How did you get diagnosed? I got misdiagnosed with fructose malabsorption, ruined my life for nearly 2 years trying to avoid fructose -which made me eat other sugars. Switched diets a couple more times (back to general, and then avoiding sucrose and starch as much as possible) and then presented this to the doctor the second time I had a colonoscopy. Succraid/your doctor can fight your insurance's decision a bit, and succraid has a program (mine was down at $5/mo.) But they did change companies recently and I had a lapse in coverage so I haven't had the enzymes yet since the new company. Get the prescription and then try to get it to an affordable cost.

It feels so weird to me that there’s only one medication out there! Maybe I’m mistrusting but the fact that my GI doctor had me breath into a tube, mail it to the company that makes the meds, and then get told by that same company that I need the meds? I don’t like it at all.