Showing posts with label inclusion. Show all posts
Showing posts with label inclusion. Show all posts

Let's see Adults with Disabilities in Advertising?

The tide is shifting. More and more companies are following the lead of household names such as Marks and Spencer and Sainsbury's and including young models with disabilities in their marketing campaigns. Hoorah!



Seb fronts Marks and Spencer campaign


Natty joins Sainsbury's Back to School Campaign


This week our little Natty's face once more peeked from the pages of Frugi's catalogue, as she advertised a glorious yellow cotton cardigan. 

Frugi Shoot for Downs Side Up Model Natty: Under Wraps

Over three years ago a little model with Down's syndrome burst onto the scene! This was such an important step for inclusive advertising and you can read more about the Pioneers for change here.

Inclusion: Natty and big sister Mia in the Frugi catalogue

During the Easter holidays we were super excited to be asked to return to our friends at Frugi for another photo shoot. 

A Year of Advocacy, Collaboration and Inclusion


What have we achieved? What have we learned?

The highs, the lows, the collaborations and challenges that made, or nearly broke us. 

Where will the next year take us? 
Who knows. But here are just a few of the moments from 2014 that have shaped our campaigning and advocacy.



The highs and lows of 2014 for Downs Side Up


Inspiring, Inclusive Blogfest

"Why am I doing this?" I thought to myself as I stood cold and alone on an empty station platform in the pitch 6.30am darkness waiting for my train to take me forward 4 hours to Blogfest.

I reminded myself that today was going to be a day of learning, my brain primed like a sponge to absorb writing tips from the finest in the game.  It was also about sharing some thoughts on inclusion and diversity in blogging at a round table at the Mumsnet Blogfest event in London.


Hayley, Soraya and Swazi discuss inclusion at the Blogfest round table.

"The next train to arrive at platform two is the 6.47 to Plymouth."

I felt uneasy, vulnerable, watching out for any sign of railway staff. A shiver of cold ran down my spine, made worse by my damp hair and the urgent need for the first hot drink of the day. 
I sheltered on the bridge, watching the heavy rain fall in vertical cords and flowing like urgent waterfalls from blocked gutters.

A Blogfest for Inclusion

I'm honoured to have been asked to join a group of leading writers and speakers at Mumsnet's #Blogfest2015, a huge one day event that promises to be a 'glittering celebration of great writing and sharp ideas'.

I've watched the You Tube clips from last year and they aren't exaggerating!

mumsnetI'll be joining Swazi Rodgers of Chocolate is Not the Only Fruit and Soraya Cotwal of I Happy Now 2 talk at a round table about creating diversity and inclusion in the predominantly white, middle class, non-disabled world corner of the internet that is the blog world. Blogging holds such power to create change when we work together, that it's important to harness that for all.

Chatty Natty on ITV Lorraine Show: The Face of Representation

Did you ever have a moment in your life that was so exciting, so surreal that you weren't sure if you dreamt it up? 

The kind of moment where you are plucked from your ordinary life and sucked into a parallel universe for the briefest of whiles, before being plopped back safe and sound, albeit exhausted and clutching a few souvenirs?

Well, if it weren't for two pink Lorraine clocks in the girls' bedrooms, I would indeed be wondering if I had dreamt up our trip to London to feature live on the ITV Lorraine Show.

We Need to See Disability in Advertising

'It's meeee!' she squealed excitedly as we drove round the roundabout.

We manoeuvred round one more time so that she could get a closer look at the huge banner outside our local supermarket urging us to get organised for the new school term. This time we all squealed. 'It's yoooou!'

A third lap. Just for luck. Just to be sure our eyes could be believed, smiles stretched across every face in the car.



2014-08-20-14897_895124300515958_5865978186038347800_n.jpgI fell silent as I fought back a tear or two, my heart swollen with pride as I allowed the true significance of what I had just seen to sink in. This was so much more than a Mum seeing her child's face on banners outside every Sainsbury's in the land. For Natty has Down's syndrome and this is the first time that a child with any kind of disability, physical or intellectual has featured in a major Back to School advertising campaign. For me the posters might as well have shouted:

• All children have a right to quality education and the skills to enable them to lead full independent lives. 
• All children have their own unique personalities and our classrooms benefit from that eclectic mix. 
• All children, regardless of their abilities or disabilities, love a shiny new school uniform!

Make Positive Choices for Learning Disability Nurses: Together we are Better

The force for change that is the wonderful Helen Laverty recently hosted the 10th Positive Choices Conference for LD Nurses and professionals in Kingston #10PC14.

