Hi everyone,
So I live in Australia, and my parents live in the UK. My dad has early stages of Alzheimer’s and my mum is feeling a little overwhelmed with things and isn’t really engaging with possible care routes. They have had a social worker come round to assess their needs a few weeks ago, but apparently she is “still researching options as everything is shut down due to Covid”. It is so hard for me to understand, through googling, what services are immediately available to my dad. Is there a one stop shop that I can contact to get all of the services that are still available ? I just can’t believe that everything is shut down. I’m looking for some clubs, regular groups, interest groups etc that could improve dads quality of life in a responsible at, whilst giving mum a bit of a break? Could someone point me in the direction of a central resource for dementia care during covid. Mum and dad live in south Hampshire- would there be a local organisation as well? Anything would be better than what’s happening at the moment, which is nothing. It’s been a year since dads diagnosis and nothing has happened. I’m finding it so frustrating and I feel powerless. Thanks so much for any help or advice!
So I live in Australia, and my parents live in the UK. My dad has early stages of Alzheimer’s and my mum is feeling a little overwhelmed with things and isn’t really engaging with possible care routes. They have had a social worker come round to assess their needs a few weeks ago, but apparently she is “still researching options as everything is shut down due to Covid”. It is so hard for me to understand, through googling, what services are immediately available to my dad. Is there a one stop shop that I can contact to get all of the services that are still available ? I just can’t believe that everything is shut down. I’m looking for some clubs, regular groups, interest groups etc that could improve dads quality of life in a responsible at, whilst giving mum a bit of a break? Could someone point me in the direction of a central resource for dementia care during covid. Mum and dad live in south Hampshire- would there be a local organisation as well? Anything would be better than what’s happening at the moment, which is nothing. It’s been a year since dads diagnosis and nothing has happened. I’m finding it so frustrating and I feel powerless. Thanks so much for any help or advice!