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dory

636d

well hello there my alikes. I was diagnosed with gastroparesis back in 2013 and I've had various and numerous roller coaster rides with it as I'm sure you all know who has it it's not pleasant but they've been telling me the last I don't know however many years that if it keeps flaring up they're sending me the Cleveland clinic to get to j tube and a pacemaker put in and I really been putting it off and putting it off and putting it off but it's been coming and going and I don't know what to do any input

Top reply
    • DaveLaw

      617d

      I'm actually being treated by the Cleveland Clinic now and moved here from Texas/New Mexico just for that reason. If I can help you with the processes or anything let me know. You're definitely not alone...

    • DaveLaw

      617d

      I'm actually being treated by the Cleveland Clinic now and moved here from Texas/New Mexico just for that reason. If I can help you with the processes or anything let me know. You're definitely not alone...

    • Jkersmom

      627d

      J tube is a feeding tube I believe!

    • Rice.Cakes

      634d

      What is the j tube and why a pacemaker not for the gastropareisis is it

      • xxARYN420xx

        627d

        @Rice.Cakes j tube is a feeding tube. And they use a gastric pace maker for the stomach. It makes the stomach spasm to imitate digestion. My old gi told me it was my only hope... I'm now scheduled to see a different gi to get a second opinion

    • Rachelliz

      635d

      Have you actually been seen at Cleveland yet?

☝ 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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