Please enjoy my article published in emagazine Crixeo for October which is Sensory Processing Disorder Awareness Month.
Please enjoy my article published in emagazine Crixeo for October which is Sensory Processing Disorder Awareness Month.
“It’s been a very bad day Mummy” was the phrase repeated continually yesterday evening after I collected Little Miss H from school.
Standing in the playground I knew it had been. I could tell by her gait, by her facial expression, by the purple bags under her eyes against her too pale skin, by the sadness of her aura. As she slowly walked towards me, scuffing her boots along the salted concrete of the playground, her eyes downcast, her hand up to her mouth chewing her sleeve and her water bottle hanging forlornly from her other hand, I knew we were in for a tricky evening.
I suppressed the urge to say “stop scuffing your boots” (do you know the damage the salt does to the leather?), or “stop chewing your sleeve” and instead just held my arms open for her. She doesn’t usually like public displays of affection especially at school (“It’s against the rules to hug and kiss at school”) but I could see she needed some overt love.
She didn’t come into my arms for a cuddle but she was demure and allowed me to touch her arm.
Her water bottle had been broken that day and she was frightened she’d be in trouble. Mostly though she was just sad. Disproportionately heartbroken actually. You see change is hard for her. Saying good bye to things is really hard. Her stuff is her portable safe space that she attaches so much love and importance to, it keeps her grounded so to have a piece of it broken is like someone throwing a brick through your window. It is devastating for her.
Of course I reassured her that the broken water bottle could be replaced. [No it won’t be the same one, it’ll be a new one but you can choose it. No I can’t fix the old one. Yes I know X person gave it to you for your birthday and yes I know it’s the fourth one that’s broken in however long. Yes I know it matched your pencil case and yes I know it was a ‘Frozen’ one].
With an unexpected burst of energy she was suddenly confrontational. These shifts come out of the blue.
We were due to take Tiny Miss H to Rainbows and this was suddenly proving too much for her.
She was shouting at me that she didn’t want to take her to “stupid rainbows” and it wasn’t “fair”, that she’d “be bored” and why should she have to go with us just because Tiny had an activity…. And so it went on. The real issue is she wanted her safe space, she wanted to hunker down after an exhausting day.
The challenge is enabling Tiny to maintain an ‘ordinary’ life, which includes after school activities, at the same time as supporting Little’s needs. If anyone has the answer on how to get the balance right please let me know.
There isn’t an option, she is eight years old, she was coming with us, so with my arm wrapped tightly around her shoulders we walked towards the car. The deep pressure, once she’s ready to let me touch her, is very reassuring for her and being hypo-sensitive she needs a very tight squeeze. So it was that I held her as firmly as I could with one arm whilst holding Tiny’s hand with my other hand and walking clumsily as if in a sort of three legged race, bags bashing against my shins, all of out of sync, we somehow managed to get to the car!
That’s when she said it “it’s been a very bad day mummy”
Chats in the car are usually the most successful; no expected eye contact, the crowd and melee of the playground has dispersed and we are away from the source of stress.
It turned out that she had been “mobbed” and crowded around at lunchtime in the playground and she didn’t have the ability to extract herself. She didn’t know what to do, what to say, who to go to for help. So stuck in the mob, she drowned. She’s carried that with her all afternoon.
The physical toll it had taken on her was visible to see. She was anxious, stressed and absolutely exhausted.
This on top of the broken water bottle made it “a very bad day”.
Within the 7 minute journey home she had told me it was “a very bad day” about twelve times.
This is echolalia, repeating herself is a form of stimming. It helps her cope with anxiety.
When she has bad days we have a ritual which helps her get from the car to the house and that is a “Mummy squeeze” once in the kitchen – a prolonged super tight cuddle. It physically hurts me she is so strong, but it is what she needs so squeeze away we do. I feel like a tube of toothpaste being squeezed, I can barely breathe, she feels like I’m lightly holding her yet I’m using as much force as I can muster! “It was a very bad day” she mumbles into my chest.
This helps her calm and from there I was able to persuade her that whilst Tiny was at her Rainbow’s Pyjama party we would go and choose her a new water bottle.
Meanwhile she’d also clocked the box of books in the hallway that we inherited a while back from cousins and I’d been storing in the garage. Luckily they proved a timely distraction! “It was a very bad day mummy” she muttered to the books as she rifled through the box.
We successfully deposited Tiny at her pyjama party but with all the distraction I had forgotten her cuddly toy and blanket…cue a mini tantrum from Tiny!
