True inclusion is endemic within your practice

Jen Blackwell and dancers with disabilities together showing inclusion in action

Inclusion, or rather the lack of it as a given has been the challenge of our lives. So much lip service paid, so much time, talk and energy poured into it, so much money spent, so many claims made, about something which in essence is so simple; in practice can be daunting.  But is it of necessity such a huge … Read More

Holidaying Blackwell style

What a beautiful summer at the end of a beautiful year from nomadics living our lives of choice. I feel like the luckiest person alive as Malcolm and I celebrate 46 years of marriage. Pity about the weather! Depression after depression after depression this August 2024, but the right place for us to be is out on the water. Otherwise … Read More

Do you see me

The business of changing lives

For Learning Disability Awareness Week 2024 this question, “Do you see me?” posed by Mencap is so deep and so profound, whilst simultaneously distressing, disappointing, and painful that it even merits consideration. It is a sad travesty of the 21st century, an inditement of the way society has stood idly by as people who happen to be learning disabled or … Read More

We are all different

Donna Jen Sophie ready for Buckingham Palace Garden Party May 24

Just a few days ago Malcolm and I were camping with our trusty ‘big’ car tent (top left) by ourselves as it turned out, soaking up the glorious view over Lostwithiel in Devon. Whilst Jen, was loving living in style for a couple of days at the fancy Rubens Hotel, Buckingham Palace Road. She loves the whole experience of being … Read More

Friendships – good for our mental health

Jen and friend Peter celebrating together

Friendship is something most of us take for granted. Even though I’m naturally shy and introverted, and didn’t easily make friends in the playground, preferring my own company, I now have a wide circle of friends and acquaintances around the world. Some I don’t see or speak to often, but that doesn’t stop us from picking up where we left … Read More

Changing lives one person at a time

DanceSyndrome impacts families

When the idea for gathering dancers with and without learning disabilities together to learn skills, create choreography and support each other to develop it was because nothing existed to support our daughter Jen to do what she wanted to do – Dance. Jen, with a her support team at that time, came up with idea in her bedroom, then put … Read More

Express Day 24 review

Dancers with and without learning disabilities Express Day 24

Dodging the cloud bursts we arrived at Blackburn Empire Theatre excited to watch Express 24, the annual show of the multi-faceted talented dance charity, DanceSyndrome. The Sunken Forest was an opportunity to put aside the cares of the world, allow yourself to be enveloped by finely wrought, enthralling, enchanting spell binding ballet.  The dance was absorbing as dancers shared their … Read More

Working together

Donna and Jen working together. Photo by Melissa Cross for Empower Housing Association

It’s fascinating what the two words, “working together” conjure up  isn’t it? Does it really mean two or more people joining together in an equitable relationship to create something? Or does it mean that someone is wanting to do something for you that really only benefits them or their organisation, but because it may be seen as “helpful” it can … Read More

Is every relationship equitable?

Jim Thomas and Sue Blackwell in conversation with Tracey-Jane Hughes - Equitable relationships

In my experience the simple answer is no. But should every relationship always be equitable? I believe every person has the right to be seen and heard in the language appropriate to them, with every voice and person of whatever age, ability or background, being able to contribute their thoughts, ideas fairly and equally with those they are in relationship … Read More

Ending stereotypes

Ciara and Jen conversation

We don’t care that Jen has Down’s syndrome. Jen is Jen and that’s the bottom line. For Jen, celebrating all those around the world with an extra chromosome, or Trisomy 21 is important. For Jen, it’s a celebration of her and people like her being recognized and valued for who they are. We have strict instructions to wear odd socks … Read More