We believed that with the right information, the right community, and the right medical partnerships, we could fundamentally change what it means to receive a Bell's Palsy diagnosis in America.
Bell's Palsy can strike anyone — overnight, without warning. One day you wake up and half your face won't move. Doctors give you a prescription, maybe a pamphlet, and send you home.
And then what?
Facing Forward was founded because that experience — the fear, the isolation, the complete absence of clear next steps — doesn't have to be the standard. We believed that with the right information, the right community, and the right partnerships with medical professionals, we could fundamentally change what it means to receive a Bell's Palsy diagnosis.
We spent months building a knowledge base unlike anything in this space — cataloguing 46 treatment approaches, reviewing 17 peer-reviewed studies, tracking 20 active research pipeline projects — so that when patients come to us, we can give them something real. Not false reassurance. Real answers.
We are based in New York. We are small. We are serious. And we are just getting started.
Founder & Director, Facing Forward
Executive Director, Facing Forward
Our research team spent months cataloguing every known treatment approach for Bell's Palsy — evaluating evidence levels, clinical stages, safety profiles, and real-world outcomes.
Corticosteroid therapy, antivirals, and vitamin B12 therapy — foundational care pathways with clear clinical guidance on when each applies.
11 approaches including mirror therapy, EMG biofeedback, facial neuromuscular retraining, and knowledge mapping — graded by evidence level.
18 treatments including acupuncture, moxibustion, low-level laser therapy, hyperbaric oxygen, and mind-body interventions — evaluated honestly, including conflicting evidence.
We track the frontier — hyperbaric oxygen, nerve growth factor therapy, and stem cell biofeedback. Local market application or potential future options.
Every decision we make runs through one filter: does this make life better for a Bell's Palsy patient or their family? If the answer is no, we don't do it.
We don't tell patients what sounds good. We tell them what the research shows — including when it's limited or conflicting. Honesty is our core clinical value.
We share our financials, our failures, and our learnings openly. There are no hidden agendas, no sponsored content, and no decisions made behind closed doors.
Bell's Palsy doesn't discriminate based on income, background, or geographic location. Neither do we. We actively ensure our resources are free and accessible regardless of background, language, or insurance status.
The loneliness of a Bell's Palsy diagnosis is as real to us as the physical symptoms. Building connection — so no patient feels alone — is core to our mission.
Early intervention changes outcomes. We operate with the urgency this disease demands — because every hour in the first 72 matters for patients.