This Time Around I Won’t Take Things for Granted

It’s a peculiar thing watching your baby pass up your kindergartener.

I really began to notice when our youngest was 6 months old. I watched him sit and not topple over. I watched his curious eyes take in the world around him while his older brother laid on the mat.

I watched his 4 finger grip change to a pincer grasp in no time at all. I taught him to use a straw in one sitting.

One. Mind blowing.

To say that I am in awe of typical development is an understatement. I am blown away at how much a child learns in the first year of life. We have an 8 year old as well but I took it all for granted.

Every single milestone. I was under the impression that kids just ​did it.

Don’t get me wrong, I know that not all children are born typical….but mine certainly would be. They would learn and grow and thrive. Roll, sit, crawl, walk. That’s what they would do.

We learned with our second child, who has PMM2 CDG (congenital disorder of glycosylation) that not all kids ​just do it.

Not all children check milestones off of their list.

Not all children learn to suck a straw in one sitting. Not all children learn to clap. Not all children will sit, crawl, and walk. All of the milestones I took for granted with our first son are milestones our kindergartener still has yet to meet.

And to be honest, I’m not sure that many of them will be met. I don’t know if he will ever speak, and I’m not quite ready to let that dream go. I know deep down in my heart that he’ll never walk unassisted, but that doesn’t stop us from trying.

Watching his baby brother pass him up has only made me realize just how many things he does not do.

But it has also made me realize how much his brother does do.

This limbo of grieving the things one son does and celebrating the same exact things for the younger one is so confusing. I am stuck in a place where I can’t wait for our baby to get to the “next” thing because it is simply amazing, and then in the same moment I tuck away a tear for his big brother.

Yes, it saddens me to watch our soon to be one year old doing countless things our 5 year old can’t do but this time around I promise I am not taking one single thing for granted.

Crawling up the stairs. Sent multiple videos to grandma.

Sticking his tongue out. Countless photos and videos.

Eating food. Instagram posts daily.

Saying “mama” and “dada.”

Treasured and held close to my heart.

I know now that none of these things are a guarantee. I know that not all children do these things on time, and like our middle son, some children may never. I am treasuring all of it.

The mess making, squirming during diaper changes, fake crying, and pulling up on my leg constantly when I am trying to get tasks accomplished. Even all of that. Even the hard and annoying parts.

All of it. I am enjoying it all.

And as much as I can’t wait for him to get to the next thing I am doing my very best to sit back, take a deep breath, and remember that not all kids​ just do it.

10 Christmas Gift Ideas For Children with Special Needs

There’s under 3 weeks to go until Christmas, and if you’re anything like me, you’re starting to panic about what to get your kids for presents this year.

I have two boys, Jude (10) and Tommy (7) and I always thought Christmas would be the most magical time of the year.

But for them Christmas is quite different.

You see their autism, and global development delay has meant that both boys have no real understanding of what this time of year means.

For them Christmas is just another day, only full of disruptions to the usual routine, with more people and flashing lights.

When it comes to presents there’s never been a list to Santa, and, especially in the early years, most toys bought for them have gone unused.

Each year it can be a bit of a challenge knowing what to get them, and with family and friends all asking what to buy them as well.

It can be easy to run out of ideas.

So, here’s a few ideas that might help you or your family, either presents I’ve bought in the past, or ones that I’m hoping will be a success this year

1. Sensory Basket

For my son Jude he doesn’t really have the motivation/motor skills for opening presents, so for the last few years I’ve made him a sensory basket and given it to him unwrapped.

This will have a few different sensory toys in that light up or have different textures to explore.

Some ribbons to flap, balls to throw, and toys to squeeze

2. Mini trampoline

This has always been a big hit in my house, an activity both boys love.

It gives them the sensory feedback they crave from bouncing, and also burns off some of their endless energy.

It also means they get to bounce all year round!

3. Body sock

I tried one of these recently whilst on a course, and it’s something both boys use at school.

