To My Beautiful Boy

Guest Post by Lauren Morfett

To my beautiful boy, 

I hope you realise as you grow up how special you are, to us and to everyone you meet. Know that your little footprints will make a massive impact on this world. Know that your smile adds colour into my grey days and that your laugh is my favourite sound in the whole wide world.

You make us so proud in everything you do, life can be really hard for you but you never give up and that amazes me. I love watching you as you go about your day, you see beauty in everything you touch, you take notice of the little things that I am often too busy too see most of the time. I love the way you watch the way the trees move in the wind with pure amazement on your face and the way you spin around really fast but never get dizzy. You remind me to just take a minute and stop what I am doing and just breathe in the fresh air and really look at the good in the world.

When you sing it makes my heart melt because your voice is something we waited so long to hear, it’s beautiful and I could listen to it all day.

These last four years you have come so far, you have learned so many new skills and you have opened up your world and allowed us be a part of it, we are so thankful of that. Always know you can do anything you want to, the sky is your limit, I have no doubt in my mind you will do great things. I hope you know that nothing you do will ever go unnoticed, we will always celebrate every single thing you do because you are an absolute star to us Isaac and don’t ever forget it.

You have been lucky enough to not have any understanding of the painful things that happen around us,  I am grateful for the innocence you will keep because of that. You have no concept of fear and whilst that can be scary to us it also means you will never be held back by it, fear won’t control you like it does so many others and that’s kind of amazing to think about.

Always know that being a little different does not mean you are less than anyone else, don’t let other people defy who you want to be. Autism is a big part of you but that doesn’t mean that is all you are, you are so much more than that, to us you are just Isaac, our perfect four year old little boy who loves the outside and who has known the alphabet since he was one years old.

The struggles you face can leave you feeling lost but know that mummy will always find you, no matter what, I will always be there to pick you up and bring you back home every single time. Know that on days like that mummy tries her best but sometimes that isn’t good enough, it just means tomorrow I will try even harder for you.

When you are sad it breaks my heart, when you cry because your emotions are bigger than you at the end of the night when your asleep I cry too, for the things as a mother I can’t make better for you, that kills me the most. Know that even if I can’t make it easier for you I will always hold you tight and stroke your hair like I always do until your beautiful smile returns to your perfect face.

Know that we will always be there fighting your corner, we will make sure you get the best of everything this world has to offer. We will be your voice when you need us to be, we will make sure we shout when you are not being heard. We will always fight for you to have the same opportunities as everyone else because you deserve that, it is your right.

We will always be thankful you chose us to be your family, you changed our lives in the best possible way. You gave us a purpose, I can’t remember what life was like before you, it’s like you have always been a part of us. I am so excited to see where you end up, never change baby, your absolutely perfect. I hope Know that we love you and your brother so much more than you will ever know ❤️
All my love foreverMummaX

Written by Lauren Morfett: Wife, blogger and Mummy to two little boys aged 4 and 11 months in the UK. Learning from my beautiful son Isaac every single day ❤️

TOTS100 - UK Parent Blogs
TOTS100

The Music of Autism

It was a lonely experience, as I watched other parents in play groups laugh while their children screamed, rowing their boats down a stream, or leaping up from the floor as the group leader shouted “wake up bunnies!” My boy was oblivious to any of the surrounding noise and interaction, he just sat and spun wheels on a car. A car which I had had to fight the playgroup leader to leave out after the previous game of tidy up.

As the song segment came to an end, I picked up my son and nodded goodbye to the other parents. They would wait around chatting and arranging visits to the park, as their children chased each other, developing friendships that would last a life time.

We left and I sat in the car, feeling the tears well up in my eyes, other times when the tears didn’t come I would uncontrollably hit the steering wheel in a bid to realise the anger and hardship of our situation. I had no control of which direction my brain would decide to release it, my body always just took over.

Then I remembered a nursery worker’s words from the week before. I took a deep breath and turned the keys in the ignition.

“Sing to him” she had said. She explained the interaction of singing, the tune and the vocabulary all combined together. “He will start to interact, then hum the tune, and who knows, maybe add some words in time” she had added.

So I open my mouth and through the sobs I sang! And I didn’t hold back. I only had one audience member, and any reaction would have made my day.

But nothing happened that day. I constantly flicked my eyes up to the mirror to seek any engagement, but there had been none, my son just continued to stare at the seat in front of him. I did however feel slightly better after a good belt out of “She’ll be coming around the mountain”, by the time I got home I was in full on performance mode.

Even though I didn’t get interaction or even a flick of eye contact from my back seat passenger that day. I never gave up.

