For example, in order to get meaningful results from a trial like this you need to choose your definition of success before the trial starts. The plans for the PACE study did have such a definition, and while it wasn't great it also wasn't terrible. The final study didn't use it; it used a new and much weaker definition. So far this is all sadly pretty commonplace.
Then the patients involved in the study got wind of this and tried to find out what the results were if they used the original, planned methodology. According to the researchers, this was a dangerous and vexatious attack on science by activists - and because they were respectable scientific figures working for major institutions, and the people questioning their research were mostly disabled women who were, according to the mainstream consensus, nuts, people believed them.
This article is basically a direct extension of this tactic, and it's working. I can already see a few folks elsewhere in the comments calling on universities to sack the few scientists who questioned this...
But regardless of whether we agree medically or otherwise, we should treat each other with courtesy.
[1] An internist who participates in and coordinates significant research, she specialized in CFS and fibromyalgia after her (late) sister had CFS. They have quite an organization with resources for doctors, patients, and families: http://batemanhornecenter.org/ . Over time I have gained a high opinion of her and the organization.
EDIT: clarification in 1st paragraph.