In 1991 my MIL had an MS attack for the first time. After some time in hospital she was diagnosed with the MS and over time that diagnosis has been changed to relapsing remitting MS.
Ever since 1991 she has been on a disability benefit, moving benefits as the system changes. She hasn’t worked since 1991 and has three years to go until state pension age.
She has brain fog, falls a lot and is often incontinent of urine.
She found out yesterday that her benefit was being withdrawn.
What can we do? She is appealing but any help or pointers would be hugely appreciated.