Good afternoon. Well, it looks like I’m joining the club of people living without a spleen... I actually lost mine when I was 17, and now I’m 33. Up until this point, nobody ever bothered to give me any specific guidance on what I can or can't eat. Since the surgery, I’ve ended up in the hospital more times than I care to admit, hooked up to IVs because the pain, vomiting, and diarrhea were just too much to handle. The doctors always brushed it off as lingering complications or internal scar tissue. The last time I was admitted to the hospital was back in December. Now, I finally got to see a doctor who replaced my regular physician, and she suggested that I might actually have celiac disease. It turns out that before this, no one ever bothered to run proper tests; they just assumed everything was a leftover consequence of my ruptured spleen. Honestly, what is there even left to say?