These are my salad days….

Once upon a time there was a person called Mum. Mum originally had a name but Mum had ended up having so many children that she was now just known as Mum or for a spot of variety: G-Man’s Mum, Minx’s Mum, eldest teenager who must not be named’s Mum, Famalam (a whole new level of confusion brought about by the “yoof of today’s” obsession with roadman speak) and other variations on a similar theme.

Mum suspects that her local authority may also have some pretty choice names for Mum but they are unlikely to be printable (or provable!) here and that is a story for another day.

Before Mum actually had her own children, she was actually a very good mum even though strictly speaking she didn’t qualify for the title role. At that point in her life she only had 2 tri-coloured cats so unless you considered the phrase “who do you think you are, the cat’s mother?!” applicable, she was reaching somewhat.

It turns out it’s much easier to be a brilliant Mum when you have imaginary children (and real cats) and only occasionally baby-sit other people’s or smirk at other parents whose children are having a public meltdown, smug in the knowledge that you could do the job SOOOOO much better.

However, Mum knows that she was indeed a very good mother pre children because in those halcyon days she spouted such wisdom’s as “There’s no reason at all that ANY child should have a crusty/snotty note when its so easy to wipe with a tissue” or “my child will eat all the things we eat, just in smaller, less seasoned versions.” She also proclaimed  sagely to her fellow thinking- about-becoming- Mum friends that children wouldn’t really change her life as it was so important that children learnt to be adaptable and behave in all manner of situations, accompanied by a tinkly little laugh. Mummy was indeed the epitome of smug…

Then Mummy went ahead and had THE CHILDREN. Mummy wasn’t entirely daft/(un)lucky to have 4 little darlings all at once. No, she thought she would spread the misery joy over a period of years. And then they all lived happily ever after. 

So child number 1 was born and Mummy spent her days between feeding/crying/elation and exhaustion with her head buried in such bibles of wisdom as Annabel Karmel, Penelope Leach, What To Expect the 1st year, Toddler Taming and other such patronising fabulous tomes of parental guidance (no I don’t mean the film category) so that she could qualify as The BEST Mum EVER.

Since I don’t want this to be a bedtime story that bores you to sleep, I’ll spare you the blow-by-blow account of children 1 through 4’s every waking moment as it goes on for many (many, many, many) years but one skill that Mummy found accompanied her through the early childhood years and surprisingly still lingers today is something called THE GUILT.

Guilt was and is her ever-present ‘frenemy.’ It’s amazing just how guilt can raise it’s cocky little head at any given moment and Mummy feels sure that if universities offered degree courses in it, she would have more than qualified for not just a BA (hons) but probably an MA and possibly even a PHD too!

Mummy you see very early on discovered that guilt was there to keep her occupied in the small hours of the night (why does this child never stop crying/screaming…have I broken it?? Did I actually want a child/ren after all?? ) and was especially good at loudly shouting when she pontificated if her children had an off button once they had found their annoying dear little voices that she had waited so patiently for to utter their first babble.

Guilt was there when Mummy went back to work for the first time and everyone else she knew was a stay at home Mummy. Guilt joined her when she resorted to controlled crying. It sat heavily on her left shoulder (I’m pretty sure that’s the explanation for all the pain in her neck anyway) as she sat with her fingers in her ears when at her wit’s end she decided to try controlled crying in sheer, utter desperation. That didn’t go very well to start with as Mummy was unable to control HER crying and it very nearly became competition as to who would tire out first…..

Over the years Mummy learned that THE GUILT had an uncanny talent for sneaking up on her at times she would least expect it. Mummy thinks back and wonders if THE GUILT is what is responsible for driving her to wine every night…then she remembers an interview on early morning television that suggested that if you have a glass of wine every night – even if it is only the one – that you are actually an alcoholic and THE GUILT laps it up. It has a very good appetite does guilt and it isn’t picky what it feeds off.  Mummy tries not to let it be an appetite for destruction and I am pretty sure she isn’t referring to the Guns ‘N’ Roses album of the same name…..

One of the things THE GUILT has an extra special relationship with and most likes to taunt Mummy with is THE FOOD; specifically feeding THE CHILDREN.

Mum studied the various Anabel Karmel books from cover to cover and invested in more ice-cube trays that you can possibly imagine  – originally for the purposes of storing and freezing micro amounts of home-made, pureed baby food in but now mostly used for the ice in a gin and tonic.

Over the advancing years she resorted to google too. Technology being handily available at all hours meant she could consult this oracle getting tips on baby led weaning et al and make notes about delicious recipes even in the middle of the night!

Nonetheless, it appears that Mummy’s precious darlings weren’t reading the books and despite being capable of reprogramming the Sky box/DVD recorder etc (something Mummy still struggles with today) definitely didn’t seem to understand the guiding principles and ethos of those internet articles showing happy, smiley pictures of  babies/toddlers eagerly scoffing down quinoa and edamame dip, chia and lingonberry smoothies and that piled on the guilt still further.

Mum is pretty certain even over 10 years on G-Man still hasn’t forgiven her for the polenta/spinach loaf she lovingly created (what was she thinking?!) When served he deigned to take the teeniest of mouthfuls, then threw it disgustedly as the freshly painted wall. Mum watched in dismay as it “walked” itself over and over like a possessed rubber man toy down the wall to land with a splat forlornly on the wooden flooring. G clapped delightedly at the ensuing greasy slime mark.

You see, back in her earliest (judgemental) Mum days, Mummy made a solemn vow to promote healthy eating choices and to cook all organic, exciting, varied meals with plenty of vegetables from scratch! She thought that manufactured baby foods were the devil’s spawn.

