I have been having pain in my right side, middle chest area and it radiates to my left and middle of my back. This has been going on for a year or better. I have had so many tests. I have
MitralMitral regurgitation - chronic
Mitral stenosis
Mitral valve prolapse Valve Prolapse also, I have been to the hospital on two occasions because of chest pain. I have been diagnosed with diverticulitis also. But this pain will not cease and desist. I just recently had an EGD and a Gall Bladder scan. The EGD was
normalNormal saline flush and when they called on the Gall Bladder scan, they referred to it as basically
normalNormal saline flush. I would like to know how precise the scan is in detecting abnormalities in the Gall Bladder and if there is an additional test that can be done to determine if the pain that I am experiencing is due to a bad Gall Bladder. I cannot in my logical mind just say, "Okay the test prove nothing so there is nothing wrong." There is pain and severe at most times, where it radiates across my chest to the left and the middle of my back. I just want to know what is wrong and have it taken care of. Is that so much to ask. Any help would be appreciated at this time.
Thank you.
~Ellen~
I know exactly what you are saying. I have the same set of symptoms and all the tests are negative also. They went in with a laparoscope last fall and found a bleeding ovarian cyst and removed it. I improved for a couple of months and then it was back. They went in again and found more cysts, took the ovaries out. Now, here we are (since February), I have daily discomfort under my right rib also. The past month and a half it has gone into chest pain and radiates up into the shoulder and back. He is planning an ERCP for two weeks.
Have you had several bowel movements a day? Is yours aggravated by activity. Can you wear a waistband around your middle or panty hose? I can't stand my jeans and haven't been able to for a long time.
Well thanx for listening. Hope you are feeling better.
~Ellen~
I also have had a hysterectomy in 1995 and the ovaries last year. Do you take estrogen? Have they done an ERCP on you? Have they tested the sphincter of Oddi? Are you seeing a gastroenterologist? Have they done an ERCP? You can e-mail me and we can talk more privately: ***@****-net.com
Tracie
I have been having uper abd pain since May of this year. I have posted a question- Upper LEFT abd pain. I am just writing a reply because I am sharing in your frustration! I am part of that medical profession. I am an RN in an ICU. Even having access to so many physicians doesn't help. No one is willing to listen and just say well maybe you should do this or that.
Anyway, I can't believe the number of people who post that have unexplained abd. pain. On one hand it makes me feel better but on the other hand it is very discouraging(sp). I am going for a second opinion with a GI specialist on Nov. 1st. I made that appointment back in Sept. I think that is pretty ridiculous too! At first I had great hopes of finding the problem with this MD but now I'm not so sure.
Please let me know if either of you find out anything more about what is going on with you and I will do the same.
Elizabeth
Have you ever heard of the use of Nitroglycerine for suspected gallbladder disorders? My doctor gave this to me. I get some relief from it for an hour or two. I do wonder about sphincter of oddi dysfunction too.
Tracie
Thanks,
Elizabeth
I really think he is giving me the nitro to cover two of his areas of thoughts of what is going on. I think he feels it may be sphincter of oddi dysfunction or else calculi in the biliary ducts. The nitro opens up the ducts through the whole body and for some strange reason it gives me relief. That tells me that it probably is not the gallbladder itself. All of my tests on the GB have been normal. I read further in the archives of this forum on the sphincter of oddi and the symptoms described there are exactly what I have going on. (That helps me so much to know I am not CRAZY!).
I too was having the same pain. Still am actually. Finally I went in for a CCK Hida Scan. This test is specifically for the gallbladdder - done in Feb.99. Came back fairly normal. Then 2 wks ago I had another one done due to the pains coming back badly. The repeated Hida Scan showed that now my gallbladder's ejection factor(which is what they measure) went from 30% to 12%! It should be at 35%. Which is why the doc questioned whether or not it was gallbladder after the first scan. Well, it is and it is coming out!!
So, what I am trying to say is keep on the doc about the pain. I DO NOT have gallstones. So, dont let them tell you because all these tests show NO stones that it is not your gallbladder. I am living proof it is.
The pain I have goes from rt upper back, rt shoulder, rt upper quandrant (under ribs), lft shoulder and back and mid line stomach. So, just keep after the doc!
Just by the by, I have read that once the gallbladder is removed and they do a pathology on it, gallstones are usually found. It is just they were too small to be detected by any of the tests.
Good Luck!
Is there more than one kind of Hida Scan? I am not sure if they looked at the ejection thing on mine. Is a CCK a certain type? I don't know if they know how much mine emptied. They said it filled and emptied fine, not how much. It was quite large on the scan. (?????????) Can distention stretch it out?
We are a mystery. Thanks for your input. More to think about. Will be curious to see if this does indeed take care of your pain. God Bless You!
