That's probably why it's taking a while I would give it a fortnight and if no luck then get in touch with pals they will help give a kick up the bum x
Hello,
Have you tried going through the Patient Advice and Liaison team at the hospital to voice your concerns - it may be worth trying this route first. The hospital switchboard will be able to put you through to them.
I understand how frustrating and worrying it can be waiting on results. I had to wait 6mths for the results of my first biopsy but then only waited 4 weeks to get results of my second one, although they were carried out 2 years apart. Never knew why it took so long with the first but I just kept ringing the Consultants secretary second time around, so maybe that speeded things up. Hang on in there and hope you get answers soon.
It’s very frustrating waiting for the results - especially the RCH as they have fewer specialists. I’m sure once you get past the first few stages and should there turn out to be something major wrong with you I’d guess they will refer you to Derriford as, as far as I understand it, they are the regional centre of excellence for dealing with liver related issues. They also work directly with Kings and have a good working experence.
The team at Derriford are excellent - huge workload but they seem to manage very well and with good humour.
I guess if you don’t get an answer soon then ask either your GP or RCH to transfer you to Derriford - hopefully it’s not too far to travel for you.
Hi I am in exactly the same situation 😥. Nearly 2 years ago I was very poorly and was admitted to hoaitial and it was found on fibroscan I had chirossis as well. After discharge and go till before Christmas I was well but became unwell again. I had an ultrasound and was in fact told that he couldn’t see any sign of chirossis so sent me for MRI. Nearly 3 weeks on and lots of calls to my consultant I am still waiting. He and his secretary are on leave till Monday. I have been told report has been reported but have to wait.... Now I sit here waiting and worrying ?? Do I or don’t I have it? Worst of it all is I work for the NHS as well so knowing too much makes it worse. Hang in there and hope all goes well. Be great to hear how you go x
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