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.
Tribunal Evidence
Options
salty1212334
Community member Posts: 145 Courageous
Hi would a letter from lcwra assessment count as evidence. At my lcwra assessment she said I spoke with flat effect and believes I have schizophrenia. I have been diagnosed with aspd/eupd and osteoarthritis in my knees. I got these diagnosis after pip appeal can I also use these as evidence. I am also taking quetiapine I keep getting dry mouth at night I keep getting blisters on my tongue. I did tell pip I had bad knees they didn't believe me so I went to see a rheumatologist and got a diagnosis I have always had problems with my knees I was diagnose last year I was 32 I am 6.2ft and 11stone 6 pounds I am not overweight. I fell off a roof when I was younger landed on my back from about 15ft it gave me a bad concussion ever since then my back hurts I haven't told my doctor I keep forgetting. I have knocked myself out about 6 times doing stupid things I never went doctors or hospital I just dealt with it I have had a lump the size of a egg on my head it's all catching up with me now. I got 0 points on my pip appeal I am now waiting for tribunal. Will I get points for being around others and behaving. I sent pip a letter from LCWRA and my medical records. I also keep zoning out people keep asking me if I like them. I go to a warehouse with my brother once a month when I have to pay I zone out my brother has to nudge me and remind me to pay would this count as being prompted. I also get a fever when I have to go out my body crashes every time about 5pm my fingers start aching then my whole body aches I have to go sleep then I wake up sweating really hot I take propranolol for it but it don't work
Comments
-
LCWRA and PIP are different benefits with differently criteria, there are some descriptors that are similar though. You can send the WCA report if you want to.
If you've had a new diagnosis since your PIP assessment because you mentioned the problems related to that they you can send the diagnosis letter, if you haven't already. Though please note that PIP isn't awarded based on a diagnosis.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. -
Hello @salty1212334
I'm so sorry to hear your health hasn't been good recently. I just wanted to comment and ask if you were getting support? Have you spoken to your GP about the propranolol not working well for you?Hannah - She / Her
Online Community Coordinator @ Scope
Concerned about another member's safety or wellbeing? Flag your concerns with us.
Want to give us feedback? Complete our feedback form now. -
poppy123456 said:LCWRA and PIP are different benefits with differently criteria, there are some descriptors that are similar though. You can send the WCA report if you want to.
If you've had a new diagnosis since your PIP assessment because you mentioned the problems related to that they you can send the diagnosis letter, if you haven't already. Though please note that PIP isn't awarded based on a diagnosis. -
Hannah_Scope said:Hello @salty1212334
I'm so sorry to hear your health hasn't been good recently. I just wanted to comment and ask if you were getting support? Have you spoken to your GP about the propranolol not working well for you? -
You will need to speak for yourself during your hearing. You really shouldn't be taking more medication than what is prescribed to you. If you feel suicidal at anytime you can always speak to the Samaritans on 116 123.
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. -
Hi the pregabalin aren't prescribed I spend £80 a month on them the others I get given to me I am prescribed amitriptyline quetiapine and propranolol. Should I even have the tribunal if dwp says I have schizophrenia I don't think it's right that they make someone with severe mental health to speak on the phone. It would be 2yrs total from when I first applied I will probably have to reapply if I only get 2yrs on my claim
-
PIP isn't awarded based on a diagnosis.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.
-
Hi I no it's not based off diagnosis but they backup what I am saying I have sent about 50 pages of evidence. I see other people getting a decision before tribunal from evidence they have sent
-
Hi @salty1212334, sorry to hear about all that's happening with you, it sounds like you're going through a lot. I'm going to drop you an email today, so look out for that, but I just wanted to say hello here first
Have you ever talked about your prescription drug abuse with anyone? I know it must be difficult to discuss it, but it's really important that you let your GP know what you're taking daily so they can help support you. They might be able to connect you with services that could help you feel more in control. We are with you and Turning Point might also have some worthwhile resources to have a look through.
As Poppy mentioned above, with PIP it's often more about describing how your symptoms affect you day to day and giving detailed examples of this rather than just giving them your diagnoses and evidence. Some people do find that providing lots of evidence helps their claim, but not always. Citizens Advice can often be helpful if you need some support with your claim.
Have you managed to get through to your GP today to chat about your propranolol?Rosie (she/her)
Online Community Coordinator @ Scope
Concerned about another member's safety or wellbeing? Flag your concerns with us.
Want to give us feedback? Complete our feedback form now. -
Rosie_Scope said:Hi @salty1212334, sorry to hear about all that's happening with you, it sounds like you're going through a lot. I'm going to drop you an email today, so look out for that, but I just wanted to say hello here first
Have you ever talked about your prescription drug abuse with anyone? I know it must be difficult to discuss it, but it's really important that you let your GP know what you're taking daily so they can help support you. They might be able to connect you with services that could help you feel more in control. We are with you and Turning Point might also have some worthwhile resources to have a look through.
As Poppy mentioned above, with PIP it's often more about describing how your symptoms affect you day to day and giving detailed examples of this rather than just giving them your diagnoses and evidence. Some people do find that providing lots of evidence helps their claim, but not always. Citizens Advice can often be helpful if you need some support with your claim.
Have you managed to get through to your GP today to chat about your propranolol? -
Hello @salty1212334
I'm so glad you found Rosie's email helpful
Please let us know if your appointment with CGL went well and if there is any way we can help further. I'd also encourage you to mention the fever to your GP. I hope you are having a better day today?Hannah - She / Her
Online Community Coordinator @ Scope
Concerned about another member's safety or wellbeing? Flag your concerns with us.
Want to give us feedback? Complete our feedback form now.
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
- 202 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
- 593 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 744 Transport and travel
- 32K Talk about money
- 4.4K Benefits and financial support
- 5.2K Employment and Support Allowance (ESA)
- 17.3K PIP, DLA, and AA
- 5.1K Universal Credit (UC)
- 6.3K Talk about your impairment
- 1.8K Cerebral palsy
- 875 Chronic pain and pain management
- 182 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 317 Sensory impairments
- 822 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.