Mummy didn’t quite think this through however with baby number 1 as she had gone back to work near enough full-time, was still having to get up for feeds in the small hours and was pretty much totally exhausted after a day at work away from her precious one (child, not wine for the avoidance of doubt).

Very quickly Mummy discovered that if she spent all her waking hours peeling/chopping/boiling/mashing and pureeing, it left very little time for doing anything else, especially playing/reading and interacting with her dearest first born…and that made Mummy feel MORE GUILTY than ever.

So Mummy got the stick out of her ass  relented and decided to buy some JAR FOOD thus freeing up some of her time and hoped that it would assuage some of THE GUILT. Surprisingly at times, this seemed to quite nicely pile on THE GUILT and Mummy may or may not have decanted jar food into baby bowls and sprinkled a few cubed bits of veg on to the top when she took it to nursery in keeping with the (myth) homemade baby food plan that she had…

Child number 2 helped Mummy on her journey with THE GUILT by being sensitized to dairy proteins once she had given up feeding herself  and put him on formula. This took the form of eczema so horrific that child 2’s back would weep open sores which made him very sad and cranky and the stealer of all the sleep for months at a time. He also started with asthma at the same time. Co-incidence? Possibly but it accompanied her special friend, guilt, very nicely.

Mummy subsequently found that an extraordinary number of every day items contain milk or dairy in some form or another and therefore spent a great deal of time of her time reading labels in supermarkets and working out how she could make alternative versions of favourite pasta sauces that Child 1 would also eat so that she wasn’t cooking herself into the ground and could at some point attempt the art of conversation with The Daddy. Mummy is pretty sure that at some point the art of conversation led to child number 3 but at that place in time she was so sleep deprived she can hardly recall.

Child number 3  – G-Man – had extremely horrible, painful reflux. Mummy knew this by the high-pitched screaming and the contorting and jerking of his back that exhausted his poor little body. He was also able to vomit at will, projectile and prolifically, even hours after a feed.

The Daddy didn’t really believe the Mummy at first when she insisted it was more than a bit of baby puke until he witnessed with his own eyes the baby upchucking so violently it hit 4 separate walls, the floor and the ceiling all in one go. Mummy was just waiting for his head to start spinning in the style of The Exorcist but at that point the Daddy had seen enough and agreed baby G should see the Doctor.

After several bumps in the road, poor baby G was hospitalised as his blood tests showed his chemical balances were completely out of whack and the medical bods suspected a condition called pyloric stenosis.

A few days of tests and investigations disproved this and thus began the ‘interesting’ journey of trying to get infant Gaviscon powder into a breast-fed baby.  This was not in reality a very fun game and by the time The Mummy and The Daddy had actually mixed it up, spooned it in, chased it back into the mouth from the drooly-chinned screaming baby, he had cried so much and gulped down so much wind, it all seemed pretty much pointless anyway.

Mum and Dad were assured he would grow out of it and that moving onto solid food would be the making of him. He didn’t and it wasn’t. There isn’t a single baby picture of him for the first 3 years of his life without a bib in situ.

Fast forward many years to present day, reflux is still hideous and painful and despite the maximum doses of antacid medications and motility speeding drugs, G Man has ended up being fed by a naso-gastric feeding tube since last October and no one is quite sure where this is going….Certainly the last 3 months of paediatrics appointments have shown he has lost weight, albeit very small amounts, and the medical bods are again scratching their heads as to the best way forward.

Child 4  – Minx – for a variety of reasons was born at a time that had been accompanied by much stress and worry. In her early weeks of life when her numerous difficulties and quite significant medical issues became apparent, Mummy was pretty sure that THE GUILT was responsible for what had happened and that made her feel it even more which was a bit counter productive in the end.

Minx’s first foray into actual food rather than breast-feeding definitely didn’t go to plan.  Frequent chest infections, coughing and choking during feeding, poor weight gain and a seeming inability to maintain a good suck reflex meant she had been assessed by a speech and language therapist (SALT) by the age of 4 months.

After listening to her feed via a stethoscope, the SALT was concerned enough to ask for a video fluoroscopy to be carried out. A video fluoroscopy is a form of x-ray imaging which examines the mechanism of chewing and swallowing using barium sulphate and this is  added to a variety of foods and drinks. Tasty… Whilst eating/drinking occurs, a series of images are taken at different stages and the barium makes it easy for the radiographer and SALT to view what is happening and pin point any areas of concern or difficulty.

Although the test is not in any way painful or invasive as such, since the body is exposed to radiation, it is not something that is undertaken lightly, especially in very young children.

Since Mum and Dad were very new to the world of special needs, they hadn’t really absorbed the ins and outs of it all and were most definitely in a haze of unaware, uninitiated denial. They certainly hadn’t thought through the why’s and wherefores of how this test would be carried out. In fact, since it was scheduled at short notice, they hadn’t even been given a leaflet or chance to look it up on-line.

On the day itself, it became apparent that getting barium liquid into a child who was solely breastfed, had never taken a bottle in her life and had no experience of “eating” not even a taste off a spoon was going to be interesting problematic.

Fortunately as both parents were present, The Dad was promptly dispatched to the nearby pharmacy to pick up a ready sterilised bottle, formula and jar of pureed baby food so that the procedure could get underway.

For many parents, no matter what number baby you are on, their first foray into tasting food off a spoon is a moment to be cherished, photographed and exclaimed over delightedly.  Watching a baby’s varying expressions of suspicion, doubt, grimace and/or delight is usually a fairly monumental occasion.

