Looking Forward not back!

Looking Forward not back!

by Alienhippy

If I had a time machine, where would I go in time?

It’s quite simple really, I’d go back to 1969

I would befriend my own Mother at the age of 19

She’d be pregnant with me, my face yet unseen

~

I wouldn’t tell her who I was, but…I’d tell her I’m an Aspie

I’d tell her all about the problems my Aspie life has dealt me

She wouldn’t have a clue but her nature would be loving

I saw her hospitality all the time when I was growing

~

I saw how her personality would really confuse my Dad

His inability to socialise made him get really mad

But he couldn’t express in words or write how he felt down

So…we would have the aftermath of his Autistic meltdown

~

I’d explain to my Mom how important it is, to look out for what is the trigger

I’d mention about the damage done, when hearing people snigger

I’d talk to her about how it was when I was just a teen

So she could be aware of reasons why I go off into my daydream

~

I’d tell her what objects she needs to hide make her aware of my depressions

Be aware of all the times and why I skived off so many lessons

I’d tell her all about my dyslexia, so she’d get me all the help I’d need

She’d find a way to help me cope and…maybe learn earlier to read

She’d then understand that I’m not shy just fearful of rejection

She’d learn to broaden my horizon not smother me with over protection

~

But if I had a time machine and I went back in time

And changed the person who I am…this life would not be mine

All the stuff I’m learning the things I share with my friends

And all the love I feel inside as God helps me to mend

~

All the memories God can use the bad ones and the good

Would not be mine, I’d not be me, so I don’t think I should

Even think about a time machine, because now God helps me see

That His plan is I’m an Aspie and I can help by just being me

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NOTE: This poem was written two years ago, my blog is helping me to see patterns in my meltdowns and shutdowns. I will write more about what I have learned over Christmas when God helps me find my words again.

Love and hugs. Lisa. xx 🙂

ASD, who do you see?

I still feel at a loss for words

Everything I am seeing and hearing in the autism community is too much. I have shared before that when negativity hits me I can’t switch off my brain and this is not good for me or my family. My way of coping is to retreat. A lot of over sensitive aspies/auties are all doing the same, afraid of our own words and saying things wrong, we focus on what keeps us functioning and happy. This I feel can make us look like we don’t feel, for me this is so untrue, I feel intensely. It’s not that we don’t care it’s that we can’t process what we are experiencing at this time. Our thoughts are with the families of those who died in the event of last week, but also the negativity that has been irresponsibly placed on who we are. We spend our lives trying to understand why we feel so different, why we feel so isolated. Then we start to understand why and claim our place on the spectrum. It’s hard to tell people because so many refuse to acknowledge it or even accept what we are saying. This week has hit quite a few of us extremely hard on so many levels. Some of us have kids and the visuals of this haunts our loops, and we can’t switch off our loops no matter how hard we try.

I wrote a post some time ago, my reflections on Autism and Empathy an explanation as to why a 10 year child would give all her toys away. I had no choice I wanted to help and in my mind I solved a puzzle, a problem that hurt me deeply. My toys would save the lives of little children, so I gave them all away. I know who I am and Aspergers is part of who I am, who do you see when you read me?

I can’t find a way to express any better my feelings of what has happened than with my own words from that old post.

ASD’s and Empathy?

I know that over the years I have had to shut down to my feelings because they are so intense. I can get so overwhelmed by emotion that I can barely function. I know that when I love a person they become as important as myself. My children are more important and I would die for them.

Because I have visual reruns of things that either hurt me or confuse me, I end up rehearsing and chatting and analysing, this can be quite tiring. I will have so many conversations going around in my head. I have managed to stay in touch with my feelings, emotions and show empathy by being careful what I feed my brain with. Being careful not to overload myself. I know now what will replay in my constant thought loops and which things to avoid. I can also praise up the less noisy loops and help myself to do the things that are hard to do.

