Question : On Oct 15 I noticed a 
hearing loss in my left ear.  At first I thought it was a defective phone.  Later that day I tried using the phone using my right ear.  I called my ENT office & asked to move up my annual hearing exam & an audiologist tested my hearing.  I am 69  & always had less hearing in my left ear but  the loss was significant .....  30 to 40 % more than last year.  She showed me the comparison & then I saw the PA.  He said I either had an 
inner ear infection or a tumor,  called in a script to local pharmacy for 60 mg. for 7 days, 40 for 7 days, then tapering to 20, 10,5 & 1/2 in 5 day intervals.  He also said I would be called about an MRI.  I took the medication because he said if I didn't I could have a permanent hearing loss.  I began taking the pills on Oct 18.  I have an anxiety disorder & take 1&1/2 mg of 
Klonopin per day.  When under stress, I don't eat.  I have had almost every side effect except hunger, 
bloating & swelling of face/throat.  I lost my appetite immediately, felt like I was on 
amphetamines 24 hrs a day.  I increased to 2 mg of Klonopin  per day.  I began taking one 5 mg of Ativan at night so I could sleep.  By Oct 22 I called to ask when I would have the MRI.  I was not scheduled until Nov 21 & I am leaving for Paris on Nov 27.  I got it changed to Oct 29, saw the hearing specialist on  30th.  I told him if he didn't get me off the pills I would commit suicide by overdose of all my pills.  I am type 2 diabetic with all levels in normal,range with meds.  I was told it was an inner ear infection of unknown origin and he changed timeline to 8 days : 4 of 20mg, 2 of 10, 2 of 5 because they had to taper them.  I stopped taking them 4 days ago.  I still live on I granola bar, I banana all day long & then I finally get hungry & eat weird stuff for dinner - not typical of me at all.  I am still hyper all day long, smoke twice as much as before I started the pills, tapered coffee to only 2 cups per day.  I have lost energy, fine & gross motor skills, focus and forget  what I'm doing a lot of  the time.  I also could not sleep more than 3/4 hrs when I stopped taking pills.  I finally called my 
primary care Dr & he sent in a script for Ambien I mg at night.  I slept 8 hrs last night even going back to sleep after using toilet but do not want to take another pill to sleep at night.  I require 8 hrs per night.  I believe I have suffered permanent brain/ neurological damage because of taking 
Prednisone  for 21 days.  I will never take them again even if it is a matter of life or death.  I am furious that a PA can prescribe pills w/o first consulting with a real Dr.  I did ask the Dr what he would have done when presented with same symptoms & he supported the PA.  What I didn't ask is the initial dosage of 60 mg  for 7 days.  Why couldn't I have taken an antibiotic instead of steroids?  I am afraid I will never get better in time time for my trip to Paris on Nov 27.  Can steroids damage a person permanently ?