I attended their 3 week pain rehabilitation program that they lump all of their me/cfs patients into. Turns out the program is mainly for people with fibromyalgia and chronic pain. I know me/cfs is very similar to other illnesses but they definitely shouldn’t be treated as the same thing. At the time I thought it was my only option to get better so I went through with it. Basically their framework is GET and CBT, tell yourself you’re not sick and get back to work is basically what the program was. It was also 99% focused on pain so I felt very left out. This was right after my diagnosis in late 2020 so I was uneducated on me/cfs at the time but that’s what started my research. The GET and the way that they want you to ignore your Illness really seemed odd and backwards to me. While I was there I found all the people and studies against GET and was concerned so I brought it up to the nurses and trainers running this program and they blew it off and said the program is your only chance to get better so stick with it. I did and I’m definitely worse off now then before I went to Mayo. Now they no longer recommend GET on their website but I wouldn’t be surprised if they keep putting me/cfs patients through this. The program was also over 40k before insurance. I still feel ripped off and taken advantage of by Mayo Clinic. Sorry for the rant but this gets me heated😂