We finally got the diagnosis of fronto temporal dementia I expected for my partner (which was copied to our GP surgery). While at the Memory Clinic, the doctor there discussed with us the importance - indeed, my partner’s right - to have in person follow up from his GP. I was staggered today when he received a letter from the surgery offering him a PHONE appointment. Do they know nothing about the condition? His main symptom is difficulty communicating. If they look at his records, they will see he is already referred for Speech Therapy. He can barely communicate face to face. If they talk to him on the phone, he will just murmur agreement with everything they say - because it’s the easiest thing - and they will learn nothing. Although his understanding is still good, and his memory not bad, he is unlikely to follow up on anything the doctor recommends, or tell me what was said, so I can help him to. He may retain and pass on a few random elements of the conversation, often missing the central points. So … with his agreement, I’ve emailed the surgery, as politely but clearly as I can, and asked for a face to face appointment, saying we’re prepared to wait as long as we have to, But I’m still tearing my hair out