Gastroparesis

[Jeannine]

Hi,I have posted here in the past and appreciate you service its
been a great help.I have had ideopathic gastroparesis for over
2 yrs now and have progressivly lost aprox 20lbs.My weight now
is 100-104 flux. Every time I get sick it drops and after some time it will get back to 104.I can not seem to progress beyond this status. I have been on disability since 11/99.
My doctor said if I dont see improvement in June,
when I was going to return to work,he will just continue the
disability.I feel weak most of the time and have been having
episodes of hypoglycemia due to what I eat or if Im not able
to eat enough.This is getting very upsetting for me.

*If I dont see any improvement do I just have to
"get by" like this?How long do I wait...........

*I am very concerned about the long term effect
of staying at my current weight and minimal activity level.
Is it harmfull to my body?

*Any suggestions as to what might be a "benificial next step"
would be greatly appreciated.I feel like I need to do something,
I cant stand watching my life go by..........

Thank you for your time!
Jeannine
(***@****)

[Kim Q: new gastroparesis meds?]

Hi!  I have posted a few times in the past.  Recently my gastroparesis/GERD (non diabetic) is worse.  I get totally full from eating 1/2 banana even.  I'm 41.  Should I ask my gastro guy about domperidone (? sp) in that does it help this?  Every time I eat anything, I end up burping it back up. This is raising havoc on my esophagus and emotions.  I am now living on gatorade and vanilla yogurt, which also leaves me feeling full.  I take prilosec 20 mg in the morning, Axid in the evening.  Nothing seems to help.  I can't take Reglan, it makes me feel nuts!!
HELP!!!  Does anyone know of studies/good gastroparesis doctor in the So. NH/Boston, MA area??  Thanks.   Kim

[carissa]

Hi again jeannine,

I was writing you a long response, and got kicked off, so I will have to shorten it.  I also have idiopathic gastroparesis...I've had it for about six years. I've written you before. My doctor (Dr. Koch at Hershey) told me that sometimes people get a lot better, sometimes they get a little better, and sometimes they don't.  I think I'm a don't.  I haven't improved over six years...if anything, gotten a little worse.  I have been on TPN since December when I was in the hospital and I really hate that. I'm having a rough time with my last semester of college.  I am supposed to graduate in three weeks, and I am way behind in all my classes because I've been so sick this semester!  I'm supposed to go to grad school in the fall, and I don't want to be this sick!  You're taking domperidone right?  That's the only drug I can take with no serious complications (cardiac arrest because of my heart problem, prolonged QT).  I don't have any other suggestions...it's trial and error with the food.  I think Dr. Koch is thinking about sending me down to John's Hopkins for another opinion.  I am also very concerned about my low weight and activity level.  At one point i lost 31 pounds and weighed 78!  I usually run around the 90's (I am 5'3")  I have minimal activity because of the combination of gastroparesis and my heart probloem and have HP parking, which i hate because I used to play sports.  I have not heard to much about the long term effects of malnutrition (in my case, my effects have been more short term, related to low potassium and then cardiac arrest).  I am scared about the future though.  I don't know about the next step for you, because I'm at a loss myself...I'm having a rough time and don't know what to do either.  I heard the gastric pacer was approved by FDA a couple of weeks ago, but I think it is still for very few people.  That might be an option.  I am trying small bits at a time, and it's hard because I usually have a huge appetite, but then eat two crackers and almost throw up!  I am craving real food and it's tough because I can't have it!  I think that is my biggest struggle lately.  The huge appetite, and then not being able to eat it.  

I have a question for you though...I tried to get on disability a year ago because there's no chance I will ever be able to work enough to support myself.  They told me that I am not disabled enough because I used to work in retail (10 hours a week, and not a chance I could do that now..it was before I got worse).  i appealed it, and they still said I was not disabled enough.  I know it is always difficult to get approved for this, and I'm not pursuing anymore at this point, but will have to in the future.  My parents are also trying to keep me on their insurance plan by claiming me as a Handicap dependent, because I will gewt kicked off when I turn 23 in October, and I won't be able to work full time to have my own insurance!  they are having difficulty getting me approved for that too.  How did you get on disability?  Was it really difficult? Did you have to go to court?  I am not going after that now, but know it may be my only option in the future.  I really want to work, but don't think I ill be able to full-time, or even close to it.  

