I just got diagnosed with Celiac Disease after 20 years of stomach and digestive issues. I really wish someone had cared enough to test me for it sooner. However I'm so grateful for the new doctor I have. She has Endometriosis and Celiac just like me, so she knew what steps to take to figure out what was wrong and she's very understanding. My biggest concern now is that I'll still have underlying digestive issues even after changing my diet, as well as the high possibility I simply won't be able to change my diet effectively. I live in a poor household with limited ways of keeping and storing food, due to pest, horrible house conditions, and my family not willing or understanding I can't eat most of what they eat. My diet was bad and limited before in hopes I could better my health, so now that I know I have Celiac idk how I'll ever be able to eat fully gluten-free and non endometriosis triggering foods.
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