Made from lycra, once inside and you press against it, it provides some really nice deep pressure that many of our kids crave.

I can see this being a fun game, and also a tool to help our kids when they need to regulate their senses.

4. Bubble tub

A favourite in sensory rooms all over the world, and great for kids of all ages.

The flashing lights and movement of the bubbles can have a real soothing effect, perfect for a bedroom to create a calm place for our kids to relax in.

5. Projector Lamp/Nightlight

An alternative to the bubble tube, they project a light show onto your ceiling or wall, and can also play music too.

With lots of different settings, they can help create a place of calm, and are easy to take with you when visiting family across the holidays!

6. Indoor swing

We’ve had an indoor swing for about 5 years now, and it’s been one of the best purchases I’ve ever made.

The almost cocooned feeling it can create combined with the movement of being swung back and forth or side to side, is a great sensory activity.

It’s also a great place to encourage interaction between you and your child too as there’s so many games you can play with them whilst they’re in there.

7. Chewable jewellery/toys

Many of our children love to chew on or mouth toys or different items.

The oral sensation they get can be calming and help them relax.

It can also be a worry though as often it might be with items that are dangerous or inappropriate.

These days there’s so many fun alternatives out there, with safe, chewable toys, or even jewellery such as necklaces or bangles that can be easily accessed and more discrete.

8. Sensory bottles

For the more creative among you, this is the perfect home-made gift.

Using a combination of an extra strong bottle, water, glue, glitter, and whatever other fun stuff you want to include, you can make a great present.

Google ‘sensory bottles’ for some inspiration, there’s so many cool ones you can make.

And if your kids aren’t into them, I’m sure they’ll help you calm after some of the stressful moments we go through.

9. iPad/Tablet case

If your family is anything like mine then the iPad is an essential piece of kit that you can’t live without, and that gets a lot of use over the holidays.

So the last thing you need this Christmas is for it to be dropped and broken.

Invest in an extra-strong case.

Take away any chance of that one drop ruining your holidays (and costing you a fortune to replace!)

10. Wireless Headphones

Whilst you’re at it, if a tablet is so essential in your house, invest in a pair of wireless headphones too.

We’ve all listened to Baby Shark, or some other random YouTube video 6 million times this year, well hopefully a pair of headphones will be a gift that both you and your child can enjoy!

I hope some of these ideas help the stress of finding the right presents a little bit easier this year.

Merry Christmas everyone!

Dear Paraprofessional

Dear Paraprofessional,

Thank you for all you do day in and day out.

You are the unsung heroes of our schools. You are the champions of our students.

You are worth so much more than what is reflected on your pay stub.

Those who work with you know you are the heart and soul of the special education programs. Day after day you advocate for our children, treating them with dignity and respect. You show by your interactions with those who are differently-abled that you see no differences.

You see a person who has feelings, thoughts, and personality. We catch you laughing, singing and sometimes even dancing to engage these kiddos.

The eye contact, the meaningful touches, the intelligent conversation you practice tell students and the others nearby that different doesn’t mean less than.

Thank you classroom aides, teacher’s assistants and support staff for tirelessly wiping noses, changing diapers, giving feedings all with a smile on your face.

You may not have the title of classroom teacher but we see the care you provide and the love you give every single day. Thank you for your patience, your energy, your compassion and your enthusiasm.

You are willing to learn new tricks and go with the flow daily.

You give your body in service by repositioning, lifting, carrying, pushing the most vulnerable.

You may not write the goals or the lesson plans, but you are the ones we rely on hour-by-hour to make these goals a reality. If it weren’t for you, the daily walks in the gait trainer wouldn’t happen, legs would not get stronger from standing in the standing frame.

If it weren’t for you, those with mobility delays might not get out of their wheelchair to stretch their legs, those with fine motor delays may not get their clothing fasteners done, and those with speech impairments may never get to practice using the communication device.

You are these kids’ world. Yes, you are seen.