This first tasting experience in a freezing cold, sterile in more than one sense of the word, environment was somewhat marred; a most inauspicious start.  Suffice to say it didn’t go well on multiple levels; not the least of which were exacerbated by the SALT and locum radiographer having a bit of a barney difference of opinion about whether it was acceptable to expose such a small baby to radiation from the procedure.

I think I did promise further up that it wouldn’t be a blow-by-blow account of each child’s developmental journey…. I seem to have spectacularly failed on that front as this piece is already much longer than I had anticipated when the mood to put pen to paper or rather finger to keyboard originally struck me, so I’ll try to get to the point of why inspiration struck to write the dang thing anyway.

Mum remains nagged insistently by THE GUILT and despite all the reasons she should know better has endeavoured to continue making as many delicious,  varied home-cooked  meals as she can possibly muster….that of course is between the myriad of appointments/admin/general assorted crappery that comes from managing 4 children with additional needs and the day-to-day running of the house.

Contrary to at least half of the children’s falsely held beliefs that Mum spends ALL DAY every day on Facebook, Mum was inspired watching Gino D’Acampo on a well-known known morning TV show (whilst doing the ironing honestly and not at all checking out she of the Willoughboobby’s fame fabulous wardrobe – total lust envy ) talking about a family favourite meal from his childhood which was so easy and so delicious and could be made up from leftovers too AND incorporate all sorts of hidden veg! Genius!

Mum watched Gino and crew waxing lyrical over various stages of the preparation and thought to herself how quick and easy, cheap and HEALTHY it all looked.  Indeed her own mouth was watering and discovering that she had near enough all of the ingredient already in, save some courgettes and the conghiglione (that’s large pasta shells for the likes of you and I) Mum vowed to pick up the extra bits for dinner. *

Several shops later, Mum had scoured the local area for the blasted conchiglione without success. Waitrose had a blank space on the shelf as did M&S (although a price tag revealed that the shells were over £3 for a mere few hundred grams!!) and Ocado had plenty of alternative suggestions but nothing useful. If Mum had stopped to think for a moment, she should have realised that this was a SIGN and stopped right there and just served up some chicken nuggets goujons with nutritious vegetables chips.

Mum however was still lost in a thought- haze of smiling, pink-cheeked grateful children thanking her for such degustation and how the dinner time conversation would flow with abandon about all the new and varied food stuffs they would try together.

So Mum went to the overpriced deli and purchased the conghiglione then set about this veritable feast of gastronomy. About 2 hours into the process Mum reflected that the ba**arding recipe hadn’t looked nearly so time-consuming and complicated on the TV, forgetting of course that Gino had one of those handy “here’s one I made earlier” bods for at least 3 stages of the process that had been condensed down to a 10 min slot on TV.  Nor had Gino used every single item in the kitchen as she appeared to have done. Mum surveyed the unholy mess surrounding her with gritted teeth but glibly anticipated the raptures of delight from her children and knew it would all be worth the end result. She did however decide at that point if she was ever going to make this again she was bloody well going to buy béchamel sauce rather than make it from scratch!!

Fast-forward to dinner time, and the family gathered expectantly round the table, Mum anticipated their reactions excitedly. It certainly looked fantastic and smelled amazing! Plates were piled high and for good measure Mum had made a large salad and served some garlic dough balls on the side as an extra treat.

Child 1 promptly reminded Mum that he didn’t eat pasta (except on camping trips with friends as a “necessity”) and mooched off to make himself scrambled eggs. Child 2 wasn’t home and child 3 point-blank refused to eat anything. Sigh. All hopes pinned on child 4, she did at least raise a spoon to her mouth….then informed Mum that actually she “wasn’t a big fan of this muck” and would just stick to the dough balls, salad oh and the shop bought orzo pasta ready salad in the fridge

Mum could have just put her head in her hands and sobbed but she was far too busy shovelling in mouthfuls of the food to care at this point and The Dad seemed to be enjoying it anyway.

The dog put his paw lovingly on her knee with big, pleading mournful eyes and told her without the need of words that he would happily scarf down any portion she was willing to give him.

Although Mum has a STRICT(ish) ban on feeding the dog from the table, she did briefly contemplate putting something on his own special plate….and then she remembered it contained onions which are very BAAAADDD for doggies and cheese which was the equivalent of about 5 hamburgers or something  so she had read in the vet, so that was that.

Mum has learned many a valuable lesson from that last venture into making meals off the tele…..and she won’t attempt it again for a while….but she might just tell the guilt to do one…at least temporarily….

*in case like Mum you fancy trying the recipe it’s this one:

Mum made the largest quantity using the vegetarian option and also used up some smoked salmon & sauce in some of the other shells. Note if you are serving strict veggies or those with dietary restrictions eg Kosher/Halal, you will need to substitute the pecorino or find a vegetarian version.


When is an EHCP not an EHCP?

For the avoidance of doubt or for those who may be unfamiliar with the UK and it’s education system in general, I will outline what an EHCP is supposed to do.

All children and young people who have a learning difficulty/disability which makes it difficult for them to access education and need more specialist help than a typical child or a child with educational needs over and above that which the school/college is usually expected to provide from their nominal budget, should be assessed for an EHCP.

As it stands, if a child has a relatively low-level learning based difficulty/disability/need, their school would be expected to fund specialist support out of their own budget before making an application to their local authority for additional top up funding.

The Governments own website outlines the EHCP in more detail:


Rather succinctly this little gem  sums it all up in a very appropriate nutshell:

The EHCP should identify, as detailed on the UK governments own website:

educational, health and social needs and set out the additional support to meet those needs

So there you have it!

