Survey results: stress




"Stress and its impact on MS is clearly an issue that is largely ignored my the healthcare workers involved in caring for MSers. Based on recent posts and comments this is something that needs to be addressed in a formal way. I am not sure how to do this at this point in time. How do we implement a stress management programme with out resources? Is the evidence robust enough for payers to give us the necessary resources? What do we tell MSers to do in relation to stress? These are all issues that we will have to comeback to you on. If you have any suggestion in the interim they would be most welcome. Thank you."

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