Hello, wondered if anyone has had anything similar or has any advice. Went to GPs day due to fly on holiday to Middle East as felt I had a UTI and should get antibiotics. They said they’d never seen a urine result like it (didn’t match any colours on their leukocyte or nitrate charts) and has blood and protein so gave antibiotics but then said because I have ‘special medical needs’ 🙄 and can deteriorate very quickly and am on so many drugs, I couldn’t fly until they knew exactly what it was. I said I’m sure it’s just a little infection and wasn’t get to let another health thing of mine ruin my children’s holidays again and they said they were writing in bold on my notes, going against drs instructions and that my insurance was now invalid! I said I’d get the blood test results then decide but the bloods didn’t come back in time so went on holiday anyway with the antibiotics.
BUT I now have obvious blood in urine and frequency (annoying my husband having to have loo stops!) and abdo pain so probably should see a dr here 🙄 (but feel fine and non - lupusy apart from that)
Does anyone know if there’s any way around the insurance invalidation issue? Anyone claimed and the company not asked the GPs?? We had to pay £800 last year for my son to have an injection and antibiotics overseas last year - obviously insurance paid but that’s quite a lot to pay myself.
I do understand why they made the decision but do think they should have spoken to rheumy first to decide as they are very nice but don’t know much about lupus and as many of us find, I either get the ‘we can’t see it, it must be imagination’ or (more often) the ‘you’re dying, go to hospital, too scary for us’ (seriously there is one who looks at me in such fear - I told her she’d send me to hospital even if I said I’d come about a veruca - we did laugh!), so I think invalidating insurance of someone who’s more likely to need it seems a bit counter-productive (except for medico- legal reasons and getting patients to do what they’re told!!)
X