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We’ll fight the NHS – Sunday Mirror

Categories: Campaign, Children, family, hot topic, Illness, Inspiration, Latest Stories, life changing, Medical, Sell My Story, Story
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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

Love these ladies! Here’s Emma, Sheryl and Hannah reflecting on the lessons they learned while dipping their toe in married waters back in their 20s. Their ‘starter marriages’ taught them so much about love, life and long term relationships, it was a fascinating piece to put together.

Out now in Best.

I had over 200 people get in touch wanting to be a part of this report – which goes to show what a mess we’re in! Too many kids are being passed around the system yet overlooked, while their parents are being made to feel like they are the problem.

This report, which I worked on for Scope, the disability charity, is in Take a Break this week. It is a very interesting, and sad, read. If you are affected by the details in this report please do visit the Scope website – they are a wonderful charity.

Divorce statistics hit an all time high at this time of year, as couples emerge from difficult festive challenges and start the new year determined to build happier lives – Judith shared her story with Bella to inspire people going through just that. Judith’s own new year divorce set her on a course for a happier life and it shows – she radiates happiness and is loving discovering who she is now she’s flying solo.

Out now in Bella.

Always brings a proud smile to my face to write about the Down’s syndrome community. This piece for the Sun was one we organised back in March so it’s great to finally see it in print, just in time for World Down’s syndrome Awareness Month. Four mums tell readers why their children deserve to be celebrated for bringing sunshine into their families.

In the age of NIPT (non-invasive prenatal testing) the Down’s syndrome community fear that terminations will increase and the community will begin to shrink. What a sad world that would be. Let’s hope that alongside the new testing technique, we’ll see an improvement in the ‘bedside manner’ of medical professionals, who need to offer a realistic portrayal of what life with the condition actually looks like, in today’s world, not the 1970s.

For advice and support, Future of Downs is an excellent website. And you can read the Sun story in full here.

So proud to write about incredible people like Kim – after contracting sepsis all four limbs were amputated but Kim has not once lost her wonderful spirit, courage and strength. Yesterday the Sunday People covered her latest milestone – a 3D printed bionic Hero Arm.

As you can see from the picture, this means that Kim can now fist-bump grandson Oliver, as well as brush her own hair and hold her own cutlery – little every day tasks we all take for granted.

Kim desperately needs donations so that she can afford another arm for her left side. If you can donate, please do, every penny counts! Click here for her campaign. 

You can read the story in full here. 

This is the beautiful, poignant story of Aimee and Daniel and their mum Theresa, who sadly passed away after a battle with breast cancer when Aimee and Daniel were kids. Years later, Aimee is looking back on her memories and how her mum shaped her into the woman she is today. It is a powerful read, with Aimee sweetly reminiscing and going into detail about all the little things she misses.

Aimee is raising awareness and funds for Walk the Walk – a brilliant breast cancer charity. Her story is out now in Bella.

It’s postnatal depression awareness week and to mark the campaign, we shared Amber’s story in Reveal. Amber’s an extraordinary woman who is determined to tell her story in order to help other mums realise that motherhood is really hard – and that’s okay.
With searing honesty, Amber explains how she just did not like being a mother. It’s a role she has come to love and her journey to where she is now needs to be heard. Too many women feel the burden of ‘perfection’ coming at them from all corners. (Instagram has so much to answer for!)
If you need support through the early steps of parenthood, visit PANDAS for support,

This beauty is Kate, a 19 year old model and now, crowned winner of Teen Ultimate Beauty of the World. Kate has Down’s syndrome and is on a mission to advocate equality. She is beautiful inside and out and an absolute joy to work with. Humble, kind, funny and so charismatic, I can see why her mum could hear the judges laughter through the walls during Kate’s pageant interview!

To find out more about Down’s syndrome, this website is the absolute best: The Future Of Downs

If you’d like to enter the fantastic, inclusive and wonderful Ultimate Beauty pageant, check out their website here.

Kate’s story was in the Sunday People and you can read it in full here.

For this glorious piece, mums Pippa, Emma and Vicky wrote themselves an open letter, going back in time to the day they found out their beautiful children had Down’s syndrome. The letters are poignant, powerful, funny, sweet and so lovely. Just like their children! I am so proud to work for the Down’s syndrome community, doing what we can to represent the reality of Down’s syndrome in the media so that families of the future understand that it’s not to be feared. Down’s syndrome has made these incredible children who they are.

Out now in Best. I worked on this piece in partnership with The Specials, which is a wonderful project. Check out their videos here.