I am being driven to breaking point by the obstructive nature of my mums local surgery.
Yet again mum has a uti. I know she has a uti because after six years of dealing with her utis I can smell one a mile away.
Her surgery will not allow anyone to drop off a urine sample to be tested. I have to make an in person appointment and take someone with zero mobility so the doctor can tell me she doesn’t have a fever so she doesn’t have an infection. I then have to argue that she never presents with a fever and beg them to please let me bring a urine sample for testing.
When I eventually get the prescription for the antibiotics they send it to her online pharmacy that take a week to deliver. I have to make another appointment to ask them to send the prescription to the local pharmacy so I can pick it up the same day. Then when I get the prescription I can 100% guarantee it’s gel caps despite requesting a liquid antibiotic because she can’t swOllie the caps. Last time I asked for it to be changed my request was denied because it wasn’t “cost effective”
I have asked repeatedly for her to be put on prophylactic treatment. I’m always told no. This is despite people I know using the same surgery being given prophylactic treatment. We talk about these things down our dementia group.
She used to have a repeat prescription for LBF barrier cream. It was removed. Despite repeated requests to have it back I’m told no. I have to buy it myself.
The district nurse requested a prescription for duo derm patches to help with a problem sore. I never got them. I had to buy them myself.
I’ve asked to speak to the practise manager 4 times this year. Each time they have refused to speak to me.
i can’t change her to another surgery because they’re all run by the same management company.
I don’t know what to do anymore.
Yet again mum has a uti. I know she has a uti because after six years of dealing with her utis I can smell one a mile away.
Her surgery will not allow anyone to drop off a urine sample to be tested. I have to make an in person appointment and take someone with zero mobility so the doctor can tell me she doesn’t have a fever so she doesn’t have an infection. I then have to argue that she never presents with a fever and beg them to please let me bring a urine sample for testing.
When I eventually get the prescription for the antibiotics they send it to her online pharmacy that take a week to deliver. I have to make another appointment to ask them to send the prescription to the local pharmacy so I can pick it up the same day. Then when I get the prescription I can 100% guarantee it’s gel caps despite requesting a liquid antibiotic because she can’t swOllie the caps. Last time I asked for it to be changed my request was denied because it wasn’t “cost effective”
I have asked repeatedly for her to be put on prophylactic treatment. I’m always told no. This is despite people I know using the same surgery being given prophylactic treatment. We talk about these things down our dementia group.
She used to have a repeat prescription for LBF barrier cream. It was removed. Despite repeated requests to have it back I’m told no. I have to buy it myself.
The district nurse requested a prescription for duo derm patches to help with a problem sore. I never got them. I had to buy them myself.
I’ve asked to speak to the practise manager 4 times this year. Each time they have refused to speak to me.
i can’t change her to another surgery because they’re all run by the same management company.
I don’t know what to do anymore.