We have just been through the reassesment and even the assessor agreed their script did not capture the reality of how cfs effects daily activity. They did not wish to discuss reliability repeatedly etc as it was off script. Saying ME was not an option it was called cfs . So I suggest you need to weave In to you answers ...I cannot do the question due to ME causing me to not be able to repeat x activity reliably or safely as occures and give an example. I felt the assessor was supportive but had no option to enter ME type replies on their form.  But arthritis replies were readily  accepted. We had a positive result but in no way did ME count for points in any category.  I do to want to identify here but it's almost a case of Nelson I see no ships for ME.  I despair of the work the charities say they do with the dwp it's clearly not reaching the script writers .  I feel examples hammer home the reality and should be given during the assessment.
				
			 
	 
 
		 
 
		 
 
		