The CCK component in the hida scan I had, is a hormone your own body makes. It is directly linked to the gallbladder and liver.
If you have had a hida scan and were told it filled/emptied fine, then you may have a problem other than gallbladder.
From what I was told, the CCK hida scan, is pretty much the final diagnostic tool for checking gallbladder disease.
Good luck to you.
Phyllis
I have been experiencing a pain in my right side, beneath my rib cage for about 18 months. It is not a constant thing but stress seems to aggrevate it. Sometimes it is like a sharp knife in my side and I can't even manage to take a normal breath for about 5 minutes. I have been tested for hepatitis (every kind), mono and have had a liver biopsy. After the liver biopsy the doctor said that I had a fatty liver and to lose twenty pounds and it would go away. I lost 40 pounds and I still have the problem. I hate to go back to the doctors because they act like I am a hypochondriac or something. I also have elevated liver counts, has this been a problem for you?
My blood counts and serum amylase and everything is normal so far. Nothing, I mean nothing, is out of the ordinary. I am not overweight either. You didn't mention your gallbladder. Is it okay too?
I went to Mayo Clinic in Scotsdale and spend 15 days on test. The doctors said all test were ok but I was feeling terrable. I coudn,t eat and have a lot of nausea.
Well, at last do you know what I had ??
* Superior mesenteric artery syndrome *
Tell your doctor to check this on you.
Hope to be help you on some, and also hope that you don,t have this syndrome. Carmen.
I went to Mayo Clinic in Scotsdale and spend 15 days on test. The doctors said all test were ok but I was feeling terrable. I coudn,t eat and have a lot of nausea.
Well, at last do you know what I had ??
* Superior mesenteric artery syndrome *
Tell your doctor to check this on you.
Hope to be help you on some, and also hope that you don,t have this syndrome. Carmen.
I am now 48 year old and this problems starts when I was 23. Please, ask your doctor about this Syndrome or look it on internet to see if this is your case. It is a very rare case, but it happens. Carmen.
Were you always so sick that you didn't eat or did it get progressively worse over time. Did you refer yourself to Mayo Clinic or did your doctors send you. How do you know when to give up and quit after the tests are all negative? Was it ever just a dull, constant aching? What did they do to help you?
After all the negative tests, today I had results with my ERCP. They found stones in the gallbladder that for some reason wouldn't show on anything else. I hope and pray that when they remove it the pain is finished.
I am so glad they found results with your ERCP! No problems after the procedure? I ended up with pancreatitis after mine. What is your next step then? Will you be having your gall bladder out? Nothing has shown up that points to gall stones or gall bladder problems. I am going to a new gastroenterologist on Monday. I hope he can help me.
Take care,
Elizabeth
Again, I am so glad for you, let us know how things go for you. Good luck and God Bless.
~Ellen~ :)
I also have same basic pain as everybody on this forum. Mine started 1 day after I worked out with weights, I hadn't worked out in over a year and I pushed myself way to hard. When 2 weeks went by with no improvnment, I started getting worried. Went to doc he examined me and ordered bloodwork, urinalysis and wanted me to go for a sonogram of abdomen. My pain is dull and constant in the URQ, sometimes it feels worse (more sharp) right under my ribs on the right side, close to the center. But the dull pain is there always. Blood and urine came back ok but I was petrified to go for scan. Three days ago,(this has been going on for 2 months I got up some courage and went to the E.R. I didn't tell the er doc that I saw a doctor previosly. He also ordered blood, urine and sonogram of URQ. Gallstones were found (many) also he thinks rectus muscle may be torn. Like other women on this forum, I didn't think it was my gallbladder because I dont have severe pain and it doesn't seem to be related to food. Sometimes its so vague that until I think about it I dont recognize it. For the record I'am 37 yr. old white female that doesn't drink but was on pain meds (vicodan) for many yrs. for an unrelated injury. One more thing I was very relieved to know that there are other women out there like me, not that I want any of us to be sick. This is going to sound crazy but when the doc told me I have gallstones, I was almost happy, do you know what I mean?
I am writing this to you from Australia.
I have had almost the same problem as you. Though I had my Gall Bladder removed about three years ago.
this problem had had me spent the 3 weeks of last month in hospital. Prior to that since june 99 when this all flaired up. I was spending about 4/5 days in hospital just seeking pain relief.
I have had all thetests: Catscan,gstrography,colonoscphy,utrasounds,xrays.
There have shown that there is no evidence of irritable bowel, and that there are no stons not sludge in the bile duct.
my liver funtion tests we abnormal only on the first attack in june, but not since then, I have now been placed in the Chroinic pain catorgery, not that that make me happy.
My GP must now apply to the Director General so that I can continue to recieve the narcotics that I need to keep the pain manageable.
