I had the blood tests for LADA 3 weeks ago and as I'd not heard anything I've just phoned them to ask if the results are in yet, and they said they weren't done! Apparently the blood should have been in the fridge or frozen within half hour of being taken and they weren't so they didn't do the test. And no-one bothered to phone me to tell me.
So I've been waiting 3 weeks for results that were never going to come! Not happy
To be honest, I'm certain you could make your point, quite elegantly and eloquently, leaving nobody unclear about how you feel about things, without insult or name calling.I've written a lot of protest letters and quite a few complaints, but I'm a bit wary in this case because I've got to keep them on side, they're the only surgery I can go to and they do prescribe testing stripsI'll think about it though, and see what they have to say tomorrow - but if they don't call me back by the time I've got my gander up they'll be getting a letter!
That's terrible! Can I just ask, why is it in England you have to go the one specific surgery? We are lucky in that we get to choose our own doctors, and if one p***ses you off you just find another. There's only the one endocrinologist in my area and I saw him once and didn't really like him he was rather pompous ... so I'm trying out a new one next month. Will see if he passes muster!
Oh I see ... I've just noticed most people on here indicate that they have to stick to a particular one.Many people do have a choice of surgeries but it depends where you live. I'm in a rural village with one surgery, which is run by the main practice in the nearest town 8 miles away, so has the same medical staff. There might be another one in the town but it's impractical for a disabled person to get to, especially if I can't drive for any reason. I can go to the local one in my powered wheelchair if necessary.
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