What are people's experiences of switching from DLA to PIP?
Comments
-
Thank you0
-
I have spastic monoplegia CP.
I recently completed the forms for PIP (high rate mobility, low rate care). I was not fazed by the questions but struggled to decide how much information I should provide.0 -
Hi @Louise2001 and welcome to the community!
I can relate to that, it's hard to know about the level of information that is provided. As long as you have showcased your ability and level of independence then that should be fine
Is there anything else the community can do to help?0 -
Chloe_Scope said:Hi @Louise2001 and welcome to the community!
I can relate to that, it's hard to know about the level of information that is provided. As long as you have showcased your ability and level of independence then that should be fine
Is there anything else the community can do to help?1 -
Louise2001 said:I have spastic monoplegia CP.
I recently completed the forms for PIP (high rate mobility, low rate care). I was not fazed by the questions but struggled to decide how much information I should provide.Hi,When filling out the PIP forms, you should provide as much information as possible about how your conditions affect you. Adding a couple of real life examples of what happened the last time you attempted that activity for each descriptor that applies to you. Relevant evidence should be sent to support your claim because they rarely contact anyone for this. If you're transferring from DLA then you can ask for your DLA file to be used as evidence.Expect a face to face assessment because most people have them. It's rare to have a paper based assessment. Waiting times depend on backlog in your area but there's no timescales. Good luck.1 -
apollo11cdr said:I have had a paper assessment ... then 2 x assessment centre gone past the point were i usually get reassessed which is usually April May .....
Is there an issue with assessments my current award expires next April ...I do believe that the PIP reviews are now taking place 6 months before your award is due to end, rather than 12 months before.If you were awarded by a Tribunal then you'll be contacted 14 weeks before your award is due to end.1 -
No problem. It's because of the backlogs i think. My review is supposed to be due in October this year too and i'm also wondering when i'll be contacted. Lots of people have said it's now 6 months but i've yet to find any confirmation regarding this.
0 -
I think maybe I got a home visit because I had an asthma attack when going to one of my hospital visits, I got very anxious and it came in the best place ever to have one! although not pleasant. I mentioned this on my pip application.0
-
The first time I had to sit down and complete the forms I almost sobbed. Too many of my responses to the questions were blatantly negative and depressing. To cut a really complicated story short, I learned weeks later we were awarded low rate care and high rate mobility based on my responses to the questions. The whole thing is depressing. Don’t know why I cannot just email them a video of his movement instead. Some of the questions don’t apply to us personally.0
-
I had a positive experience with my DLA to PIP transfer. My appointee was sent form, he sent it to my supported living manager, she fill in form best she could, In a short time a assessor rang her and asked her some more questions, she was told I wouldn't have to attend a face to face medical, about 4 weeks later I was awarded PIP, high on both awards.2
-
I understand DWP are way behind schedule for completion of transfer from DLA to PIP.2
-
As a community champion here on scope i'd like to remind you to please be mindful of your comments. If you don't like someone then please put them on ignore, this way you won't see their comments.
2 -
@ilovecats has never hidden the fact they were a former assessor and has always been honest with everyone here.I've never found their comments to be anything but honest, truthful and very helpful, which is what this forum is all about.I totally understand mental health having suffered with it myself for over 20 years.As for deleting your own posts, it's impossible to do this, only admin can delete a post. You can edit a comment you've made but you only have 1 hour in which to do this, after this time it's can't be edited by yourself. Only admin can do this.As i previously advised, if you have issues with forum members then simply add them to your ignore list and then you won't see their comments. Ignore lists have been increased to allow more people to be added.2
-
@apollo11cdr -
When someone uses phrases such as 'people like you' it's a good indication that they are directing personal comments at an individual based on an assumption that they behave in the same manner as members of a particular group. Quite often these assumptions are wrong which is why such comments are unfair and unhelpful. All posters should be treated respectfully.
I had a bad experience with my assessment - but that doesn't mean that all of the assessors are bad, it just means that the individual that I dealt with was.
I am sorry that you have mental health issues that make you feel like this - can I suggest that it might be an idea to read through what you have written before pressing the 'post' button?2 -
Scope's online community is a supportive space to get disability advice and information 24/7, and talk to people with similar experiences.
1 -
Hi everyone,
Some of the comments recently made on this thread have been removed by a moderator due to breaking rules within the community guidelines. Please do be respectful and understanding towards other other users.
We understand that everyone has had different experiences and we are sorry if this has had an impact on your mental health. The community is a forum that is here to support all users.
Many thanks,
Chloe2 -
Julie how did your f2f go.?
0 -
I couldn't find this thread! I felt it was ok but then the next day I thought about what was said and it was not OK. The assessor was a very young girl and in a mad rush, because I'm a bit slow, movements and talking, she was irritated by me, well that's how I felt. I've either done very well, or I haven't got any points at all. She was here for an hour and a half, very curt and efficient. But if she was under pressure I can understand that. She questioned my ability to move about as I don't use an aid in my home but do so when I go out, I use the furniture instead to grasp hold of if needed. I felt embarrassed and uncomfortable in asking for help but know I'm not alone now and thank you all for being there and able to just read others comments does help even if those comments that are not good, they make you feel you're not alone. We keep our fingers corssed that anything we get is better than nothing. I do not want to go through this again. x0
-
http://chng.it/7sZm4dTs
Please sign this petition against the DWP to take them to the priminister and please pass it on as much as possible
thank you
-3
Categories
- All Categories
- 14.5K Start here and say hello!
- 7K Coffee lounge
- 77 Games den
- 1.6K People power
- 64 Announcements and information
- 22.7K Talk about life
- 5.2K Everyday life
- 116 Current affairs
- 2.3K Families and carers
- 844 Education and skills
- 1.8K Work
- 472 Money and bills
- 3.5K Housing and independent living
- 958 Transport and travel
- 676 Relationships
- 69 Sex and intimacy
- 1.4K Mental health and wellbeing
- 2.4K Talk about your impairment
- 854 Rare, invisible, and undiagnosed conditions
- 907 Neurological impairments and pain
- 2K Cerebral Palsy Network
- 1.2K Autism and neurodiversity
- 37K Talk about your benefits
- 5.7K Employment and Support Allowance (ESA)
- 18.9K PIP, DLA, ADP and AA
- 7.2K Universal Credit (UC)
- 5.3K Benefits and income