Does anyone have that vomit-ty feeling?

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Regular Member

Date Joined Sep 2007
Total Posts : 29
   Posted 9/14/2007 11:06 AM (GMT -6)   
I know this is usually related to obstruction but I don't think so in this case. I'm not sure if it's the Prednisone or the Protonix weakening my stomach juices too much but every once and awhile I get this kinda feeling like I want to toss - but it never gets that bad. I wouldn't call it reflux cause there is no pain, and I don't think I'd call it nausea because, I don't know, it just doesn't seem that bad. It comes and goes seemingly at random - no tie to when I eat or my position that I can figure. Testing shows I'm mostly inflamed in the large colon. I do have alot of bloat going on.

Veteran Member

Date Joined Feb 2007
Total Posts : 1010
   Posted 9/14/2007 12:41 PM (GMT -6)   
Nausea is one of the most common symptoms of crohn's disease. I know I have gone through periods when I had episodes of nausea every day. As you say not so bad that you are in danger of vomiting, just queasy. I had to learn to eat even though I never felt hungry during these times. Otherwise I would have been anorexic because I forget what it felt like to be hungry.

I'm not feeling that way anymore. After years of mostly being the other way it is a wake-up call in retrospect. I think it is a significant symptom if it is pervasive, not just once in awhile.

30+ years living with Crohn's.

Regular Member

Date Joined Jul 2007
Total Posts : 456
   Posted 9/14/2007 1:19 PM (GMT -6)   

Ginger is a natural nausea remedy.  I've tried ginger tea, but didn't notice a difference.  I may not have brewed it strong enough.  My mom found some ginger candies called Ginger Chews, and they seem to help with queaziness.  I haven't felt run-for-the-bathroom bad since I got them, so I don't know how much they'll help if it's really bad.

Peppermint is supposed to be good for settling the stomach also.

Elite Member

Date Joined Apr 2005
Total Posts : 14995
   Posted 9/14/2007 1:31 PM (GMT -6)   
I have nausea all the time. I have to take 8 mg Zofran every morning and Phenergan everynight before bed. Mine is no longer really caused by a blockage, at least my GI doesn't think so, its more related to a mechanical problem I have since my resections. (Things move differently thru my system now)I have to make sure I eat every 2 hours or so or I can get really nauseous really quickly. I am suspecting the Pred is more than likely the culprit in your case. It does it to me too. The Ginger idea is a good one too. A old GI of mine told me about Ginger Altoids that help too. Those are recommended to pregnant women when they have morning sickness.
Been living with Crohn's Disease for 32 years.  Currently on Asacol, Prilosec 60 mg, Estrace, Prinivil, Diltiazem, Percoset prn for pain and Calcium.  Resections in 2002 and 2005.  Recently diagnosed with Fibromyalgia and doing tests to see if I have Inflammatory Arthritis or AS.

Veteran Member

Date Joined Mar 2005
Total Posts : 4305
   Posted 9/14/2007 2:15 PM (GMT -6)   
I have been dealing with nausea for a long time now.I take phenergan for about for years now and I don't know what I would have done if it had not been for it.I have now been up graded I now have crohns in my stoamach (sp)this is why I have been throwing up so much.But even way befor I was told I have in my stomach I had nausea all of the time and out of know where I would throw up with no warning what's so ever.I also have Gerd and that does not help either.

Veteran Member

Date Joined May 2007
Total Posts : 1284
   Posted 9/14/2007 2:21 PM (GMT -6)   
That's funny... I remember when I was having nausea all the time, the doctors thought it was unusual for someone with Crohn's disease... //@.@\\'... *I don't get as nauseous anymore... since I've eliminated milk products from my diet...*
I think I am being picked on by life, sometimes. But's that okay. Life and I are good buddies... I know life doesn't mean no harm. It just is the way it is. I can accept that.

Veteran Member

Date Joined Sep 2006
Total Posts : 2527
   Posted 9/14/2007 7:58 PM (GMT -6)   
Since my surgeries this year I feel nauseaus a lot. After my ostomy I had abscesses in my abdomen that when they went in for the reversal they actually had to scrape my abd walls down to rid it of the infection. Since my reversal I have vomited 2 times once was within a month post op the other was this morning.

After my ostomy Sx I was nauseous a lot but I actually didnt vomit until one day a banana I ate didnt agree, that was in april the week of the 21st. Today I ate a banana for the first time since then....granted I vomited many times between the 2 incidents ...but I vomited again , no visable banana but makes me want to turn those on my table into banana bread instead. They use to cause heartburn in me prior to having my gall bladder removed in 99 but besides that they were always a safe food for me
Dx with Crohn's 1987, symptoms as early as 1984.
Temp iliostomy February 2007, reversed June 2007, Ovarian cysts, migraines, allergies (incl food allergies) , oral allergy syndrome (diff than true food allergies), Asthma, Gall Bladder removed 1999, Inguenal hernia 1987

Regular Member

Date Joined Nov 2006
Total Posts : 281
   Posted 9/14/2007 8:08 PM (GMT -6)   
I am pretty much nauseous all the time. It is so hard to deal with. On one hand you feel like you are going to puke all the time but you know that eating might potentially make things better. I'm just scared to eat because since this DD I VERY easily puke. It is so annoying. I was on a date the other night and got nauseous. Great. I had to jump out of the car and run around the side of a building to puke. When I came back my date asked if I was ok. Thank GOD his dad has CD so he totally understands!
I take phenergan when my nausea is TOTALLY out of control. Phenergan makes me really zoned out. If I take just a half of a pill it doesn't do much. If I take a whole pill I sleep for 2 days. I think I'm going to have to ask for some zofran next time I see my GI. I'm hoping that starting Remicade soon will also help with my nausea. Has anyone had success with that?

