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My daughter was first diagnosed with systemic sclerosis 7 years ago. After two years had a re-diagnosis to morphea generalised scleroderma. She was on disability with a blue badge etc until this new PIP system came in. She has gone from full award to absolutely nothing. She has appealed and went to tribunal today, but nothing new. Anyone else had a problem proving an invisible illness or do you have a different forum for discussion? Thank you in advance.