Hello. My caree suffers from ME/chronic fatigue syndrome (CFS) and will be unable to attend her PIP tribunal. However, I understand that paper-based appeals are less likely to be successful. As her main carer, I would be happy to attend the tribunal on her behalf and represent her/answer what questions I can if this would help.
Is this acceptable? I can't quite work it out. If so, has anyone else done it, and do you have any useful hints and recommendations for me, please?
Thank you.
Carer for a long-term ME/CFS sufferer 
