you can choose to have the face to face assessment in your home.
i didn’t get to choose because they had already decided it was to be in my home.
i actually felt disappointed because i’d planned/dreamed of sh*tting myself in their office!
food (disgusting food) for thought there!
get help from a welfare rights advisor, CAB or similar.
they will help you with the form, questioning your answers to make sure that you fully understood the question.
make yourself familiar with the criteria that they are looking for.
key words are - can you do this safely, repeatedly and in a timely manner.
so if you can shower and dress yourself, ask yourself are you safe?
can you do it again tomorrow?
does it take you the same amount of time as it did before you had ms?
one of the trickiest things is to let go of that positivity that you have cultured.
be realistic instead.