Sorry I wasn't much help...Hope it was a little help and support at least!  Please feel free to e-mail me agian anytime.  Good luck.  ***@****

[MICHAEL STORY]

I AM A 50 YEAR OLD MALE.OVER THE LAST TWO YEARS I HAVE HAD SEVERE ABDOMINAL PAIN.THIS PAIN WOULD START TOWARDS THE CENTER AND RADIATE TO THE UPPER RIGHT.I ALSO HAD BACK PAIN BETWEEN THE SHOULDER BLADES.EVERY TIME I WENT TO THE EMERGENCY ROOM,THEY WOULD RUN A EKG.WHEN MY EKG CAME OUT GOOD,THEY WOULD DIAGNOIS ME AS HAVING ACID REFLUX.I HAD A ULTRA SOUND,AN UPPER GI,A CAT SCAN,ALL CAME BACK SHOWING NO PROBLEM.IN MAY OF 1999,AFTER MANY OF THESE ATTACKS,I REQUESTED TO SEE A SURGEON.AFTER SEVERAL MORE TESTS,HE REMOVED MY GALLBLADDER .HE SAID IT WAS DISEASED AND THAT I HAD SLUDGE IN IT.I HAD NO MORE PROBLEMS FOR APPROX 5 MONTHS.THEN I STARTED HAVING THE SAME PAIN AGAIN.ALL DURING THIS TIME I WAS DRINKING ORANGE JUICE ON A DAILY BASIS.I QUIT DRINKING THIS AND CARBONATD DRINKS 2 MONTHS AGO AND I HAVENT HAD ANY MORE ATTACKS SINCE THEN.I FEEL MUCH BETTER AND BELIEVE THE SPASMS AND PAIN WAS OCCURING IN MY ESOPHAGUS.

[PATTY]

hi,
i am not able to help you with your questions. but i am wondering if you can help me. I have just recently been diagnosed with Gastropareisis. I am 26yo., can you tell me what i am in for?...What meds. you are taking?...Any suggestions would help...I have been soooo upset and frustrated since I have been diagnosed, there doesn't seem to be much help out there...

Thank you in advance...

...if you just want someone to hear you vent your grief, email me at ***@****

[Pat]

Check at Mayo Clinic in Rochester, MN.  They are doing research and tests there dealing with gastroparesis and are using different meds for this.  Last I heard about Domperidone it was not all it was supposed to be.

[Sharon]

I have been seeing the gastro dr who said that since my throwing up ahs stopped i could try to stop using the reglan when this has happened i get a pain in my back about even with my shoulder blades which seeds me back to the medicine cabnet for the Reglan that stops the pain. I have let it go and then become sick..could you help me with this. i am also not eating hardlyany red meat and am also bordering on hypoglycemia at times
i eat it seems like all day very little.I was told this could last for 6months to 2years he thinks it was from a virus.Also has any one have diahrrea and constipation with this I never know if it is from the medication or other wise I have also gone from 205 to 185 in a short amount of time. I hate feeling druged all the time. I have tryed riding my bike short distances to build my stamina back short hopes and lots of stops.could you all help with some of these questiions!!I have used the gicare diet and cut my faat intake to about 30 to 40gms a day. My E-mail if you care is ***@**** thanks

[Carissa-to Patty]

Hey Patty.

