experiences.

Would taking away his autism change these other things? I don’t really think so. Autism is a part of who J is but it’s not the whole. He is so much more than his autism, so capable and resilient in spite of the difficulties and challenges it throws at him. Maybe having these challenges helps to shape in into the little character he is but when I see him distressed and in full meltdown mode I can’t help but wish it was different for him.

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How well do I know my child?

J recently celebrated his sixth birthday. He seemed more aware this year that it was his day and that things were for him. It got me thinking about his thought processes and just how well I understand them and if I get it right most of the time.

When your child is non-verbal it can be very difficult and frustrating for both them and you. It is hard to fully understand what they want or need. Often it’s a guessing game of elimination to figure it out and finally give them what they are looking for. We have taken part in many activities, workshops and courses to try to help us to meet J’s communication needs, to try to support his development and to try to understand him and his world a little better. It’s been a long road with many ups and downs and bumps along the way. Being honest, we’re still on the journey and finding out new things as we go. 

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Benefits of being an Autism Mum

Firstly, the title is for effect. I’m not a big fan of the term ‘Autism Mum’ and only use it when it’s the only succinct way to describe what I’m talking about. I don’t mind other people using it, I just try not to use it myself. I’m just a mum. I have a child who has autism, so it is a big part of our lives. I’m not however a mum to autism, I’m a mum to my boy. I’m here to help him with his difficulties and celebrate his achievements. Not to label him and allow it to limit him as a result. Secondly, I use the word benefits in a loose, tongue-in-cheek way to describe the following list!

1. The ability to function on only a couple of hours sleep.

Most parents of young children will relate to this one. It’s the role of the young child to keep their parents awake or to waken them at regular intervals throughout the night. If you have more than one child they will usually take it in turns throughout the night to do this, thus keeping you awake for as long as possible with minimal disruption to their own nocturnal routines. If you are a parent of a child with autism, it’s likely this will continue long past the recommended time limit found with ‘neurotypical’ children.

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A tribute to the most selfless woman I knowΒ 

Last week my mum celebrated her birthday. I agonised for ages over what to buy her before eventually just asking her what she would like. The reason I find it so hard to get something is partly because I want it to reflect how much I think of her, how much I appreciate everything she does for us and to show her how much she is loved. Is there something you can buy that truly shows all of that?

My mum is amazing. She’s always around, always a shoulder to cry on and a rock to depend upon. I honestly do not know what we would do without her. From when we were little she has always put my siblings and I first, herself last. Now that we have children of our own she does the same for them. My mum and dad look after our kids whilst I work. Without them I would have to give this up, as J wouldn’t cope with a child minder or after school club environment. Instead of relaxing, winding down and enjoying retirement my parents are back to doing what they did when we were young (possibly more, as they help with looking after all 7 of their grandchildren!) They are so great with our kids and I don’t think we will ever be able to fully show how much we appreciate it.

To help with the kids’ routine and mine, my mum picks them up in the morning and they get dressed at her house. This saves them being dressed too early and allows me to get ready and go to work. They are then ferried to their relevant place of learning or looked after by my parents through the day, sometimes until fairly late by the time I pick them up when I finish work.

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A rose by any other name…

I’m changing my name! Ok not me, literally but I’m changing the name of the blog. My wee blog, awetismblog, and its name have served me well so far and I really appreciate all of the follows, likes and comments. Thanks everyone. I hope you will all continue to follow me under my new name. The content will be still be the same and the layout, at least for now, will still be similar. I have just been having a think about things lately. About our lives, family, the purpose of the blog and what it means for us and says about us.

When I started blogging it was purely to share my thoughts and experiences of autism. I think as it has progressed, it has become a bit more than this. It’s more a story of our lives and my thoughts/feelings. My purpose has always been for me to try to find the positive in things and learn lessons from what has gone on. Where I am definitely in awe of my son and his personality and progress in spite of his difficulties, I don’t want autism to be what defines him, or us. Yes autism has a big impact on us and what we do, but it’s not what I want our whole lives to be about.

This is not because I have an issue with the label or that I am in some way ashamed of it. Anyone who knows me knows that I am extremely proud of my family and what they all achieve. I regularly highlight issues associated with autism and its effects. I celebrate the good and learn from the not so good. Life is full of ups and downs, it’s hard, but it’s also rewarding and full of moments that make it all worthwhile. Therefore I see myself as a person who prefers to try to look on the bright side, the upside, and that’s why I’ve chosen this as my new name.

Everyone needs a makeover or fresh start once in a while, this is mine. I really hope that you will all stick with me in my next chapter of my blogging life and continue to lend me the wonderful support you have shown so far. It really has helped me to pick myself up after the hard days and feel good about the better ones.

Thank you!

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