Sell My Story with Phoenix Features - Getting you The Best Deal Available For Your Real Life Story. Fun Fast & Friendly Service. Call Kim @ Phoenix features on 01380 850 860

All posts in hot topic

Ah, isn’t this gorgeous? Four daughters and one son who were adopted write open letters of thanks and adoration to the mums who adopted them and helped shape their lives for the better. I love adoption – it is not easy but it is incredible and these five families are testament to the rewards.

Out now in Take A Break.

The Restaurant That Makes Mistakes took a group of people with varying forms of dementia and gave them the opportunity to work in a restaurant – the results are on 4od now. It’s a great concept for a show and an experiment – incredible people have been written off as incapable of working but the show asks what happens if you give people responsibility again?

Lorayne was one of the participants and has early onset frontotemporal dementia. Here she tells her story in Best and it was wonderful to work with her. Lorayne has lost none of her wit, strength or courage.
The title refers to the film Still Alice, which is a devastating but poignant watch. Lorayne’s story is out now in Best.

Donna shares her story of how she watched Parkinson’s disease overwhelm her grandmother and her mother. Now battling it herself, Donna is such a brave and courageous woman, determined to give her own daughter the best life she can. It’s too soon to know if Beau has inherited Parkinson’s too but Donna lives in fear that she has.

With donations, research into Parkinson’s will find a cure before Beau grows up. Please visit Parkinson’s UK to donate.

Donna’s story is out now in Bella.

This was an inspiring story to write up for Best magazine – Toni saved for years before carefully selecting a surgeon she trusted to give her a facelift which has not only taken years off, but also given her confidence she’s never had before. You can’t argue with that!

The lovely Toni shared her story in Best, out now.

We’ll fight the NHS – Sunday Mirror

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

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.