I am on patches at the moment to try to keep me out of hospital.
the next step is a Biliory Mamnometry (I think that is how it is spelt). This is where they measure the pressure of the sphinter of oddi t(that is the one at the bottom of your bile duct). they THINK that it could be disfunctioning.
so can feel all that you are going through. may be request a mamnometry with your GP
Take Care
Suzanne
I just wanted to let you know that I had my second opinion visit yesterday. I am much happier with this MD then the last. The bad part is that he thinks my problem is chronic pancteatitis. He isn't ready to 'label' me with it yet. I have to go for an MRI and MRCP and then he wants me to have some blood work done. I am glad that he is leaning toward a diagnosis this time. I am also glad that he isn't planning anything like another ERCP or the sphincter manometry. On the other hand, chronic pancreatitis isn't the best news either. He also put me on large doses of pancreatic enzymes with each meal and wants me to take two tylenol every 6 hours around the clock. I say tylenol? I don't think that will do anything but I am willing to try.
How is everyone else doing? Keep me updated if anyone has anything to share.
Elizabeth
but I still had to be put on Pain medication as I have been dealing with chronic pancreatitis for years. I do hope the enzymes will work for you as they can increase how many you take with your meals. Have they told you to take them with a snack in between meals? This is what they have suggested for me.
I hope everyone of you are feeling better.
Since the surgery I have continued to have the pain. I have had a CT-Scan on the Abdominal Area to Pelvis, Cystoscopy with x-ray of the kidneys, EKG, MRI-Brain Scan for headhaches, x-ray of the small intestines, Liver Function Test, Chem 7 test, and a MRCP to check the bilary tree for stones. All these test came back negative.
I experience nausea and dull pain in my URQ and middle back constantly. Headhaches come and go. I am at the end of my rope and do not know what to do. Does anyone out there have some suggestions or ideas. I do not drink, I am 34 years of age, male, and not overwieght.
Thanks,
Sam
I've been sick for 9 monthes: heartburn,weight loss, some reflux, nausau every morning....but the worst is the chronic pain in my URQ. Have had way too many tests: ultrasounds, x-rays, scans: nothing showed anything until I had a HID-A-SCAN that showed my gallbladder was not working. The normal score should be 35, mine was a 9. I was so excited to find this out. Planned to have my gallbladder out and then be fine !!! Well, had it out 2 weeks ago and feel exactly the same. Now the doctor thinks it could possible be the sphincter of the oddi and I'm awaiting an appt with a doctor to perform a test for this. Does anyone have any information about this ? I am at my wits end. My quality of life stinks as I know most of yours do, too.
Also, they found no stones at all in my gallbladder, although they said it was inflamed and had scar tissue. What would cause this ? A problem with the sphincter of oddi ? I'm wondering if all my symptoms point to one problem, or are more things wrong ?
Any information is truly appreciated.
Out of curiosity, how did they treat your pancreatitis?
I hope you get better really soon, what are the symptoms of pancreatitis? I hope they find out your problem soon.
Take care.
Ellen :)
I just wanted to answer some questions I've seen. An ERCP is a test where they put a scope down past your stomache into the duodenum. Then they visualize the duct from your pancreas to the small intestine by injecting dye into it. This way they can tell if there is an obstruction...usually a stone from the gall bladder. Unfortunately just by manipulating the pancreas one can get pancreatitis from the procedure. I was one of those people. The test itself was negative but I ended up in the hospital for 5 days. After I was out of the hospital they really didn't 'treat' me with anything. My MD was at a total loss as to what caused my original pain which returned as soon as my pancreatitis pain resolved. I was lucky in that the pancreatitis that was due to the ERCP resolved quickly. Still and all I was out of work for 3 weeks.
Tracie, I hope you are feeling better. When did you first realize that something was wrong? You went home after your ERCP, right? Did you end up admitted through the ER?
Fran, I am taking the enzymes with snacks also but I find that I am just not eating because I HATE taking pills. I know that I really shouldn't complain but i just hate it. I will however, admit that it is helping. The pain is still there but at least I can stand it.
Take care everyone....
Elizabeth
Whomever would like to talk about this, you can reach me at ***@****
I work for a large gastroenterology practice and we see quite a few people who seem to present w/symptoms of gallbladder distress however after the usual processes return w/normal; work-up, ie. u/s, hida scan, ct scan neg for gallbladder stones etc...the next step would be to evaluate for a motility problem such as gastroparesis. This diagnosis would leave you feeling pain under your rib cage right side (b/c this is where your stomach is located), a feeling of fullness after eating (even a small meal), nausea, etc. A solid phase gastric emptying study could rule this out. Good luck.