Because of all the hours you spend up close and personal, you are the one who gets the special giggle, the messy hugs and slimy kisses, and the well-earned friendship and trust from some of our most valuable players.

You matter in the life of a child!

As a school-based physical therapist, the paraprofessional oftentimes carries out my physical therapy plan for a student.

Whether it be lifting, transferring, standing or stretching a child, I rely heavily on the classroom staff to implement my therapeutic activities.

Whereas a physical therapist has a student for 30 minutes a week…

A teacher’s aide attends to the student’s needs the entire school day.

Without a para repeating similar tasks as a therapist a child may not make progress toward his goals or, even worse, he may not be able to participate in educational and daily life tasks.

Similarly, a classroom teacher makes lesson plans and educational goals, but without the assistants, growth may not occur. The paraprofessionals are the ones in the trenches: on the playground, in the lunch room, in the bathroom and wherever else the student goes.

Behind the scenes, they make things happen.

Rarely getting the glory, most aides I know love what they do even though it is exhausting and not financially equitable to the work they do.  INVALUABLE best describes their role.

So, the next time you see your child’s or school’s paraprofessional, thank them!

From me, Maria, Haley, Shayne, Felicia, and Kara-you guys are the best!

In the Mind of a Special Needs Mum

It’s night-time. She cleans her face and stares at reflection in the mirror; half focused, half somewhere else entirely. “Your eyebags are awful” she thinks to herself. Another harsh judgement.

“Really,” She thinks, “these are marks of honour for many sleepless nights endured.

They’re also signs of dehydration – drink less damn coffee” she reminds herself, knowing full well that her first morning instinct will be to make a hasty retreat to the coffee machine before facing the day. She lets out a sigh and plods to the kitchen to prepare the last medicines and feed of the day.

Her legs feel heavier and each step reminds her how exhausted she is both mentally and physically. Her back is sore from lifting and her limbs feel weak and each task feels laboured.

Though she is tired, her mind is racing. Out of nowhere a memory pops into her head. She’s lying on a hospital bed wailing for help as she’s rushed down a corridor for an emergency c-section.

Her only sight is the passing lights above her head. Her grip tightens and her heart races, her eyes become watery. Quickly she suppresses the thought.

PTSD. Birth trauma. It never leaves you.

She feels a lump in her throat and is overcome with emotion – fear, panic, grief… relief. She swallows, takes a deep intake of breath, and refocuses on the task in front of her. “It’s over. Everything is fine.” she chants to herself in her head repeatedly.

Snapshot images continue to flood her consciousness – probes, beeping sounds, incubators, it’s dizzying, but she perseveres with the task in hand. She keeps herself present by acknowledging objects in the room. Microwave. Kettle. Toaster.

“Am I losing my mind?” she wonders to herself, trying to re-affirm her grip to reality. The whole scenario was enough to remind her to take her own medication, and to check when her next therapy session is.

She wants to get better desperately, she doesn’t want to have these thoughts. They can come at any time, and with no warning. It can be debilitating. She feels sorry for herself, but also frustrated at not being able to control her own mind.

She pops out 3 tablets from the strip and puts them into a purple 10ml syringe.

She draws up the water with almost robotic precision. She does this so frequently in fact that she can afford to let her mind drift elsewhere again. She glances around the kitchen counter as the tablets dissolve, and notices a letter. It’s an appointment letter for an important hospital appointment next year.

In her mind she begins to plot potential outcomes and what she is hoping will be achieved. She thinks about the journey – it’s a hospital she hasn’t been to before.

Immediately the anxiety awakens as she plans in her head the conversation of asking her partner to take more time off work to accompany them. She wonders about the parking, the facilities, and whether they’ll be able to find where they are going.

Leaving town scares her. She knows how irrational it is… but home is what she knows, it’s her safety net… she has relative control here.

Funding, waiting lists, unreturned phone calls, paperwork, clinics – all key words in her repertoire now. She thinks of the weeks ahead.

