Opinions needed please, I am trying to be succinct. Back in May my Dad had a fall & we knew he’d broken himself somewhere due to how he was moving. I called our doc, who is great, and then went to the local hospital to get him checked over. (FYI I didn’t put him in a wheelchair as it was likely to make him panic/ think he was really ill/ being left and refuse to walk, I was also exhausted and had arranged to go away the next day so I was aiming to check all was OK before swapping carer duties.) Once at the hospital I led him the short distance into the lobby, with a frame, issuing clear blunt instructions and repeating them, as you do. I was standing in front to encourage him to straighten up and ensure he didn’t topple. (On one side I am used as a leaning post and can’t risk further sciatica.) When I turned round and saw the expression on the receptionist’s face I knew I had been judged, so unfortunately the next hour and a half we spent there I was subjected to the usual messed up verbal multiple choice to assess my state of mind. Fair play- doing their job BUT my poor Dad wasn’t diagnosed...they just said his gait was due to the seriousness of his dementia. Well of course it wasn’t! Sadly it took my son a further visit to our doctor & then driving his Gd into a further afield hospital to get the X-ray which I said we needed in the first place. Finally they.worked out he had a fractured pelvis. Poor old guy, shame carers are often treated so shoddily.
I have filled in a feedback form at the hospital...no response of course...no apology! Any views on chasing this up anyone? Should I get back to them again/ Someone else...anyone know who? I would hate this to happen to someone more eroded than myself if you know what I mean.
I think this is an indication of how difficult it is to get care for your PWD (esp when there are 2 involved) BTW this is our 3rd year of dealing with both pretty much 24/7 and no social worker, (except once in in February when I insisted we needed an interview to cover my back so to speak.) Amazing really considering the effort put into quizzing me and running safeguarding procedures...little follow through. What do you reckon anyone? Are the family best off without any SWs anyway. Keeping away from hospitals as much as possible seems to me to be the best path. However, sometimes families need help and Dementia seems to rob a person of their ability to know where their nerve endings: pain etc are. ????
I have filled in a feedback form at the hospital...no response of course...no apology! Any views on chasing this up anyone? Should I get back to them again/ Someone else...anyone know who? I would hate this to happen to someone more eroded than myself if you know what I mean.
I think this is an indication of how difficult it is to get care for your PWD (esp when there are 2 involved) BTW this is our 3rd year of dealing with both pretty much 24/7 and no social worker, (except once in in February when I insisted we needed an interview to cover my back so to speak.) Amazing really considering the effort put into quizzing me and running safeguarding procedures...little follow through. What do you reckon anyone? Are the family best off without any SWs anyway. Keeping away from hospitals as much as possible seems to me to be the best path. However, sometimes families need help and Dementia seems to rob a person of their ability to know where their nerve endings: pain etc are. ????