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739d
any advice for someone with a new eds dx?
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Ehlers-Danlos Syndrome (EDS)
Gastroparesis
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729d
@Bijoux_bean22 it absolutely does. I'm sorry you are struggling. I finally convinced my gp to see up with a dietician
1
732d
@crunchyoddball I am currently existing on soup, applesauce, baby food, juice, pudding ect. It’s only made a 7% difference and I feel like all my nutrients are missing. I hate it. Gastroparesis sucks sometimes.
735d
Find a PT that is very familiar with EDS and will listen to you and your body.
738d
I am also trying to find balance with EDS and gastroparesis among other things. It’s not looking good though. With how its progressing I would be very surprised if I went back to school in the fall without a feeding tube of some kind.
737d
@Bijoux_bean22 so sorry to hear that. Are you on the gastroparesis diet? It's helping me tons.
What do you do for the gastroparises
@Bartender I take entocourt and stick to a gastroparesis diet. It sucks, but it makes a huge difference
I'm still trying to figure it out myself. Hopefully someone else will have some experience?
@Bartender it's a scary new world, for sure
@crunchyoddball yes and there are other illnesses that can be connected to EDS. Do you have anything else
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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