Hopefully this makes things clearer to you than mud (please read that in an ironic tone) but the whole EHCP process is such a lengthy, demoralising fiasco, so forgive me if it’s still murky. Anyway, I digress….

EHCP stands for Education and health care plan. I’ll say it again and in bold, just in case and for the avoidance of doubt:


Let’s take a moment for that to sink in.

Okay then. Got it?

If you saw those words at the top of an important document, with your child’s picture beaming out at you from the front page, what do you think you might expect to find reading on?

I may not be the sharpest tool in the box, no contender for Mastermind or MENSA but even I don’t need a dictionary or google translate to understand those 3 little but ever so important words.

I would expect a to-the-point, concise yet detailed report outlining what and how all my child’s EDUCATION, HEALTH and CARE needs could be best met.

I would assume (& yes my dad did teach me the adage about assume making an ass out of you and me) that such a document would clearly state what steps/methods/therapy or such like would be put in place to accomplish this and help the child achieve the best possible outcomes, uniquely tailored to their own specific requirements.

There would be bullet points stating  identified needs. And to each of these there would be a response detailing how those needs can be met, who would provide the support and how. Quantifiable, specific. Defined.

As you may have guessed by now and if you have read my previous blog posts: ( and😡😡 we lost our educational tribunal case as the judge decided after hearing the evidence that we couldn’t prove a waking day curriculum (residential school mon-fri) was solely necessary on educational grounds, which is the ONLY aspect of the case he could rule on.

The judge however did stipulate verbally on the day of the tribunal hearing itself and in his subsequent summation that there is a clear, identified need for both the bodies representing children’s social care and health (ie CAMHS) to step up to the plate and that a tri-funded agreement would have been in our son’s best interests.

Regrettably because the latter 2 aspects are not enshrined under current legislation and despite the overhaul of the whole statementing process which took place in 2014, leading to the creation of EHCP’s, the judge was not able to rule on any other factor than education and he also had to balance his judgement with the best use of public funds.

We found all this out last October but there has been so much other assorted 💩going on in our lives that I’ve needed time to step back, lick my wounds, retreat, repair and decide what to do next. It is still an ongoing process.

So as it stands, it turns out I really should have listened to dear old Dad because assuming anything positive about the EHCP process really did make me an ass.

I naively thought the 3 very specific words of education, health and care would formulate the basis of MY child’s frame work of specialised education.

That those in authority and tasked with facilitating the EHCP would recognise not just his needs but his fundamental RIGHTS to access appropriate care and support to his emotional, social and educational needs as an entirety. Ha!

Essentially it seems MY child’s needs are pretty much irrelevant in the document that stands as HIS EHCP. Furthermore how his needs interplay and merge with those of ours as a family – because we are a functioning (debatable!) unit – seem totally irrelevant.

How egotistical of me to think all these things should be reflected and factored in as a holistic approach in his plan?! I think wishing for unicorns and rocking horse sh%t would have been more achievable.

As I was succinctly reminded the local authority do not have a duty to provide the best possible outcome for our son or our family, just an outcome. So let’s disregard what could have been a fantastic opportunity; a way forward that would promote his independence, resilience, friendships and enhance every aspect of his life.

Let’s ignore the fact he’s bright and potentially capable of achieving highly academically (as stated by an independent professional) Lets disregard the lack of ‘real’ life contemporaries, social skills and tasks pertaining to daily living that would best be achieved by supporting him in a residential school placement. In fact let’s knee cap him before we even start.

Because what we wanted for our son costs too much… and shame on me for appealing to the powers that be that providing the best possible support in EDUCATION HEALTH and CARE right now would reap dividends in the future.

I was told by “management” that long term goals/achievements aren’t even considered when looking at the costs right now!! So what the bloody hell is even the point????

Silly, silly old me! Bottom of the class for me. Do not pass go, do not collect £200 and straight to the jail!

Only we are not playing a fun game of Monoply (if the way you play Monoply is anything like the way my lot do, I accept I might be playing fast and loose with the word fun) I suppose if we are using paradigms as an example, we should choose The Game Of Life as a better synonym.

Forgive me if I’m coming across a little over zealous with the italic button. But the unhappy little fact is, we aren’t playing games and our story isn’t unique.

We are talking about REAL life, REAL children, REAL families being put through the mill and being spat back out again. Crushed, devastated, lost.

In fact those 3 words above would far better sum up the plan that is now recognised as the official EHCP document, prescriptive and responsible for shaping my child’s future.

Our legal representation has reviewed the decision made in law and reluctantly concluded there have been no errors in interpretation of the legal aspect. And just because we don’t like the decision, it doesn’t give us the right to appeal.

I’m still deciding what to do next and how best to proceed but in the interim if we refuse to accept and send him to the school stated in the plan, then we are in breach of the law and could face a fine and/or prison sentence. It saddens me beyond belief that legally I cannot do anything other than comply obediently in the interim.

The irony is not lost on me that on 24th October 2017, the Minister of State for Education department in the UK – Robert Goodwill – issued a statement advising that with effect from March 2018, every local authority in the county should ensure that all EHCP’s encompass the health and social care needs of the child in addition to those of education.

Whilst this is not mandated in law, a previously trialled scheme of 17 local authorities demonstrated an overwhelmingly positive response and therefore Robert Goodwill has announced that it should be adopted as best practice on a trial basis going forward for the next 2 years.

