Diane Peterson, Group Founder, Victoria, BC, Canada

This group was founded in 2008 when I discovered there was next to no information about May-Thurner Syndrome on the Internet. My first goal was to find others like myself, who had been diagnosed with this “rare” condition, as it was called back then. And interestingly it is still being called “rare” today in 2024, although judging from our growing membership it is actually not all that rare. We add at least 40 to 45 new members each week in our Facebook group, which has grown to over 6,400 members as of April 2024.

Please feel free to look for us on Facebook. The link to my MTS group is on this website.