Special needs dentist for a descaling without sedation – will she aspirate? Paediatric clinic – how soon will we get the home nebuliser? Flu vaccine – will she be well enough for this one? We’ve rearranged 3 times already. Ordering more tube feed supplies – will we have enough giving sets until then?

So many logistics, so much planning. There is never a quiet week…

She finds herself part amused at the irony of so much planning when actually life couldn’t be much more unpredictable. Every eventuality has to be considered, every worst-case scenario must be prepared for. There is always a contingency plan. She can’t afford to be unwell.

She is struck by the paradoxical nature of being so busy and meeting so many people; yet earning so little and feeling so alone. She misses normality, and yet she feels guilty for complaining – she knows how lucky she is, how privileged she is, but still her heart feels heavy.

These conflicting emotions take a toll on her – they almost justify the eyebags.

Her mind goes back to when she worked in retail. Her favourite customers were the ones who seemed the loneliest.

It had always pained her to think that she may be the only person that the customer gets to interact with that day. To remedy this, she always made extra time and effort with these people. She is now one of those people – those people she pitied and wanted to help.

The loneliest people are usually the ones with the most interesting story to tell

You can see a visible change in their faces when they’ve been validated as the important person that they truly are. It’s beautiful but bittersweet. She hopes that others feel that way towards her, because sometimes now she feels invisible, unimportant, even an inconvenience.

She shrugs off the thought… don’t think about work and normality, don’t get nostalgic… it wasn’t always easy back then either.

She washes her hands and goes to administer the meds. “Administer” she thinks. What a medical term to use. She’s not a nurse, she’s mum… she’s not even just mum, she is her own person.

She goes to give the meds… every word is a potential trigger for her to start over analysing, every topic is a sore spot. She has become over sensitive and irrational. She wishes she could leave her own mind for a while, to take a holiday from herself.

The bed is hard to open. It’s a huge high sided bed with multiple openings.

She feels her eczema on her hands pulsate with pain and burn as she puts pressure on the latch of the bed. “Stupid giant bed” she thinks to herself whilst feeling simultaneously so grateful to have this piece of equipment. Beds like this don’t even exist in hospital for her. She can’t help her child be safe there.

She is sick of feeling “grateful” for basic necessary provisions and feels full of anger at the lack of facilities in the world.

Home is the only safe place she can keep her child. She feels isolated.

Why is it a privilege to have the same accessibility, dignity and quality of life as everyone else? As she closes the bed, she also tries to close down her persistent angry thoughts. She stops for a moment to admire her sleeping child. Her anger and resentment are quickly replaced with a deep love and pride.

What an angel. She watches her breathe and works hard to not think of the times she has struggled to breathe. “This is a peaceful moment – keep it that way” she instructs herself. She hopes for a better night than the last 30 nights. Medically, it has been an exhausting time. Interventions throughout the night have been constant.

She wants to go to bed, but she knows that the insomnia, the nightmares, the need to suction her child and give her an inhaler will take over. Going to bed seems futile and yet so necessary.

The used syringes are thrown into the sink to be cleaned tomorrow, the light is switched off, and she retreats to bed. She would love to read a book to take her mind to a different world, to a place of escapism, but she can’t.

She’s too tired to indulge… there are also more important things to do than read a book. Reluctantly she turns off the light and struggles to get comfortable.

Every night as she tries to get to sleep, she tries to replay the day in her mind.

It helps her feel productive to know how much was achieved. It triggers her to think of the next day – what needs doing, what will the day hold in store? Will she manage to do it all? So what if she doesn’t… and yet at the same time she has such huge expectations of herself. She feels a compulsion to prove herself and justify her role in the world.

She often imagines her mind as a brain full of little people working away. They work really hard, but they are underpaid, overworked, and short staffed, and this makes them a bit scatty and disorganised. She is amused at the idea that this reflects the health system and also the world that she lives in.

Every sound outside the bedroom reawakens her. Does she get up and check? She wants to conserve as much energy as possible, but she doesn’t want to take any chances. The decision making continues into the night as she and her partner navigate their way through the early hours intervening when necessary.