So, I can tell you and more importantly, the bean counters in their ivory towers: I won’t retreat, withdraw or go quietly. Of that you can be sure. One way or another I’m coming for you.

(Wo)Man’s best friend ❣️

This is a post I didn’t think I’d write for many years to come. One I shouldn’t even be thinking of composing. It’s not right. It’s not fair but here it is.

I am also acutely aware that this ramble may be perceived as very self-indulgent. Far too many of my good friends have lost their children. I would not dream for one moment of comparing my grief to theirs. But nonetheless the sudden and very unexpected loss of our much loved dog burns white hot and I am hollowed out with sadness. For all intents and purposes, our pup was a fully paid up 7th member of the family. Well technically 8th I guess if you count the cat. (We do love her too!)

If you have read any of my past blogs, you will know some of the difficulties and battles our family has faced over the last few years.

Whilst it’s not a competition, no top-trumps fest, the day to day demands of medically complex children, the amazing quirks but also relentlessness of autism, endless appointments, clinics, surgeries, battles for and with various agencies and services takes its toll. You Buddy (or Sir Budston of Burnarrrr as we sometimes referred to you!) my wonderful little dog, helped alleviate some of those burdens.

Please don’t misunderstand me. I recognise there are many people, probably some of them reading this, who would give everything they have and then some to be facing those same fights and difficulties I mentioned, having lost their precious loved ones far too prematurely; but oh my boy, I thought we had so many long and happy years ahead; wondrous walks to stroll/pad through, delightful or disgusting (depending on your perspective) smells to sniff and cuddles on the sofa to sneak in at any and every opportunity.

Buddy, much admired by all who met you, faithful four legged companion. How can we only have celebrated your birthday a month ago? How can it be that we never even made it to a whole year of you being in our lives, in our home?

You were my birthday present almost one year ago. We had talked about having a dog for over 5 years before taking the plunge. A bit like having a child, it was never quite the right time to introduce a dog to our chaotic lives.

Enlarging the family, moving house, redundancies, working abroad, relocating and leaving the island of my birth and the only home our children had ever known followed by house rentals before finally having a settled(ish) house of our own.

Quite out of the blue and having been a steadfast, most resistant party, I’ll never forget the day my hubby, Martin, turned to me and asked if I wanted a puppy for my birthday!

Minx was about to go into theatre for surgery number whatever and was giggling woozily from the pre-op medication. I recall being so taken aback I asked him if he had actually downed the pre-med instead! I was ecstatic and not about to give him time to change his mind.

Although it had been a long time coming, I knew exactly what kind of dog would suit our family, our crazy-hectic-bonkers lives and had done quite a bit of research in the hope that one day… maybe…just maybe… we would be lucky enough to have a pooch of our own.

We saw your picture first and a flurry of emails were exchanged before THE BIG DAY: your homecoming; my 40 something birthday. The moment I picked you up, cuddled you to me and laughed at the thought of putting you in the enormous crate in the back of the car, you filled our hearts so entirely. The void you leave behind is a chasm of epic proportions. I don’t know how or if ever it can be filled.

It doesn’t seem possible that I’m writing about your passing over the rainbow bridge when we should be looking forward to so many more years of mischief and mayhem. More days fretting about what you might have managed to scarf down if one of us wasn’t quick enough to stop you – I lost count the amount of Lego I scooped up just in time; how many bits of this and that I retrieved from your doggy jaws. Your quivering nose whiffling along always seeking out, questing and foraging. You could smell a dropped blueberry from a 100 paces and hear the rustling of the treats bag in the kitchen no matter where you were in the house or garden; a pretty useful tactic when you were being cheeky and not wanting to come to us when called!

You brought so much happiness. Joy, laughter, giggles and fun. And so much poop too! Martin tells me he cleaned up 12 doggy bags worth yesterday. Considering I last did it on Saturday morning and yesterday was only Wednesday, that’s quite an achievement. Especially since you were nil by mouth from Monday night on. And you were at the vets all day Tuesday….

We joked it didn’t feel right to get rid of all the 💩; perhaps we should create some poo-based monstrosity altar dedicated to you? Your legendary pooping out an entire, intact nerf bullet still makes me smile now. (NB definitely not to be encouraged responsible readers/dog owners – the children learnt the hard way that I meant what I said if they left things like Lego/nerf bullets lying around = bin)

A lot of expectation on such stumpy little legs. Not just the 6 people in your immediate family cuddling you, loving, and petting you. So many people that had the pleasure to meet you – our favourite coffee shop by the river and all the employees therein, our lovely groomer and her dog Poppy, friends and family and the seemingly never ending stream of delivery people with medical supplies or equipment, Amazon deliveries and so forth. Always an action packed day in this wonky-old household and you always ready to greet them with a deep woof, occasional bark and a wave of your magnificent plume of a tail. We often remarked your tail was bigger than you! It looked like it should sit in pride of place on a hat worn by one of the 3 Muskateers. And now I have a small piece of it saved in a memory box to remember you by. It smells still of the grooming, pamper session you had just last Friday. I’m glad it is of that and not the clinical smells of the veterinary practice, their kindness not withstanding. Your grooming sessions over the year cost more than my haircuts!

You were my secret keeper extraordinaire. Too many nights I muttered oaths into the top of your sweetly curling fur when dealing with the latest co*k-up from various services, be they special needs, medical bods or utility companies. So many times I poured out my heart and soul to you, you listening attentively with your head on one side, adopting the classic cava tilt that all other cavachon owners will recognise in its uniqueness. When I was saddest you snuggled that bit closer. When I was happy you were delighted that there were extra treats and cuddles and when it was all just a bit too much, you expected nothing but ensured your presence was always felt.

