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May 22, 2012, 10:53:15 AM
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left side pain with IBS diagnosis at present  (Read 641 times)
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Hello, 

New to the site and think this is where I post for newcomers.  Here goes.  I read the undiagnosed illness webpage and felt some similarities, some differences in terms of the actual symptoms, but mostly resonated with all the pushed aside feelings and frustrations of doctors and having that rather paradoxical optimism of being told there's something wrong with you. 

Anyways, I've had bowel problems at least since I was 12, probably longer but know for sure since then because it was the first time I ever saw a doctor.  I hadn't "voided" for 2 weeks and mentioned it to mom (she was concerned).  The norm for me is actually diarrhea.  Lack of voiding is much less common now, but happens sometimes when I've been sick a while.  The diarrhea is embarassing, annoying, triggered by stress, not really related to specific foods (although sometimes specific restaurants which is weird).  No, that's not really what bothers me. 

What bothers me is the double over squeeze your eyes shut pain I get in my left side behind my ribs when I have an attack.  If I'm lucky, it will only last a few minutes, I'll be sweaty and feel very ill, then I hear and feel my stomach area gurgle and shift, have diarrhea, and feel better.  Other days I don't get diarrhea and just have random cramps in my side with alternating dull pain.  Mornings are always the worst.  I'm currently diagnosed with IBS, and I take a cholesterol medicine that induces constipation and dicyclomine for the spasm pain, but they only reduce frequency.  I still get diarrhea frequently, sometimes bloody (which my GI doctor was quick to say no big deal), and always this left side pain.  I also can feel a pea shaped something, but it doesn't really change and the pain feels more internal than that. 

I should say, I don't have debilitating pain.  I can function on a daily basis, but it will interfere with work and social life.  Going to a restaurant with friends only to leave after everyone else ate while you spent the entire time in the facilities is rather depressing.  I don't know how many times I've told my husband I want to stab myself in the stomach just to have it looked at properly.  But, I know other people have things worse. 

So, my hit and misses:
Helico bacter Ab negative
Ulcer meds no help
Colonoscopy clean
No parasites in stool
Celiac test negative
Diabetes test negative
Liver enzymes negative
Blood tests indicate cancer not likely
Probiotics don't help
*I once took this non-absorbing antibiotic and thought it helped for a few months, then got bronchitis and took broad spectrum and went back.  I tried the non-absorbing antibiotic again, but it didn't help.  I don't know if the two were so close together that the first time ever truly worked. 

I'm tempted to try other theories: nutcracker syndrome, hiatal hernia, weird allergy to common forms of yeast (yeah, even I think that one's a stretch), but mostly I've been dealing with this for 16 years now and don't know what I do and don't want to try anymore.  I've moved several times, so sticking with one doctor hasn't been an option.  Transferring medical records is a nightmare and some doctors take one look at a 60 page file and say they don't see anything in there of interest (or are probably just skipping it all together).  Maybe I just need to switch doctors, but that's just depressing as well.  (SIGHHHHH) 

It's nice to hear other people feeling similar frustrations that I'm not alone, not to say for all of your sake I wish I were :)   

Anyways, thank you for posting this site.


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I Will Be Diagnosed !


 welcome to the forum

I can very much relate to your comment
"I don't know how many times I've told my husband I want to stab myself in the stomach just to have it looked at properly."
I said almost the same thing to my partner Sad

I can relate to some of your symptoms too  Sad. Despite testing negative to Celiac I actually suffer if I eat gluten but have only realised this over the past 6 months or so. Im trying hard to stick with gluten free because it has a huge impact on my bowels and also skin rashes etc. Just a thought maybe cut back on certain foods even though you tested negative.

I hope you find some answers Im still waiting for a diagnosis too almost 7 years now
 Huge Hug


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It's at least worth a shot.  I just picked up a couple of gluten-free foods to try out for a few weeks.  I've had a rough few days, so ANY improvement will really be worth it!  I also picked up some generic "one a days women's" vitamins so that I don't get mixed signals from any deficiencies a change in diet might bring.  If I don't see any change before Christmas, I might try to cut out one of the other common food allergens systematically (soy, milk, etc.).  I'm glad P.F. Chang's has a gluten-free menu so that I can go out for my birthday without much worries of what I can/cannot eat. 

Anyways, thanks and happy holidays!
Lindsay 


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I have a very similar case.  Left side, right under rib cage.  I also have a pea sized bump there, but as you know the pain is intense!  I also have the episodes like you described - get sweaty, feel like you are gonna die, your stomach makes these amazing noises, you stumble to the bathroom, you go & it's over.  I have other symptoms too that no one dr has been willing to put together.  I've even had a bowel ressection so I piece of my jejunum could be removed.  The tests showed nerve damage but from an unknown cause.  My theory is that the same virus that causes Gatroparisis is responsible for some of the nonsense a lot of us go through that is dubbed IBS.  It gives me hope to see I'm not the only one out there. 


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wow, your symptoms sound so like mine it's scary. Check out my post on polychondritis/Behcet's syndrome. Do you have mouth ulcers - you say something about ulcer meds not working for you. It might be worth reading up on the symptoms. Like I say in my post almost always overlooked....many docs have never heard of it. My symptoms are definitely worse at night or in the morning. This is common as inflammation is worse at night. Hope the description of my illness may help you and give you some insight into what might be going on. It took me a very long time to get a diagnosis and I know what it's like to go through that unidentified illness struggle. It's a syndrome in itself and I'm very glad to see this site because hopefully it can bring some things into focus for sufferers.

Problem with something like Behcet's is it's so under the radar and a lot of medics don't know anything about it or have misconceptions about who can get it. I'm not sure whether or not you have it - obviously I can't make any diagnosis but I think that you certainly seem to show some of the common symptoms. Have a read up about it. good luck Margaret


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The trouble with alot of our symptoms is they match alot of "Diseases" but getting a diagnosis and treatment is so hard.  aggressive


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Agreed - I have symptoms across the board as well.  I've been told everything from "it's in your head" to "it's your menstral cycle" to "sounds like carcinoid".  I've had soooo many tests that come out "normal" yet I have these issues. 

The main "problem" that has been found is that most of my jejunum is "thickened".  It causes my food to back up sometimes (ER calls is a psuedo-obstruction) & incredible pain.  The pain is ongoing.  A piece of my jejunum was sent to several labs that had no clue.  Johns Hopkins came back with a report saying they could see nerve damage but the cause was unknown.  They hypothesized that I had a virus at some point that caused the "damage".  This has been causing me issues since I was 19 but the last 5 years have been the worst. 

I think this mystery virus is the same mystery virus that causes gastroparesis.  The connection between the vagus nerve is another link to that, in my mind.  When I've had those episodes in the past where I've almost passed out, make my way to bathroom (usually at this point I start losing my vision, cold sweat, etc.), sit on the pot & have a bowel movement & POOF - I feel better, yet exhausted.  I also have waves of nausea everyday & my left side always hurts. 


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