Talking Sense blog
People like you, writing about their experiences of complex disabilities, deafblindness and all things Sense.
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Four things disabled people need to know about new voter ID rules
If you live in England, there are new rules that mean you’ll need photo ID to vote in the local elections on 4 May. Here's what it means for you if you’re disabled.
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Jacob found his groove through our dance workshops
Jacob is exploring the world of dance through our arts programme. He’s been able to build energy, confidence and a love of music and movement.
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On Sense Holidays, U’nite gets to find her inner adventurer
U’nite’s mum Althea tells us why Sense Holidays are so important to their family.
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Remembering Sheila Anderson, an important part of our history
Sheila Anderson, who was daughter to one of our founders and a dedicated member of our staff, passed away. Her colleague, Geoff, reflects on the brilliant and lasting impact Sheila had on Sense.
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Dieumerci is boxing his way to a bright future
27-year-old Dieumerci had to win personal fights with anxiety before getting into the swing of a more independent life.
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How we make sure that every Sense Holiday is as unique as our holidaymakers
Jess, a Sense Holidays coordinator, explains all about the care that goes into making every holiday special.
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How play unlocks the world for disabled children
From infancy to adulthood, people with complex disabilities gain profound benefits from both structured and independent play. Sense specialists Jade and Laura discuss all that play offers.
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From language to golf, becoming deafblind hasn’t stopped me learning
Simon knows what it’s like to feel excluded and unable to access the world around him. But with support from Sense, he’s broken every barrier.
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How learning to bake has helped Luke grow in confidence
Luke attends Sense College, where he’s learning about life skills like cooking. Here, his support worker Della explains how learning to bake has helped him grow in confidence.
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For disabled people like me, the effects of the Covid-19 pandemic are still going on
As we mark three years since the first Covid-19 lockdown, Natalie shares this timely reminder of the ways the pandemic is still impacting her, as a person with complex disabilities.