Well since my last posting I have been in Hospital yet again, This is now to me beyond a joke, as I work full time ,and I have spent 2 months of the last 6 months in hospital. The stress levels not only on myself but on my partner are beginging to show as he only wants to here if I am pain free, which I have not been since the begining of SEPTEMBER. My Last visit to hospital resulted in a Pethadine fit (gee that was interesting), so I am on a diffrent opiate, which seems to be the only way to control the pain, oh yes I am now considered a CHRONIC PAIN sufferer.
I went to see a Associate Professor, who specialises in a condition known as sphinter of odddi disfunction, and I can say that is what I have. I can at least put a name to it.
I have a small problem though, because I have had the previous sphintorotomies, trying to find a surgon to preform an other is a bit like finding teeth in a chook, damm near impossible.
So I stand at the 15th dec 99 traveling over 150km to have a BILLIARY Menometry, from there I am either going to have the Slash down my tummy and be inhospital for the next 6 weeks or I will go home.
The doctors have given me a 50/50 chance that there will be
A)no problem from the menometry
B)that further nicks to the sphinter will solve the problem.
so those are my chances. I'd like to know how GP's are treating you over there once they consider you are suffering from chronic pain??
I am trying to cope with out the opiates, and with out any of the stronger pain killes as the contraindications are really really frightening, the other thing is that all the opiates also can cause the spasm of the sphinter of oddi, so I guess that I am back to square one.
I have tried the alternate medicine and threw up for 2 days straight,resulting in a lot of maxalon being thrown down my mouth,and ingected into to feew spots left on my body that are not alrady bruised, from previous injections.
hope to be able to get some feed back
What is Sphincter of Oddi, Jane is that what you
do have, I know you wrote that is what the doctors
would be checking for. Suzanne,2 questions, why
are the doctors skeptical about a second treat-
ment if I understand your post correctly. Also what
are the condradictions of opiods? Did either of you
have pain in URQ which is like a dull pain most of
the time? The doctors still have not given me a
diagnosis. Even though the scan did find gallstones
they say I would have sharp pain that was more like
a heartattack, but they will not say my pain is not
do to a bad gallbladder. I really hope we all pull
through these bad times. P.S. the reason I asked about
the pain meds is because I'am currently and have been
taking them prior to this problem for something un
related. So I dont know if I'am excasberating the
problem. I wish you all the best. Please respond.
The sphincter of oddi is the valve around the bile duct and duodenum. It is supposed to open in response to a meal to let the digestive juices through to the duodenum for digestion. Evidently when the sphincter is too tight, there is a backup of bile, which can lead to pain. It can also lead to jaundice, pancreatitis and abnormal liver function tests, from what I understand.
I saw a new gastroenterologist (I like this one !!!) on Thursday. Supposedly he's the top dog around here. Anyway, he doesn't really think I have a sphincter dysfunction. He said I would be throwing up, which I have never done. He feels my URQ pain is most likely a cartiledge imflammation. He gave me some Celebrex pills, and said if nothing changes in 4 or 5 days, he will consider giving me some kind of shot in that area. I forgot what the shot will be. Anyway this sort of makes some sense to me. I was pretty violently sick in Feb. of this past year, and that's when the pain started. If that doesn't do the trick, he said he would then consider gastroparesis, although he said with that dysfunction a person would feel EXTREMELY full after a few bites of food.
So, I guess I'll just wait and see if these drugs work. He also told me to take Prevacid. I did last night and today is the first day that I can remember that I woke up NOT nauseus. So, maybe I do have reflux too. At the very least I have too much stomach acid.
I hope I answered your questions about oddi. Good luck. Let me know how you feel.
And if anyone has had cartiledge imflammation, please let me know how things worked out.
Don't ever feel like you're going crazy. Your pain is real! I doubted myself after being in the hospital for 5 days with pancreatitis after an ERCP. It is an awful feeling to doubt yourself. Don't give up looking for an answer! Switch MD's if you have to. I did and I am so glad!!!
Take care,
Elizabeth
Courtney
They are not sceptical but rather worried doing the 3rd proccedure via an ECRP, as there is a great risk that they will pierce the douremum, this is potentially life threating. there is also a chance that they will do this during the menometry. apparently they give me a odds on bet, 50/50 that this will happen during any of the proccedures. Also that this will solve my problem
The contridictions of the opiods are the side effects, and the things that you cannot mix,here in Australia we have access to a book called MIMS which lists all the drugs avalible on the market here and their potential side effects. Reading up on all the drugs that I am on has just scared the DOO DOO out of me.
The pain for me is like a clamp that is fixed on my body from my right side rib cage to my back,it some times feels like it will hurt to breath, sort of like when you have run a lot, but it does not.On its bad days,it feels like some one is squeezing tighter and tighter, on its good days it is a nagging ache.
I have, since being out of hospital tried to cope with out the opioids but that has not been successful , so I am on the patches all the time.