Eventually, she drifts off.

Her mind calm enough to let the resting commence.

Goodnight.

A Hairy Dilemma

Hair. It’s more than just a head covering. It is something that sets us apart as individuals. It can reflect your personality and how others see you.

You can have a bad hair day, a blonde moment or let your hair down.

Hair is part of your identity.

Hair can also be a major life challenge. Especially when you have a child with additional needs.

My daughter Z has hair that is as crazy and unpredictable as she is. Her hair is thick and wild and grows in a million different directions.

It defies hair clips and buns and all but the strongest and stretchiest of hair bands.

Z’s wild and crazy hair is one of the things I love about her. It makes me smile and it truly seems to reflect her personality. I would never want to change it.

Managing Z’s hair is hard, however.

She hates having it washed. Or dried. And she particularly hates having it brushed. Surprisingly, she isn’t too bad when it comes to haircuts, but she will get cranky and wiggly if they last for more than 2 minutes.

To make matters worse, Z pulls her hair when she becomes upset or frustrated.

At its worst, this has left her with bald spots, but more commonly these days, it just means that her hair is shorter (and thinner) on one side than the other.

Z also prefers to spend her time lying down, which coupled with her tendency to dribble, means she usually has hair stuck to the side of her face.

Add a head cold to that mix and the hair is cemented onto her face.

She gets terrible knots in her hair as a result of rolling or rubbing her hair.

I’m pretty sure the neighbours have come close to calling the police on the occasions I’ve tried to brush the knots out.

I am constantly at a loss about how to style her hair. I’ve tried several styles throughout the years, an undercut being the most successful.

However, as she gets older, Z now has her own opinions about how her hair should look. For her last haircut, I was hopeful she would agree to cut it short (“like Mummy’s hair!”) – not realising no self-respecting seven-year-old wants the same hairstyle as their mother.

Instead she used her communication book to declare she wanted “long hair”. Sigh. We compromised on a bob.

However, no matter what style we choose, we always seem to come back to a “palm tree” type ponytail on the top of her head to keep her hair out of her eyes.

I don’t think we will ever get rid of the palm tree ponytail because it is the only thing preventing her from looking like Cousin It from the Addams Family.

I’ve resolved to think of it as her signature style now.

So, it looks like my future will continue to include industrial amounts of spray conditioner, strong and stretchy hair bands and apologies to the neighbours when a vigorous brushing becomes unavoidable.

At least the palm tree style provides the opportunity to buy her lots of cute hair clips and accessories for Christmas.

And for Halloween, she can always go as Cousin It…

One for the Dads

Any time you read a blog online about children it’s usually from a mum, when you see pictures on social media of children it’s usually with their mum or the picture was taken by the mum.

But dads need a mention too!

My husband is amazing, I could talk about him all day long but the only time you’ll see a picture of him on our social media is on a weekend, and that’s simply because he works all week.

When my son was diagnosed, I made the decision to stay at home and care for him which means my husband has to work so hard to provide for us all, I know he has a stressful job but he never lets it show.

As soon as he comes through the door on a night, he steps straight into dad mode, he does everything I would and always reads a story to our children before bed.

He then helps tidy up and often cooks for us too (did I mention how amazing he was?)

He has never once complained about the mess when he comes home and always reassures me when I’ve had a bad day!

Everyone always tells me what an amazing mum I am and admires how much I do for my children but I don’t do any more than my husband does!

It’s only because he’s out working that it looks like I do more.

When our son was diagnosed, he was the one spending hours and hours researching everything we could do to help, he was the one who called and wrote emails to professionals when we needed to see them more because I was too shy and too polite to do it myself!

There are so many dads out there that don’t get the recognition for what they do for their children but what’s even more special is that they don’t mind!

They just carry on with what they do and do anything in their power for their children just as mums do, because the love between a father and child is equally as incredible as the love between a mother and her child.

