Hello! I just recently have bed. Diagnosed with mobile cecum syndrome too.. after 13 years of dealing with the pain and no doctor has been able to figure it out. I’ve felt so alone through this whole thing! When I explain the pain to my friends/family they have no idea what I’m talking about 🙁 i guess I just wanted to connect with someone who knows that pain I go through! It’s excruciating and so isolating since it’s not common!