Multiple Sclerosis (MS) Support Group
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ilotusflower
I am confused!!!
Were to start...about 5 months ago I started to vomit for no reason ( not often but often enough to notice) and as the months went by that became more often. I already have some bowel issues due to MS...I have lost the feeling of pushing when taking a poo...plus I have to take miralax every day other wise I will not be able to go. Anways...on top of all that now i cant keep any food down. It feels like my food just piles up in my tummy till when it comes to dinner and there is no more room so it all comes up (everything from all day) and my stomach hurt all the time. Now I feel soooooo weak...I went to see my GI Dr and he is worried and I am having a colonoscopi and endoscopi, really worried about my ileocecal junction. I know I have heard on here before that people have vomiting issues...but is this really an MS thing or is it something else. I think I am wanting it to be something else....cause then they may be able to fix it? seems like if its MS then...I will have to just deal with it. And another thing...I never know which Dr to call anymore...GRRRRRR!!!!!!
Thanks for letting me vent ;)
Were to start...about 5 months ago I started to vomit for no reason ( not often but often enough to notice) and as the months went by that became more often. I already have some bowel issues due to MS...I have lost the feeling of pushing when taking a poo...plus I have to take miralax every day other wise I will not be able to go. Anways...on top of all that now i cant keep any food down. It feels like my food just piles up in my tummy till when it comes to dinner and there is no more room so it all comes up (everything from all day) and my stomach hurt all the time. Now I feel soooooo weak...I went to see my GI Dr and he is worried and I am having a colonoscopi and endoscopi, really worried about my ileocecal junction. I know I have heard on here before that people have vomiting issues...but is this really an MS thing or is it something else. I think I am wanting it to be something else....cause then they may be able to fix it? seems like if its MS then...I will have to just deal with it. And another thing...I never know which Dr to call anymore...GRRRRRR!!!!!!
Thanks for letting me vent ;)
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Good Luck, and keep us posted...
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Hugs, Owlxxxx
My first symptoms of whatever I had started when I was 32 and I've since had one relapse. This time I have more abdominal problems: trouble feeling when I need to go and when I do it's usually loose, some urinary incontinence, intestinal - and quite pronounced upper abdominal - pain.
Get tested no matter what. Like smathie said, it could be co-occurring with MS or something totally separate.
All the best.
Here is a link from a different forum on autonomic dysfuntion and gastroparesis.
http://www.medhelp.org/posts/Dysautonomia-Autonomic-Dysfunction/Gastroparesis/show/1108422
'http://www.medhelp.org/posts/Dysautonomia-Autonomic-Dysfunction/Gastroparesis/show/1108422'
called the Dr again today to tell them that there is no way I can wait 2 more weeks...having test on Monday. I will let u know what they say. This SUCKS!!!!
Smooches!!!
Smooches!!!