Tell us what’s been happening.

The first conversation

Most people begin by telling us how things have been: what it’s like day to day, what they’ve tried, and what they hope might change. You don’t need to know anything about TMS to call.

Our New Patient Coordinator will ask a few questions, answer yours, and explain plainly whether we think we can help. If you’d like, we’ll check what your insurance covers while we’re at it. If we’re not the right place for you, we’ll tell you, and we’ll try to point you somewhere that is.

Many people call for someone they love: a partner, a parent, a grown child. That’s welcome. We’ll talk with you first, and with them whenever they’re ready.

What happens next

• An evaluation, arranged for you.

  A consultation with our clinical team, who’ll get to know your history and what you’re living with now.

• Assessments, where they’re useful.

  Depending on what’s right for you, that may include an MRI at an imaging center near you, a brainwave map (qEEG) in our clinic, and a few short questionnaires.

• A plan, reviewed by Dr. Liker.

  Your plan is built from your own results and reviewed by our medical director, neurosurgeon Dr. Mark Liker. We’ll walk you through it, and nothing starts until you’re comfortable.

If you’re thinking about suicide or are in crisis, please don’t wait for a call back. Call or text 988, any time, day or night, or call 911.