Sorry to hear about your diagnosis.  I remeber when I was first diagnosed and it was very
difficult to adjust.  Although it still really sucks having to deal with this, I have learned
to adjust and it has become part of my lifestyle. Every case of gastroparesis is different, so
it's hard to say exactly what you are in for, but I will give you my experience (and I have a
lot of it!).  I have been dealing with it for six years.  Is your gastroparesis idiopathic, diabetic
or postsurgical?  The reason I ask is because prognosisis can differ between the three causes.  
Idiopathic gastroparesis has a little hope of improving, in some cases, and typically does not get
any worse.  Diabetic gastroparesis usually gets worse.  Postsurgical usually does not have the hope of
improving, but will not get worse because the damage has been done.  As far as what you are in for...Nausea
and/or vomiting after eating, early satiety, occasional abdominal pain (maybe), weight loss, malnutrition,
bloating, dehydration, etc.  That's my main symptoms.  Some cases are not as severe as others.  Some people
are able to maintain their weight by eating small meals all day long.  Other people can't even keep small meals
down and eventually end up on nutritional support (like me).  I have been on TPN through a midline 5 years ago,
a j-tube for two years, and now I have had in a PICC line for five months. There is no cure for this disease, but
the doctors are currently working on a pacemaker for the stomach which was recently approved by the FDA for a
small group of severely ill people.  Drug research has been slow, and they are not sure about ever discovering a
new drug.  I take domperidone which I get from Canada, and in the past have taken reglan, e-mycin, and propulsid.  
I had severe neurological reactions to reglan, and went into cardiac arrest several times in reaction to propulsid
and e-mycin (I also have a heart problem).  this all started when I was 16 and now I am 22.  None of the drugs
have been really effective...basically the reglan only blocked out my nausea until the drug wore off and then I
felt it full-force.  The other drugs have not given me tremendous benefits, and the domperidone alone certainly
doesn't do the trick.  As far as what you are in for, like I said, it depends on the nature and severity of the
disease.  It is very difficult to treat, but if you are not real severe, you have more hope.  I can't say you will
lead a normal life, because you won't, especially if it is severe.  It has had a tremendous impact on my life and
some days I can't even get out of bed, which is hard as a full-time college student!  I don't work, barely take a
full-load, and still take incompletes every semester in my courses.  Of course, I am on some pretty high doses of
heart medication also which makes it especially difficult and tiring. As far as foods...eat low fat, low fiber, low
or no meat (some people can handle some fish), and careful on the fruits and veggies.  Some good foods to try are Frozen
yogurts, low fat cottage cheese, eggs (one of the most easily digestible foods), pasta, soups, mashed or baked potatoes,
hard candy (for calories), some breads are ok (a lot of carbohydrates are good), puddings, soft white meat (if you can
tolerate it).  You have to get creative in order to add variety.  For example...I have had very low fat cheese pizzas!  
I have to make them of course and only eat a very little bit, but they are pretty good and it adds variety.  Sometimes if
I feel up to it, I will eat low fat waffles with high-cal syrup.  On a good day, half a bagel goes down ok. Some low fiber
cereals in small portions can work well too.  I hope this is helpful...Sorry if the news is not that great, but there really
is no good news with this disease.  Some hospitals to check out (depending where you live) are Hershey Medical Center in PA (to
see Dr. Ken Koch), Johns Hopkins in Baltimore, University of Kansas Medical Center (to see Dr. richard McCallum).  Dr. McCallum
used to be at the university of Virginia, but he left so I don't know that they are heavily involved in the research there anymore.  
I hope this helps.  If you have any more questions (I also have other food ideas if you are interested...you have to get creative,
and even then it gets boring and you REALLY start craving a McDonalds Cheeseburger and fries), feel free to write me at
***@****.  Good luck.

[Jolene]

I have a three year old son who has always refused to eat solid food and his fluid intake was minimal from day one.  He was finally sent to a GI doctor a few months ago who diagnosed him with gastroparises and a motility problem.  His stomach is always bloated he is very gassy.  His weight has always been very low and finnaly was off the charts when he was about two years old.  He also has cronic ear infections, speech delay.  His GI doctor put him on Peptamen Jr. which is about 30 cal.per ounce.  It is pre-digested, lactose free and gluten free.  In just two months time he put on 6lbs. which placed him in the 25% for his age.  He has steadly gained about a lb. a month since and looks very healthy.  Although he does eat a tiny bit now we depend on the formula for his total nutrition.  He is on pepcid and pariactin syrup for an appitite stimulant.  We did try Propusid for about 3months with little response and so after the warning about it we discontinued it.  Thankfully we haven't had to put him on a tube but I spend my whole day dealing with his feeding.  When he will accept food he won't feed himself.  Although he can drink from a cup he refuses to drink his formula from a cup so he is still on a bottle.  Which he won't hold himself so I have to give it to him which is about every 21/2 hrs.  We have tried taking the bottle away but he loses weight every time because he doesn't eat.  When he does he is in a lot of pain and becomes very very bloated.  He has done very well on a very strick routine that suits him.  We tried putting him in Nursery school this year but it would have messed his schedual up to much.  We don't try to make him fit into other peoples ideas of normal.  He sleeps quit a bit so we are home bound pretty much.  and of course being on a bottle at 3years old is not considered acceptable but it works.  It sure seems better than a tube.  His doctor wants to put him on Reglan but we are hesitant.  He does very well if he only drinks the formula and stays away from solids.  We are seeking alternative treatment for him.  We have taken him to an Envirmantle allergist.  Who is a Holistic Doctor and just had a consult with an ostiopathic doctor who has given us some hope.  He says that the trama of being born did damage to his cranium therefore the brain doesn't send the correct messages to the stomach.  He also thinks that he may have an over growth of yeast and is doing a complete study of his stool.  Both of these doctors are old and belive in finding out the cause of the problem rather than treating just the symptoms.  Not to many insurance  pay for these services so it can get expensive.  Our insurance doesn't pay for the formula eaither (they would if he was tube feed) which is costing us $721 a month (four cans a day).  It can get tough financally plus a am going through a divorce.  I am so glad I found this site because I am alone in this.  My mother brother and sisters want nothing to do with him.  Which is hard for me. I would appreciate any feed back or suggestions.  His GI doctor said that it will probably be lifelong.  I am getting so sick of battling doctors and insuance companies.  