I was so very sorry that I could not attend to speak as invited, I was so very disappointed not to be able to meet the medical angels that support us all, and the incredible, inspirational speakers she had lined up, such as actress Sarah Gordy (who has DS), who has become an online friend. Infortunately illness and storm-damaged railway lines conspired to keep me in Cornwall, so in lieu of my speech, I made a little film for the delegates, a film outlining the role of learning disability nurses for our family, what they have done for us and what they mean as we move forward through Natalia's life.I wanted them to know how vital their job is. 
You can watch it here:



             

What Did World Down Syndrome Day Achieve?

On the 21st of March, 2014 we joined forces to celebrate the 9th World Down Syndrome Day together. The charities Down's Syndrome Association and Down Syndrome International decided that the theme of the day was health, and as a way of getting everyone involved we wore our funkiest socks... 

'For we are all colourful and unique.'
(That's a phrase I coined as a stock response when people ask what the sock theme is all about.)





But I was conscious of mutterings in the wings:

Little Red Riding Hood: A hero with Down syndrome

ONCE UPON A TIME...

in a quiet clearing in a faraway wood, there lived a wise, brave and beautiful young lady named Natalia. Because of her fondness for dressing in a velvet cape of crimson rose, and a frock adorned with pictures of her favourite woodland friends, she became known by all who loved her as Little Red Riding Hood.

Little Red Riding Hood had fought valiantly to become strong, overcoming battles of health and development with a smile. And each day she worked as hard as she could to learn the skills she needed to go out into the big wide world by herself, and each day she drew others in with her humour and vivacious spirit, so that she could teach them all about her inclusive community, her determined family, her zest for life and her famous way of turning Big Bad Wolves into the gentlest of puppies.




Gorgeous Inclusive Calendars




Look no further than Shabang Theatre or Down Syndrome Centre, Dublin for your calendar for 2014. 

Sahabang Theatre include 3 useful Makaton symbols and signs to use at home for each month.




Down Syndrome Centre, Dublin includes a lovely story about each child featured.



Not only do they make a great gift and promise to organise your life simply by hanging in your kitchen (I'm clinging to that hope anyway), but they will bring sparkle, joy and a set of beautiful role models into your lives.

Proceeds go to charity of course. You can purchase both calendars via the weblinks links above.

I wonder if the Makaton Charity will be bringing out an interactive advent calendar again this year. That was such fun too!

Sports Day Sunshine

Last Friday saw Natty's first ever Sports Day! Woohoo! 

Egg and Sppon gentleness

Last year we had planned and practiced, mainly what was expected of her, what each activity entailed and how to wait her turn, cheer on her friends and so on. 

Well, if you can cast your mind back to last summer, it rained. It rained a lot. It washed out 3 scheduled Sports Days and then we ran out of term time. The weather matched my mood, I was so very very disappointed that Natty and her classmates didn't get their first experience of this tradition.

Pippin is smuggled in
However, straight after half term (nice and early in case the weather decided to change its mind) we received a slip giving us the date of this year's event. Straight in with no time to plan or dilly dally.

Sun cream and hats were the order of the day and we turned up proud and excited to watch Mia and Natty enjoy the fun together. They had been put in the same team which pleased them both greatly. In fact it was the first time Mia hasn't complained about not looking forward to Sports Day in her 5 year long school career.

We even brought Pippin with us (Dogs, we later discovered, weren't allowed, so I hid him under my arm and pretended he was a fluffy handbag with legs.)

Now for those who think Sports Day is about being competitive and sporty and excelling and winning, well there is that element, it is brought out in some more than in others. But there is so very much more to it. This Sports Day was very inclusive; every child competed in every event, including the ice lolly pit stop. Older children worked with younger children to encourage and support them. There were future athletes, children who shun excercise and wouldn't put team sports at the top of their list and children with LDs and physical disabilities. 


The sense of achievement for all involved was all too plain to see. Look at Natty's face when she threw her last and 5th hoola hoop and it when over the pole. Priceless. A boost to any child's confidence.

Hoola hoop over pole result!

I was nervous about the 100m race. What would she think as her long-legged friends tore down the straight ahead of her? Would others look on and feel sorry for her 'bless her'. 
Not a bit of it. As Natty tore down the straight as fast as she could, watching her friends disappear over the finish line ahead of her, she looked from side to side at the crowd, with a grin as wide as the Cheshire Cat, and she waved. The crowd roared with cheers as she finished and many other Mums had tears, making my wracking sobs slightly less conspicuous. Pride doesn't come close to describing what we felt. Sports Day being one of the events we wondered if we would ever watch when Natty was born.

