This patient support community is for discussions relating to Dysautonomia (Autonomic Dysfunction) including: Postural orthostatic tachycardia syndrome (POTS), neurocardiogenic syncope, mitral valve prolapse dysautonomia, pure autonomic failure, autonomic instability and others.
You might try calling back to Cleveland, explain the situation, and see if they'll move up his appointment or if they know another GI in your area who is decent.
In the long term, it would be nice to find a GI doc closer to home that can work with you, but this may be a solution to the short-term issue of getting the test done in a timely manner while you work toward the long-term goal of finding a GI doc that doesn't have his head attached to the wrong end of his gastrointestinal tract. ;-)
When I called our GI doctor (now ex GI doctor) and told his nurse the findings in Cleveland and faxed over all of the doctors notes, you would think out of curtesy to another doctor they would run the test. It wasn't his dime paying for it. Anyway, the notes also state that he has lost reflexes on the right side of his abdomen. That to me tells me something is wrong with those nerves. If it turns out that indeed he does have gastroparesis, this doctor is going to get a very, very, long, not nice letter.
So, now I'm waiting to hear from the hospital so we can schedule the test.
If it turns out he has gastroparesis, don't write the letter to the former GI, write it to his boss or an ombudsman. Letters to the doctor have a way of disappearing or just getting shoved in your file. Better to get them in trouble with their bosses.
My sons test is scheduled for Thursday.