Remaining politically neutral during General Election 2024
Under guidance from the Electoral Commission and Charity Commission, it's important that Scope remains politically neutral during General Elections.
While we understand that this period will see many passionate discussions and do not want to discourage open discussion, we cannot allow discussions which are purely intended to influence voting.
As ever, please make sure that your comments remain respectful of other people's opinions and keep to our online community house rules.
Dropping my working hours due to Ménière's disease. Am I entitled to any financial help?
Options
Deekay
Community member Posts: 1 Listener
Recently diagnosed with Menieures after 7 years of hearing loss in right ear. I struggle daily with Tinnitus and vertigo and desperately trying to remain in education work . I am not sleeping well at all . I'm about to drop fro.a 5 day week to a 4 day week to manage fatigue ..
Will i get financial.disability help ?
Will i get financial.disability help ?
Comments
-
Hi @Deekay. A warm welcome to Scope's forum from me. Thank you for already finding the courage to reach out to us. I appreciate this is never easy especially as you are new and finding things tough.
Are you currently in the UK? If so, you might be able to get financial disability help (e.g., PIP) but this will depend on how your disability affects you and the evidence/decision of DWP.
It is unlikely that you would receive LCWRA (or anything similar) because you will still be working (and showing the capacity to work). You have mentioned you are desperately trying to remain in education work. Would you like to tell us more about this?
Have you considered things like reasonable adjustments and Access to Work? I am asking because I can identify you wish to work but are finding this tough at the moment, especially with your health and not sleeping well at all.
Please don't hesitate to let us know if there's anything else we can do to support you, even if that's just extending a listening earCommunity Volunteer Adviser with professional knowledge of education, special educational needs and disabilities and EHCP's. Pronouns: She/her.
Please note: if I use the online community outside of its hours of administration, I am doing so in a personal capacity only. -
Hello @deekay and a warm welcome to our online community, how are you today?
I'm so sorry to hear that you're struggling with your Ménière's disease. Are you receiving support from a healthcare team with it? And also, are your employers able to implement any reasonable adjustments that will be able to make your working life that bit easier?
You might want to try a benefits calculator to see if you would be eligible for any financial help, based on your circumstances. Whilst, you can also speak with a welfare representative for free, whom you can find via the Advice Local - selecting Welfare benefits and entering your postcode, to scroll down the next page.
Just to let you know, I've amended the title of your thread and moved it to our Benefits and financial support category to help make it more visible to others.
Wishing you the very best. Take care and I look forward to speaking again soon.Online Community Co-ordinator
Want to tell us about your experience on the online community? Talk to our chatbot and let us know.Concerned about another member's safety or wellbeing? Flag your concerns with us. -
Hi Dekay,
Sorry to learn of your Meneirs disease, I just thought, that I would reach out, as I have a little understanding of your condition.
My Son was diagnosed with the same a few years ago, he receives medication now, & hasn't looked back since.
He was referred by his GP, prior to this, he was having awful attacks, & missed a lot of days from work, which was a great concern for him, but since the medication, he hasn't missed a day's work.
I hope this little information, may offer you some hope, good luck for your future....
Best wishes,
Ps you've come to the right place, for advice & support. -
durhamjaide2001 Community Co-Production Group, Scope Member Posts: 11,128 Disability GamechangerOptionsI'm really sorry you have got this horrible disease and I hope you get back to your usual hours soon.
Categories
- All Categories
- 13.3K Start here and say hello!
- 6.9K Coffee lounge
- 72 Games lounge
- 394 Cost of living
- 4.3K Disability rights and campaigning
- 1.9K Research and opportunities
- 205 Community updates
- 9.5K Talk about your situation
- 2.2K Children, parents, and families
- 1.6K Work and employment
- 785 Education
- 1.7K Housing and independent living
- 1.4K Aids, adaptations, and equipment
- 602 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 755 Transport and travel
- 32.5K Talk about money
- 4.5K Benefits and financial support
- 5.3K Employment and Support Allowance (ESA)
- 17.5K PIP, DLA, and AA
- 5.2K Universal Credit (UC)
- 6.3K Talk about your impairment
- 1.8K Cerebral palsy
- 880 Chronic pain and pain management
- 194 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 319 Sensory impairments
- 824 Rare, invisible, and undiagnosed conditions
Complete our feedback form and tell us how we can make the community better.
Do you need advice on your energy costs?
Scope’s Disability Energy Support service is open to any disabled household in England or Wales in which one or more disabled people live. You can get free advice from an expert adviser on managing energy debt, switching tariffs, contacting your supplier and more. Find out more information by visiting our
Disability Energy Support webpage.
If we become concerned about you or anyone else while using one of our services, we will act in line with our safeguarding policy and procedures. This may involve sharing this information with relevant authorities to ensure we comply with our policies and legal obligations.
Find out how to let us know if you're concerned about another member's safety.
Find out how to let us know if you're concerned about another member's safety.