Egoscue Method, Physical Therapy, massage and treatment for a 'possible' ulcer helped me - also I stopped carrying a heavy purse over my right shoulder. Who knows for sure-- only God! I just praise Him for my being out of my worst pain.
..folks really should be sure to check out bodywork especially when other things are dead ends...
I could not afford much testing, and well, I don't have a whole lot of faith in conventional medicine today -- they are too specialized and looking at folks from their specialty only not the whole person. The last time I looked all my parts were all connected and when one part hurts the whole body is uncomfortable---
I personally think dehydration might be a factor with myofascial pulling on our muscles and messing with our overall structure.
Lots of considerations-- thanks again for your thoughts!
Wow, you shared a bunch of good things to consider.
BTW I am almost 60 female and into menopause 2 years.
I was at 56 on my last Vit D test- last year. But alternative doctors want folks at 70 or 80. I know it is important to ask for the 25 Hydroxy+25OH-D2 Test (Dr. Mercola has lots of good information on this on the web) I was as low as 27 in '08. I supplement and also get little bits of sunlight and like taking cod liver oil in wintertime. I would like to get my levels up!
My URQ pain got better at once with Pepcid but help wore off after a while Plus I think Pepcid and similar OTC or prescription drugs are not healthy and they can cause other problems.
I was finally helped (over 1 year) with remedies for ulcer, Egoscue Method bodywork, Chiropractor and massage visit and physical therapy.
Will talk to my "Alternative" friendly Endocrinologist- I am hypothyroid and am wondering about the thoughts you shared...
In the 90s I had blood transfusions and 6 months later was told I had Hep C. I have pain in my upper right quadrant where my liver is located. I did a year of interferon for the Hep C, cuz my liver counts started rising, the treatments were successful. I'm having the pains again so I am wondering if my Hep C is back. I will have liver function test ran in Augsust.
Somewhere below in these comments, someone posted something about Flaxseed Oil and boiling it and taking a few swigs of the stuff each day. I didn''t have the time yesterday to do that, so I bought a bottle of Flaxseed Oil Gel Caps. I took 2 caps 3 times yesterday and I already noticed a difference this morning. Dr's don't know diddly - just read these postings about how many people have had procedures that did nothing !
It is Aug of 2012 as I write this and I have now been pain free eight months from the Upper Right Quadrant pain that I had had for 1 1/2 years prior.
I am still studying my health and believe that I reacted to Nightshade Foods (some of nightshades are Potato, Eggplant, Tomatoes and Peppers). I had become a vegetarian 6 months before my pain began and I had been eating a lot of these. And I was taking a bunch of herbals that had cayenne pepper in them. I believe I developed an ulcer from the peppers and the tomatoes. I was on a protocol to heal my ulcer for about 6 months and I know that was a big healing factor, but I was also helped when I gave up gluten and when I did Egoscue body work. If you go though my posts you will see all the things I tried.
I hope my experience with this pain helps someone else. I was one of the worst pains I have ever had and I cried myself to sleep many nights.
On the plus side my health quest has yielded many great lifestyle changes and most importantly my spiritual life excelled.
Just to let the guys know - look up Epididymitis on Wiki if you ever have sore testicles combined with pain radiating into the abdomen - the vas deferens can get infected when the little check valve that is supposed to stay shut when urine passes through fails slightly - I had this happen during a hockey game - I am in my 40s and thought I either had a groin pull or hernia - it suffered for a couple years with that on again off again dull pain - turns out the only "doctor" that could figure it out was the PA at work (former military) that suggested an infection - it took the second treatment of antibiotics to cure it but it worked -
With me I decided to test eating gluten and see how that feels - I have felt URQ discomfort but so far (one a few times days apart) no way near what I had at its worst--
for me I think I had an ulcer caused by nightshades and gluten-- This is just a strange theory so I am still trying to sort it out. It was so very painful and I dealt with it 1 1/2 years. I never want to go there again, will avoid nightshades and most gluten to be careful.
Because of faith in the Lord Jesus Christ and serious study of the Word of God I am coping with life stresses so much better and my system is more alkaline (Stress is very acid to the body). And I also think that and Earthing, grounding, (going barefoot on my walks) has been healing.
Faith Alone in The Lord Jesus Christ Alone has healing for now and eternity and natural things like checking reactions to foods, getting the body into a more alkaline state and going barefoot are safe, simple and Free.