Hurtling down the track, waving to her public, after all her friends had crossed the line
Another little girl's wheelchair had to pull over for a pitstop as it was experiencing 'technical problems' because her TA was pushing it so enthusiastically down the straight, so high was the feeling that afternoon. I'm not sure it was made for such speeds ;)

Javelin Thrower par excellence

The egg and spoon race was a similar story. Natty carefully and gently tiptoed down the track, only dropping her egg once. Slowly but surely went that tortoise.

So, new skills were learned, confidences were boosted and our little community was again brought together, brought closer by the variety of children we have in our midst sharing a common goal that afternoon. For, as Mia says, 'Everyone is different'.

I reflected on our Sports Days, when I was always the last to be picked, made to feel chubby and useless, with sadness. Thank goodness those days have gone for our girls, although some schools have yet to fully embrace a properly inclusive Sports Day so I understand.

It's amazing how events like this rake up the past isn't it.
Tricky bean bag event

We returned home happy and with sunshine in our hearts, a few millimetres taller, our chests puffed out far. Mia was beaming. Natty was unusually quiet. When we looked around she had fallen asleep in the car...



The Significance of the Birthday Party Invite


The Party Invitation

Children's birthday parties...

"Noise.  Other people's kids.  Sky high little ones on a sugar-fuelled trajectory headed for mahem and destruction.  A couple of hours eaten into your precious family weekend.  Small talk with other parents you barely know.  All those scary germs lurking in the ball pit that are bound to make your child ill.  The stress of hoping your child behaves better than the worst of them."

That may be what some people think when their children are invited to a classmate's birthday party.  Certainly when they are before the age of the 'drop and pick up later' phase.

Here's our story...

Last week, when I dropped Natty at school, her friend Bella bounced up to me, beaming from ear to ear and proudly holding a large pink envelope aloft.  On the front, it simply said 'Natty', written in her own 5 year old hand.  Natty and I took the envelope and I asked what it was. Bella replied, "It's a birthday invitation."  From what I recall, there was much whooping and hugging all round.

You see, Natty attends mainstream school. And Bella is a gorgeous, bright, funny, confident, 'typically developing' girl in her class.

Immediately the birthday invite became a symbol to me.

Today we attended the party, and what a fabulous party it was. There were games and a disco and a soft play bit and a buffet Nigella would be proud of, tears, tantrums, party bags and even a glass of bubbles for the mums! 

But this is not the overriding, enduring image of the day for me.

I am sitting here with an picture in my head of Natty right at the front, joining in the game of musical statues.  Of her climbing through the soft play area without me on her tail.  Of her going up to the buffet with a plate in one hand and her friend Fin holding the other (he also happens not to have Down's Syndrome).  Of her saying thank you to the parents of her host before she left.

What I saw today was a little girl who was not completely identical to her peers, perhaps because of her speech, perhaps because she is head and shoulders shorter than them, but a little girl who took part in all the same activities and felt part of the group.  Not for one minute did I observe an outsider.  Not for one minute did I see her stand apart. And not for one minute did I see her classmates treat her with anything but love and respect.

I did observe that other little 5 year olds instinctively understand that she needs a little more time, or help, or translation.  But to them, this was just part of the party, part of daily life with Natty in their midst.

And suddenly I realised at once, that the full power of inclusion is a 2-way thing.  It's not just about our kids with special needs being accepted.  It's about a new generation growing up with others who are 'different' alongside them, learning acceptance.  It about all of us looking out for each other.  Our children give back something too. Every time someone cried today, Natty's radar was activated and she was by their side in seconds, comforting.  And they welcomed, wanted that comfort.

So, for me that party invite was a symbol of true inclusion.  I hope they never stop coming...


Read about how Natty celebrated her own 6th birthday with a party here in Natty's 6th Birthday.


Watch Natty's Mum tell friends and family what to say when a baby is born with a disability, here: 

Advice for SENCOs - The Parents' Viewpoint


Natty at her fully inclusive Pre-School


I was recently asked to address a group of SENCOs (Special Educational Needs Co-ordinators) as they neared the end of their 3 year Masters Degree Course. Their tutor hoped I could provide the missing ingredient to the course: that of the Parents’ Perspective. 

I put my thinking cap on and set to work to come  up with something that would change the way new SENCOs think forever.

