Our GP refuses to, leading to delays of between two and five months while they are referred to the community paediatric team. I want to check whether it would be reasonable of me to complain to the ombudsman about their policy.
The background is that my DD (6) has had 5 episodes of fever lasting 4-6 days each time over the past two months. No other symptoms apart from headache and achey joints (eg no cough, cold, sore throat, vomiting or diarrhea). After the third episode I went to the GP (but they actually made us an appointment with the nurse practitioner) and asked for blood tests. I explained that my daughter had been losing weight and was pale and tired all the time. I asked for a full blood count and if it was possible to check for glandular fever in particular. I was told that it definitely couldn't be glandular fever as she was too young, and that they couldn't send a child for blood tests, and that they'd have to refer her to the community paediatric team which could take up to 18 weeks. I then asked if there was no quicker way to get a blood test and was told there was actually an "urgent" community paediatric triage service. When my DD had her 4th episode of unexplained fever and we still hadn't heard from this "urgent" service I then rang up again and had an emergency phone appointment with a GP. He confirmed that nothing more could be done and that we just had to wait.
I sent a formal complaint to the GP practice and was told that this was their policy, and that "we feel if a child is unwell enough to need blood tests then it is prudent to see a paediatrician for a holistic assessment".
In the meantime I paid for her to see a paediatrician privately. We had the blood tests on the same day. She tested positive for Epstein Barr virus -- it's been glandular fever.
It's really useful to know, both so I don't think she's dying of leukaemia but also so her school understand why her absence rate has been so high and why she is still so tired and also so they allow her to skip PE. It turns out that it's important to refrain from exercise for 4-6 weeks after having glandular fever in case your spleen ruptures!
We've finally had a letter through about the NHS community paediatrics triage and the appointment is in January, 2 months after we went to the doctor and asked for blood tests.
Without a diagnosis, I could have been continuing to push her to cycle to school each day and do PE, putting her at risk of rupturing her spleen. It also worries me that another child could have similar symptoms but these could be symptoms of leukaemia. I feel it's really dangerous that they can't do basic blood tests for a child without waiting for 8 to 18 weeks for a paediatrician referral.
AIBU to take my complaint further, to the Ombudsman?