Off and on for 13 years I would episode that were not painful--that overrode my darvocetN--I would just get extreme bloating right below my ribcage. The first one happened 1996, I couldn't vomit, no diarrhea, just like something was blowing up my ribs. After hour-or so-, I broke out in extreme sweat.
And then I was fine, except little tummy distress. Six months later same thing, but of lesser endurance. Every 18-24 months I would have these episodes. I just became diabetic, but all over excellent health..on heart healthy diet, lost weight-40 lbs, etc. In 2009 I had one of these episodes and went to emergency room. I had a gallbladder attack, with possible pancreas involvement. Given antibiotics for 8 days then had laproscopy.
Test shows stone, crystals, sludge. After surgery, I had extreme diarrhea, no matter what I ate, but then at same time prior to the surgery I had had a total knee replacement...so my antibiotic level was on overload..steriods, biotics, herparin, etc. I ate some yogurt--good for gut, and went on with life..Ate anything I wanted. Also have had 3 colonscopies within 15 years..negative. I never had PAIN, vomiting, diarrhea with my gallbladder. My liver enzymes were up before, Now all
my lipids, TSH and heart readings are normal.
My paternal grandmother, father, and now me have had gallbladder problems, grandmother died from it, but back in 1945-1948, screenings,
CATs, MRI didn't exist.
I have just completed one of the most agonising weeks in my life.Like many other posters on this site, i have been plagued by URQ discomfort also accompanied by upper stomach discomfort, bloating, belching and loss of appetite.Its sad to say but at some point i began to suspect the worst.The doctors i first saw thought nothing of it and prescribed antacids.They did not work.After doing numerous blood work I got fed up and saw another doctor who referred me to an Gastro who told me that he would not comment until I had an endoscopy done.It was done.Almost everything was negative save for some slight irritation.That was a breath of fresh air thank God! I now have tonnes of medication just to deal with the symptoms.For all those undergoing the same, take heart.
The burning sensation is exactly like mine!!! Yay! Mayo says it's more than likely a chronic muscle injury due to incorrect weight-lifting movements.....I'm guessing you lift free weights to improve your upper body. Get someone to watch your technique to see if you're doing it correctly...otherwise, dunno....
I am 62..and am in the forum of indentions on my head, neurology. I too live in florida..where there are plenty of chemtrails. Here is what I found:'ve been on this forum for several months..I think we all have morgellons ...which includes Nanno Technology parasites. There are 10's of Thousands of children and adults afflicted with this new unresearched or undiscovered affiction. I have been treated this last few weeks and am getting much better. My doc doesn't have all the answers ...but a blood test with the microscope showed all the parasites. If any one has questions, I will give them information. Our doctors are not familiar with Nanno Technology parasites...they are being used to kill the real bugs, pests in corn, cotton and wheat fields...all over the world and can nest in the cotton clothing...you can breath them into your nose...they look like a piece of pepper and very very tiny. But they can bite..kind of like a tiny dart....They link together with fibers inside your body, kink of like the picture below of "new gene discoveries". They are a cross between Garden "scabies and spidersWEBS" I think they come from Chemtrails. This is an assault on Humanity, animals and mother nature...
in Florida: my story (I'm on the Indention forum in Neurology: 've been on this forum for several months..I think we all have morgellons ...which includes Nanno Technology parasites. There are 10's of Thousands of children and adults afflicted with this new unresearched or undiscovered affiction. I have been treated this last few weeks and am getting much better. My doc doesn't have all the answers ...but a blood test with the microscope showed all the parasites. If any one has questions, I will give them information. Our doctors are not familiar with Nanno Technology parasites...they are being used to kill the real bugs, pests in corn, cotton and wheat fields...all over the world and can nest in the cotton clothing...you can breath them into your nose...they look like a piece of pepper and very very tiny. But they can bite..kind of like a tiny dart....They link together with fibers inside your body, kink of like the picture below of "new gene discoveries". They are a cross between Garden "scabies and spidersWEBS" I think they come from Chemtrails. This is an assault on Humanity, animals and mother nature...
I have right side pain for past 2 years. Had my gallbladder out, still pain. Had an angiolipoma on my rib cage just about bra line right side, had that removed still pain. Came down with cdiff from antibiotic use and pain got worse. Very hard to get rid of but also prevalent in our community. Now on flagile, vancomycin taper and lots of benibiotic probiotic. When pain is better, cdiff symptoms are better. Never really gone. I've come to associate pain getting worse as cdiff coming back. Ulcerative colitis, inflammation of the colon causes pain. Feels like someone pushing on my rib from inside. Even painful to touch on outside, not as bad. Only way to know is cdiff stool test. Took doctors almost a year to do the test. Btw, acid rescuers for stomach make cdiff worse as stomach acid helps keep cdiff in check. You can get it from community or taking antibiotics, kills natural flora in colon.
