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Archive for March, 2019

Happy World Down’s syndrome Day 2019! It’s become my tradition to collate all the stories about all the legends of the Down’s syndrome community I’ve written about in the past year, to mark this wonderful, worldwide celebration. I have written about amazing children like Max, who I wrote about over Christmas for Best and Chat, who is just about the most gorgeous little elf in the world. I wrote a lovely feature for Best in the style of an open letter from mums Emma, Pippy and Vicky to themselves, offering advice on the day their children Corin, Leo and Audrey came into the world. Remember the Carpool Karaoke video that went mega-viral? We placed a story about a few of the mums involved, in Bella. And then there were a few stories about older people who had Down’s syndrome and are blazing trails – beauty queen Kate shared her story in the Sunday People and huge, happy congrats to Heidi, who shared her story in Best just recently, detailing the day her fiance proposed. I look forward to writing about your wedding, Heidi!

For more information about Down’s syndrome, visit www.futureofdowns.com an online community offering friendly support for parents and an up to date, balanced view of life with the condition.

Click ‘read more’ here to see all these fantastic stories in print! Read more

How adorbs is Henry? Emily had to fight to have her voice heard when she found out prenatally that he had Down’s syndrome. She was urged far too many times to have a termination… but she knew her own mind and her love for her unborn son was never in question. Once he was born, Emily was asked if she wanted him adopted. Would you just leave the poor woman alone already! Look at his beautiful, mischievous grin – Emily knew Henry was her world.
The first of my stories out this month to celebrate World Down’s syndrome Day on the 21st. Out now in New!

We’ll fight the NHS – Sunday Mirror

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Comments Off on We’ll fight the NHS – Sunday Mirror

I’ve worked with the incredible Rich family before, but last time, the story had hope and promise… We thought the pioneering treatment little Jess and Nicole were on might change the world for generations of kids with rare genetic diseases.
But now, the NHS has refused to fund the treatment which leaves these girls at a perilous crossroads. I love the NHS – what I don’t love is the government budget cuts which put lives at stake. It’s heartbreaking. The treatment works and the girls and many other kids in England (Wales and Scotland have made different decisions on the matter) deserve to stay on it. You can read the full story in the Mirror