Currently 3 x per day 1000mgs Pentasa, Entocort (3mgs), Prilosec, multi vitamin, biotin, Lortab, Librax (for spasms) & VSL#3 (for probiotics) or activia yogurt.

Preparing to start Remicade because I am steroid dependent now.

Veteran Member

Date Joined Jan 2007
Total Posts : 656
   Posted 9/14/2007 10:06 PM (GMT -6)   
Hey, me, too! I'm nauseated a lot of the time, and it's kind of a relief to know that so many of you are, too. I haven't taken anything for it, but I'm reaching the point where I may want to. I really really hate the nausea.

Regular Member

Date Joined Oct 2006
Total Posts : 121
   Posted 9/18/2007 9:18 AM (GMT -6)   
I have trouble with the nausea, too. I try ignore it as much as possible and then sip on COLD peppermint water (Metromint) to help it if it's really bad. My doctor gave me metoclopramide to help it, but I don't like the way it makes me feel. Hope you feel better!
DX W/AS 1996

DX of CD 8/2006

Taking: Pentasa (1 Gram 4 x Day), Humira (1 Shot Every Other Week), Entocort EC (6 mg), Ultram and hydrocodone as needed for Pain, Advair for Asthma, Synthroid for Hypothyroidism, Metoclopramide as Needed for GP and Nausea, Forvia (2 X Day), Calcium (1200 mg) W/ D Each Day, Milk Thistle (1000 mg daily for liver support), Ambien as needed,

Elite Member

Date Joined Apr 2005
Total Posts : 14995
   Posted 9/18/2007 10:18 AM (GMT -6)   
Hey Opossumgirl, I can't take the Reglan (metoclopramide) either, makes me feel like I want to jump out of my skin. Gives me the heebie-jeebie's. Ask your doc about Zofran, it works great for the nausea, but doesn't make you loopy.
Been living with Crohn's Disease for 32 years.  Currently on Asacol, Prilosec 60 mg, Estrace, Prinivil, Diltiazem, Percoset prn for pain and Calcium.  Resections in 2002 and 2005.  Recently diagnosed with Fibromyalgia and doing tests to see if I have Inflammatory Arthritis or AS.

Regular Member

Date Joined Sep 2007
Total Posts : 160
   Posted 9/20/2007 11:01 AM (GMT -6)   
mad  the nauseas hell get shot of the kfc the pizza huts and the maccy ds tongue the smell alone makes you want to vomit.
i was prescribed domperidome but found they did not help so i went into the health shop and bought bags and bags of crystalised ginger yeah
it truly works only problem now is partner wont come near me for the smell!!!!!!!!!! better than hallitosis haha.
joking aside i thoroughly reccomend it to all crohnnies

Veteran Member

Date Joined Apr 2005
Total Posts : 3763
   Posted 9/20/2007 2:32 PM (GMT -6)   
I was almost never nauseous until about a year and a half ago, now all the time. When I said something to my GI in the city he said that nausea wasn't all that common in CDers, Ha I don't believe that. What I find strange is that my presentation of symptoms would change so drastically after almost 20 years. I still believe that they will eventually find that all of my gastritis issues were CD in the stomach that just wasn't showing on biopsy and that is why I am nauseous all the time.

As for how to deal with it, I'm at a loss. I take Zofran, Tigan both orally and suppository but sometimes none of those work and I end up worshiping the porcelain god. YUCK!

CD 19 years offically, 29 unofficially. 3 resections '93, '95 '97
Symptoms constantly but all tests show only minor ulcerations. Currently having multiple episodes of gastritis with no known cause.

Prednisone, 6MP,Prevacid, B12 shots, Bentyl, Xifaxan.....

Regular Member

Date Joined Apr 2007
Total Posts : 217
   Posted 9/20/2007 2:55 PM (GMT -6)   
I feel the most nauseous when I wake up in the morning....I kinda feel ok during the day....but the morning are horrible...I feel like I am pregnant all over again!!!!

35 yrs female, dx with crohn's on july 13th 07 increasing my  entocort 9mg . starting imuran 250 mg  pariet ,dx with depression in 2002 ,effexor tappering off, welbutrin,resperidal and lemotrogine.

Regular Member

Date Joined Feb 2004
Total Posts : 77
   Posted 9/27/2007 1:16 PM (GMT -6)   

You know when I feel the most nausaus? ( lol how DO you spell that word ) after I go #2.Whats up with that????? Anyone else??? It's like my system has to recooperate after I go,I feel bad for a little while after.THis mostly happens at night for me.


Elite Member

Date Joined Apr 2005
Total Posts : 14995
   Posted 9/27/2007 3:02 PM (GMT -6)   
Another thought is maybe the Protonix isn't working as well for you anymore. I had it quit working for me and had to change to another Proton Pump Inhibitor and things improved. Just a thought!
Been living with Crohn's Disease for 32 years.  Currently on Asacol, Prilosec 60 mg, Estrace, Prinivil, Diltiazem, Percoset prn for pain and Calcium.  Resections in 2002 and 2005.  Recently diagnosed with Fibromyalgia and doing tests to see if I have Inflammatory Arthritis or AS.

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