According to Urban Dictionary: A Helicopter Parent is a parent who hovers over their child, is controlling and extremely over-protective.
Well yes, I guess that term is very fitting when applied to a parent who is unwilling to cut the apron strings from their typically developing child and let them discover life on their own BUT, in my opinion…..this term should not EVER be applied to parents of children with special needs.
For most of us – it is definitely NOT a choice but instead – a necessity.
I would LOVE to be able to just drop my child off at school in the mornings and go about my business but you see….this is a pipe dream for me. I don’t hover because I don’t trust the teaching staff or the school…..I hover for MY SON’S sake…..NOT mine.
And that my friends, is where I believe the difference lies.
When God blessed the parents of spectrum kids with these children, he also gave us enough grace to deal with the massive responsibilities that come as part of the autism package.
The simple fact is that with autism spectrum disorders- part of the diagnostic criteria is that the child has impairments in socialising, communicating and has restrictive or repetitive behaviours.
And in essence, what that means is that throwing your child in the deep end and letting them dog paddle their way through is not only stupid but very very cruel!
***
I have a very emotional story to tell now and I need all of my autism mother friends to wrap their virtual arms around my shoulder as I write because I’m particularly fragile this morning.
Ok?
Thanks..
I sent Harley to school today with both of his hands bandaged up because he has let his anxiety overwhelm him again.
He has licked, sucked and literally chewed his knuckles again until they bled. They are red raw, weeping, bleeding and really majorly gross to look at. He is in dreadful pain and was whimpering as I gently bathed and dressed his wounds this morning and it broke my heart to see him like this.
He looks like a little teddy bear with his paws all wrapped up and as a result, is unable to perform simple tasks like cleaning his teeth and getting dressed unassisted.
I went up to school just before recess to drop off his blazer that he had forgotten and signed in and went down to his classroom to change the dressings on his hands.
The beautiful office ladies would have done this for me but I knew that Harley wouldn’t have responded well to someone else touching his sore hands so I opted to go in myself. (yes, that’s right…..hover, hover, hover).
He was SO excited to see me and Lucas. He ran over to us giving us both HUGE cuddles and announced loudly that his Mummy was here and telling all his friends how much he loves me! (I developed a speck of dust in my eye as you could imagine!)
I hugged him back, took him aside and re-dressed his hands and helped him to get his blazer on. He went back to his desk and sat down and arranged his books in front of himself proudly.
I told him that it was time for me to leave now and that Mummy would see him in a few short hours. He nodded and said his goodbyes to us.
I walked over to the teacher to say goodbye and she started chatting with me about the great progress that she’s noticed in him lately and I beamed with pride.
All the while, Lucas was tugging on my leg so eventually I followed his pointed finger with my eyes and then I saw it.
Harley was leaning forward with his head down, staring at his work. He had his pencil awkwardly grasped in his bandaged hand with tears streaming down his little face. He was TRYING SO DARN HARD to be brave but the tears kept flowing. I watched him wipe some of them away with his little white paw and I could tell how much strength this required on his part.
I walked over to him, crouched down and put my arm around his shoulder and asked him what was wrong.
“I can’t do what everyone else does Mummy” he answered.
“What do you mean honey?” I replied.
“I can’t even hold my pencil, I can’t read and I can’t stinkin write, I’m so stupid” he sobbed.
“YOU ARE NOT STUPID” I practically yelled, LIVID that my boy’s anxiety was consuming him and I started to wonder if coming into the classroom was such a good idea after all.
His gorgeous teacher stepped in and assured me that she would look after him so I thanked her and gradually made my exit once I knew he was ok.
I DO trust that his teacher can deal with this. I DO trust that she has only his best interests at heart but I want everyone reading this to know:
My kid ALSO needs me.
Call me whatever you want. A helicopter parent, a smother mother, a freak, WHATEVER, but when my child is in this much pain just from a task as simple as “being” in a classroom full of kids who can naturally do all the things that he struggles with….. I will not back down and leave him to his own devices.
It’s not a simple case of parental separation anxiety here.
I am not trying to control the school, the teachers or the environment.
I just want to parent my child responsibly and effectively and for ASD kids – that means hovering, asking questions, making requests and sometimes….being a pain in the butt.
I WON’T apologise for being my child’s biggest and loudest advocate. I do not want to look back in five, ten, fifteen or twenty years time full of regret that I didn’t do more to help him navigate this frightening and overwhelming world that we live in.
And I will ALWAYS be the parent that you see waiting patiently by the classroom door to “have a quick chat” with his teacher.
I don’t want to know if he aced his spelling test, or ate his sandwich or got all his sight words correct….I couldn’t care less about these things…..I just want to know if my little boy managed to simply survive!
So if you’ll now please excuse me ….this helicopter needs to go and re-fuel – tank is getting empty : )

(((hugs)))
I don’t know what else to say, Fi. You’re a fabulous mom.
Thanks Laura…..that IS the perfect thing to say
If only we could drop our kids off and leave like everyone else! If ONLY life were easy for us just like everyone else! It bothers me. And yes I pack my 16-year-old’s lunch each day because he WILL FORGET and going hungry for a day just won’t “teach” him anything.