Finally extricating myself from the clutches of the Tiny tirade – I escape outside frazzled and on tenterhooks to persuade Little to walk with me to the butchers before going on to buy her bottle. Reluctant to walk anywhere normally I was braced for the fall out but in response all I got was “It was a really bad day Mummy”. She was so well behaved in the butcher’s that they gave her a fudge. She decided it had been worth walking! “Still a bad day?” with an eyebrow raised, “Mmm” she shrugged, “it’s getting better”.
On to the supermarket to buy her bottle, I managed to persuade her to make a practical and useful choice that would withstand at least some playground action without too much argument. We’d been playful and chatty walking round the supermarket. Things had turned around. I was still on edge keeping it light, keeping her happy. Then we bumped into Tiny’s class teacher who stopped to chat. The transformation from playful and chatty was marked. Little Miss went quiet and couldn’t make eye contact. Out of the context of school, her confidence had melted away and her anxiety kicked in. To a stranger this would appear as ‘shyness’ but it’s different.
Selective mutism is an extreme social anxiety that results in an inability to speak. It is involuntary and more than simple shyness. I’m proud though as she did manage to squeak something to me as the teacher was walking away. Then straight back to being chatty with me once we were safely alone again.
At the till, the cashier told us the amount and Little Miss repeated it in various voices, over and over and over again. Anxiety making her repeat the words. Again, her echolalia. The opposite if you like from selective mutism. Still anxiety driven and not necessarily ‘appropriate interaction’. I could see the anxiety ramping up so a quick distraction technique was needed. Her forte is maths so I made it her job to tell me how much I still owed each time I produced a coin and that busied her brain but in between each amount she still repeated the total amount in a strange voice. The cashier was so patient, smiling and friendly and put absolutely no pressure on her, instead only complimenting her on the maths. The fact there was no queue and no one else around at that moment helped all of us enormously. I didn’t feel stressed or self-conscious, and Little Miss just did her thing.
Once back in the car she asked for water and I didn’t have any. I, almost flippantly, suggested she run back in to buy some. My genuine intention was to buy time whilst I was finishing putting something away in my bag before going back in myself but to my utter astonishment she said “OK”!
So…We talked about what she would do, where she would go, how to choose what she wanted, where she would pay. We talked about the change she’d wait for, the route back to the car and the fact I would not move from the spot I was in. We land marked where I had parked for her to reference it. It was a HUGE amount of information we covered.
She hesitated. She took the coin. She ran. She went round the corner…… I watched and watched and watched, heart hammering and holding my breath until finally there she was running back with a bottle of water in her hand, a smile on her beautiful face, pride in her eyes and flushed cheeks to show for it.
She had gone round the corner to the door of the shop, walked in, turned right to the fridge, chosen still water (not flavoured, not fizzy, just plain , it’s all she drinks), she stood in the queue with two people in front of her and waited calmly (“feeling very nervous mummy” she told me), and when it was her turn the same lady recognised her and helped her through, I’m still not clear whether she actually spoke, but she waited for her change, and ran back to the door, turned left, round the corner and sprinted back to the car “7 spaces down” she told me. Climbed in out of breath, heart hammering (or was that mine?), asked me to open her water and drank it. “I’m so proud of you darling” I told her, “I’m really proud of myself” she said.
SHE DID IT. I smiled with tears streaming down my face as we drove to collect Tiny.
“It was a very bad day mummy” she told me at bedtime, “but it ended well” we said in unison.
The burning question I always have as a mum is how do I know I’ve got it right? How do I know my decision is the right one?
My daughter’s autism manifests in many ways but one of the main ways is anxiety. She has enormous trouble decoding the world, processing the information and coping with change.
She can’t explain herself and self advocate when she is experiencing stress and it’s always with hindsight that the facts come out. While she is experiencing stress she is in survival mode and doesn’t even recognise she is stressed until the stress stops.
This goes some way to explain how she holds it together at school and appears ‘fine’ and sometimes appears better than fine, she’ll be laughing and engaging but still comes home to fall apart.
This week has been so hard for her with staff illness and absence meaning unexpected substitute teachers. Her week is not going to plan, it’s unfamiliar and the level of stress it causes impacts on everything. She came home from school last night subdued and tense. She was pale and clammy and being winter I suspected a bug, I took her temperature and it was normal. She was not unwell, she is just exhausted and drained from the emotional toll of all the changes. The evening was erratic, she was vacillating between tearful and angry, she was refusing school the next day and refused to go to ballet that evening.