My Gall Bladder was removed 3 years ago, your doctor is right when you have an attack of BILLIARY COLIC, the pain will be so intence and unlike any thing that you have ever suffered before.You will belive that you are having a heart attack trust me on this one.
The joy of all of this is if they slip I will be in Hospital for 6 weeks rather than overnight, so in there for Christmas, which I suppose is not a bad thing as I will atleast be in
airconditioning, as it gets real hot over here in December.
Jane
Tell your doctor he is talking through his nose.
Since june of this year I have not once thrown up because of this dysfunction, rather from the opiods that I have been given for the pain.My Gastro at first did not belive that I had SOD as my liver function tests were as close to perfect as can be. But I think that he has changed his tune now. The thing of feeling full after a few bites of food, gee I wonder how I got up to 80kgs in hospital if all I could have was a few bites of food.
I have been through the shot in the area and it was a local anasetic, did not work for me. also tried a test to see if the pain was nerve pain, where they give you 3 injections, in no particular order one is saline, one is fentonal, the other I forget. to see if there is any change in the pain. Well I Flunked that one too.
The only way that the dysfunction can be totalt rules out is when a memnometry is done.
I wish you luck.
Pat
You sound a lot like what I have gone through,good god if your sphinter had closed off then you are really a candidate for SOD
has you Gastro performed any sphinterotimies? (where the duct is nicked) if not why not.
Stress has not a drop in the Pacific to do with it. If it is SOD there are no triggers, not food , not stress, not sex, not anything. Tell your doctor to wake up smell the short black, then drink it.
Has the irritable bowl been dragged out yet, that is always a good convenient answer to any unexplainable pain.
Do not belive every thing that you are told, ask them to justify their diagnosis. Watch them stammer and stutter.
Keep on trying
take care everyone
Suzanne
My primary doctor (I have that awful kind of insurance where I need to ask her for permission every time I want to go see someone else) says she has nothing else to offer me but the shot of lanacane in my ribs. She says I've had the best people look at me and they cannot find anything to be causing the URQ pain.
I have been on Celebrex for 7 days now, with not much relief.
Write me back here or you can mail privately to me at champagne.***@****. Thanks, Jane
and IBS. I have had a pain under my lower right
rib cage and around my lower right ovary area.
The pain is further complicated due to a
pinched disk in my lower back found when I was
admitted to the hospital for four days of tests
recurrence of these problems has gone on for
one year last october and finally got to the
point I couldn't handle anymore. I also had a
Colonoscopy-camera inserted up to see inside of
intestines and was diagnosed with the
Diverticulosis. I currently still have the
problems of constipation and then the attacks
of the Diver. It has been a nightmare that no
one seems to be able to understand. i still do
not understand why my intestine paines are on
the right side vs the left. I also had tests
for my liver, gall bladder etc etc-they are
normal. I am on medication twice a day at
present, very high fiber diet, exercise for my
back one hr a day and walk 30mins which is two
miles each day. I cannot sit for more than 20 r
30 mins at a time due to my back and haveto
wear tennis shoes all the time. If my back is
bad it starts the stomach problems, if my
stomach acts up-my back goes which also effects
my right knee, ankle and foot due to the siatic (sciatic)
nerve. I am 50 I have had to resign three jobs
due to the events of this past year. I cannot
sit at a desk, work a computer etc. Good luck
to all of you-Please advise if my pains on
right are shared by anyone vs the normal left
side with these problems. Is this unusual?
May God touch each and every one of you with His healing hand.
Yep that’s right I’m off for another visit, though I feel that I know the health system fairly well by now. My mother god love her has sent me down a tapestry to keep me busy.
The symptoms that I have are :
Pain in the upper right quadrant, this pin feels like as if I am having an attack of Billiary Colic.
The pain is pretty constant most of the time. It well on a bad day be a level 5/10 then it will wave to 6/10 back to 5 ½ /10 ., then 7/10 back to 6/10 etc.
My liver function test has been normal. (this is apparently a dead give away to the condition)
My potassium level has some times been very low.
Previous sphinterotimies have solved the problem for 3 years. (where they nick the oddi sphincter) though this has now put me in the position I now face.
So yes I have been diagnosed with SOD, aside from the fact that that I have not displayed the classic signs of this dysfunction except for the on going pain in my URQ, that cannot be associated with my gall bladder. (ain’t got one no more so try again doc) or with the muscles in the area as the test with the pain team proved negative. I have had every ultrasound xray and ECRP that they can throw at me. I do not have stones/sludge in the bile duct, nor in the kidney. The flip side to this is that I am now a chronic pain sufferer, and I now wear narcotic patched 24 hours a day. The patches are under the name of dorogesic or fentonal. They use them here for cancer patients to help with the pain, apparently over there in the US you can get them as 25 to 75 microgram patches , with the added bonus of 12microgram lollies for break through pain. We cannot get the 12 microgram here in Australia yet. They also have me on Trammal. Again this is a narcotic but a synthetic one, this I use for the breakthrough pain.
