What do you think? If I write more for MEaction it will probably mean fewer posts here, but I will post the links as a mini-post.
I’m also attempting a patient piece for the British Medical Journal. I don’t know if this will be accepted or not. I’m writing about how cognitive difficulties in ME/CFS combines with GP time constraints to create a barrier to effective communication. Adjustments can be made to overcome this though. Do you have any suggestions?
I write down what I want to say to the GP. If it’s complicated I may type it and print a copy for them to keep.
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