I decided to allow her not to go to ballet this time. I usually push her outside of her comfort zones and insist she sticks to her commitments. It was her choice to take up ballet and she’s really good at it, she has just achieved a high merit in her exam and was really (rightly) proud of herself. This term every week she’s tried to get out of going to class and I’ve not caved once. It’s exhausting always battling and cajoling but it’s the right thing to do and furthermore we’ve paid for it, so she’s going! She can never explain why she doesn’t want to go and I can’t get to the bottom of it so, commit she must.
After all the school changes this week however I felt that rather than fight that battle I’d keep her home and let her rest and hopefully increase the chance of her managing school the next day.
All evening her stomach was churning with anxiety about the following day at school. A totally new teacher she has never met is taking them and this is all too new. There are too many unknowns that haven’t been planned, prepared and practised. It’s overwhelming for her.
She woke up this morning claiming illness. It’s really avoidance.
My main aim is to get her to
We have spent a lot of time talking about ‘the little boy who cried wolf’ over the years, we’ve read the book more times than I can count. On an academic level she understands the concept but she is not equipped to manage putting it into practice. So every time she experiences anxiety she claims illness.
She is eight years old. Now is my time to teach her to recognise what her body is telling her. To teach her how to self advocate for that. To teach her that she will be believed when she says she is feeling anxious and that it’s nothing to be ‘embarrassed’ about [her words]. It’s our chance to prove to her that she will be respected for the recognising her feelings and limits. It’s our chance to nurture her, to build her into a strong person who can identify and manage her body’s signals.
We also have to be careful not to be manipulated every time she wants to get out of doing something for any reason other than her crippling anxiety. She’s very bright, she’d make the connection and employ the tactic if she felt it would work.
So, as a mum, how do I know when to push her and when to nurture her?
Mental ill health in young people is on the rise. The amount of pressure our children are under is at an all-time high and is in some cases damaging their psyches. The amount of help available is minimal as the NHS mental health service is at crisis point. Prevention is better than cure, especially when ‘cure’ relies on patchy service availability.
Autistic girls are a particularly vulnerable group and I’m very conscious of that.
Am I harming her or helping her by pushing her out of her comfort zone, by making her go to school?
What is the right answer?
I’m so proud of her, that today, with my and the school’s help she managed to go in. I managed to tread the fine line of ‘coaxing without demanding’ well enough to get her to school and then with their help through the door, they are managing her transition into and through this tricky day.
Are they doing it right? None of us truly know. Are they doing their best? Absolutely.
Am I worried that my daughter is suppressing her anxiety to meet expectations? Yes, very.
Do I feel conflicted about this? Yes, incredibly so.
Suppressing her anxiety is different from coping with it. Suppressing it is quashing it, ignoring it and denying it which leaves it simmering deep down causing damage and delayed presentation. Coping means addressing it, solving it, learning from it and leaving it behind. It’s a fine line to find the balance. How do I know I’m getting it right?
Little Miss H is having a very tricky week (And it’s only Tuesday!)
We’ve had to miss ballet this evening as a result and she’s not coping brilliantly at all. She’s currently decompressing with her “tool kit” of sensory toys. She’s been incredibly erratic changing from argumentative to tearful to quietly angry and I’m exhausted, so goodness only knows how she must feel. It’s different from a full blown explosive, aggressive melt down, it’s more an implosion of anxiety.
It is all because her teacher and the usual substitute both of whom she knows well and trusts, are both off ill. As a result both yesterday and today she has unexpectedly had a different teacher. It’s someone she knows (and likes) at the school but hasn’t been taught by before. This change has caused her immense anxiety and this prolonged build up has culminated in this implosion. It’s involuntary and she can’t control it. Yes it seems irrational to me, does that frustrate me? Absolutely. Does that matter? No. I can not let my frustration inform my reaction. It does of course because I am human, but I do my best to count to twenty and mutter under my breath behind the cupboard door to enable me to be patient with her. I vacillate between calm and sympathetic to irritated and impatient. Which in turn leads to me feeling guilty and defensive. You see I am tired, sleep deprived and poorly so this reaction and the resulting unpredictable behaviour from her have me like a cat on a hot tin roof. Furthermore some of her calming toys are noisy and with my headache they are driving me nuts!!! Obviously I can’t react so here I am, telling you lot about it, hoping you won’t think I’m horrid for not just being a bundle of sympathy for my blessed child. Obviously I’m sympathetic but I’m nearing the end of a frayed bundle of nerves I think…
To really add sprinkles to the cherry on top, the teacher she currently has needs non-contact time tomorrow so it means a further teacher is coming in. It is a teacher she has heard of but doesn’t know. She doesn’t even know her name and is beyond worried about it. This has tipped the balance and she now can’t cope with it all. She’s anxious about every aspect from uncontrollable variables to things that just wouldn’t cross my mind. I’m so impressed with her that she is now able to (partially) vocalise her concerns but she doesn’t at school and it all comes out at home.
