Clear, understandable information is important to help you make the right health and care decisions.
Medical and healthcare information can be complex. But, if you’re disabled or have a sensory loss, you have a legal right to this information in a way you understand. You also have a right to communications support if you need it. For example, if you’re D/deaf, you should be able to use a British Sign Language (BSL) interpreter at appointments.
The Accessible Information Standard has been a legal requirement since 2016. Yet many NHS Trusts are not supporting equal access to care for deaf and blind patients.
That’s why we’ve launched a new campaign, ‘Your care, your way’. We want to ensure services are taking their duty seriously to provide information in a way that people understand.
The obstacles people face trying to access information they understand
The lack of support from services has a negative impact on people who need it most. The views of 6,200 people shared with Healthwatch show the incredible difficulties and obstacles people face trying to access care. This leaves them frustrated, concerned about their health, and reliant on others.
Just a handful of examples people shared include:
- Dental practices not getting hearing induction loops installed
- GPs refusing people access to a sign language interpreter
- Low staff awareness, with D/deaf people reporting that staff communicated by shouting
- The lack of accessible information prevented people from understanding national COVID-19 guidance.
- Physical barriers, such as face coverings, made it harder for people to understand healthcare staff.
“I feel forgotten, ignored and not taken seriously”
Student, Connor Scott-Gardner, who is blind and requires healthcare information in an electronic format as well as in Braille, said:
Trying to get information about my own healthcare, in a format I can understand, has often been difficult. I can’t read letters that come through the post, or prescription medications. I feel forgotten, ignored, and not taken seriously. All I’m asking for is consistency, training on accessible information for staff. A few minor changes would make the world of difference to people like myself.
What rights do you have?
If you have a disability, impairment or sensory loss, or are a parent or carer of someone who does, you should expect:
- To contact and be contacted by services in ways you find accessible
- Services to give information and correspondence in formats you can read and understand
- To be supported at appointments if needed.
- Health and care services to support you to communicate.
Find out more about your rights and support the campaign.
Published on 24 Feb