We don’t have the same sort of insurance problems that you guys do as it is totally voluntary to be a member, and you get to pick who your doctor is, and I am so lucky that I have the Gastro. From heaven and also the GP from heaven. Nothing is really too much bother for either of them. They go into bat for me when I have problems with A&E. We are headed for a health system like yours but it looks like there is a big fight to reject it. Though I have to admit the public health system here is in a lot of trouble. Interns who work 20 hour days, nurses on strike., not enough pillows for the beds sheets with holes in them, the list goes on. Though you would bet that if a politician ever presented they would have it all at their finger tips. Still that is life I suppose, and that is why I pay into private health insurance.
I have been like this since June of this year, and this first attack was the only time that my liver function tests showed that they were abnormal.
Apparently some of the other give always to the condition are poor circulation, well I’ve already had to have veins stripped from my legs, and I have not had any children. Get around me in winter and I am blue in my extremities.
Has you doctor looked at a condition called Loin Pain Hematura I think that is the spelling for it. This also creates pain in the URQ , they though I had that possibly, as I when I presented to A&E I had blood show in my urine samples. But apparently my kidneys are not enlarged, so they ruled that one out.
When I had my gastroscphy my Gastro found that my esophagus was enflamed., but could not explain it, I meet a girl who was in hospital this last time who had the classic signs of SOD. And she was in this time with ulcers on the bottom of her esophagus. I found that quite interesting.
I estimate I am about 18months behind her, in treatment at the moment.
So at the moment I await the memnometry, with all of it’s associated risks. But I figure anything to stop the pain right now would be a real good thing.
Good luck with this
Take care
Suzanne
ps tried your e mail did not work probably my system
I have to say that i have not had those problems, just the pain in the URQ. What you have discribed with the bowel problems, sounds like, irritable bowel syndrome, and in spite if what every one is told, a high fiber diet does not make a scrap of diffrence to the condition. I am 34 years of age, I have lost weight but not fast.I was never considered obese, but at my worst I was 20kg's over. I am currently about 10kg's over.
This week is shaping up to be a bad one as I am fighting nausea 24hours a day, and I always seem to be very very tired. This I put down to the narcotics I am on to control the pain. I am fortunate that I have no children. But the stress of all of this is telling on my husband. Though what can one do? I suppose that one does as one can to resolve the situation.
good luck Kris
Suzanne
Thank you for being such a source of comfort and encouragement to many on this forum. I am going to do more research on SOD and search for another doctor in my insurance coverage area. I continue to keep all of us in my thoughts and prayers.
Cher-- What kind of tumor does your mom have? My e-mail is ***@**** Anyone else who has questions about this, or any information for me please e-mail me. Thanks Sandy
I never drank or smoked.I have had my blood tested 4 times and it come up adnormal. I have a appointment with a gastrolis Dec.3. Hope he has a answer. I have been out of work since April with legs.( to do with a blood condition ). I don't sleep good at night. Feel worn out all the time. I don't talk to friends because I feel thay don't want to hear it any more and that it in my head. I have had all the test you can think of. If you have an answer for me please let me know. you can e-mail me at ***@**** Thanks Elinor
P.S. Don't mined my spelling I'am not good with it.
I am so glad I found this site and after reading all your comments I now don't feel like I am going crazy. I too have URQ pain going on 8 years. I finally had a CCK test done and my doc said it was normal. He said it was probably stress HA!!
The pain I feel is very real and seems to get worse when I am very tired or feeling under the weather. It is a dull ache in a particular spot just below my rib cage exactly where my gallbladder is. Sometimes it is very intense and sometimes just a dull nagging pain. Sometimes it goes away for days but it always returns. I don't know where to turn for answers. Please lend me your thoughts. I often think my liver will fail and have a beautiful 2 year old daughter I want to see grow up. I wish there was someone out there that could figure this out so I could get on with a "normal" life. I am 37 years old and only feel it will get worse as I age. Other than this I have been in perfect health my entire life. I am a social drinker but don't think this is exasurbating my condition as I see no difference if I do not drink anything. There must be some type of medication available to ease the pain. I did have Mononucleosis last July that affected my liver function and enzymes. I also became jaundiced. My doctor said that is not common but is possible with mono. All my liver tests were back to normal after a few months. If anyone has any feedback I would welcome it with open arms. Oh yeah, the area where I feel the pain sometimes feels very tight like something is pulling on something inside. No doubt something is up but what could it be and why can't anyone figure it out? Thanks for listening !!!
HI
The last two weeks have been, interesting to say the least. last night I went out socially for the first time in 6 months,actually felt like it. I had a severe case of gastrointestinitis (vomiting& runny stools) for 5 days, no amount of maxalon (a drug used here to combat severe nausea) helped at all. Started to feel better finally on saturday last. I have had the Fentonyl patch off for 2weeks now, and have been coping with the Tramal.