I too have had under the right rib pain for several years. Sometimes it makes me nausious. The pain spreads across my mid-section under my ribs and makes me bloated. Hurts. Dr. put me on Omeprazole. I take it for about 14 days then go off. It is still tickling me though up under that right rib. Mother and her Mother had their gallbladder out. I don't have stones, but have not been tested to see how it is squirting. Guess that's my next test. Ugh!!!!
problems after gallbladder removal, I've had all the test MRi, ERCP ultra sound,Catscan , Endoscope,Barriam test, straight shot all the way down no blockage.etc. The docs find nothing, Must be scar tissue,final answer. Pain pills and home. This October will be 1 full year of extreme pain. I have Doctors bill up the yang yang, Thank GOD for Medi-care. I feel so bad using all that money from Medi-care. Pain and or pulling down from under rib cage, right side, hip to the back, sometimes I can't stand up so severe,also been to the emergency hospital they find nothing. Was planning a trip to GERMANY to visit daughter, now can't go. Its miserable.
If anyone has an answer to my problem plse call. 559-471-5301, th u
Thanks so much for sharing and all the great insights and info. you've given here. I just developed this symptom a few months ago for a week or two and now today it started again. I was tested last year and my pcp Dr. found that my calcium and vit D levels are low. He does prescribe me a prescription vit D3 off and on . when i have the vit D 3 script,I take one pill a week on the same day,so I choose sunday. I take them for about 4 to 6 wks. Then, when I'm off them for a while,I've been retested and the findings are the dame ,low vit D and calcium. My Dr. also had me buy viactiv calcium chews with vit D and k. when using those,I'm to take two a day;one in the morning and one at night,12 hrs apart,so that I get the recomended amounts of calcium with the benefit of vits D and K. I've been disabled since spring of 2003,when after having IBD since march of 1988,I kept getting worse again,but now with lower back pain,left leg sciatica, fibromyalgia, chronic fatigue immune disfunction,chronic epstein barr virus,chronic gastritis(had gastritis since I was 5 yrs old and was always constipated as a child and teen),I had untreated ADD as a 10 yr old and think I still have it, hypothyroid,nausea,migrains,multiple chemical sensitivities, low level asthma,lactose intolerance,bad bone density,going through menopause,depression,gerd and many overlapping symptoms,illnesses, medicine side effects and misc. And,my dentist says the reason my teeth are decaying ,chipping and falling out,is due to dry mouth caused by my medications. I've lost 6 teeth within the past 6 months and some fillings and parts of teeth too. One of which is my right front tooth,and the two beside those and some others. It seemed to me that everytime I'd go to the dentist,especially to have my teeth cleaned,and if when i was there my dentist didn't fix the small loose teeth,fillings and cavities right away,they's get worse. Not wanting to blame anyone,but,I've watched it up, three of the teeth I've lost,were right after I'd come home from a cleaning within a day to a week afterwards. White fillings won't stay in either. I wonder if there's more than one reason why I'm literally loosing my teeth.like those dreams you often have of your teeth falling out: mine actually are. I'm now going to have to have oral surgery in a hospital about 2 hrs away from my home,due to dentists and oral surgeons not wanting to accept my UPMC medicare advantage special needs plan and/or pa medicaid,since I'm low income and a duel eligeble patient. It's always like I'm chashing my tail,or constantly putting out fires,or trying to with all my medical problems. I'm worried about going under ,being put asleep to have all my teeth taken out,then get dentures. I didn't do well with a laproscopic gallbladder surgery in spring of 1993,when i was 33 yrs old,in Palmerton ,Pa hospital. I had complications,was in alot of pain and was in the hospital hooked up to tubes and ect. for several days,and then after a week ,I was discharged. then,to find out that there wasn't anything wrong with my gallbladder afterall! So, why on earth did they remove it then? They'd done a prior sona gram or ultrasound. They should have just closed me up,if they were in there and knew it was a healthy gallbladder. This might have been a case of unneeded surgery. I'm not sure ,if i survive the oral surgery,if and how I'll adapt to and afford comfortable dentures. I don't own a vehicle ,so i must depend on others and pay them to take me to my dr's appointments and ect. Sorry to go on and on,but I'm wondering If I'll ever be able to get out of bed,for several hrs at a time,without alot of pain and other symptoms. I need and would like to find out how to get a better "Quality of Life"../ Then,My ex and some others,are on me for having to take prescription narcotics and going to a pain management clinic. I was on tylenol since 1988 for my ibd cramps and leg pain. Dr's tell me it could have a bad effect on my liver and heart,if i take tylenol. I weaned myself off all narcotics for 4 to 6 months in spring and summer of 2011 and took OTC Aleve liquid gel caps. They did help some,but they also ended up making my upper stomach much worse too. So, when I'd gone back to a pain management center in Aug or sept. of 2011,they'd told me that Aleve is very hard on the upper stomach. So, I'm dammed if I do,and dammed if I don't. Again,so sorry to go on and on,but without going into some detail and explaining most of everything I'm dealing with every day and night,it's hard to get the total picture of me and my medical probs. Don't get me wrong,I know there are people out there much worse off than i am.And I'm very greatfull for all my blessings as well as the blessings of others. If anyone has any insights,info or comments,please feel free to post them. God Bless,Meldy
All posters, ithurts constantly and bman1973 and Jim_Dandy particularly
I am having the same symptoms for a few weeks now and it is mind blowingly annoying ...irritable pain URQ just under rib cage radiates and follows to scapular region in back, sometimes dull, sometimes sharp and more bothersome at night time. Also some indigestion and gas at times (my diet isn't all that great but I try), I am slightly overweight but no where close to obese (20 pounds left over from 2 year old), I am age 42, feels like a racket ball is under my rib at times and new the last 2 days is itching at the site URQ. I am female, a nurse and relate to the drill of test after test but I have decided to skip all that and not even see a doctor right now (not anxious for them to want to remove any of my parts or insert objects into them) and go for the raw garlic/hot tea and flaxseed gel caps. Wish me luck. If this works out maybe I will learn to quit smoking and eat even more natural and organic foods because I do believe the variety of processed foods we eat are slowly killing us all.
Have you found out any results because it sounds like what my son is having, he has every test you can imagine and nothing, The catscan reports inflamation (inflammation) and fluid in that area, but they still can not figure it out. He is 23 years old and is depressed, misreable and sleeps all the time. He is thinking the worst also. Please HELP US figure this out.
Has anyone considered that it could be chronic lyme disease. I have had the same right sided pain for months. 2 emergency visits, cat scans, hide a scans, sonograms, sec. All blood work is fine. I did go on antibiotic 2 times and felt much better, my psoriasis on my palms completely disappeared but came back 3 weeks later upon stopping the treatment. I just finished another round of antibiotic and felt great til I stopped now the pain is back and the hand is itching again which means the skin condition is returning. Everyone is puzzled. I am doing holistic treatment for lyme disease no even though I tested negative the last two tests. If anyone comes up with an answer please post ASAP. It is making me nervous. So afraid at this point that they are missing something and this bug is getting stronger against the antibiotic and will take over some day. N
I had the same problem for over a year I went and had a hida scan found out my gallbladder wasn't functioning properly. Doesn't empty properly. to fix the problem I eat less fat I did not get it removed cuz that causes you to get heavy & sometimes some people still have phantom pain after removal.
I had my spleen removed in 1980 due to being a goalkeeper on a marine/navy soccer team and rolling onto my right side to make the save. this was in 1979, the surgeon told I was lucky my spleen did NOT rupture because they found 2 severly weak spots on the spleen, Since then I have In 1980 I was totally open from sternum to 3 inches below my belly button I expected major scar tissue, since then they have had to go in 2 more times for scar tissue removal. Could this be more scar tissue given all of the tests have come back negative, they did a contrast CT and it did NOT reveal anything but on palpation the hospital doctor could feel it. I need help, any sugestions?
Have you considered bodywork? I would recommend Egosque,MELT and massage. These can eliminate pain and work to hydrate Myofascial. These helped me when I had un-diagnosed upper right quadrant pain for over a year. Health seeking came from my suffering and by the grace of God I have improved my health in many ways and have learned better how to listen to my body. No doctor or even close loved ones live with your body 24/7 and no person can solve your issue better than you can. I pray you get rid of your pain and get blessed in the process.
