As a healthcare provider that has worked and helped Bell's palsy patients for the past 18 years, I can't say I am surprised anymore when a patient or prospective patient mentions they feel lost, alone... Feel like they have not been given much guidance besides, and even not always, been prescribed steroids and antivirals....
They mention how they don't know what they should be doing to work on improving their condition. Should they take vitamin? Should they have massage? Should they use electrical stimulation? Should they continue exercise? Can they continue jogging? Should they just rest, and lie down for the next months crossing their fingers their face will start moving again?