I decided to ask other parents and disability groups what they would say to a room full of SENCOs if they had the opportunity. I did this via Twitter and Facebook, and the response was overwhelming. I printed the replies off, cut them up and spread them on the kitchen table. Interestingly they fell into 3 distinct categories, and echoed my own initial plans for the talk.  I weave the quotes from these parents into what follows.  Thank you to all of you that helped.

This article has since been published in SEN Magazine.



Advice for SENCOs - The Parents' Viewpoint

I am a former language teacher and learning support assistant and am now a stay at home mother of two. Our youngest, Natty, has Down's Syndrome.
When I looked back from the parental side of the fence, on my time as an LSA, I realised that I may have been good, but that I was not quite good enough. So I decided to ask other parents and disability groups what they thought of the professionals who support their children; what they would say to a room full of SENCOs and SEN workers, if they had the opportunity. The reaction to this was overwhelming and the responses fell into 3 distinct categories, which echoed my own thoughts.

Consider the parents

By far and away the most frequently mentioned and passionately   discussed point was that professionals must consider what parents think and want.  All families differ, some need more support than others, but the vast majority know their child better than anyone else.  After all, it is the parents who have sat up into the wee small hours researching their child's condition online, fuelled by worry, fear of the future and a desperate need to know that they are doing the very best they can.
It is they who have been the experts from day one. It is vital to involve and accept help from parents. SENCOs who recognise this have the most valuable resource at their finger tips.

"Realise that the parents are experts and be open to suggestions of new ways of doing things that have been successful elsewhere."

"I would like to be treated as the lead professional."

"I would ask the SENCOs to take 5 minutes to listen to the parents (very different from talking). I may not have any O Levels, but I want my child to go through school in the best way possible. This means being regularly involved in planning and forward thinking."

It is so important to see things from the parents' perspective sometimesand understand the pressure they can sometimes be under.  They live with the child's difficulties every day, they may not get much sleep, might have been through worrying episodes when their child was ill, hopitalised or undergoing surgery. At times this will take it's toll, and recognising this will go towards creating a better working relationship.

Teachers and SENCOs should take the time to look for potential problems within school, so that the parents don't always have to be the ones to mention what is not going to plan. Suggestions should be taken seriously the first time because as one father mentioned;

"By the time I raise an issue at school, it is because it is really important and because I have already let a lot slide. I will have been mulling it over for a very long time."


The Pupils' Advocate

"For inclusion to be successful, a teacher must provide for the needs of every child in the class and this includes children who have teaching assistants (TAs)." says SENCO trainer Angela Redman. "The teacher should work individually with these children so that they can fully understand them. Pupils will often work harder for the teacher and this also models how the other pupils in the class view that child."

Most parents realise that the role of a SENCO is a difficult one. They are employed by the school, report to a head of department and headteacher, and work within ever increasing time and financial restraints.  Primarily though, they work for certain children within that school, often some of the most vulnerable, and they are their advocates.

"Sadly, a SENCO's role is to run with the fox and bark with the hounds."

"First and foremost they should be an objective advocate for our children."

"As an ITU nurse, I attended a Critical Care conference each year, listening to survivors of disasters, so that we culd understand the trauma whn patients came in to us.
At the end of the day, I was the patient's advocate first and foremost as they are always the most vulnerable person in the room. It was my priviledge to keep that patient safe in every conceivable way at all times. I always considered them with the highest possible regard and if I had to lose my job to whistle blow I would.
To me, anyone involved in SEN should be the same."

Sadly bullying and disrespect towards SEN pupils can and does occur within schools and sometimes staff members are the perpetrators.  This could be a peripatetic teacher, a dinner lady or receptionist whose ideas are a little 'old school', so you need to be vigilant.  All staff need to be made aware of the school's Disability Equality Policy, and trained to follow it.

"Make sure all staff know that just because a child has additional needs does not mean they are a problem, just that you need to think differently and change your way of working."

SENCOs need to get out into the classroom and go on learning walks around the school. They need to spend time with the children with SEN, to assess needs and determine which advice servises and interventions to recommend.

One TA I have worked with summed up the SENCO role rather well: "An efficient SENCO would have the ability to promote effective teamwork. They should be aware of their team's individual expertise and have in place methods to deploy them across the school, ensuring teachers, teaching assistants, supervisory staff and parents have access to a higher level of support, and providing service users with a flexible, efficient and competent workforce. This dynamic approach to teamwork allows for the identification of gaps in provision and highlights areas for professional development."