I’m not convinced I’ll get her to school tomorrow but it’s bedtime now and I’m not even sure she’ll get much sleep, so we will cross the school ‘bridge’ tomorrow…..
What Autistic Adults have taught me about Parenting my Daughter
As a parent to an 8 year old girl we have our share of frustration, cross words and clashes. We also have a strong bond, a close relationship and enjoy each other’s company. Obviously I love her more than words can say and am beyond proud of her (yeah, yeah – blah, blah, blah!)
I have noticed however that traditional parenting techniques are not always successful with her and whilst being ‘strong willed’ is one of many positive traits she seems to have inherited from me, there is more to it! Another factor that adds a different dynamic to the relationship is that I am Neurotypical and she is autistic. I am conscious that I don’t always respond to her the way she needs.
In an effort to gain some insight into what I could do to improve my parenting of her, I turned to Autistic adults on Facebook and asked ‘what is one thing you wish your parents had known when you were growing up?’ This is what I learnt.
Acknowledging she is Autistic is the first and most powerful message that came across. To accept her for who she really is. “The chances are she already knows she’s different” so giving it a name and recognising it is empowering for her. Acknowledging her for who she is is vital.
Calling it something isn’t enough though – it is about recognising what it means. It is about recognising that;
Something else that came up was “don’t be embarrassed to have a child that is different” – whether we mean to or not I think sometimes as parents we change our approach based on what setting we are in and that is often driven by the fear of what others will think. This exercise has taught me to try not to care what others think! (I will add that I have never been and will never be embarrassed by having a child that is different).
2. To Respect that her struggles are legitimate and real. Respect that;
One woman explained that she wanted her caretakers to understand that she wasn’t “highly strung” as they called her, in fact she was “baffled by life and society itself”. Truly humbling to hear those words when you are neuro-typical, how much we take for granted.
3. To Teach her everything. Not to make assumptions that she will just ‘pick things up’.
4. To be Available to her
5. To continue Learning together as we go. I need to learn at each stage;
Some of this, we as a family already know and do, we are fundamentally on the right track and mindful of doing our best. The rest of this we need to remind ourselves and work harder on. Much harder!
Having neurodiversity in a family is fabulous and challenging in equal measure for all of us. We won’t get it right all of the time but having the intention and motivation to at least try our best has to be good enough. Then we can trust in the fact that ultimately her happiness will come from being her true self.
With thanks to the Autistic Women’s Association and other facebook users who answered the question!
*Autistic Inertia is basically a state of wanting or needing to do something, but being completely unable to do it, almost like a paralysis. (https://nolongerinabox.wordpress.com/2013/03/12/autistic-inertia/)
This time of year is busy for everyone but we find it exceptionally so.
We have birthdays as well as Christmas to plan and prepare for, five on the same day but we also have step- and parents, nieces and nephews, aunties and uncles, god-children and friends’ birthdays in December and early January so we have to organise for those. We have the usual school commitments and Little Miss H’s Ice Skating shows to prepare for and be available for, as well as the usual ‘Christmas Chaos’, as I call it.
It means that it can all be very exciting which in ‘autism speak’ means ‘different’ and ‘overwhelming’ which then has a knock on effect on all of us.
It’s also a poignant time of year, as it was when Tiny Miss was diagnosed and whilst we have so much to celebrate, there are still challenges that can’t be ignored.
So please forgive my recent relative quiet spell. I am still here, sharing and recommending my good friends’ pages. I’m still answering emails. I perhaps am not quite so forthcoming with as many FB memes just at the minute, so please forgive me and bear with me.
There is an element of ‘I can’t outrun it’ going on in my life as I am attempting some self care too so that I can cope with all that is happening and yet to come. My health means I need to pace myself and pick and choose and allow plenty of recovery – sometimes its a waste of energy to try and outrun things that you know are coming. Sometimes just letting it wash over you is the best course of action. We’ll see if I’ve got the right approach after the fact but regardless I need to manage as much as I can for as many people as I can, including myself.
You see I’ll let you into a little secret – it’s my birthday on Wednesday (same day as Tiny Miss) so I try and manage to enjoy MYSELF as well as look after everyone else 😉 xx