I kept singing.

I would sit him on my lap facing me, and do every nursery rhyme and children’s song I could think of. Over time he began to look at me, and then allow me to show him the actions with his hands.

I sang all the time, wherever I went. I was Maria, just without the guitar or perfect pitch! After months of solos and crazy individual hand jives, one day my son gave me his interaction. His reward back for all my singing.

As he sat on the carpet clutching Teddy, I watched him rock back and forward to the rhythm of my voice. He listened and did the actions. There were no words, but after every verse he would look towards me for more. It was the first step to an amazing journey.

That was three years ago, and today I don’t sing as much as back then. My pitch is still pretty shocking, and Rhys is only accepting of the perfect note.

He however sings every day a tune he has learnt or something from the back catalogue. I love to sit outside his door, in an attempt to not disturb him and listen to his singing, remembering all those hours I dedicated just a few short years ago.

Never give up.

Always remember to ignore strange glances from neighbouring cars when waiting at a red light and rocking the latest nursery rhyme. Trust me, you are having a lot more fun than they are. Also you most probably will never see them again.

Belt out those tunes. Its worth it.

Music is magical, even when you are a bit out of tune.

TOTS100 - UK Parent Blogs
TOTS100

Why I stopped Saying “My Son is Autistic”

“Autism. My son is autistic.” Those were words I said to myself, over and over again, as I tried to let them sink in. They had come as a shock to me, I was someone who had never had any experience in additional needs.

Autism had just been a word I had heard of, but had no context. It had never featured in my life and there had never been a need to research about it.

But my son, who was still the same little boy before the diagnosis, was autistic. This wasn’t a delay or something he would grow out of, it was part of who he was.

“You don’t need to tell anyone if you don’t want to.” said the paediatrician across the table from me and my husband, “that is your decision. You can call it whatever you like. A communication condition or social complex need. But you will have the formal diagnosis to get the support he needs”

As the days and months passed, I only told family and close friends. I felt like I was living in a parallel world where other people’s lives moved around me in a haze while I just thought “Autism, autism, autism”

I needed that time. I needed it to process the reasons for my son’s meltdowns, communication delay and absence from our world. It had come as a shock to the system. A shock I had to take time to process.

I talk about myself and my need to mentally process the diagnosis, even though it was not my diagnosis, it was my son’s. My son was only three, and to him nothing had changed. He still did what he did every day, sorting out his number cards and watching the motion of wheels as he spun them on his toy cars.

On the outside I carried on as I always had.

In the park I would refer to my son by name, “This is Rhys”, I would respond to a stranger during an impromptu conversation. His muteness was easily overlooked. He was only three, where ignoring adults could be easily seen as acceptable.

It took me six months to finally say the words, “My son is autistic”.

I started to tell strangers about his diagnosis when I mentioned my children being at different schools, or when Rhys would gently push a small child aside to get past, or when he would not answer to a question an adult had directed at him.

It started to give me closure, and I felt relief as I started to share a ‘secret’ I have buried away for so long.

It allowed me to share awareness, show people what autism was. My son was just like every other child in the park, the play centre, and the supermarket, and I wanted people to know that.

I spoke about autism whenever someone asked questions about Rhys, it was part of him and something that would grow with him as he got older.

But then something changed.

I stood in the park last week. Rhys spun on the bucket seat, absorbed in the motion of the spin, and I watched him from afar.

“How old is your son?” a lady asked, her daughter starting to climb up the steps to the slide, alongside us.

“He’s six” I answered, “how old is yours?”

We exchanged details of our children, our crazy lives, the local area and the weather. Then we bid each other farewell.

I then stopped and replayed our brief conversation in my head. Not once had I mentioned Rhys’ autism, not once had I said, “He’s autistic”.

I had just spoken about my boy and who he was – his age, his school, his siblings. I realised that I didn’t need to jump in and announce his diagnosis, and give examinations to strangers, or let everyone know. I never give a run down of my other children’s characteristics, strengths and challenges, so why should I do that for Rhys?

I will always educate about autism and talk about it when there is a need, but I feel I have moved to the next phase. Years ago I took time to accept my son’s diagnosis, then I found the courage to talk about it and share his differences, but now I have realised that not every situation is about his autism, it is about him and who he is as a person.

I want to talk about my son. About the amazing things he has accomplished. His cheekiness. His sneaky and quirky character.

He is autistic, but that is not what he is, it is part of him.

Autism doesn’t define my son. Nothing defines my son, except who he wants to be.

TOTS100 - UK Parent Blogs
TOTS100