Fow few days I have persistent pain in the right side just below ribs, painfull on touch area about 2 inchhes in diameter close to center. 2 months ago I had CABG replacement surgery. Another problem groin hernia. Do you have an idea, what it could be
I too am suffering from these symptoms and after reading the first page of comments (many comments) I came across a post about SOD, Sphincter of Oddi. I have had my gallbladder removed in 2002 and have suffered from abdominal pain ever since. I am currently being treated for acid reflex but even that doesn't do anything for the pain under the right side of my rib area. Research symptoms of SOD and you will be surprised on how this will copy many of the issues you are dealing with. As with everything this is not the answer to all but I'm sure it is for many as it is in my opinion for myself. I am making a doctor appointment for verify and although I have been let down by our western medicine doctors for years it seems that God does answer prayers and yes he uses those he sees fit as vessels.
I am also hving right side abdomen pain for abt 1year.after went to doctor(5doctors,2 gastro,3 medicine) some found it to be gastric ulcer,one liver problem,one found IBS.blood test,amylse,syrume,LFT,CT scan,upper endoscopy,colonoscopy,ultra sound all done.But they are not confirmed what is happening to me!now i still feel the pain sometimes.So i am now on very strict diet,boil...left drinking ,meat,milk ,high protein.So all of you if you are also tired of going to doctors i ask them to make a habit of very selected diet.
I am a 53 yo Male that has had RUQ pain for 5 years! Gallbladder removed in 2010 for insufficient empting, Ultrasounds, CT all neg except for fatty Liver. All Blood work normal, I have High Cholesterol. SOD was discussed and I tried a anti-spasmatic drug that did not work. I have had colonoscopy and Upper endoscopy with some erosion in stomach probably caused by NASID. I ma getting tired of this pain. any ideas??
That is the same thing Im dealing with.....I don't have a clue whats going on ...went to hospital and they said stomach bug or food prison...but it was really bad that time ..most of the time it just feels like a really bad heart burn with pain ...feeling nausea and I have the diarrhea .......
I have been suffering with pain right under my ribs right side, all organs are fine, no infections, doctors cannot find anything wrong but now that I read your post I pressed deep right under my rib and found a tender spot.
I am going to examine this possibility closely.
I have had pain on my right side below my rib cage going for 2 years I have experienced many test but last test I had was a chemical stress test. When testing I experience no pain in my heart but the faint constant pain that I had in my right side below rib cage really was really intense and couldn't stand the pain but once the test was over my intense pain went away. Dr. didnt want to address my pain because they said it not a heart issue. But my mother had the same pain before dying and Dr.'s told her that she had blockage in her artery that goes to her kidney but my mom didnt die from that,she only had the pain there she died from pulmonary fibrosis . I have experienced that pain for 2 years. About a year ago when pain developed . I began exercising and stop eating fast food and making everything fresh at home,staying away from carbs anything that was white like breads and pasta.I Eat or drank anything with the last name berry on it. Eat papaya,mango also try to stay away from alot of sugar and sodium . I bought juices that were not concentrated plus apple cider that was all natural. I put spices in my food like turnike, ginger root,basil. I also paid for B-12 injections at a lose weight clinic for ten dollars each week for my depression. Once i did all this I lost 45lbs and the right side pain went all away. But after 6 months of loosing weight I have gone back to eating fast food every day , I have gained my weight all back plus my pain has come back as well.Could not stay away from fast food for long. Hope this makes sense or helps.
I am experiencing the same thing. I have endometriosis and had surgery. than I got sick again. I just had surgery and they found 4 tumors and 27 cists. Unfortunately this surgery didn't help I am scheduled to see a NEW doctor to do an exploratory surgery. The pain if electrifying. It comes and goes whenever. If you can tell me anything I would be so happy as well as my family and friends. The pain is totally disabling.
P.S. Been going on since October of 2013.....
I have had the same pain and symptoms ever since I had my gallbladder taken out in 1986. Have had ultra sounds, mri's, cat scans, and numerous ERCP's with stents placed in the pancreatic duct over the years. Tons of lab work and many hospitalizations. Surgery at the Mayo Clinic in 1993, which helped for awhile and then the pain & spasming started all over again. I have spastic pancreatic and liver ducts, and it is all connected to the gallbladder being removed. Have had elevated enzyme levels and had sphinterotomy and sphinteroplasty's done. What I believe I have is Sphinter of Oddi Dysfunction. Right now I am trying to find a Dr. or Clinic who has done studies on the type 111 Sphinter of Oddi Dysfunction to find a medication to control the pain and spasming besides pain meds., which I have to take now. I currently am being seen at the U. of MN. and recently heard that they had done a study on Sphinter of Oddi Dysfunction. My appt. is in July, 2014, so hope they have some other answers.