I have now got to survive the next week without any of pain killers as I go for the Memnometry on the 15th Dec and my specialist in Sydney has advised that they will cloud the readings, gee I can tell you I'm looking forward to the next week. My husband and I have named the problem ODDI, he asks each day how Oddi is, I suppose it gives us some thing to laugh about.
I have been able to compleate a full week at work, so things are looking up.
I'll post further after the 15th
Take care
We all seem to be in the same boat or at least the same bay.
Rhonda yes I do have upper shoulder pain along w/ the URQ pain.
The surgeon does not want to operate? You sound like you are
also on a roller-coaster!!! Emily its not in your head, I have
heard that too, anti- depressants are going to relieve our pain?
Well than I'll buy stocks for it!! HAHA. Rhonda does the Hida-
scan hurt? How long does it take? Do any of you find that cafeine
aggravates your syptoms (symptoms)? What about exercise? My e-mail address
is ***@**** Please write me, anyone on this
list, maybe we can help each other. Thanx...Georgie
I still however have the URQ pain that radiates. I don't know what to tell you. Certainly having my gallbladder out cleared up alot of my problems, however I still have that pain. A GI thinks its imflamed cartiledge. Could be...I had no stones, but the gallbladder was imflamed and full of scar tissue. I'm going in to my surgeon soon for a shot of Lanacane. It's like a novacane to numb the area. Supposedly if the pain goes away, then we can be certain it's imflammation. I'm curious as to why the doctor said you have IBS. I've sometimes wondered that myself. Are you gassy at all? P.S. George, sorry to say that my hide-a-scan hurt ALOT. But it's bearable. Good health to all of you. Jane
After I had my gall bladder out to relieve pain, I too still was in pain. It still felt like my gall bladder was still there. We went the route of inflammed cartilige also but after several years and many anti-inflammatories I have just about given up. IF you find out anything about this pain, please post it. Thanks.
Stephanie
Karen
My Primary Physician tells me not to worry, it's stress, it's my imagination, see a pshycologist. I want to slap him!! I have finally seen a GI specialist out of my area. He wants to do a biliary scintography to help determine whether I have SOD. If so, He will do an ERCP and cut my sphincter of Oddi. I would like to hear from anyone who might have any thoughts on my case. I wish all of you health and answers to your problems. I know how frustrating it is to see doctor after docter only to find no answers!
Kathy
As they say in the Classics "I'm back"
first of all sorry it took so long for me to post my updated but I have just got the test results back on Tuesday 25/1/00.
Well the news is as suspected I have SOD. The next option is now the surgery and to this end i am off the see my Surgeon on the 8/2/00 to oganise that.
Christmas was ok not a lot of pain and i was abe to cope with the drugs.
The interesting thing was that during this whole time I did not show the classic signes of SOD in regard to the liver function test.
please everyone do not be afraid of your gp's or speciaists, you know what your problem is. I have to say that my specialist is a lot more sympathetic to me now.
Jane
How are you? has the pain Settled any ??
take care
Suzanne
I've been having urq for two years now and have had all the tests. I've seen a GI and a Kidney doc. Everything comes back normal. I've been on anti inflammatory meds, pain meds of all sorts. Nothing has seem to help. I see the doc every few weeks I'm am at the point of exhaustion due to the pain. I feel like noone seems to understand and that the docs don't believe me. I'd appreiciate any info you guys can give.
I guess the bottom line is that I understand what all you are going through and also I wish like you all do, that I could get a definitive answer. Please feel free to e-mail me at ***@**** if you have any thoughts or would like to discuss anything like this.
Take care & good luck,,,,,Christopher
the position of golden time of surgery from the onest of syptoms (symptoms)
Treating specialists and their studious colleagues mean well and Modern Medical Technology has saved many I'm sure. Still we appear to be proven a medical nightmare to all who dare treat us.
I have suffer twenty years of intermitent pain in the upper right quaderant of the abdomin (abdomen) not to mention the referals, diaognosis, second opinions, medications, x-rays, therapists, pyschologists and psychiatrists etc.... and everyone else who can make money out this pot of gold.
Here is my gift to you all DON'T GIVE UP!!! Quality of life may well be down but your are alive. And thank you for taking the time to share your personal experinces so we can all learn and find a cure or aleast minimise the pain swiftly together. I will post more interesting things to consider soon.
I went back to the doctor & he sent me back to the doctor who did the colin surgery. You know, I didnot even know the intestine was part of the colin. When I saw the nurse she looked up my file and said, oh yes, you are the one who had the colin surgery, I WAS SHOCKED! All I could think about was cancer of the colin and prayed to god that was not it. They did tests after tests and all came back negative, but I am still in pain, like something is pinching me in the side constantly. I am so scared, who will take care of my family, my grandchild.
