I'm engaged on a piece of self-advocacy that has reached the point where I must explain how serious the effects of cognitive dysfunction can be in ME.
I'll be writing a summary of my personal experience of this symptom, which has been crippling right from the start of my ME.
I'm also considering seeking out a specialist medical report on the subject.
But I'd also like to include any good general piece that's been produced. Is anyone aware of a statement from any of the charities on this subject? Or anyone else who could be considered an authority? Is there any good research that I could cite? Thank you.
I'll be writing a summary of my personal experience of this symptom, which has been crippling right from the start of my ME.
I'm also considering seeking out a specialist medical report on the subject.
But I'd also like to include any good general piece that's been produced. Is anyone aware of a statement from any of the charities on this subject? Or anyone else who could be considered an authority? Is there any good research that I could cite? Thank you.