My father has been recently diagnosed with PSP he is 80 and has always been active in thought. A very intelligent and successful electrical engineer. My mother and I care for him at home but are finding it very difficult his deterioration has been rapid and we are requesting support from social services. Thankfully we believe we are on their radar but I fear we are entering late and are ill prepared. In the past week alone we have increased concerns over his mobility finding we are using a wheelchair rollater more and more often.
My fear this evening is that the Doctor has given him medication to relax the brain at night to help with agitation and sleep deprivation - we have noticed that although he has never been violent he is forming fists to defend himself and is scared. He is verbally abusive. We have stopped the medication on Day 3. Has anyone else experienced anything similar and can offer advice.