So to my husband, thank you.

Thank you for everything you do for not just our children but for me too, just know that although I don’t often tell you, you are amazing!

I really don’t know what we would do without you.

What to Get – SEN Christmas

My son is ten and it took me nine of those years to get the Christmas present purchasing just right.

Yes, NINE whole years, well I suppose the first few up until he was diagnosed at four were easy enough.

At that time, I was just purchasing the latest Cbeebies cartoon toy of the moment or any type of vehicle.

If it had wheels of any kind then it was a winner – preferably wheels that he could then proceed to chew off in the coming weeks and I would have to follow him, prizing them from his mouth.

I am just thankful he was never one of those children that chose to stuff these up his nose or in his ears – although the fear of him choking was real.

So, fast-forward to the years six, seven and eight.

These were the years that his speech was much more formed, his vocabulary was amazing and his writing was coming on.

This is where the lists started.

How hard can it be – to follow a list! that’s what he might as well have said to me for the next couple of years.

Christmas at six Cameron had most things on his list except for a bike.  He was growing so much at this stage and my logic was that I would wait until his birthday in May as he would not get much use of it during the winter months.

A wonderful day was had by all and when I asked Cameron how was his day – he said, “it was ok but I didn’t get everything on my list – I didn’t get a bike”.

I was crushed – no one wants their child to remember not getting something they really wanted.

Christmas at seven was where I got everything on the list – we all know how rewarding this is as parents.

We would have no repeat of the previous year.

Yes, I even managed to get retro micro machines discontinued in 1993!! in addition though I bought him extras, you know bits that I thought he would like.

Since that Christmas, if I have ever only given one piece of advice to my fellow SEN parents that I hope they take on board – STICK TO THE LIST; No more, no less.

This was the year that he opened gifts and announced, “I didn’t ask for that” and this wasn’t just reserved for me and dad, this gem of information was also extended to family’s gifts.

I was mortified, I literally cringed, I was so angry at how could he be so ungrateful, but why though – in his logical mind he hadn’t, he was being truthful.

Its only society that tells us that you can’t say those things as it is rude.

Fast-forward another 12 months to Christmas age eight!!

Only list items were purchased; when family asked what to get him, they were also given a list item or asked to pop some money in a card as this is also something that he was starting to quite enjoy receiving.

As with previous years I asked, “how was your day today baby?”…… BEST CHRISTMAS EVER, I got everything I wanted.

It worked an absolute treat, genius and so much more stress free.

At nine I felt he was old enough and had come on so much in these last 12 months.

He knew about his autism now and was fully embracing this.

I made a suggestion to him: “How about you don’t make a list this year, I think between me and Santa we can figure out the things you like – lets have surprises this Christmas” and you know what, at first, he wasn’t sure.

He told me he would get back to me and that was fine, as he needed time to digest this massive change.

He eventually agreed!

“How was your day baby”………..”mum it was the best day, I’m actually quite surprised at all the amazing presents I got”.  SUCCESS!

So, yet another 12 months have passed and as we were on approach to xmas 2018 he said………….

“Mum can I just have surprises again this year like last year”

All I Want for Christmas is… to Stop Comparing

It’s December. The festive season (or whatever you refer to it as) is here. It’s absolutely in-your-face, unavoidably, here.

I really pity those who truly despise this time of year.

You can’t even hide away in your home for fear of checking social media or switching on the TV and having tinsel coated pigs in blankets pelted into your face.

Me? I’m a wreck.

I am forever oscillating between hopeless grief ridden despair and determinedly optimistic.

“We WILL find our own way” one moment but then the next moment, buckling under the immense pressure I put on myself, and the strains of day to day life.

Christmas is a fantastic opportunity to socialise, form traditions, and explore super sparkly sensory play.

However equally; it is also a time of nostalgia, reflections, loneliness, illness, and… last but certainly not least… comparison.

With each seasonal obligation, I’m forced to find a way to “make it work”.