I think that the lack of empathy thing is just a shut down mechanism of self protection because emotion is so intense…it will overload the system and cause sensory difficulties and eventually complete shutdown. But this is just a whole load of Lisa Lingo from my babbling thought loops.

No mentions here

I am only linking this post to ASD and Empathy. I do not want search engines hitting my blog with people seeking out ridiculous Google searches. We all know what I am writing about so I am not going to even write the words. Instead I offer prayers to those grieving the loss of loved ones and I share a poem for all children everywhere, those on the spectrum and those who are just a little different. Also all those who are childlike in mind or heart who cannot comprehend the pain, confusion and fear that this tragedy has brought.

 As a child

by Alienhippy

As a child I would call to you, I knew you were always there

I had the words and a way to speak, I understood you’d always care

But as I grew the words got lost, the light then left my eyes

So at the floor I downward looked, I put on a masked disguise

˜

I tried so hard to live like this, to fit and not be seen

A daily battle to wear a smile, in my mind I still had the dream

That one day you’d come and sort me out, and make my life make sense

You’d take away the pain I carry, freeing me from feeling so tense

˜

So you called to me when I was hiding, by this time I didn’t even care

But you pursued and did not give up, knowing I’d meet you there

You took my hand and gently guided, you understood that I was weak

You walked the path and checked the way, giving me the heart to seek

˜

You showed me love when I was alone, and filled my life with hope

Explained the way that I’ve been made, you now teach me to cope

You are my friend you are my Lord, and Autism is part of me

You really love me “JUST AS I AM!” so now I can just be free

It’s so easy to take me apart!

wonderfullywired.wordpress.com

Hello my lovely Bloggy friends,

Wonderfully Wired is what I’m learning to see

My wonderful friend Fi helps me so much with this. How? It’s so very simple really….she loves and accepts me for me! She accepts my quirky ways and doesn’t put unrealistic expectations on our friendship. She also prays for me and my family. This is something I have never had in a friendship before, but it is something I have always prayed for.

In my last post I said I’d been inspired by one of the photos Fi had sent to me. So I’m going to share some thoughts I had about it.

Let’s talk about an Autistic trait of mine…

Analysis

Analysis is the process of breaking a complex topic or substance into smaller parts to gain a better understanding of it. The technique has been applied in the study of mathematics and logic since before Aristotle (384–322 B.C.), though analysis as a formal concept is a relatively recent development.

The word is a transcription of the ancient Greek ἀνάλυσις

(analusis, “a breaking up”, from ana- “up, throughout” and lysis “a loosening”)

Taken from Wikipedia

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Taking things apart is something a lot of ASD kids do

Not just kids though adults do it as well, I really enjoy taking things apart it’s like an adventure into another world. It’s a time of discovery and learning in my own way and in my own time. Not too long ago I took an old computer apart, just for fun, and collected all the pieces that I know I can use in a sculpture one day, when I get the time that is…. 🙂

When I’m taking something apart I can see how it all works. I can imagine rebuilding it in new ways. My brain just comes alive and I don’t notice anything else around me. Or anybody actually…I get lost in there, in the WHOLE process of it. AND….it’s so very lovely. 🙂

Putting things together is different

Why?

Instructions…expectations…a feeling of failure and disappointment.

Confusion, complications and always someone telling you you’re doing it all wrong.

I do love solving puzzles though, I just like to do it on my own with no help at all, away from everyone.

Having someone around “hovering” while I am building/making/solving something is very distracting. I have my own way of doing things, but because of how people have been in my past, I’m used to feeling like I do things wrong all the time. So having someone watching me build something (like a flatpack) while trying to follow instructions, actually throws my brain into meltdown mode.

I can keep this in for quite a while now, but as a kid the model, puzzle or board game would get kicked into the air or thrown across the room. I would then stamp off in a vile mood to a safe place, this made me feel guilty and wrong. I would then get REALLY told off for having a “temper tantrum” Yes…that’s what happens unfortunately when you are high functioning or undiagnosed. People have expectations of how you should be, because who you really are is unseen.