I am a 23 year old female. my pain starts in the upper right side of my stomach and wraps all the way around my right side under my arm pit and to my spine. happens a few times a week. the pain seems to last for a few hours at a time. I have tried everything. nothing seems to work. I don't like going to the ER. kinda scared its my gallbladder. both my parents had theirs out due to stones. Anyone have an idea what this could be.
I suffered what we think was a duodenal ulcer Aug 2010, I called it upper right quadrant pain. I was neg for h. pylori. Finally got the ulcer diagnosis to work on in June of 2011- so I suffered for a year before I even began to take things to heal. I began a protocol of a whole bunch of things, Took three rounds of Prilosec ( that otc drug help at once but then began to wear off after 3 rounds). Then I went gluten and nightshade free food wise, did Egosque body work and took lots of supplements DGL, L- Glutamine etc (search my former posts if you want to see more things that helped me with that pain). After 6 months from June of 2011 to the first of 2012 I was finally free of pain. And I was pretty much pain free in 2012 and until Dec of 2013. Unfortunately I began having abdominal pain again. A little different feeling this time began as a mild cramping gawing like discomfort. Maybe because it was a little different pain (more lower center abdominal pain) I did not even consider to try the ulcer protocol until 4 months later...Then I did try the same protocols but this time I was not getting better. Also this time I did test positive for h pylori but my doctor did not think that would be a cause an ulcer. It has been 6 more months now Oct 2014 and I am still having pain. Was better on a beach vacation so I've wondered about earthing (walking on the beach), was constipated then so no movements, was not eating the fiber or taking the boat load of supplements I normally do, did not have to worry about what to eat because we were eating out each day, did not have A/C but host had a wonderfully open beach house with ocean air and we had great mild weather. The Host had one other thing that I now consider a factor. He had 3 great dogs two labs one weimaraner. We loved on them and they loved on us. We had lost our little Iggy (Italian Greyhound) about the same time my pains began. He was almost 16 when we had to put him down. I think the doggies at the beach were giving me Oxytocin the feel good, love, trust, bonding hormone. I remember changing our little dogs food from grain based to meat based (Blue) dog food in 2012 and walking with him- this may have helped him feel better (he really rallied- coat and appetite came back and he loved our walks). I think this in turn helped me to heal. I am considering asking my doctors to get a prescription for Oxytocin. I found out about Oxytocin some time ago when a friend gave me an article by Dr. Jonathan V. Wright about Oxytocin helping gut pain. I would rather have a dog. Sadly at this point my husband says we will never have another dog. Hope and Pray he will reconsider for our health and physical well being. If you google 'dogs and oxytocin' you can learn more about that phenomenon.
But for some supplement helps I have found that within minutes of taking Black Seed Oil my pain is gone or greatly reduced. This is really a puzzle to me but I was also taking it while on the beach vacation because it was in the fridge and easy for me to access. I never bothered to dig out my other supplements in the bottom of my luggage. I only take 1 tea a day usually in the evening. I've only used the Amazing Herb brand that you can get at most all health foods stores. Coptis (a chinese herbal) I got from my Chiropractor also takes my pain away. Not as good as the Black Seed Oil. BTW both the Coptis and the Black Seed Oil taste horrible! I am not sure if these are healing my problem but am thankful that they take my pain away as I cannot take pain meds of any kind. Pain meds cause me bowel bleeding.
Until you get to the bottom of your pain Hope these ideas might help you and others who may see this.
I know God has a reason for our suffering - it is in some way to bless not to hurt.
hi I have pretty much the same pain as your self for the last year now but when ever I go see my gp they keep saying its ibs or muscle pain I had my gallbladder removal many years ago , so iv ruled that out my self , are u yr self any closer to finding out what it is
Was your pancreatitis caused by your ERCP procedure or did you have pancreatitis beforehand? I know that pancreatitis is one of the risks involved with ERCP, among other things. I will also list some doctors (below) that might offer you some help.
I also hope this will be helpful for anyone who might be suffering from Sphincter of Oddi Dysfunction (SOD). So, for others reading this & have had your gall bladder removed, or have other biliary disorders, you might ask your GI about the possibility of SOD. One thing I would advise anyone who thinks they have SOD (or their doctor suspects they have SOD) would be to try meds before having an ERCP or surgery on the duct itself.
I will try to make my story short as possible. (I have a tendency to over state things sometimes). I began having pain 2 years ago & the only way I could describe the pain is as if someone was stabbing me under my right rib cage & it exited out my back. My GP sent me to GI doc, who initially thought I had an ulcer. I knew it wasn't that, because I have had ulcers & reflux in the past & the symptoms weren't the same. The pain was so severe, that it literally affected everything aspect of my life & I found myself avoiding going out at all, if I didn't have to.