We joked often that you were not so much a dog – more part goat, part sloth. Your dislike of vigorous, brisk walks was the cause of much frivolity and it was remarked upon more than once that you were the perfect companion for a fair-weather not terribly exercise motivated owner such as myself. Too many times at the site of your harness and lead you would feign sleep or rush back to your bed refusing to come out, especially if it was cold. and dark. and raining. and there was a ‘Y’ in the day…..

Of course now I know my darling boy, you weren’t just faking it; you weren’t trying to make me feel better about the dislike of walking in the 4-seasons-in-1-day climate of Yorkshire. You were tired. Your little body was constantly battling a build up of toxins that in the end would be your downfall.

I try to take comfort from the fact that you are no longer suffering. That we could afford you the peace and dignity that is so often missing when our human loved ones are terminally ill. It makes a small dint in my grief.

At the moment there is too much sadness in this household. Too many reminders everywhere we look: your water bowl empty, toy box neat and tidy, not strewn all over the kitchen. Your place on the sofa vacant. I think even Tilly the Cat in her own feline way misses you; after all she can no longer take a swift munch out of your breakfast or dinner when she thinks none of us are looking.

Members on a wonderful Facebook web site I belong to for cavachon lovers have provided me with enormous support. An out pouring of love, empathy and sympathy. A stunning bouquet of flowers was delivered from them to me today. It made me cry again. But the tears were underscored by gratitude too. After all as Alfred Lord Tennyson said it best: “Tis better to have loved and lost than never to have loved at all.”Buddy 04/10/2016 – 14/11/2017 🌈❣️


How do you sleep at night… part 2 😡😡

I’m a bit less ranty today but no less passionate so let’s get this done and written before I lose my impetus… never mind the will to live. 

I like to think I’m currently  channeling my inner Taylor Swift and her pals in the Bad Blood music video: 

(*above image may be subject to copy-right) 

But in reality I should be so lucky. I’ve spent far too much of the day with my youngest son on a hospital ward, wallowing, sat on my butt, scrolling social media and eating chocolate. Less Swift, more sloth;  I can feel the helplessness wanting to swallow me up; shut me down again. 

(sorry sloths everywhere who are probably outraged at the comparison) 

I’ve been extremely touched how many people have commented/got in touch or shared my previous post. Thank you. 

I wish what I had written didn’t resonate with so many but I am also grateful for the support and the sense of solidarity. 

I recognise the issues facing my family are far from unique. Judging by support groups I belong to, friends, social media and so forth, this utterly deplorable battle for services to provide and protect those most in need, those who don’t have a voice of their own, those with the least ability and energy to fight are being waged up and down the county. 

Whilst the difficulties faced may be slightly different, they all share a common denominator: the vulnerable, those in crisis, those society should be protecting and empowering. 

Forgive my Whitney Houston moment but our children ARE the future and if we don’t invest in them and secure the best possible pathway, what hope is there for society moving forward? 

I also know the elderly, infirm, mentally unwell and so on deserve their cause being championed in the same way. 

I recognise on a deeper level my attitude is simplistic and that something policy-wise, fiscally, has to give or change dramatically going forward. 

How do we achieve this? I don’t know; I never professed to have the answers as to what this should look like in terms of the bigger picture. 

All I do know is a seismic shift is necessary, society is screaming out for it. How we approach this, how we can achieve it is for somebody/ies far more qualified than I. (Otherwise I probably should be standing for government….🤔) 

The demands of a large, aging population who are living longer, the epidemic of obesity, drugs/alcohol/cigarettes, the advances in medical science meaning those who once would have met their maker because of cancers, heart disease, prematurity of birth and the terrifying increase in the so far unstoppable dementia are well documented. There can be no escaping the fact that expectations and demands for provision will increase year on year. 

All the while the funding for front line services is being reduced or in some cases done away with all together. Departments asked to find millions in cost savings, balance the books and yet still pull it out of the bag, somehow. 

Morale is at an all time low as evidenced by the mass exodus of Doctors, nurses, emergency services and so forth. 

I’m not naive. I know the country is on its knees financially and floundering in uncertain times: Brexit, the future of the NHS and government but the refusal to engage, instead throwing up wall after wall, challenge after challenge means there’s less money in the pot to provide even the most basic of services. 

Is it just me and people like me that can see the irony in money being spent on disputing and denying care instead of the care itself? 

We are informed of cuts to services/benefits/ grants every time we switch on the tv, open a news paper.  The effects of austerity on all aspects of social care, health and education (and of course the ripple effect on our police force, armed forces and such like) have been hiding in plain sight for many, many years

Why is it that the major political parties seem far more invested in scoring points at each other’s expense and plotting a coup to oust their leaders than implementing change and securing services for the greater good? 

I want to believe the bean counters genuinely care, that there is an appetite for change but they have become so blinded in covering their backs, their departments and their funds, (actually the tax payers funds) they have forgotten their original purpose. The other alternative: that they enjoy the power trip, playing god and causing abject misery has to be some dystopian fantasy…. doesn’t it?…

I do know that continuing with this ostrich style approach, riding rough-shod over those of us trying to cope day in, day out and strangling us in a bureaucratic nightmare, (presumably in the hope that parents/Carers will give up) ISN’T helping. 

If as much effort and emphasis was put into providing and fulfilling services, identifying and enabling children, parents and the wider family before they reached crisis point a great deal more would be achieved. 

I can’t help thinking that in fact the overall financial outlay would ultimately be a lot less, nevermind the impact and fallout on the family which ultimately add to the spiralling costs. 

