I have a friend that has been undergoing THOUSANDS of dollars worth of treatment for TMJ and jaw issues and is still having symptoms (like 25k+ worth of out of pocket treatment for ONE dentist). She's getting into the space where random rare syndromes are being thrown at her (Eagles syndrome) which I understand to be because of a structural abnormality - though I'm not a doctor, I know these abnormalities don't have to cause pain (open to more info from someone that's heard of this disorder - don't google it, i made that mistake lol. I tend to get the symptoms I google about). I want her to feel the freedom that this work and community has to offer. If anyone has ideas about how to gently suggest or bring a friend into information about this work, I'd love ideas. Thank you so much! It's heartbreaking to watch someone struggle from doctor to doctor.