My Dad was recently in hospital with aspiration, he was making gurgling noises and holding food in his mouth.
The SALT team assessed him and he is now on a puréed diet.
Unfortunately he is back in hospital again, he has kidney issues that have sped up the deterioration of his Alzheimer’s, and they uncovered a huge abscess on his kidney that is being drained. Because of this, he’s on IV antibiotics and fluids… and his appetite has improved! He’s also not been making noises when eating, and he seems to be swallowing a lot better now.
I’m wondering if infection and pain can make dysphagia worse? And if he needs to be on puréed foods? We’re on a waiting list now for the community SALT team to come back and check on him, so until then don’t feel we can just change his diet without support.. but we’re just left a little confused (as we always are with this cruel disease).
Wondering if anyone has had any similar experiences?
Side note: so many times in hospital his meds have been left on the side for him to take himself (which he obviously can’t do!!) and they keep giving him in tablet form!! Despite us consistently saying he has liquid medication - because he is on a puréed diet!!! The care people with dementia receive in hospital is just so poor and heartbreaking, they have no voice and consistently forgotten about.
Sending love to any of you feeling helpless too xx
The SALT team assessed him and he is now on a puréed diet.
Unfortunately he is back in hospital again, he has kidney issues that have sped up the deterioration of his Alzheimer’s, and they uncovered a huge abscess on his kidney that is being drained. Because of this, he’s on IV antibiotics and fluids… and his appetite has improved! He’s also not been making noises when eating, and he seems to be swallowing a lot better now.
I’m wondering if infection and pain can make dysphagia worse? And if he needs to be on puréed foods? We’re on a waiting list now for the community SALT team to come back and check on him, so until then don’t feel we can just change his diet without support.. but we’re just left a little confused (as we always are with this cruel disease).
Wondering if anyone has had any similar experiences?
Side note: so many times in hospital his meds have been left on the side for him to take himself (which he obviously can’t do!!) and they keep giving him in tablet form!! Despite us consistently saying he has liquid medication - because he is on a puréed diet!!! The care people with dementia receive in hospital is just so poor and heartbreaking, they have no voice and consistently forgotten about.
Sending love to any of you feeling helpless too xx