Hello zamalek: just want to wish you all the best for this procedure. I hope you've got an answer to your question. Sorry, but I can't answer it. I just want to thank you for asking this question, because I think a contrast CT scan of my lower GI is in my not too distant future, so I'm interested in the debate re barium vs gastrografin. I hope you'll let us know how you get on today
Glad it went smoothly! Thanks for letting us know what it was like.
No I'm not on warfarin. Over the decades, I've had what you may have meant by 'invasive' investigations (colonoscopy 2x, gastroscopy 2x, all with biopsy): are these what you mean? The NHS has never hesitated to investigate because I have immediate family history of GI cancers.
My lupus is infant onset, and my sjogrens is also relatively early onset + I'm ehlers danlos hypermobile, all of which seem involved in my GI issues. Daily systemic prescription treatment for lupus etc only started 5 years ago when my infant diagnosis was recovered. So, I've been managing my chronic upper & lower GI symptoms & conditions from childhood via conscientious lifestyle techniques & gastrolgy's prescription meds. am now 62. Things GI-wise have been very reactive, and a constant preoccupation all my life, but also relatively bearable & cooperative to management...until these past few months when quite severe lower GI symptoms have set in. As usual, am coping via lifestyle stuff, and I do think my daily systemic prescription lupus meds are helping up to a point....but, due to these past few months of recurring flares of severe lower GI pain followed by more persistent symptoms, my GP has organised an abdominal ultrasound scan. Meanwhile, I recently tested neg via my 2nd 2 yearly BM smear postal lab test.
My husband has early onset crohns, so I have my lower GI stuff firmly in perscpective. The main reason I'm push ring my stuff now is that he is alarmed by my symptoms, which he feels are down to inflammation. And he is a very stoic guy who knows my health patterns well and has good judgement.
anyway, I saw my Urologist last week, and she doesn't think my urological/renal system is involved in my current stuff. So, now it's on to checking gyn & vascular (for AAA) organs via this UltraSound scan in early jan. Am expecting everything will be normal. Then I'll ask for referral to gastroenterology, intending to lobby for a CT.
Meanwhile my urologist suggested I see the specialst gyn physio again to review my long standing pelvic floor exercise routine in case there is any chance I need to change how that's going. But she wrote to my GP & me that she suspects my pelvic floor isn't actually involved in this lower GI stuff (I was trained in the early 2000s by NHS gyn physios, and reviewed ok after 10 years). Whatever, I'm glad she brought pelvic floor dysfunction up, because I had no idea this can be relevant in the sort of lower GI symptoms I get. I'm wondering if my rulers danlos hypermobility could make this type of dysfunction more of a possibility. Have you encountered this?
Apologies for going on about myself at such length in your thread! But I suspect you have more gastroenterology experience than me...
I'd be very interested to learn more about your version of lower GI stuff - am hoping you'll keep us updated. Is lupus your primary condition? Do you also have sjogrens?
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