SM & Digestive disruption

Have a question about a symptom, procedure, medication, diagnosis, research, or coping? Ask questions and share what you know with others

Moderator: pmaxwell

SM & Digestive disruption

Postby Debbieducati » Wed Mar 13, 2013 1:34 pm

I have had SM for 8 years, I developed an H-Pyloric ulcer the doc's didn't catch and purferated. Since then I have had to go off all my medication because my stomach dosn't work any more. Gastroparesis 90%. The pain medication was not an option anymore because of how much it slows down your GI tract. Been off for 2 years. I have seen so many specialists that no one knows why my intestines are is havic. I'm seeing a neutritionist now and found out through her testing I had been suffering from malneutrition for years. Which I knew and no one would listen. Lost my job and insurance.
Have any of you herd of Neuro-transmitting testing. To see if the vegas nerve is causing some of the GI Havic. I'm not responding to the diet as well as I should, and my Neuro symptoms are wrose then they have been. Bad hand and head treamors, blurred vision in one eye. Pain increase. Any thoughts. Anyone. (Why do doctors give up when they can't figure things out) [url]What happened to the Doctors Oth!!!!!!!![/url] Every doctor I saw blew me off....
Love to all
Debbieducati
Love to all
Debbieducati
PTSM C5, C6
Debbieducati
 
Posts: 137
Joined: Fri May 18, 2007 10:35 pm

Return to All About Chiari, Syringomyelia, and Related Disorders

Who is online

Users browsing this forum: No registered users and 4 guests