Have you ever had tests or X-rays taken and received the results in an envelope sealed with a sticker that instructs, “NOT TO BE OPENED EXCEPT BY THE DOCTOR”?
Did you know pathology companies have a policy that they won’t give the results to the patient only to the requesting doctor?
How very audacious of the medical system to keep you the patient, you the paying customer, in the dark, the last to know, waiting on the doctor’s convenience.
It’s your information, it’s your life.
You have paid for it, even if Medicare paid, you and fellow taxpayers paid for it. It belongs to you.
You will be able to understand it. After all the General Practitioner is not a Pathologist or a Radiologist. Even if the detail is not clear to you, there will be an interpretation written in clear English for the doctor to read. It’s usually in bold at the end so it’s easy to find.
If you feel you will not be able to cope with the implications of the results, then of course seek counseling and use your best judgement. However, I feel that most of us, most of the time will just want to know and that should be our option not the doctor’s. I would not want to be waiting and worrying.
Next time you get one of those envelopes, rip it open, so it’s obvious you’ve done so (it’s not naughty) and have a read, so you don’t have to wait to see the doctor. I’m not saying don’t see the doctor.
When Pathology sends your results to the doctor, get a copy. By the way, did you know you have the right to tell the doctor which pathology company you’d like to use rather than accepting whatever company provides the doctor with their stationary. The right of assignment is yours.
Similarly, when you get a script from the chemist ask the pharmacist not to put the sticker over the information about the active ingredient and strength of the medication. Ask them not to throw away the information pamphlet which the drug companies put in each packet. That’s useful information you should know. The chemist routinely throws them out so you don’t get concerned about the side-effects etc. After all, the doctor has made the judgement for you and wouldn’t want you to be unduly worried, burdened with all that information relevant to the drug you’re taking (?)
Doctors are very qualified, necessary contributing members of society but if no one complains, you get more of the same. It’s only by challenging for patient’s rights, that the culture changes.
Funny you say that about the drug info page that comes in the packet. I was reading the other day about how nurses don’t have t tell the patients all the terrible side effects of a drug unless they specifically ask for it. And even then. If they think it would worry them unnecessarily, they can tone it down a bit to spare them more anxiety 🙂
oh and I HATE it when i have to make an appointment with the Dr to hear the result of a blood test. What’s up with that? I guess if they only called you in when there was something bad, then everyone would freak out when that happened. This way it’s a bit like going i blind. You don’t know if you might get bad news…