If there is something wrong, I would like to catch it before it gets out of hand, but everyone is telling me my test are normal, that could not be with all this pain. But, If it is some kind of cancer, god I would like to catch it before it kills me.
I can't wear clothes on my stomach like pants, stocking,jeans. I get chest pains where they stop my breath, it feels like charlie horses in my side sometimes. One night it had me crawling on the floor like a snake the pain was so bad. Can someone please help me, give me some guidence.
Thanks for listening,
Connie.
Am I understanding right that you found out for sure it's ODDI in January and have to wait until August to fix it ??? That seems like a long time to wait. You must be so relieved, though, to finally be diagnosed. All the best to you; hope everything goes well.
I have found by trial and error that if I drink psyllium fiber once a day (yuk!), my pain subsides a bit and my stomach isn't as bloated. I did have an MRCP (mri) done a few weeks ago to look at my ducts, which of course showed everything normal. My new gastro, however, is sympathetic to my complaints and has referred me to a super-specialist gastro in Boston...about an hour away, so I'm excited about that. Did you have an MRCP done to diagnose your oddi problem ? My symptoms now are, of course the weird feeling in my URQ, constipation, bloating, some heartburn and a sore throat ! Luckily I am able to get to work and function very well most of the time. I am a bit concerned about colon cancer, though, as I've been doing too much reading on the web !!!! I'm a bit anxious about what's wrong, which may explain my inability at times to catch my breath; I gasp at times and feel like I can't get a full breath. I've been told it's anxiety. That doesn't suprise me at all ! Had a stress test done to rule out heart problems !
Anyway, it was so nice to read your posting. Glad to hear that you've finally discovered what's wrong. I REALLY hope things go well for you. Write back; I'll check in a few days.
PAT: Has your URQ pain ever gone away ? Do you have the same symptoms as me ?
29-year-old healthy, active female
ruq pain - almost 7 months now
constant ache - sometimes shooting - sometimes extreme shooting from back to front.
epsiodes of extreme pain - pain on the step, pain in abdomen when voiding. only way to relieve is to be completely still.
have been hospitalized.
weight loss - 20 lbs in one month - 5 back now.
loss of appetite
seizure/suspected tia (mini stroke)
middle finger left hand turns waxy white
noticed middle toe left foot did it last night.
hyperhidrosis - controlled with drysol.
night sweats
sleep apnea - wake up gasping for air in the night. heart racing.
hiccups daily
yes - i have the shoulder pain too. thought it must be from hockey, goalie (although i had taken some time off).
pain right hip - feels like a bruise but gets worse instead of better. had lasted a month now. at times i can't lie on that side. gp says bursitis.
hives on trunk of my body.
toothache that moved from upper molar to lower to opposite side of face and back to start, all within 45 minutes then gone.
my breasts are growing and my hair is curling. how's that for neat?
the past few days i have had a shooting pain on the left side of my head. not a headache. just sharp shooting pain, then nothing.
i've had all the same tests that are mentioned in previous postings, although no mri, hida scan or ercp (don't know that one).
would be interested in any input.
I have been searching the internet looking for an answer to my problem. Noone else seems to be able to tell me what the problem is, and I'm tired of trying to diagnose myself. I may not be a doctor, but I do know my own body and I'm too young to be going through so much pain and feeling like an old woman. I'm having right flank pain, daily. Some days are worse than others, but there isn't one day that goes by that I don't have to deal with the pain. I'm 34 and have had numerous surgeries. About 5 yrs. ago I had a hysterectomy/appendectomy with 1 ovary removed due to cervical cancer and endometriosis. Since that time, I've had 5 surgeries to remove cysts attached to my back on either side of the spinal cord, on the remaining ovary, and a vulvar tumor. The pain that I'm experiencing is on my right side, sort of "wrapped around" to the back. The ovary I have left is on the right. I keep associating the pain with that ovary. However, my GYN says that everything is normal concerning the ovary. Okay, so I go to my regular MD....after ruling out a kidney infection or gull bladder, we're now onto the bowels. Today I have an appt. with a bowel specialist. Could it be Colitis, Diverticulitis, or something that I can't come up with the lingo for since I'm not a doctor. I sound angry, I guess I am. I've been dealing with this for almost 4 1/2 yrs. now and it just progressively gets worse. The first time I noticed this pain was 2 mos. after the hysterectomy. I can't help thinking it has something to do with that surgery. I guess it could be scar tissue or lesions. I just don't know, but I've got to do something to get me through this pain until I have an answer and can have it taken care of. If anyone has any suggestions, please contact me at ***@****. Sorry to use this as a "sounding board", but it feels good to vent a little.