I recently posted asking if anyone had pancreatitis issues with lupus (just been diagnosed with cutaneous lupus) and I got some advise & help & support. I spoke to the hepatobillary clinic who removed my gallbladder & they agree it’s most likely the pancreatitis is being caused by an autoimmune issue that’s not showing up on tests, I asked them to recommend to my gp I get sent back to rheumatology and I had a specific guy in mind (recommended by the maxfax consultant I’m under for mucus membrane pemphigoid) so I’ve emailed the gp asking for a referral and that’s all going to be set in motion.
so a heartfelt thanks to you all. I feel like I’m finally getting somewhere! 🥰❤️