The invisible disability…“The invisible people”

Your intelligence in other things is noticed but your behaviour with so called simple things is unrecognised as a difficulty. This caused me a lot of confusion as a child. I felt so clever with some things and so stupid with others.

As a child I had no control over my reactions, my body acted in a way to protect me. I learned as I got older but I also learned to internalise TOO MUCH! I became far too quiet. Even the things I was good at, the things I had gifts with were no-longer enjoyable, I felt I did everything wrong.

Creating is different

With creativity it’s like building something while taking it apart. It gives me both! I see something being built/made/created but also feel the adventure of seeking and discovering. There are no rules in creativity, no instructions, no right or wrong way of doing (or there shouldn’t be)

School changes this, they place rules on the arts, they tech techniques and place expectations. I was always very good at art at school, but on my bad days I couldn’t meet the goals of my teachers.

Lisa is a quiet child with a lot of talent, she is naturally gifted in art, however she needs to try harder. She tends to drift off into daydreams and not finish the work set for her.

(one of my teachers)

I love this quote by Pablo Picasso

“Every child is an artist. The problem is how to remain an artist once we grow up.”

It’s so easy to take me apart!

With God’s love I am learning to put me back together.

God’s creativity flows through everything and also through everyone who lets Him in. I’m learning to use my Wonderfully Wired mind to see through my Aspie eyes. True creativity comes NOT from learning techniques and reading from books but from within, from who we are created to be. Creativity and expression are a scary thing to share, but it is also very healing when we do. I have always naturally wanted to learn about the things I love doing, the things I am interested in. My Aspie mind needs to feed on information, when I am interested in something it’s all I can think about.

Fi’s Blog title is…

Wonderfully Wired “Created to be remarkable…”

Created to be remarkable…I see this in my kids and Fi sees it in her kids.

“Different, but not less.” Those of us with spectrummy kids all see this and want everyone else to see it too! It’s not easy being a Mom to kids on the spectrum, not for NT or Aspie Moms. Our kids are unique and wonderful creations. They are blessings from God that we feel a need to protect. We see their quirkiness and we love it. The world however….well, let’s not go there!

As parents to kids with quirks we see its affect every day!

We already know how some people mock that which they are ignorant about, that which they refuse to try to understand.

Bringing awareness to the needs of those on the Spectrum is so very important.

Without people sharing what it’s like there will always be people who tear Aspies/Auties apart.

There will always be the bullies, the manipulators and the abusers. But through sharing our journeys we are building a path for others to walk on. We are making a safe place for others to share. We are telling our stories in the hope that things will change.

I love blogging….. WHY?

Because God has given me a way of taking me apart and building me back up, in a group of loving and accepting friends. In a little community I like to call Bloggyland.

“A place where I can be me!”

Love and hugs friends.

Lisa. xx 🙂

1 Thessalonians 5:11 (The Message)

So speak encouraging words to one another. Build up hope so you’ll all be together in this, no one left out, no one left behind.

I know you’re already doing this; just keep on doing it.

Why I Hate Religion, But Love Jesus

Hello my lovely Bloggy friends,

My lovely friend Angel sent me this video yesterday, I just had to share it!

Missing Jigsaws & Excess Lego

Image from Google

Hello my lovely Bloggy friends,

A sturdy cardboard box, covered with retro funky 70’s orange floral wallpaper. Can you visualise that? I can still see it in my mind 33 years later!

Inside this box is a collection of lost and missing pieces from games, jigsaws, Lego sets. Action mans missing boot and Cindy’s lost tiara. Not to mention a few marbles, ball bearings, coloured pencils and even a few toy soldiers.

