Showing posts with label photo shoot. Show all posts
Showing posts with label photo shoot. Show all posts

World Down Syndrome Day Fundraiser



Watch our film to see how and why 

DOWNS SIDE UP UNCOVERED came about.


            


JustGiving - Sponsor me now!
You can give online here


Here are a few behind the scenes shots to give a little flavour of the day. The nerves, the excitement, the giggles...



You can also text DSUU47 £AMOUNT to 70070





Downs Side Up Uncovered


It's that time of year when we begin thinking about World Down Syndrome Day which is coming up on the 21st March. The date represents the 3 of chromosome 21 that individuals with Down's Syndrome have. 

To raise awareness it is also Lots Of Socks Day, or Different Socks Day as I prefer to think of it. For we are all unique and play an equal role in life's colourful tapestry.

We can all get involved in this, wear different funky socks, dare to be bold, get your school involved, your colleagues.
I've decided to do some fundraising for 3 major charities; our local support group, the CDSSG, the Down's Syndrome Association who help families on a national level and Down Syndrome International who work globally.

What am I going to do? Run a marathon? Cycle from Lands End to John O Groats? Sit in a bath of baked beans? Sky dive? 

No. I don't have the time or the stamina for the first two options and I'm not very keen on beans, and I did a sky dive for charity when I was at college, so...

I'm going to be taking my clothes off for a photo shoot. I'll be protecting my modesty with a multitude of differently coloured socks.  Yep, that's right, I'm getting my kit off Calendar Girls style.


Yep, that's right, I'm getting my kit off Calendar Girls style.

JustGiving - Sponsor me now!

OR TEXT DSUU 47 £AMOUNT TO 70070 TO DONATE


How on earth did this all came about? It's is a question I have been asking myself the last couple of days as I nervously prepare for the hoto session.

It began last year at the Britmums Live Brilliance in Blogging Awards ceremony, where I met Kate @kateonthinice for the first time. Kate and I really hit it off and shared a giggle over a glass of bubbles. We are both quite different, but our personalities slotted together, and it felt like I had always known her. It was a very rare evening where we felt like women, friends, writers, not only Mums.

Kate's blog The Naked Mum is a wonderfully supportive community for Mums trying to value every aspect of their lives, whilst supporting one another. She's had an idea to ask one blogger a month to pose naked, a way of showing that we are not just mums, but women, wives and partners too.

Kate says we should try things outside our comfort zone. It's better than regretting not doing them later on in life. And after all, in writing a blog, one lays ones feelings bare every time you press the publish button.

But more than that I want to show that Mums of children with Down's Syndrome, in fact any disability, are just like everyone else. We have wobbly bits and bits we like to hide, there are the unwanted pounds, places we are proud of, bits we don't mind flaunting, bits that have been stretched beyond return but most of all our wonderful bodies have made and nourished our beautiful children, just the same as everyone else. I am yet to find the green scales replacing skin.

Natty gets her first taste of breast milk at 4 days old

I remember when Natty was born, that I felt ashamed of my body,  foolishly guilty that it had not got it quite right. I have also suffered 5 miscarriages. By getting naked for this year's WDSD I am burying that ridiculous notion and I hope it helps other women celebrate the wonder that is creating all and every life.

I also help to raise awareness for World Down Syndrome Day and raise some money for those wonderful charities. Please sponsor me.

Hayley x

On The Brink

Tonight I write, unplanned and unprepared.  Exhausted after an exciting and emotional week.  In haste almost, but from the heart.
I feel as if I stand on the edge of a precipice.  Below me the unknown.  Pitch black.  The world of media and putting my precious babies into the limelight.  Of critics, bigots, jealousy.  
Who knows how deep the chasm is, what obstacles we will find ourselves falling onto, what lies at the bottom.
Others are charting this hostile territory too.  But they are thousands of miles away and my ethos doesn't necessarily sit completely alongside theirs.  So I am alone when I jump.

Behind me is a queue of parents,  both friends and strangers I have met along the way and their children, some who have varying disabilities.  All waiting for me to test the water, pave the way, soften the blow, create change.
I take comfort from their support, their desperate need for the world to alter it's attitude towards disability.  I am blessed to be surrounded by such fiercely loving, supportive and protective family, friends and community members.   I also cannot believe how I stumbled upon a journalist who writes for the tabloids, but who is a mum foremost and a person with great integrity.  We also happen to really hit it off, what are the chances...?

Some times things happen in life for a reason... 
Language teacher and music biz guru have 2 beautiful daughters. (Actually language teacher, chatterbox and general lover of people.)  One has Down's Syndrome.  The other immediately takes on the mantle of fiercely loving, protective sister and mentor. 

A doctor tells me we will be ambassadors for children like this just after Natty is born.  (No pressure there then!)

We meet a beautiful photographer who takes pictures of Natty that get me thinking (Traci Giles, we adore you).  Natty is a natural in front of the camera.

Husband buys me a screamingly powerful Mac and a brilliant camera, both quite useful in this business of media.  (Thank you darling x)

Natty starts school and people ask "What are you going to do with your time?"  Another gauntlet thrown down.  I fill the time with making teaching materials and giving Natty the 'extra' stuff she needs.  That lasts 3 months before it is not enough.

Stories of teachers, doctors and midwives getting it so wrong with our kids fire up my imagination.  (Well, they make my blood boil to be exact.)  I'm an educated professional, so these people do not phase me one jot.  (However, I believe that there are two ways to skin a cat...  by shouting at it, or by gently stroking it and asking it nicely to do so....you get my drift.) 

I see a lady on morning tv talking about how she was pressured into a termination hours after her baby was diagnosed as having Down's Syndrome.  Something snaps in my head and I decide 'to make a change'.

I start the little blogette, as it became affectionately named.  I always planned a book; a kids story with a character with Down's, my husband's life story, or a personal journey map as a mum, I was never quite sure, I never had time to think it out.  But this would do as a trial run.

I join some blog networks.

I write to a few companies asking if they want Natty be in their ads, and then WHOOSH.

We clearly struck a chord somewhere along the line.

Thank you all for following us.  I am just trying to do my best for us all.  
I am jumping tomorrow and I hope I will simply dive into a warm pool of water, creating no more than a few ripples.   
I hope you will all follow in my wake, unafraid.  
I hope the world will see us basking there, relaxed and at home.  I hope they get so accustomed to seeing our children in the media that they cease to notice their differences.

As I wrote, the article came online.  It was abridged, it wasn't quite what Alison and I had planned, but it is there.  It is positive.  It is light and airy.  It will reach 5 million people over their morning cuppa.  Natty's beautiful face is shining out like a sun from the pages of the Sun.  

And a picture paints a thousand words :)