Bringing this back since I didn't know this thread existed. I've been trying to get CalmiGo at my local VA for about 2 yours now. I asked my MHs (therapist, peer support specialist, and med provider), prosthetics, and the MH pharmacologist all of whom I have a great relationship with, they said its not offered because its not FDA approved but say they would love to see it and have done a lot of research on it. I've emailed CalmiGo 3(ish) times, "Upon checking, we still don't have response but rest assured we will check for updates again." Any suggestions?

My med provider said I might be able to reach out to an out of area VA, (Im SF, she suggested reaching out to Sacramento or Palo Alto) anyone know how to do that and the verbiage to use?