Does anyone know of a good (formal) protocol which could be used as a basis for either: 1) educating a hospital on how to deal with an ME/CFS patient; or 2) to set up a specialised ME/CFS ward?
Does anyone know of a good (formal) protocol which could be used as a basis for either: 1) educating a hospital on how to deal with an ME/CFS patient; or 2) to set up a specialised ME/CFS ward?
I guess what I'm looking for is something authoritative to take to hospital staff / administrators / ministry of health to lobby for the protocol to be used with a patient, or, even better, to lobby for a specialised ward.
My general thought is that hospitals are not a great place to have to be - whether one has ME or anything else.
I don't know of a protocol but I hope others have suggestions.
Sorry I am not more help.
Does anyone know of a good (formal) protocol which could be used as a basis for either: 1) educating a hospital on how to deal with an ME/CFS patient; or 2) to set up a specialised ME/CFS ward?
My general thought is that hospitals are not a great place to have to be - whether one has ME or anything else.
I don't know of a protocol but I hope others have suggestions.
Sorry I am not more help.
I believe they have also done the CME in Michigan.
try pandoraorg.net to contact Pandora
Some of the regional orgs also work with physician education, such as the New Jersey org mentioned.
Ryan Pryor 's org is also working on physician education but I think solely via internships (so maybe not predictably helpful for a given hospitalization, but should help over time)