"I have MS and my partner has mesothelioma"

We can't get appointments or even spoken to appropriately from members of staff and feel worse after phoning because anxiety is off the scale, which means stress, which means MS is worse! Honestly don't feel like we can depend on our doctors/practice for anything and my partner's terminal cancer which you would think should be dealt with appropriately. They hadn't even updated his pain management/prescription so had to get palliative nurse to physically go to surgery and sort it out and then bring it to him too as the way they were questioning the amount he had to take was terrible but she informed them exactly what he should be taking. We have never heard of anything like this, especially with our health conditions, but obviously cancer and MS isn't serious enough to get a proper patient/doctor service!