How much do local authorities spend on retaining expensive legal council, defending cases and when challenged by parents on the attack, concede a case with moments to spare? The costs in such situations are not merely financial.

Whilst I cannot go into the ins and outs of our case in detail at the moment (until we receive the decision of the SEND tribunal I don’t want to prejudice any outcome) I can relate some of the damage and the wider implications the delays have caused us so far: 

  • Inability for autistic child to access mainstream education since March 2016 resulting in high levels of anxiety, depression leading to self harm and suicidal idealisations necessitating multiple in patient/out-patient hospital stays
  • Provision of interim specialised education package with 1:1 staff ratio/on occasion 2:1 to provide up to 2 hours study per day (where possible round child’s anxiety) 
  • Child unable to access GCSE subjects/make option choices
  • Involvement of multiple agencies on numerous occasions – police, accident & emergency, CAMHS, children’s social care, Young Carers, autism out reach, fostering team and foster carers
  • Local authority (LA) assessment and review officers to prepare EHCP, take information to specialist information panel on multiple occasions, liaise between relevant parties, issue consultation paperwork to potential schools 
  • Assessment of child by educational psychologist for local authority 
  • School transport (single occupant) with escort to ensure autistic child safely taken to and from school
  • Maternal mental health crisis triggered, medical intervention required,  inpatient psychiatric care for 3 months, multiple medications and therapies
  • Community care package to support maternal mental health, crisis team management, out of hours services 
  • Care package from disabled children’s team to provide direct payments in support of care for medically complex child thus enabling sole breadwinner to continue to work 
  • Emotional support to other children in the family necessitating pastoral support, teachers from 2 separate schools reporting back on children’s well-being and attending looked after children’s (LAC) team  meetings, approximately every 6 weeks
  • All children in family requiring support and intervention by CAMHS  to address trauma and ongoing psychological fall-out
  • Family engaging professional legal team and independent educational psychologist to prepare case for tribunal
  • LA engaging in-house legal advice and support
  • LA acquiring professional legal counsel to present at tribunal
  • Convening of independent tribunal and panel member(s) in official court to hear evidence from family and LA surrounding case 

How much does all of this add up to? This is not an exhaustive list and no doubt  there are things I have unintentionally missed/forgotten but I think it is a fair representation. It’s pretty depressing reading isn’t it?  

Has what I’ve detailed shocked you? We are just one family in a cast of thousands, dare I even say millions. 

Unless you or a loved one need to avail yourself of services, you assume it happens to others; not to people like us. 

We are now the others. 


How do you sleep at night?… part 1…

Heads up, a warning: I am enraged. White hot, scalding anger that is making me vitriolic and bitter. 

I know it’s doing me no good and I should channel some inner zen but there’s no yin in my yang and frankly I need something else to focus on; some kind of drive to power forward instead of zoning out passively. Time to create a stink. 

I don’t as a rule swear very much. Mainly because I have spent and continue to spend a great deal of time round small folk, be they my own or other people’s and the fact that mummy has a potty mouth is not the kind of accolade I want to be renowned for.  It doesn’t mean I don’t think in creative Anglo-Saxon oaths but I try to restrain myself from actually launching into a tirade that would make a sailor blush. 

Over the years, it’s been quite amusing to find substitute words for the things that have nearly slipped out & turn them into something socially acceptable before the offspring absorbed it as their latest word du jour. 

Try to teach them please/thank you/hello/goodbye in polite company, you would think I was attempting to teach them the full works of William Shakespeare… in Flemish. Yet one *almost* expletive of a wangdoodling, cowbunkerling f-bomb amd such like and they have absorbed it by osmosis. 🙄

Tonight however. I make an exception. I am angry. So fucking angry. The fact that fucking just autocorrected to ducking as I typed it, has incensed me further still. 😡😡

I feel sweary. I feel ranty and shouty and full of words my Dad would get cross with me for using (even though he taught me most of them) I’m even tempted to use the ‘c’ one (& I don’t meant Christmas) – sharp intake of breath.

But I can’t have a good shout, unleash a stream of invective because yet again we are in-patient on Hotel NHS and there are a lot of very small people around whose parents would quite understandably be distinctly unimpressed.

So I’ll do my ranting, raving and effing and jeffing here on my blog; after all I did start my musings some years back in an effort to make sense of it all. Life that is. It’s been cathartic to brain fart away.  Download and dump the crap (d’ya see what I did there?!) 

Half the time I start a blog post with some vague notion of what I want to write about but no idea what will spout forth. I usually feel better by the end. I’d love to be all coy and twee and say I don’t care if people read it or not but actually that would be a lie. I do care. I suppose I need some validation. 

Tonight however I REALLY need you to read it, share it, spread the word. Because I’m sick of the powers that be getting away with it. Letting down vulnerable children. Leaving families in crisis, drowning in despair and fracturing already fraught and taut relationships. 

3 weeks ago today we took our local authority (LA) to a special educational needs tribunal in an effort to secure an appropriate, residential school placement for our high-functioning autistic son.

This was a culmination of 18 months of fighting and battling and relentlessly dealing with the stalling, the hoop jumping bureaucratic, bean-counting process. 

Our 14 year old who should have chosen his GCSE options last school year and commenced this September term on the pathway forward to achieve his future potential has been entirely let down and cast aside by THE SYSTEM.

Would it shock and surprise you to learn he’s received less than 2 hours education per day since March 2016? I know it does me. 