Yes, it is the lost and found and I can’t be bothered to go and sort these things out right now. I’m a very busy young Mom and I have FAR TOO much to do looking after these hyperactive kids and my moody hubby….I loved my Mom SO VERY MUCH! Thinking of her makes me smile! 🙂

My Dad built an extension on our home

We called it the playroom and it was filled with all of our toys. It was lovely in the summer, it had a terracotta tiled floor and the door opened onto the back garden. Our black Labrador (RAF) would go in and out as he pleased, following my beloved ginger tom cat Sammy. In the winter though our playroom was absolutely freezing, so me and my brother would grab a box of toys…actually we’d grab a few boxes of toys, and bring them into the living room.

The contents would then get emptied out ALL OVER the living room floor and we would play quite happily or fight over things. Mom would find all our bits under the furniture when she vacuumed. Sometimes she’d find them down the sides of the furniture, under the rug and even behind the telly if we’d been throwing things at each other. She’d then put our bits in the box.

Two Aspie kids playing our own games

As we got older my little brother became even more disorganised and I became the bossy little organiser. He would use books to build ramps for his wind-up Evel Knievel and he’d mess up the playroom something terrible. He’d mess it up SO badly that I just couldn’t cope with it actually. My bedroom became my safe place, a place of calm and order. I kept my special toys in my bedroom where I knew they wouldn’t get hurt. Notice I say *hurt* and not broken. I’ll write a post about that another time.

Thinking out side of the box

I knew that if any of my toys, puzzle pieces, bricks or bits from the Lego models were missing they would be in the box. It was just a case of going and mooching through. There was always the risk of Mom saying, “Now you’re in the box you can put things were they should be!”

I didn’t realise that this method of lost and found, find and sort was something I was STILL using until a few days ago. My computer was returned and it had been rebuilt with EVERYTHING completely wiped off. Have you ever seen a grown Aspie burst into tears because her collections and projects have all disappeared. You get the picture, I went into shutdown.

I am extremely visual and I love to collect

I had so many files of images, links and quotes that I enjoyed and could recall when I had filtered through my mix up of thoughts and loops. I had slide shows I could put on of Art I had collected. Old photos I had scanned and could find in seconds to help me with processing memories. I had 100’s of fractals I had made, 3D designer projects and landscaping I had created. Also my SPORE progress was lost, I was on the last level and I really liked the world I had created there. 😦

Over the last few days I have avoided writing

I’ve not really been able to cope with sitting at my desk. I’ve just been doing stuff from my mobile and my netbook. I know how ridiculous this will sound to some people. Those who understand the difficulties Aspies/Auties have will totally understand where I am coming from. My computer is like a friend to me, now I’m having to work at getting to know it again. I don’t cope well with change and I’m really not good with loss.

I have been thinking a lot of a post I read about Lego

A LEGO Life by my Bloggy friend Richard at “Where Living Begins”

I read this post 2 days before my computer was returned and it made me really think about my life. It’s still making me think actually! The scripture Richard added was this…

To everything there is a season, a time for every purpose under Heaven:a time to break down, and a time to build up

(Ecclesiastes 3:1, 3).

Richard’s post is excellent, I love how he sees God in the everyday things. This post helped me to start putting my pieces back together. I don’t know what I’m building yet, as always the instructions have not been included, so I’m making it up as I go along. It’s an exciting adventure though. I trust God with this, He always provides what I need. I might not understand His ways but I can lean on His promises and accept His unconditional love.

I started a blog for my collecting

I didn’t intend to tell anyone about it, it is just storage really. But last night one of my subscribers from Alienhippy accidently found it and subscribed. Those who know me REALLY well know that when things happen like this, I see God-incidences. My storage and collecting blog is like my Mom’s retro box full of bits n bobs. I don’t know half the time why I collect what I collect, but I like to be able to find things easily when my thoughts start making tangent jumps and pulling together parts and pieces to help me move forward. To help me understand who I am in time and space. To help me make sense of the past and it’s pains. To help me share my journey and whatever else I feel God wants me to share.

Here is the link

Missing Jigsaws & Excess Lego

You can read more about this on my about pages.

Love and hugs.

Lisa. xx 🙂