Indefinite Dla transfer to PIP
Options
photoannie
Community member Posts: 2 Listener
Good afternoon all and a happy New year . This is my first post here.
I have been on indefinite DLA higher rate mobility and care for 23 years due to Spinal problems, RA, Fibromyalgia and various other disabling conditions, also severe anxiety/depression
Late last year I recieved the Dla to PIP transfer letter, informing me that my dla would stop if I didn't apply for pip within the month. I made the phone call (which I find terrifying) to get the pip migration process started.
I had a local disability organisation help me fill in the pip2 form, a home visit, should I need a f2f was also requested. I sent it and supporting evidence including, mri reports proving my progressive and degenerative spinal problems -( spinal stenosis, degenerative disc disease, anterolisthesis ) A letter supporting my claim from my chronic disease nurse, up to date medication list and a personal statement from myself. etc...all sent off by recorded delivery. I recieved a text message a week later to say it had been recieved.
On 31st December 2018 I recieved a letter from Person Independence Payment regarding an appointment for a f2f consultation at thier offices with Independent assessment services. Despite requesting a home assessment they have made an appointment for next week. I'm also going into Hospital next week for a spinal procedure.
I'm at my wits end, not eating, crying, anxious and quite honestly in a complete state. I'm not thinking properly at all and expecting the worst, that I will not be awarded pip. My nurse and disability case worker feel it would be preferable if I had a paper based assessment due to the detrimental effect this is having on my physical and mental health. They are both more than willing to provide letters to say so. Can anyone offer any insight or help as to what I can do . Thank you in advance.
I have been on indefinite DLA higher rate mobility and care for 23 years due to Spinal problems, RA, Fibromyalgia and various other disabling conditions, also severe anxiety/depression
Late last year I recieved the Dla to PIP transfer letter, informing me that my dla would stop if I didn't apply for pip within the month. I made the phone call (which I find terrifying) to get the pip migration process started.
I had a local disability organisation help me fill in the pip2 form, a home visit, should I need a f2f was also requested. I sent it and supporting evidence including, mri reports proving my progressive and degenerative spinal problems -( spinal stenosis, degenerative disc disease, anterolisthesis ) A letter supporting my claim from my chronic disease nurse, up to date medication list and a personal statement from myself. etc...all sent off by recorded delivery. I recieved a text message a week later to say it had been recieved.
On 31st December 2018 I recieved a letter from Person Independence Payment regarding an appointment for a f2f consultation at thier offices with Independent assessment services. Despite requesting a home assessment they have made an appointment for next week. I'm also going into Hospital next week for a spinal procedure.
I'm at my wits end, not eating, crying, anxious and quite honestly in a complete state. I'm not thinking properly at all and expecting the worst, that I will not be awarded pip. My nurse and disability case worker feel it would be preferable if I had a paper based assessment due to the detrimental effect this is having on my physical and mental health. They are both more than willing to provide letters to say so. Can anyone offer any insight or help as to what I can do . Thank you in advance.
Comments
-
Hi,It's very rare to have a paper based assessment, most people have face to face assessments. You can certainly ring them and ask for a home assessment but they may ask for a letter from your GP stating the reasons why a home assessment is needed. Also if you attend other appointments then they can also refuse the home assessment by saying that if you can attend other appointments then you can attend the assessment centre.Remember that PIP isn't awarded based on a diagnosis, it's how those conditions affect your ability to carry out daily activities based on the PIP descriptors. It's different to what DLA was.This link may help you understand what PIP is all about.
I would appreciate it if members wouldn't tag me please. I have all notifcations turned off and wouldn't want a member thinking i'm being rude by not replying.If i see a question that i know the answer to i will try my best to help. -
Thank you for your reply. Yes, I understand the differences. I'm housebound apart from appointments with consultants and surgeries in hospital. My chronic disease nurse visits my home. I've had a total of 8 surgeries in the past five years. I'm unable to walk without the assistance of someone else, I don't cook as I cannot stand unaided, have no grip, my legs give way, I cannot wash myself, go to the toilet myself, etc, etc. This has all been written down on pip2 form along with evidence from consultants and my nurse.
Thank you for the link.
Brightness
Categories
- All Categories
- 13K Start here and say hello!
- 6.6K Coffee lounge
- 104 Games lounge
- 416 Cost of living
- 4.3K Disability rights and campaigning
- 1.9K Research and opportunities
- 199 Community updates
- 9.3K Talk about your situation
- 2.1K Children, parents, and families
- 1.6K Work and employment
- 777 Education
- 1.7K Housing and independent living
- 1.4K Aids, adaptations, and equipment
- 615 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 738 Transport and travel
- 31.6K Talk about money
- 4.4K Benefits and financial support
- 5.2K Employment and Support Allowance (ESA)
- 17.1K PIP, DLA, and AA
- 4.9K Universal Credit (UC)
- 6.3K Talk about your impairment
- 1.8K Cerebral palsy
- 868 Chronic pain and pain management
- 180 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 319 Sensory impairments
- 825 Rare, invisible, and undiagnosed conditions
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.