((hugs to you))
Thanks for the hugs x
And yes…I can still see me doing all these things when my son is 16 *sigh*
thanks
((((Huge Hugs Fi)))) I guess the sermon at Church hit lots of tender spots the other day. Don’t let other people get to you, the ones who are worthy of your friendship know that you are just doing what is best for your child… Advocating for a child or a person who has not many other options is a blessing, not a curse. Those who stand in judgement should remember that God has gone before us and judged us already – it is not for them to do so. Love ya x0x0x0x0
Thanks for the hugs Mishy

it sure is xx
Yep…Sermon was a little confronting! But I also understood that it wasn’t a direct attack on me
And thank you for pointing out that it’s a blessing
My beautiful and darling friend.
You don’t ever have to make excuses for loving your child. You don’t ever have to apologise for longing to help them when they are distressed.
You don’t ever have to justify yourself for being you!
From one Autism parent to another – You Go Girl!
I love you dearly and don’t ever, ever apologise for being you. You have the strength of God’s mighty hand behind you, before you, above and beneath. He HEMS YOU IN!
THANK GOODNESS that God hems me in!
I don’t know how I’d possibly cope without Him!
You are a gorgeous friend Donna..xxxx
Fi,
You are the best Mum for Harley and that is all that matters. Anyone who thinks differently is not worthy of notice. ((((((((((((hugs))))))))))))
Thanks Sue. I appreciate the hugs x
You never need to apologise for doing your best for your child. So many children have neglectful and even abusive parents – imagine an autistic child with one of those (and it must happen). Sue is spot on: you are the best Mum for Harley. And he showed you that by his demonstration of love.
You are in my prayers. God bless you.
Thanks Tilly,
I can’t even get my head around autistic children having neglectful or abusive parents…EeeeeK!~ Scary!
Here, have my shoulder to cry on
and a couple more hugs (or squeezies as my girl likes to call them).
You are doing a fantastic job, you know that, but i know also how tiring and exhausting – mentally and physically that is. I know too, how easy it is to worry about what others think, but relly we need to not waste any energy doing that. We ‘hover’ because we have to, and because we want to as that is what is best for our children, but not because we choose to. The other mums really have no idea – to be fair that’s not their fault either. But no-one should be judging.
poor Harley, hope his hands get better soon x
Thanks Steph..squeezies sound AWESOME!
And just to clear up a few earlier comments on here as well….I wasn’t actually judged personally – this post stemmed from a “general” comment that I heard on the weekend referring to helicopter parents
So heartbreaking to watch our own kids be so upset!
With his determination, his teachers help, and your love, he will be the best he can be, and find his own joy!
I need a second comment though.
Helicopters hover needlessly. They never let their kids fall, nor fail, and in doing that they stop their kids from learning.
If you’re close enough to see it happen, but pick him up afterwards – he’s had the opportunity, and you aren’t a helicopter.
By asking your son what is wrong you showed you are concerned. By letting the teacher sort it out you gave him room to grow that a helicopter parent never would.
Helicopter mum? No freakin way. Supermum is more like it!
imawestie is absolutely right – you are a rescue helicopter, piloted by Prince William and saving the stranded climber. You are there when needed, to call upon, but not getting in the way.
Hello my lovely Fi,
Just keep being you, you’re exactly what your kids need.
God trusts you with them that’s why you have them.
I was going to write to you yesterday about something I saw at school that triggered off a memory. Funny because you have got most of it here already.
Love you and everything about you.
Lees. xxxx
You’re such a great mummy. You and your beautiful family are so lucky to have each other. I hope Harley’s anxiety calms down soon, poor kid.
Fi,
Let me just say, the image that played out from reading your post brought up many similar ones from my childhood, except my mom was unable to be there like you are.
I did not have the emotional support that you give your children. My mother simply could not be there because of work and also her own misreading of what I was going through at school and home.
It is a wonderful thing that you are so supportive and in tune with your children’s needs. Keep on hovering!
(I have been called a Helicopter mom and I don’t care!)HA!
Here are some (((((HUGS))))
Everything I read about you points to how much you love your kids and that you get them, you’re dialed into them and trul understand their needs. That is far diffrent from a hovering, meddeling parent. In my humble opinion you are your children’s best asset and the teachers as well. Keep doing what you’re doing and hover away!!!
xxoo
Your story brought me to tears. I can relate more than I would to. I hate when D beats himself up like that. He calls himself stupid or my other favorite, retarded.(thanks to a mean kid at school who got off with a warning for his name calling)
It just breaks my heart. I wish more than anything that he could see himself through my eyes.
I hear you on this one. This last week during my son’s horseback riding lessons I overheard a conversation between two of the girls that was, “Where’s your mom?” “Shopping.” “That’s where my dad is – shopping.” I thought, oh my goodness, other parents just leave… could I just do that?!” But while I would want to have a little shopping time alone while he’s busy doing something, I think I need to be there to keep an eye on things. The people aren’t trained in managing Autism (I don’t think they know he is AS)- and I couldn’t bare to just leave and hope for the best. What if the worst happened!? Hope for the best, prepare for the worst, you know? One of these days I’ll have to do that, but right now isn’t the time.
(Oops – this is lucyshouse… I was signed in at my other blog.)
hehe……the name “Josie” gave you away
Oooh, I could NEVER leave my kids and go shopping….it’s frightening to me to think that people actually DO that!
You only get ONE chance to raise these kids and to leave autistic kids with just “anyone” is just bizarre to me!