Dances4Monet

Great idea on the accessibility, thank you.

Apparently his type is so rare he’s the only one with it so it doesn’t have a name. Just calling it congenital MD as an umbrella term.

Thank you

One of my friends sons has MD, it’s a very rare type that doesn’t have a name and his symptoms started when he was very young. He’s an awesome kid and they’re a lovely family but I often feel like I don’t know what to say to my friend, or how to support her. Can you shed some insight into this?

Thanks for this AMA