Hi Natalie,
When I was on DLA, I was receiving the Mobility Component High Rate, and the Middle Rate Care Rate. This went on for years, and I didn't not expect to try and get the High Rate Care.
The conditions I suffer from become progressively worse over time, and I still did not apply to see if my entitlement could change. I just assumed I was becoming worse and did not even think about reapplying for DLA at higher rates.
Bear in mind, I rely heavily on my wife and children (all left school, I may add!!), to push me around for many hospital appointments, doctors appointments and my LifeLine 'red' button service. On top of all this I have had many adaptions done to the property over the years.
+ Driveway widened and extended (*DFG)
+ Bathroon & Toilet converted in to one room (*DFG)
+ Bath and shower fitted (*DFG)
+ Clos-o-mat fitted (Bidet / Toilet £3,100 supplied via DFG)
+ Service Contract for the Clos-o-mat is £15.00 per month.
+ Sliding doors fitted in many rooms (for easy access (*DFG)
+ Telecare 'Emergency Service' Installed (Adult Social Services)
+ Patient Care Plan (Setup by my GP)
+ Hospital Bed (with wired remote control for adjusting the bed - Setup via my GP asking District Nurses)
+ Electric Bath Lift Chair (highers or lowers me in to the bath) (*OT)
+ Electric Riser / Recliner Dual Motor Arm Chair (*OT applied for a charity grant)
*DFG = Disabled Funding Grant
*OT = Occupational Therapist - Contact Adult Social Services first).
Prescribed Medication Daily
Over 50 tablets taken daily, and through the night at 7 different times of the day.
Other Prescribed Medication
6 Botox Injections given every 10 weeks in Neurology Outpatients.
I am unable to feed myself, I have to be careful what I eat which is a real nuisance. I cannot dress myself, well I can to a fashion, but that takes me an hour on a good day.
My wife helps me most of the day, and at night times because I get muscle cramps and spasms.
It was at this point I decided to apply for the High Rate Care Component. It took awhile while everything was checked including medications, some of which are 'A' Class drugs. When I finally got a letter from the DWP that took my case on, I was shocked to read that he wished I had applied a long time ago, because he could only backdate the payment from the Application form.
There was many changes over the years, but I didn't think I was even disabled enough to even receive the High Rate Care.
One thing I have learnt is I am disabled and still become worse as the years pass by, what I have can only be controlled by medication, but never cured. I wish there was a cure for my condition, I would opt for it. I hate being on benefits, being physically unable to do virtually anything without help - mentally, I forget a lot of things, but that is down to all the medication I'm on.
But reading you OP, you should try for higher rates, pain is what many of us have to live with everyday of our lives.
If you want any help on anything let me know via PM - I have helped many people on these forums. I received many thanks in helping them winning their cases.
Regards,
Les.