The brilliant charity, Contact a Family, is from today offering an extended helpline service.
Contact a Family has long been a source of information about the benefits system for parents of disabled children, however now - thanks to three years of funding - they will be able to offer more personalised advice for parents living in England.
From today (June 3), if you get in contact with CaF, they will be able to offer you an appointment with their welfare experts to discuss your situation. They will then be able to take you through the latest relevant benefits advice and run through any other financial help you may be entitled to maximise your income.
Senior Parent Adviser and welfare rights expert, Derek Sinclair said:
"At a time of huge change to the benefit system, this will provide a badly needed source of free, confidential, high quality and up to date advice for parents. Our advisers will make sure that parents have the right information to make informed choices about issues."
These include:
- moving into work
- benefit options when a child reaches 16
- or how to use self-directed support to take greater control over how services are provided to their disabled child.
Contact a Family will also be offering a series of workshops across England to raise awareness of the new benefits system. Get in contact with your nearest office to find out more.
You can also access their quarterly welfare update in their What's new e-bulletin and a range of resources to help parents make sense of the benefits maze. Sign up to receive your free copy.
Contact the CaF team of experts on freephone helpline number 0808 808 3555, email them on helpline@cafamily.org.uk or post a question on their Facebook page https://www.facebook.com/contactafamily
You can also:
- Read more about the changes coming to the welfare system including more about personal independence payment (PIP) and universal credit
- Watch our video - meet the parent advisers and find out how they can help
Tania Tirraoro
She is also an experienced broadcast and print journalist & author. Tania also runs a PR, web & social media consultancy, SocialOro Media. She is a Rare Disease & chronic pain patient advocate with Ehlers Danlos syndrome.
Latest posts by Tania Tirraoro (see all)
- Exemplary Practice: Why this special school is PROUD of its pupil voice - December 3, 2019
- What’s a PRU to you? Busting the myths about alternative provision - November 19, 2019
- SEND Tribunal trial extended – but it needs more than just time to be a success - November 5, 2019
You must log in to post a comment.
Reblogged this on Kirklees PPS.