Hi
I dont have Lupus but am being treated for a couple of other dastardly autoimmune disorders and have found the Lupus site here one of best sources of info.
Getting a diagnosis and treatment where I was in Wales proved to be a complete nightmare. I want to possibly make a complaint and also possibly feed my experiences into research aimed at improving the diagnostic process for autoimmune diseases in general.
BUT
I received my (or a part of my) GP records last week and there seems to be more holes in the record than information provided. So I would be really grateful if folk could let me to know what should be there, so can get better idea of what has perhaps been held back. Including what kind of info you were given.
What was not there included:
1. No referral letters to consultants or for investigations
2. No notes at all relating to GP consultations I had. Is like they never occured. Should there not be some note made after each consultantion and maybe during it (including under GMC guidance), recording what was said, decided etc?
3. Apart from copies of test results, there is nothing that records the GP's clinical findings or thinking about what is or might be wrong. For example, there is no note subsequent to my consultant writing to GP saying what he thinks could be wrong.
4. No notes of phone calls, like with hospitals.
5. No notes of GP discussions about my case.
Thanks very much for any help you can give.
Kind regards