Hi again @sarahdennis87 to be perfectly honest this is beyond any GPs knowledge. I think you now need either an urgent gastro appt or more relevant maybe see a liver/pancreas specialist. If you need Creon then you have pancreatic enzyme insufficiency and that needs proper investigation and may need a collaboration between gastro and pancreas specialists. I would be alarmed to take that many Creon unless you didnt have a liver or pancreas. Why dont you adk for a second opinion and in the meantime do research on how much Creon to take. Its your health and your life so dont be shy. Good luck.
hello
Does anyone here have exocrine pancreatic insufficiency? Just diagnosed with it in December. I’m type 1, almost 16 years strong!
Struggling to control EPI. Was on creon 25000, taking 10 with meals 5 with snacks. Wasn’t working and making me vomit. Changed to Nutrizym 22, taking 6/7 with meals 4 with snacks. Still not working but thankfully no vomiting. I’m just not sure how to control it and I have zero support. Currently waiting on an appointment with my gastro
Silly question perhaps, but were you taking 250,000 per meal? Does it matter what you are eating or do you vary the amount? Have you tried lower amounts and slowly building a tolerance? I also have EPI and remember being nauseous initially but was taking 36,000 per meal initially and was able to increase it over time. What also helped me was to stagger the pills throughout the meal with the first pill with the first bite and the last with the last bite. There were a couple of books that really helped me, and I will dig up the names when I get home. I also had to address diet considerably, which was completely opposite to what my gastro had told me.
Mylan are only the distributors in the UK. There is currently a “manufacturing problem” in Germany for all but the 10,000 dose. If you go on the Mylan website today they are advising that supplies will be resuming soon.Just seen a post on UK WHIPPLE WARRIORS that Mylan are going to cease the production of the 40k tablets !!!
I have increased slowly since diagnosis, now taking 14 25k with majority of meals, I will alter slightly if I’m eating something with less/more fat and protein. I’m eating a fairly healthy diet as I’m also trying to lose weight. It doesn’t matter what I eat nothing helps. I’ve tried taking all tablets up front, staggering them throughout the meal, nothing helps. I don’t know what more to do?
I’ve been in contact with my gastro who informed me that she was leaving the trust so couldn’t offer me an appointment. I’m currently on a waiting list for an urgent appointment to get further tests done but I have to wait until another gastro starts. I’ve been told to try different medication, none of which helps and the gastro said the next route would be a gastroscopy for D1 and D2 biopsies and a colonoscopy to check for IBD.
I recently found out my stool sample from January tested abnormal for calprotectin but nothing was done with the results. I’m not entirely sure what it means but I just want to be normal again
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