I nervously navigate my way around the shops trying to look past the scooter she can’t ride. The advent calendar she can’t open, eat, understand… enjoy.

The irritating elf guy that parents tirelessly position and photograph each day to post on social media and show their child for… erm. You see, I don’t even know what reason.

The truth is I sort of presumed he wasn’t for us, and also seeing his smug little “I didn’t do it” face was enough for me to write the idea off immediately.

I mean, he’s monitoring kids’ behaviour during the day but then paradoxically practicing frowned upon behaviour himself when everyone else is asleep? Anyway. I digress…

As always, special needs parents deal the hand they’re dealt with great innovation and creativity.

I see parents make their own advent calendars with little prizes that their child can enjoy.

I see parents fundraise and campaign to get their child an adapted bike (you know, the ones that cost about 10x more than the other bikes… as if carers earn anywhere near the amount their full-time working peers do).

This all takes extra energy reserves, extra time, and extra money – something that actually many parents don’t have.

Their ability to continue to find that reserve is something that we should all admire, celebrate and respect.

Sometimes these extra efforts work… and sometimes they don’t.

We operate on unmet expectations and uncertainty all of the time but still always find that glimmer of hope that our efforts will prove worthy, and this gives us the drive to keep on trying… to capture those smiles of those little people we love the most.

The social media feed is awash with hot chocolate drinking children, families whose children would sit through and enjoy a trip to the cinema, and so on.

Even worse is scrolling through all of this from a fold out camp bed in a children’s ward in hospital.

So many of my attempts to make her happy somehow feel like a punishment to her, or something she must endure.

It’s forever playing the game of “if we don’t try, she’ll never like it” and sticking to what you know works. I want to expand her horizons, but not take her too far out of her comfort zone that we do some damage.

I’m not sure my child knows what Christmas is about yet. Every year I think maybe this year.

But then another year passes. I internalise my jealousy when I see a child half her age talk about father Christmas coming down the chimney and instead choose to smile at their adorable innocence and excitement.

I don’t mean to sound cynical – Like I mentioned earlier, I’m sad, but also bubbling with positivity.

Rising and diving between the two is actually exhausting and I wish I could just feel okay with things and not have to constantly analyse and process a huge spectrum of emotions and opinions.

I just want her to be happy. Happy for her won’t be the things that made me happy as a child.

It won’t be the things that make a lot of people happy. She doesn’t have a Christmas list. If she did it would be to be swung around and bounced until she shrieks with joy.

It would be lots of music only videos on YouTube (very specific ones, don’t get it wrong!). It would be wandering round places and showing her different things (of course, with music on).

She doesn’t ask a lot. At all.

She isn’t materialistic. Or greedy. She wants her loved ones… and a good data plan.

We have an upcoming family meal. It makes me feel guilty when occasions are centred mainly around food. She doesn’t eat. Food holds no interest for her. Nor does being in one place for any length of time.

I’m forever torn between doing what people do at Christmas, and wanting to just shun it all in favour of whatever seems easiest, even though I know I’ll yearn for what others have and take for granted.

My family are amazing though; they’ve chosen a venue that goes next level over the top at Christmas. The decorate everything. Not one inch goes un-baubled.

I am hopping she is in awe of the setting and that we can help her be part of the event by showing her the sensory delights… with of course all of her loved ones around her… and again… her music and videos!

We WILL make it work.

I need to remember that in life it is what it is. If we pile on too much pressure on ourselves then we are guaranteed to crumble under the weight of the expectations and ultimately break down when things don’t go how we want.

I need to learn to be grateful for every little success, every new activity enjoyed, every day got through that she can fall asleep worry free.

For Christmas all I want is some new socks, some strong coffee, and memories with my family – whichever way they are achieved. I need to focus more on the current moment and not future moments.

People always say “all that preparation and then it’s over in a day”, and it’s true.

All the planning, all the worrying, why didn’t we just relax and enjoy the build up? Why compare ourselves to social media.

