Guest guest Posted March 26, 2004 Report Share Posted March 26, 2004 Dear Jen, I'm sorry you're feeling so awful. I know all too well. I know some people like a heating pad, but when I use one, it makes me feel more nauseated. I don't eat anything solid, & just concentrate on staying hydrated. I've learned to stay away from sugared drinks, & when I'm feeling like I'm starting to get dehydrated, I'll sip Pedialyte. And that's all I can do is take sips. So I have fluids with me all day & by my bed at night. Stress makes my symptoms worse, so I do whatever I can to relax & don't worry about things like housework. And I rest as much as possible. WhenI'm really feeling bad, I'm usually in my bed or on the couch. I don't go ANYWHERE unless I absloutely have to. It took a couple of years for my diagnoses of CP to become definate. I think it's such a hard thing for docs to diagnose. In fact, I believe they really don't know much about the pancreas at all. But that's just my opinion. Just be sure everything is documented well. Even if your'e up to it, keep your own record of pain levels, nausea, vomiting, stress, emotions, & what's happening in your life. I didn that & it was a great tool for my doc when he diabnosed my CP. Hope this helps in some way. Hugs, Deanna Tubb New Mexcio PAI Rep Quote Link to comment Share on other sites More sharing options...
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