Inclusion and Independence

We all know that school is not just about Reading, Writing and Numeracy, but sometimes it is easy to become lost in academic targets and assessment.  For SEN children, their time at school is  more about the long-term goal of enabling them to live in mainstream communities as independently as possible.

"A good SENCO will see this bigger picture and help their staff see it too."

"Our daughter will not finish school and live in a vaccuum. Our hopes should be that we can all enable her to live within the mainstream community. And for this, her experience at mainstream school is crucial. Inclusion at school will help her be included in her future, will help others learn to include her. Schools should see themselves as mini societies, enabling children to become good citizens.'

Another parent's comment encapsulates a common concern:
"Some teachers are used to measuring success in data and feel 'what's the point in helping this child who is so far behind?' They become frustrated that they aren't making more progress. They need to see that reaching small goals are worth such a lot, that they are helping a child to live an independent life."

Inclusion is a two-way street. Classmates learn as much from our children as our children benefit from being included alongside them.  I recently wrote a post about true inclusion as I witnessed it at a 5 year old's birthday party:


Conclusion

SENCOs have a difficult role, but they are in a priviledged position: they can make an enormous difference to the educational careers and future lives of so many. It is important that they get it right for our children.





This article appeared in SEN Magazine, March April 2013. 





Open Letter to the Girl Guide Association



Once upon a time, far too many moons ago, I was a Girl Guide.
I have many fond memories from that time and I recall our group being supportive, open, warm and encouraging to all girls. We were proud of the fact we pooled our skills and helped each other where there were weaknesses. I learnt a great deal from my time there which I carry forward into the work I do today.


I'm sure the Girl Guide Association has moved on greatly over the last 30 years, as has the Scout Movement. I expect the activities are even more thrilling, the skills imparted more practical, the events better organised and the ethos even more inclusive.

I'm sure, then, that you are as saddened as I to hear of a less than welcoming Brown Owl. One whose reluctance about accepting a new Guide with a learning disability was aired.

I am always one to think of both sides in every situation, and you may well simply have a woman here who was nervous about whether she had the skills to adapt to teaching a young lady whose learning styles differ, but who expressed those concerns wrongly.
Perhaps she felt she would need additonal training or to alter her working style, and that filled her with dread.
Perhaps she has a personal experience of disability which is painful for her. After all people manifest guilt and remorse and pain in a miriad of ways.
Perhaps her ideas are genuinely not up to what the Guide Movement expects and she is in the wrong role.


Wise words for us all from model Natty Goleniowska who has Down's Syndrome

Either way I feel heavy-hearted, not only for the girl and her family who feel offended, but also for the lady in question, who has clearly been denied the benefits of a truly inclusive society. For inclusion is a two-way street which we were denied growing up in this country many years ago.  Our children's generation are lucky to have friends with learning disabilities, who teach them a different way of viewing the world and the most important lesson of all, which is acceptance, something this lady lacks.
I think the guides she is claiming to wish to protect could teach her much on this important lesson in life.

This situation is not like many I find myself writing to resolve; countering those like former UKiP candidate Geoffery Clark who called for compulsory termination of babies with disabilities (OPEN LETTER TO MR CLARK), or supporting a family whose daughter with Down's Syndrome is being forced out of a school in Malaysia by other, ignorant, parents taking legal action against her.
No, this is a more widespread, insipid kind of prejudice and discrimination but which is thankfully easier to change through education.

I do think a public response would do much to allay the public anger that has arisen from this incident and I await your reply, which I will publish to the thousands of families and professions within our network.

I would also like to offer my services as a speaker and trainer in inclusion and disability for institutions such as yours.

I very much hope that the 12 year old girl in question will feel fully welcomes into one of your groups shortly, as I hope both our girls will be when the time comes. None of should let a blip like this stop us seeking mainstream activities for our children.

I leave you with a post I wrote about the true nature of inclusion, through our children's eyes.
THE SIGNIFICANCE OF THE BIRTHDAY PARTY INVITE



Hayley Goleniowska
Author of Europe's Top Down's Syndrome Blog: DOWNS SIDE UP
Mum of ambassador and model NATTY GOLENIOWSKA, 6, who has Down's Syndrome
Speaker, campaigner, writer, trainer, educator, expert in Down's Syndrome
Facebook: Downs Side Up
Twitter: @DownsSideUp

"Changing perceptions of Down's Syndrome gently from within hearts"

---------------


The Girl Guides later responded favourably with the following statement:


Girlguiding UK is open to all girls and young women. This is one of our most important values – and we strive to uphold it in all circumstances. We are very proud to have many young members with Down’s Syndrome and other disabilities. And we would like to welcome more. We encourage all our volunteers to include young members with disabilities and we have a network of special needs advisors and specific resources to support them in this. 