We all know that Facebook, Instagram, all of them…  they aren’t true representations of people’s lives. Instead of comparing our lives to the moments people purposely select to share, we should shut our phones down and focus on what really matters.

We should be helping those who can’t afford a Christmas; helping those who are alone at Christmas. It shouldn’t be a time of comparison, greed, competition and anxiety.

It should be a time where communities come together to celebrate our many differences, accommodate and validate each other in every way we can, and work together to enjoy life and improve it for everyone else.

I am of course talking about the social and commercial aspects of Christmas.

I don’t mean to discount the actual religious element which is of course the basis for the whole thing. But I wanted really to talk about how it is for Special needs parents and our families.

Wishing everyone a hospital free, happy time. If it can’t be hospital free time, then I wish for you to still be surrounded by those who matter most. It is after all one day out of a whole 365, take it easy.

What Your Car Says About You

You can tell a lot of things about a person by their car, or at least narrow down some options to likely outcomes.

If you see a really flash sports car you can assume, the person is rich or in lots of debt and quite possibly a man in a mid-life crisis.

You don’t stick around to see if it’s true but that’s who you pictured, and you move on.

A large 7-seater car however will leave you considering that this is a young family, particularly if the windows seem to have attracted lots of finger marks and smudged smiley faces drawn on.

Cars with large boot space and a cage styled between the boot and the top of the backseats would belong to a dog owner (or at least you hope so).

On top of the car itself you can find out about the owner based on some of the contents, a pink fluffy dice hanging from the mirror doesn’t say older business man and seats covered in clutter give you a very busy person.

Where the car is also gives some clues – outside a school could be a teacher or a parent, on a driveway means they’re at home and maybe their house is a new clue, or if they’re parked outside a hospital, they could be sick or a carer or they may just be a visitor.

Doctors and nurses have their own car parks so that is a bit of a giveaway.

Why have I suddenly started talking to you as if I am the Poirot of automobile investigation?

Well, my car can tell you a lot about me, its not particularly flash, I don’t have a fluffy dice and it can be found outside the school, on my drive or in the hospital.

My car is tall, it has a blue badge on the dash board and a blue tax shaped sticker on the front windscreen with a disabled sign.

It has another sticker on the back windscreen saying leave space for wheelchair and a big door at the back to roll a wheel chair in and out on the ramp.

Its usually parked in a space with yellow hatched markings next to other cars that are very similar.

From my car it’s likely that’s somebody could tell that we’re a young family, that a member of the family is disabled and unable to drive as they roll in at the back.

It would tell you that we need space around us and patience as we’ve got to do a lot more than just step out of the car.

We’ve got a lot of equipment to get out and buckles to undo before we can get everyone out and go anywhere.

It would take a shorter time to see and figure all this out than it has for you to read this paragraph.

The extra space afforded to the disabled spaces in my local hospital (Morriston, Swansea, Wales) has either side have been taken upon by able bodied people without a blue badge to park in which means rather than the disabled car users having MORE space between them as intended by design, they actually have LESS space than every other row of cars.

How helpful, unfortunately these people never get fined or stopped so it’s likely to continue. This tells me a few things about the people parked in the middle:

1. They have never struggled with disability for themselves or a loved one (Unfortunately it sometimes takes this to open people’s eyes)

2. They are selfish people who don’t care about anybody else as long as they’re ok

3. They know they’ll get away with it

4. They care more about money than they do about people (If there was a fine implemented that space would never be full of cars)

As well as this the pavements on the way into the hospital are covered in cars which means unassisted wheel chair users have no chance of accessing THE HOSPITAL.

Just think of the insanity of a world where we were so self-involved that we don’t notice that we’d made it impossible for a disabled person to access a hospital without rolling themselves into the road.

I wish we lived in a world where fines weren’t needed to inspire people to behave decently but we don’t.

So next time people get out of their cars and leave them where they are, I would love if they took a second glance and thought, I wonder what my car says about me?