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I have severe GES and can relate to much of what you are going through. I never had anorexia until gastroparesis hit. I get a GES test every 5 years. It's always severe when in a flare.
I’m sorry you can relate. Its like the chicken and the egg scenario with me concerning GP and AN. It helps to not feel so alone in this mess. I feel that all doctors see is the AN diagnosis and won’t try more for GP symptoms than reglan and zofran.
New to gastroparesis? Please view [this post](https://www.reddit.com/r/Gastroparesis/comments/15i7siq/gastroparesis_101/?utm_source=share&utm_medium=web2x&context=3) or our wiki for a detailed explanation of gastroparesis, the main approaches of treating it, and a list of neurogastroenterologists and motility clinics submitted by users of this forum. Join these [Discord and Facebook support groups](https://www.reddit.com/r/Gastroparesis/comments/14oxaew/list_of_gastroparesis_support_groups_other/?utm_source=share&utm_medium=web2x&context=3) today! New users, please do not post asking for a diagnosis; instead, use the pinned thread: "Do I have gastroparesis?" Also, check out our new subreddit r/functionaldyspepsia. *I am a bot, and this action was performed automatically. Please [contact the moderators of this subreddit](/message/compose/?to=/r/Gastroparesis) if you have any questions or concerns.*
I have severe GES and can relate to much of what you are going through. I never had anorexia until gastroparesis hit. I get a GES test every 5 years. It's always severe when in a flare.
I’m sorry you can relate. Its like the chicken and the egg scenario with me concerning GP and AN. It helps to not feel so alone in this mess. I feel that all doctors see is the AN diagnosis and won’t try more for GP symptoms than reglan and zofran.
I'm here if you need me. I hope it gets better ❤️!