It is very difficult to comment on an individual circumstance without knowing the details. However, we are very saddened if any potential young member, and their family, feels they have been excluded from joining us. We very much hope to have a conversation with the family and the volunteer as quickly as possible to support them both to find a way to include this girl in guiding – and be a full part of everything we offer. 

We would encourage anybody with concerns to contact our membership support services: msswebconcerns@girlguiding.org.uk 

Julie Bentley 
Chief Executive

Natty's 6th Birthday

Children's birthdays are wonderful yet emotionally complex markers of time for me.
I've decided therefore to do two posts about Natty's 6th birthday, and this is the light-hearted one about parties, presents, jelly, tutus, Pass the Parcel, friends and family....

This time last year when Natty was 5, her Dad was unfortunately working away. I did a simple party at home but it's hard to take pics and cook and organise games and stop kids crayoning on your walls and smile and enjoy all at the same time. It was a lovely day, but passed me by in a slight haze. Read about it here in An Unexceptionally Exceptional Birthday.

This year was very different. We had celebrations over 2 days. A mini tea party with just our immediate family on the day and a party for school friends at the weekend.

Mini celebration on Natty's birthday with simple cake number 1


Not only was Daddy Downs Side Up here, but Natty's big brother and his wife were visiting too. We had an army of help and it meant we could all enjoy the tiny details of the day.

A very happy birthday girl

For the first time I think Natty understood that her birthday was coming. She got excited and chatted about the party both before and after the event. I'm so happy that she clearly loved every minute of it. Pictures speak louder than words, so here they are...

Cheeky Monkey!

The birthday girl donned her favourite tutu and big sister  Mia set up a facepainting station for all the guests, starting with hearts for Natty.






















Natty then then painted some of her friends' faces before decorating her big brother and turning him onto a rosy-cheeked elf!

I adore the look of concentration and love here


No party would be complete without a selection of games: Pass the Parcel, Pin the Purse on the Mermaid, (please excuse my feeble art skills!), and every parent's favourite Sleeping Fish (there was a vague swimming theme), as well as colouring in a little thing that shrinks in the oven, doing your own puppet show and decorating your own party bag.

Pin the Purse on the Mermaid, Pass the Parcel and Puppet Show




The children were all beautifully behaved and worked together, instinctively allowing for each others differences; explaining, calming, comforting, dancing, laughing, hugging, cheering up, consoling, asking for help if necessary. Wonderful to see, and exactly how it should be.

When it was time, they sat down for tea. I decided to swap traditional party food, which is always more time consuming and costly than you think to prepare, for a starter of cubes of cheese, pineapple and grapes on sticks, then a bowl of pasta and  blitzed homemade veg and tomato sauce (so easy to knock up in advance) finished with mini trifles in cups (fruit and sponge with jelly, then custard and sprinkles). All so easy and enjoyed by the kids and when their parents picked them up they knew they had eaten a 'proper' dinner too.

But enough waffle about healthy birthday banquets... the main player in this stage of the party was... the much anticipated... CAKE!!!

The cake, the reaction and the fingers in the ears during the very loud singing!
I am no baker. It takes me a whole day to make a birthday cake, but having bought them in the past I have to say I prefer the shabbier looking variety that is infused with the secret ingredient - LOVE. Well, it was a swimming pool affair with splashing Peppa Pig and George amidst a bright blue jelly (What a to-do making that I can tell you! Many a night was spent consulting friends on Twitter to work out how to do it), complete with icing floats and lilos. It wasn't perfect, but it was 'good enough' to please the children. (Phew!)

And there you have it, another unexceptionally exceptional birthday, like many taking place in homes up and down the country every weekend.

Birthday parties are a wonderful time to see the joy of inclusion first hand, to see how our children just accept each other for who they are. It always means so much to me and I see what I was denied as a child growing up in a more segregated society where people with disabilities were hidden away. Read The Significance of the Birthday Party Invite for a light-hearted look at this.


Jojo Maman Bebe Xmas Catalogue: Models with Down's Syndrome

Jojo Maman Bebe's Facebook banner


Natty and Seb (M&S) in the Christmas Edition of the Jojo Maman Bebe catalogue



I still adore the outtakes!