No CHAT GPT or AI
Fibromyalgia Syndrome (FMS) write a question or comment about the social factors impacting this disease. Include enough depth to your question/comment (about 200 words) so the readers will understand your perspective.
You are free to take this in many directions. I provide a few suggestions below, but please do not limit yourself to these topics. I am also NOT looking for you to start a post, list these four questions, and then comment on all four at once. Focus on specific issues. For example:
· How does someone come to know they have FMS? Are symptoms identified or defined?
· Consider how the self-help literature impacts the disease and its diagnosis.
· How do you think this reading/analysis impacts the validity or skepticism of the existence of FMS?
· Can you think of other diseases with similar “illness narratives” in our society?