So I was told I have NAFLD after my GGT kept rising and then two ELF tests within a year of each other has risen to from moderate to 9.5 severe I was sent for US which didn’t show anything .
I spoke to my GP Who agreed because my ELF test had risen we should get a fibroscan
I expected a scan but had a letter to say it was a call for today at 2pm - I logged onto the NHS site earlier to check timings all good - 2.05 pm came along no call so I logged onto the site to see if I was supposed to call but no the call has been moved to MARCH 2022 !!!
I will get back onto the doctor but I think it’s because NICE guidelines sat you only need to be tested every 2 years - that’s all well and good but things changed quicker than that !
Has anyone else experienced this in the early stages ! How quickly can it change and what should I be doing in the meantime !!
Thanks in advance
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Tiaday
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Hi Tiaday
that is not good, I understand they can say every 2 years ,but, when something changes, there should be a need to know what is going on. Not just for us, but also for our consultant/ doctor.
Is there any possibility of you contacting your GP and asking if it can be brought forward?
A fibroscan obviously requires us to be nil by mouth that day and only water (or black tea or coffee) for 3 hours before the scan. It would be a long shot and require a little effort, but you could try contacting the appointments and let them know you will be nil by mouth every day until 12 noon, so if there was a fibroscan cancellation, you could attend provided you are contacted by 12 noon.
I think cancellations used to cost us (the hospital where I worked) around £150 and we were always happy if we had someone who could attend at short notice.
I was talking with an ex colleague last night and he said, he thinks lockdown has probably led to an increase in alcohol consumption. I do not know but, if that is true, I'm sure it will mean an increase in waiting time for an U/S, fibroscan.
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