PIP/ADP?
I wanted to know what people’s experience of applying for (previously known as PIP) ADP?
I applied for PIP the year I was diagnosed and I scored 0. So to them my disability does not affect any aspect of my life. I obviously wasn’t hitting enough of their buzz words! I also think because MS is life long once you started receiving ADP they can’t stop paying it as the condition itself will never get better.
Just wondered what peoples experience of this was? I’ve been put off applying recently because I do live a normal life and I work but this doesn’t mean my disability doesn’t affect me, and at the end of the day we are entitled to it.
Thoughts/experiences below! :)