The GI doc ordered an upper endoscopy & also referred me to her partner, who ordered CT scans of cervical & thoracic spine as well as abdominal CT. I was told everything was "normal" & I was "fine". After the endoscopy, I was given pics she had taken during the procedure. Once I arrived home & the anesthesia wore off, I noticed that everything looked normal, except the tissue around the ductal opening, by the duodenal bulb, was severely red & irritated. So, the following day, I called her office & asked her about it & if she felt further investigation was warranted. She asked me why I thought I needed further testing & I told her I was a former nurse (now retired) & the pics indicated to me that it was more than likely related to bile & pancreatic juices. She finally agreed to perform an MRCP, but after that test, she again told me that both the CT & MRCP showed everything was "normal" & I needed no further tests.
Since, I am not overly trusting of medical professionals (comes from working around them for so many years), I asked for copies of the MRCP & CT scan. After I received the results & radiology reports, I discovered that not only did I have dilated intrahepatic & extrahepatic ducts, but also an adrenal tumor & a mass in my pelvis, that the radiologist "felt" was an ovary. They never told me anything about this. I called her office & told her, "why would you think the mass is an "ovary", when I had a TAH 27 years ago? I told her i had no female organs, so it would be difficult for the "mass" to be an ovary. Again, she refused to do anything, even refer me to anyone else. So, I asked her nurse for copies of my entire patient file. This is exactly why I would advise anyone who has medical tests to ALWAYS ask for copies of any tests you have performed, so you can read for yourself what the tests show. I noticed in her notes, that she mentioned the mass & even mentioned that I had a TAH & would consult with me before proceeding. But, she didn't!
So, after this rude awakening, my GP referred me to another GI doctor, who specialized in ERCP's & also a surgeon regarding the pelvic mass. The surgeon refused to do anything, until an ERCP could be performed & a repeat CT. The new GI doc refused to do an ERCP, (he felt it was too risky). He suggested, instead of the ERCP, an EUS (endoscopic ultrasound). Since his hospital wasn't equipped to do EUS, he sent me to another hospital. That test noted that I also had a dilated common bile duct. So, that now added up to 3 dilated ducts. This GI doc still refused to do an ERCP or any surgery (sphincterotomy or sphincterplasty) until my dilation was at 8-10 mm or larger. I am currently between 5-6 mm. I asked him if he could at least try me on some of the meds used for SOD, but I received a big NO.
The repeat CT was not the same type as I had before & performed at a small, local hospital, so still not sure what the mass is, as this radiologist, failed to even mention in his report. But, he noticed another anomalies (some of which turned out to be wrong). So, now the surgeon has backed out of removing the mass, because now he says surgery is "too risky". I told him, so is dying, but shouldn't a biopsy be done to see what the mass is? He said I need to see a gynecologist. That was another waste of time as she blew off all test results. So, now my GP is now sending me to a gynecologist oncologist. I just hope I am not too late, if it is cancer as my health continues to deteriorate, without anyone offering hope or suggestions. If all else, fails,, I can always go to VA hospital. But, I know it takes forever to even get an appt. in VA hospital, let alone treatment.
Since everyone is refusing to offer any type of treatment, I started doing my own research on med options. I see my GP next week, so I have called in advance to let him know what oral meds that can be used for SOD & will he at least "try" me on meds to see if it will alleviate the pain. But, with the luck I have been having with doctors, the past 2 years, I am not holding out hope for anything. But, I will keep on fighting for treatment on not only the SOD, but also the pelvic mass & adrenal tumor. The adrenal tumor is the least of my worries, right now, because more than likely is it just a benign adenoma, that can wait & just be monitored.
For those of you who do have symptoms of SOD, some of the meds used to treat it, are Calcium Channel Blockers, Nitrates, Gabapentin & low dose Amitriptyline. I cannot use CCB, because of low B/P, so will probably try either Amitriptyline or Gabapentin.
Botox injections have also been used to treat the spasms, but that is not something I would be interested in trying. Don't really feel like waiting for an appt. & then driving 2 hours to see the doctor. For anyone interested, there is also the option to check into clinical trials for treatment.
If my GP refuses to help with oral meds or they don't alleviate or reduce the pain & I am unable to get into VA into reasonable time, I have been researching specialists who work specifically with patients with SOD & pancreatitis. They are all out of state (for me) but would be worth the travel, if the pain could be alleviated. They all come highly recommended by other SOD patients. These doctors have found a new way to use stents to keep the ducts patent longer. If anyone is interested, they are Dr. Peter Cotton at MUSC, Dr. Martin Freeman at Univ Of MN and Dr. Sherman at Univ of IN.
