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All posts tagged Supermum

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.

This is the story of Caitlin, a very special little lady who lived for just six days. Her story is heartbreaking, but her incredible mum, Nicole, is determined to live a happy life in Caitlin’s memory – because Caitlin made her so happy for the duration of her little life. Nicole has such a wonderful way of looking at the world and her wisdom is truly inspiring. It was a pleasure to write for her.

Out now in Best.

This beautiful story, out in Woman’s Own, tells the story of how Cathy came to adopt Sinead, a poorly little lady who needed someone to believe in her. Sinead has Down’s syndrome and was left pretty much alone for the first few months of her life. No cuddles, no love, no hope… until Cathy came along, fell madly in love, and gave Sinead the love, care and attention she deserved. A beautiful story of family life.

For more information about Down’s syndrome, visit the excellent futureofdowns 

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

Always extra specially proud of my stories for and about the Down’s syndrome community – here’s this week’s piece in Woman’s Own magazine celebrating Sophie and Joe, two brilliant kids who have brought sunshine and sparkle to their family and friends – and who happen to have Down’s syndrome. Their mums, Cassy and Vikki, were interviewed about the looming sense that science is attempting to eradicate future cases of Down’s syndrome – and what a sad world that would be.

Every time I write about Down’s syndrome, I hope that we help undo the tide of misinformation that has swept society for decades. Out now in Woman’s Own.

 

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.

I mean – seriously. Could Willow be any cuter? My latest Christmas themed story is about a beautiful little lady called Willow, who came along and completed her family. Hers is the sort of story Christmas is made for, because Christmas is a time for love and gratitude for those we keep close.

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.

Catch Willow in Bella – out now!

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.

I adore Tyler – he’s been through an extremely difficult and dark chapter but he’s determined to use his experiences to help other children. And he’s still only 11 years old.  Tyler has Asperger’s syndrome but for a long time, he couldn’t communicate how he was feeling or what he was going through. His dedicated, wonderful mum Tracy perservered and supported him, even sleeping on the floor beside his bed.

In time, Tyler was given the extra support he needed and he’s now flourishing – he wrote a book, Invisible Me, to help other kids, but he’s so wise, he can help adults while he’s at it. You can buy the book through the Marie Curie website here. 

Out in Bella now.