I also know if we personally elected he only attend school for this woefully inadequate amount of time, over such a long period, we would have been threatened with fines and imprisonment by the education department. But this situation is not of our making so apparently that makes it legal, ok, just tickety-boo and we can all smile sweetly, nod and wave because they are trying THEIR BEST. Except they are not. 

The powers that be are far more concerned with covering their departments backside, zealously guarding their pot of funds so they don’t actually have to put it towards what’s in the best interests of the child. 

 I hasten to add this is NOT the fault of his current school who have done everything and then some to support him and us as a family in providing him with a suitable education whilst time ticks on relentlessly. But they don’t have the resources or specialist autism knowledge to support the style of learning and can’t provide the low-sensory low-stimulating environment he needs to facilitate his learning.

Even so his mainstream school have strived to do all they can; he has 1:1, sometimes even 2:1 sessions in an area well away from the hustle and bustle of the main school. They have come up with creative and thoughtful ways to stimulate him;  to forge a kinesthetic approach that captures his imagination where they can. But it’s not working. 

On that at least the LA are in agreement on. But that’s pretty much where it ends. 

I knew I should have smelled a stinking, great dirty rat when the  placement panel convened in October last year and agreed that our son did indeed require a specialised educational establishment. 

Not for us the refusal to assess for an education health care plan (EHCP), not for us the refusal to grant such a plan and not for us the dispute over main stream or specialist placement. So I should have known. It had all come to us far too easily.

Having had the benefit and heartbreak of reading other parents accounts of the lengths they have had to go to even just to get their  LA to agree to assess, I knew we had been extremely, for want of a better word, ‘lucky’ 

But really that’s where our luck ran out. It’s much harder than you think to find appropriate, specialist education. There are a myriad of schools out there meeting complex and varied needs but how do you narrow it down?

In actuality your LA are supposed to help you with this too. They paid lip service to it so I ended up resorting to google and a pick and mix approach, narrowed down by area of expertise and geographical location. 

I’ll spare you the laborious ins and outs of the very lengthy and exhausting process. Suffice to say, after panel sat in January 2017, they decided they didn’t have enough information on our case to make a decision. Sigh.

In February 2017, although all the information from the 3 schools we had received provisional offers of placement from (we had approached more than 12 by this point who couldn’t meet our son’s needs) the panel asked to consult with yet another 3 schools. Of course if they had read the case notes properly they would have seen that 2 out of the 3 had already been approached by us and felt unable to offer a place. The remaining school was full and wasn’t suitable for reasons I’m not at liberty to go into. It would be an understatement to say I was fuming.

The assessment and review officer (ARO) acting for the LA tried her best and wanted to expedite matters instead of making us wait till the March sitting. She was new and fed duff information from people higher up the food chain who left her carrying the can after dangling false promises.

The people with THE POWER don’t like taking your phone calls. They are it seems unable to respond to email, even when you have their direct email address. Their phones must also be unable to make out going calls as they never call back and mysteriously all voicemails go awol. Or something. 

Apparently they can reply to your local MP if he/she gets in touch after you have involved them and made them aware of your dissatisfaction  but only with vague promises that matters are in hand and will be dealt with. A word to the wise: don’t hold your breath. 

So March 2017: to our dismay,  panel named a wholly inappropriate day-placement school some hour or so away from our home which they expected our son to travel to and fro on a twice daily basis.  

Having previously viewed this particular school, I had submitted a lengthy explanation highlighting why the establishment, the cohort of students, the academic remit (or lack thereof) and lack of opportunity to promote our son’s social/emotional development in a holistic over-arching approach to his education were not just incompatible but potentially very damaging and in the worst case scenario likely to exacerbate his anxiety, self harm tendencies, suicidal idealisations and more extreme behavioural difficulties. These concerns were also backed up by his psychiatrist and psychologist from CAMHS (child adolescent mental health) in 2 separate letters. 

It will hardly comes as a surprise that the school the LA had selected was the cheapest option. 

I was swiftly reminded that the LA only have a duty to provide an education for my child and if they can prove that is enough, it doesn’t matter what we know to be in his best interest, what has already proved dividends in students with a similar make up, what’s in the best interest of society over the long term in aiding him to achieve his potential, thus ensuring he contributes economically, socially and attains independence; to negate relying on the state for benefits, or support services. The school we have found and the costs associated with it are ‘incompatible with the public purse’ and therefore they can refuse to provide it. 

They accepted the school we had found is superior in every way; they accepted it could meet need and that  like on like it would (based on past performance of students very like our son) offer him the best opportunity and chance of success going forward. Indeed The Judge at tribunal was very clear on all these points.

Yet the LA refused to concede. They have played dirty; suggested we have stalled the case by refusing to ask for an earlier tribunal date – although fully aware that the independent educational psychologist we had asked for input from couldn’t assess until the end of June. Paradoxically, once the extremely enlightening report had been shared with the LA and we suggested moving up court proceedings, they couldn’t accede to our request. 

Although the statutory dates for submission of evidence were clearly set out in writing and which both parties agree to abide by, the LA suddenly found a pressing need for their own educational psychologist to assess our son, although they hadn’t deemed it necessary since the previous visit a year ago. Funnily enough they then asked for the revised report be admitted into late evidence.  

Surprisingly they also suddenly discovered a letter that had been ‘misplaced’ from our son’s psychiatrist (and which we had never been party to even though we have always been copied into all other correspondence to date) which were counter to 2 previous letters she had written supporting the need for a residential specialist school and expressing her grave concerns to him being placed in an environment such as that outlined in the LA’s chosen school. How very curious indeed that all this information had only just come to light…..

To be continued….