I'd also suggest, that if you suspect you have SOD or pancreatitis, don't do like I did & go to just any GI doc, just because they are closer. If the above docs wouldn't be worth it to you, take the time to find a doctor who specializes in pancreas & SOD issues. Also take the time, to check reviews by other patients on websites that allow patients to review doctors, such as vitals, healthgrades, etc. Your life is too important to just allow anyone to experiment with your health.
I hope this helps anyone who is still battling SOD & not finding help.
OMG....thank you so much, for 15 yrs i have been though test after test and my gallbladder removed all due to pain as you have. Sometimes so bad im screaming in pain, hot flashes, nausea, sweating, and tossing what ever i ate and drank up. Been put in the hospital a few times with pancreoues issues, sometimes when at the ER I get tests are all Normal, so drugged up with thier strongest pain med and sent home and down knocked out for days. Been told to never come back at one in San Diego, my first time mind you there but he thought i was ther just for the pain meds, my husband at the time my boyfriend got so mad. He knew i was in so much pain. Im so tired of tests. Last hospital visit the doctor put me on gabapentien. For 3 yrs no issues until around Aug 2014 i started working again andnit started it back up, even my pain doctor upped it to 4 a day. Whcih i cant see no more until i pay them what i owe them from another issue proceder, so out of pain meds also and been in pain on and off in the day for over a month now. Anyways this so sounds like my issues. Doctors have said i have IBS, Acid reflex, and pancroues issues.my pain aint sent me to the ER since i was there 3 yrs ago and hopeing my pain dont get that bad, but i lost my job cause my family doctor hasnt did my work paper on what i can and cant do, also i have discs in my back disenagrating also. So now jobless and still waiting. Now im taking this to him and see what he says, my last doctor before she left was doing every thing she can to find out what was wrong with me. I just pray this isnfor sure it. Im so tired of researching also and want it done and over with. Im only 42 andthis as i said before started when i was pragnant with my now 15yr old. Again thank you for the new hope of finding out whats wrong with me!!!
My wife's story is similar to yours. She has been struggling with this for 3 yrs now. Many tests, ER trips, hospital visits, bad drug reactions, etc. Had her gall bladder removed 3 yrs ago. Many misdiagnoses but no answers. It has been terrifying at times.
She was diagnosed with early PBC but they say that wouldn't cause this kind of pain.
The symptoms sometimes go away completely for a few months, and she can eat normally, then they will start up again for no apparent reason and go on for months. Difficult to get enough nutrition when you can't eat. When she is having symptoms the spasms start every morning, and on a good day will subside by late afternoon. Ativan seems to help the spasms and anxiety somewhat. Morphine helped the pain at first, but that seems to help less as time goes on. Diet consists mostly of Saltines, scrambled eggs, gatorade and a blend of apple juice/prune juice.
I've mentioned SOD to several doctors, but they are resistant to suggestions from the patient or family.
I was curious about the doctors you mentioned: Dr. Peter Cotton at MUSC, Dr. Martin Freeman at Univ Of MN and Dr. Sherman at Univ of IN. Other hospitals (such as Mayo, Johns Hopkins, Cleveland Clinic) also discuss SOD. Have you heard any feedback on success stories with those hospitals? For instance, Univ of MN versus Mayo?
yes the pain is just under my right rib cage. Sometimes when I breath each breath causes great pain .I've taken several Ibuprofen so can bare the pain now, but otherwise I have to breath with short breaths
The Content on this Site is presented in a summary fashion, and is intended to be used for educational and entertainment purposes only. It is not intended to be and should not be interpreted as medical advice or a diagnosis of any health or fitness problem, condition or disease; or a recommendation for a specific test, doctor, care provider, procedure, treatment plan, product, or course of action. Med Help International, Inc. is not a medical or healthcare provider and your use of this Site does not create a doctor / patient relationship. We disclaim all responsibility for the professional qualifications and licensing of, and services provided by, any physician or other health providers posting on or otherwise referred to on this Site and/or any Third Party Site. Never disregard the medical advice of your physician or health professional, or delay in seeking such advice, because of something you read on this Site. We offer this Site AS IS and without any warranties. By using this Site you agree to the following Terms and Conditions. If you think you may have a medical emergency, call your physician or 911 immediately.