There are a lot of myths and stereotypes surrounding #Autism, so for this week's blog post I tackle some of them.
❤️Lockdown & children with autism.
To say life isn’t hard would be an understatement right now,l know life is so hard for many in lockdown,but with Children with autism and our eldest Adam having chemotherapy it is a nightmare for them https://all.Our children do not understand this situation it is so hard for them,they want to get in the car and go to see their grandad their older siblings,their auntie or most of all McDonalds😂,they are not happy with just a walk down the road as it doesn’t lead to anything for https://them.Lisa wants to go to school,she still picks up her school bag waiting for her bus she also no longer sleeps at https://night.Adam will spend his 18th birthday in lockdown,in many ways it feels so unfair for https://them.But what l will say is l would rather my children be safe than sorry as if any of them got this virus their chances of coming out the other side are not very https://high.Please be patient with everything that is going on as a lot of families have a lot to lose if Covid got into their https://home.I know this will pass,but putting yourself and others at risk is not the answer,there are always people that are worse off than https://you.The quicker Covid-19 is gone,the quicker we can get back to some kind of normal,l don’t believe life will ever be as it once was,but l do believe we can make it https://better.Please be safe take care of one another and most of all be kind. 💕❤️ #Autism #Autism #AutismAdvocacy #AutismAwareness #AutismBlogs
When I first took my son for craniosacral therapy I never knew how much it would help him but also how much it would help me! I had no idea what craniosacral therapy was or how it could help but I was willing to give it a try. The practitioner explained that it was a way of working with the body using light touch which supports your body’s innate ability to balance, restore and heal itself. The first thought I had was he is never going to let you touch him in a million years so how is this going to work! She just sat down and let him be himself. He ran back and forth, stimming and giggling to himself just as if she wasn’t there. I felt the energy in the room change, I can’t explain it but it seemed calmer. After 20 mins or so Joe had stopped running and climbed onto the bed like he knew what to do – it’s the strangest feeling in the world to witness something you cannot physically see! We had weekly sessions after that for about 6 weeks and every week he would do the same, stim and run and then eventually calm down.
I started noticing changes in him almost immediately, the most obvious change was that he was less anxious. This meant that I could get him to do different things with less of a struggle. He started being able to control his emotions better, I’m not saying he doesn’t have tantrums because he still does, but he can bring himself out of them. I see the range of emotion before my eyes, anger, grief, acceptance all in about 5 minutes.
This is a boy that only ate ham sandwiches (minus the ham) at school but now eats a variety of foods, even bean wraps. We now have conversations about his day, what he did, what he ate, etc it’s amazing. Only a special needs mum (or dad) knows the desperation of wanting that connection with their child. I remember the first day it happened. I picked Joe up from school asking him lots of question and anticipating his ‘no more’ response, but that day was different, that day he answered me, I continued to ask questions trying to stop the tears rolling down my face. It was one of the happiest times of my life!
Therapy hasn’t just helped Joe, it has helped me see that if I believe something can happen it will. As parents, we are so afraid of what might happen that we let our fear take over and this has an impact on our body too! Letting go of that fear in the sessions calmed my inner turmoil and allowed me to shift my mindset and it’s made a massive difference.
We still go for therapy once a month, it is making a real difference to Joe. He has finally landed and I couldn’t be more proud!
Hey. This is my first post on here. I started writing a weekly autism blog shortly after I was diagnosed a year ago and want to share my posts with the aim of helping other autistics (whether diagnosed, self-diagnosed or unknowing) and spreading autism acceptance.
This week's post is on echolalia and is at this link.
Went to Texarkana to see Temple and put my autistic visual invention in her arm. She accepts a gift that she inspired and Amazon sells. Thinking in Pictures woke up my 1991 idea we almost patented when I was undiagnosed. 2015 finally diagnosed and read book. Designed and manufactured over 9 month period. Thanks for representing the Autism World Temple!