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.
Any ideas on pip assessment time frame?
Options
mookie
Community member Posts: 51 Connected
Hi everyone I'm up to 16 weeks waiting for the assessment for pip ,anyone have a rough idea on time frames for pip ass
Tagged:
Comments
-
mookie said:Hi everyone I'm up to 16 weeks waiting for the assessment for pip ,anyone have a rough idea on time frames for pip ass
-
I waited 4 months waited from beginning of November to mid March but I'm not sure how they do the assessments if it's just going down a list or if different places are quicker than others? Or if they do it alphabetical? I don't even know if the whole country is done by same people? But hope you get answers soon! :-)
-
Thank you for your replies , I wish I had applied now the stress of it all , after my liver transplant my back just won't stop hurting ,and just diagnosed with fibromyalgia that's effecting my legs , well everywhere!
-
I've been waiting since beginning of January (when they said they received the form) and still not heard anything. I've tried phoning a few times and just get told they are still deciding if I need an assessment. So I guess it more waiting but approaching 6 months waiting now.
I have Autism, ADHD, Schizophrenia, Gilberts Syndrome and Crohn's Disease and have knowledge in these areas. -
Blimey that's ,ages.
I did phone them just said it's being look at
Hope you get good news soon -
I waited 6 months for mine.
-
I think it depends on your area. I’m in the north east and I had to wait just over 6 months for mine. Just sat waiting for my decision now which is worse than waiting for the assessment lol.
-
Haha I'm trying to keep upbeat ,wish never applied now ,what horrible people they are
Good luck bart70 -
Yer I’m the same trying to have a happy not give a bleep attitude. But the fact is it does matter. It’s the difference between been able to cope or not. But you can ring the assessment people and get a update from them.
-
I did that ,they said it's with a assessor ,I'm not sure what that means ,I leave in bath
-
Hi mookie, I'm just over 17.5 weeks waiting for assessment, it with capita or independent?
-
Your get a date soon then. They may be writing for extra information depending on how much evidence you sent when you applied. But you won’t have to wait much longer. They may not even do an assessment, it all depends if they have enough with what you sent
-
Hi ,not idea ,I'm in esa support group was advised by cab to try ,what a nightmare ,I've been to flower hill assessment for esa ,they were absolutely horrible ,so dreading the face to face ?
-
If you need an assessment it could be over the phone or face to face. I believe their in the process of phasing in the face to face again but not for everyone
-
Yes I read that for transplant call in ,for fibromalgia tentively ask to come in ,for assessment so ,not sure
-
@mookie just be firm and don’t let them force you to do anything that will cause you pain and be honest about your worst days and your be fine. Pip is about how your illness affects your ability to do day to day things not about your illness. Your be fine and when you get it all backdated, your be able to spoil yourself ? your be good
-
I applied 28th January and had my phone assessment today 15th July. Was told I'd get the result in about 8 weeks.
-
Yes I got a text and letter 20 July app ,is it scary I glad you have had your that have the battle. At least that parts over.
-
It shouldn't be scary @mookie. The assessor should be polite and treat you with respect. You can have someone there with you if that'd help to calm your nerves, and you can always ask to take a break or get them to repeat a question if you need
-
Thank you Tori , I hope it goes well x I have asked my niece to be with me
Brightness
Categories
- All Categories
- 13.1K Start here and say hello!
- 6.7K Coffee lounge
- 69 Games lounge
- 387 Cost of living
- 4.3K Disability rights and campaigning
- 1.9K Research and opportunities
- 200 Community updates
- 9.3K Talk about your situation
- 2.1K Children, parents, and families
- 1.6K Work and employment
- 773 Education
- 1.7K Housing and independent living
- 1.4K Aids, adaptations, and equipment
- 590 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 739 Transport and travel
- 31.9K Talk about money
- 4.4K Benefits and financial support
- 5.2K Employment and Support Allowance (ESA)
- 17.2K PIP, DLA, and AA
- 5K Universal Credit (UC)
- 6.2K Talk about your impairment
- 1.8K Cerebral palsy
- 872 Chronic pain and pain management
- 181 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 317 Sensory impairments
- 820 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.