IBD nurse not pleased with me
Options

Binky1234
Online Community Member Posts: 475 Empowering
My IBD & incontinence nurse was here yesterday to do my yearly review and I told her about my PIP and she said basically what others have said on this forum I should have went into more detail, I'm kicking myself tbh.
Jackie my nurse got me to write a letter and enclose my new repeat prescription as a few things have changed since July example I'm now on 50mg of amitriptyline. Meds don't make a difference as far as I'm aware in PIP.
She also advised me to start the letter saying as your likely aware I was on DLA with a indefinite award then changed over to PIP with a 5 year award that is now up for award review. Surely the DWP know this information.
I would like the following to be taken into consideration in regards to the award review dated July 2022.
Washing and bathing hubby needs to both supervise and help due to pain and physical restrictions then explained my restrictions in detail.
Taking nutrition she got me to write that I use easy grip cutlery and hubby cuts up my food, again used a real event that happened.
Infact she got me to into detail on:
Preparing food
Taking nutrition
Managing my meds
Washing and bathing
Dressing and undressing
Mixing with others
Budgeting
Planning and following
How far I can walk
In the planning to walk she got me to write that because I suffer from bowel incontinence this makes walking extremely difficult as it takes a great deal of effort as I need to move slowly and carefully to keep the faecal matter within the pads as secure as one can.
When I get to my safe place I break down due to the embarrassment and the physiological distress I encounter.
In my review form I focused on my anxiety and pain due to arthritis and fibromyalgia and only touched on my IBD.
Surely this letter far too late to make a difference. It was sent today as hubby said Jackie my nurse knows better than me.
Jackie also said that on rare occasions it has been known for the award review to be sent back to the CM without the need of a medical, so my question is this true, surely not. I'm hoping someone will be able to tell me if this is indeed fact.
I do think this letter that Jackie advised me to write is actually fab, but personally I think it's too late to be taken into consideration as my review has been passed on from the DM.
Anyway what will be will be.
Sorry if this post is a little graphic but needed to actually write what was written to get a honest answer.
I honestly feel that some scope members will have more knowledge of the benefits system than my IBD nurse hence this post.
Jackie my nurse got me to write a letter and enclose my new repeat prescription as a few things have changed since July example I'm now on 50mg of amitriptyline. Meds don't make a difference as far as I'm aware in PIP.
She also advised me to start the letter saying as your likely aware I was on DLA with a indefinite award then changed over to PIP with a 5 year award that is now up for award review. Surely the DWP know this information.
I would like the following to be taken into consideration in regards to the award review dated July 2022.
Washing and bathing hubby needs to both supervise and help due to pain and physical restrictions then explained my restrictions in detail.
Taking nutrition she got me to write that I use easy grip cutlery and hubby cuts up my food, again used a real event that happened.
Infact she got me to into detail on:
Preparing food
Taking nutrition
Managing my meds
Washing and bathing
Dressing and undressing
Mixing with others
Budgeting
Planning and following
How far I can walk
In the planning to walk she got me to write that because I suffer from bowel incontinence this makes walking extremely difficult as it takes a great deal of effort as I need to move slowly and carefully to keep the faecal matter within the pads as secure as one can.
When I get to my safe place I break down due to the embarrassment and the physiological distress I encounter.
In my review form I focused on my anxiety and pain due to arthritis and fibromyalgia and only touched on my IBD.
Surely this letter far too late to make a difference. It was sent today as hubby said Jackie my nurse knows better than me.
Jackie also said that on rare occasions it has been known for the award review to be sent back to the CM without the need of a medical, so my question is this true, surely not. I'm hoping someone will be able to tell me if this is indeed fact.
I do think this letter that Jackie advised me to write is actually fab, but personally I think it's too late to be taken into consideration as my review has been passed on from the DM.
Anyway what will be will be.
Sorry if this post is a little graphic but needed to actually write what was written to get a honest answer.
I honestly feel that some scope members will have more knowledge of the benefits system than my IBD nurse hence this post.
0
Comments
-
It's never too late to send more information. If your form has already been sent to the health assessment providers then it would be worth contacting them for the address so that you can also send it to them.Most people have assessments even for reviews so you should expect one of those, which would either be telephone, video call or face to face at an assessment centre. Paper based assessments are rare but possible. If there's enough of information to do a paper based assessment then yes it will be done. A report will be written and returned to DWP.I think your anxiety to walk because of IBD would be more appropriate for following and planning a journey. Fibro is a physical condition so moving around part of mobility is what will be looked at for this.There are long delays for reviews so you could be waiting several more months, possibly longer. Your current PIP will continue until a decision is made.1
-
Thanks poppy123456 I did as you suggested and I was told that when they receive it they will scan it on the system therefore the health assessment provider will have access to it. Anyway I've done all I can do and now I'm going to take it easy no point in worrying as ma Granny used to say worrying is like a rocking chair it gives you something to do but gets you no where lol.
Anyone waiting for assessment I was told today that mine ore than likey mine won't be getting looked at till next February/March next year as they are so far behind they're doing new claims and going by dates of when the award review was due, makes sense really.
I can now chill out.
Thank again Poppy honestly your a star.0
Categories
- All Categories
- 15.3K Start here and say hello!
- 7.2K Coffee lounge
- 88 Games den
- 1.7K People power
- 121 Announcements and information
- 24.1K Talk about life
- 5.7K Everyday life
- 406 Current affairs
- 2.4K Families and carers
- 864 Education and skills
- 1.9K Work
- 523 Money and bills
- 3.6K Housing and independent living
- 1K Transport and travel
- 882 Relationships
- 255 Sex and intimacy
- 1.5K Mental health and wellbeing
- 2.4K Talk about your impairment
- 863 Rare, invisible, and undiagnosed conditions
- 922 Neurological impairments and pain
- 2.1K Cerebral Palsy Network
- 1.2K Autism and neurodiversity
- 39.2K Talk about your benefits
- 6K Employment and Support Allowance (ESA)
- 19.5K PIP, DLA, ADP and AA
- 8.1K Universal Credit (UC)
- 5.6K Benefits and income