[Pat]

Jolene,
Sorry to hear about your son, but as for the formula he is taking for nurishment and the cost, I can relate.  I too need to supplement my intake with a liquid nutrient.  It runs me approximately $645.00 every 2 weeks.  My insurance was not going to cover it but my GI doctor wrote and appealed it for me, explaining that it was my only real source of nutrients due to my malabsorption and motility disorder.  They, the insurance company, had their medical team review my appeal and they are now reimbursing me for this expense.  You might want to try this. (I do have to pay up front but then submit the bill to them and recieve a check from them.)

[carissa]

Jolene-

I also have had to take liquid supplements by mouth as my sole source of nutrition in the past.  My doctor wrote a prescription for it, and that way the insurance company covered it.  Otherwise they would not.  They did cover my tube feedings for two years, and also my TPN for the past five months as well as a few years ago.  I think you should be able to find a way to get this covered.  Good luck!

[Jolene]

Thank you both for your suggestions about the formula.  His doctor has written numerous letters to our insuance company but they still haven't agreed to pay for the formula.  I also call them almost every week.  They have said that if was tube fed they would.  I was wondering if someone could tell me how uncomfortable my son is with so much abdominal swelling?  He is pretty good if he just does liquids but if he eats solids it is obvious he is in pain and usually vomits.  His doctor says he is a tough boy.  If he had his way he would live on water.

[Pat to Jolene]

Just a thought.  A pharmacist once told me that sometimes if you contact the pharmaceutical company that makes the product they can help you.  They sometimes have funding for something like this.  It might be worth a try!

[Carissa- Please help...I need advice]

Hi,

Now I have a question for all of you. I have had severe problems the past few months keeping any food down (I've had very severe regurgitation).  My doctor
checked for blockages last time I was in the hospital, as well as other problems.  Basically, what he discovered was an excessive amount of acid in my stomach...
no suprise.  He also did the gastric emptying test which, of course, came back positive as it always has.  There was not much change except a slight decrease in my
emptying speed (2-3%) which he was not all that concerned about.  He started me back on nutritional support (TPN)and I began taking Prilosec.  I've heard all these
great things about Prilosec, but haven't had much success myself with it.  It has been helpful in that now when I regurgitate it is usually just undigested food
and not as acidic as it was in the past.  My food usually comes back up after around an hour after I have eaten it and lasts up to six or twelve hours later. It doesn't
seem to be affected at all by what I eat...everything I eat comes back up.  It is like vomiting, only it's not.  It's that amount though.  Depending on how delayed it is,
it will come back up in the form of bile.  I am on 20mg of Prilsec twice a day.  Even on this dosage (which my doctor will not increase) I am still losing everything I eat.
Five weeks ago I took some medication for diarrhea (which is caused by the TPN...I've never had problems before) and it made me sick, so I only took it that once.  I know it
was five weeks ago.  Twice this week when I have regurgitated my food back up, large remains of that medication have been in it.  It's really disgusting.  I KNOW without a
doubt that it is that medication because nothing else would look like that.  It has not dissolved or digested in all that time.  It really made me nervous.  I am going to talk
to my doctor at Hershey Med about this, but I doubt he'll have any answers for me.  He's scoped everything he can think of out.  He's thinking about sending me down to Johns
Hopkins for another opinion.  My questions are:

Is it possible that the Prilosec would not do the trick for me?  Why would everything (even six hours later) be undigested food and not acidic if my problem is acid reflux?
Also, if it's acid reflux, why would the Prilosec not help much?

Second of all...why would this medication sit in my stomach for five weeks without being dissolved or digested.  Is that possible?  I KNOW it was that medication, and I know
my stomach is slow, but that's ridiculous.  

Also, why would this regurgitation problem just show up five months ago when I have had gastroparesis for six years, and my gastric emptying has not changed much?

Oh yeah...besides the Prilosec, I am also taking Domperidone and Tenormin (for prolonged QT...a heart complication).

Please help me if you have any ideas.  I will talk to my doc about it, but I don't think he will have any new ideas either. My e-mail is: ***@****
Thanks.
Carissa

[Cindy Keefer]

I posted this reply under another question but received no answers.  Can someone please help me?  Since I posted the reply, I have tried to eat and ended up so sick that I do not want to eat again.
"Hi, everyone! Sorry that you are all having these health problems. I do know what it is about.
What is gastroparesis and how is it diagnosed?
Here is my story. Started in January with the Flu which went to Bronchitis then Asthma. Next I had menstrual bleeding and a kidney stone at the same time which required a D & C and Cystoscopy/Ureterscopy (also at the same time). Came home from the hospital to find my dog sick (he was old), he collapsed outside and I picked him up to carry him in the house (did not want him to die out in the cold by himself) which was not a good idea because I popped a ventral hernia repair. I went to the doctor about the hernia and because I had diarrhea and nausea and vomiting since I had gotten the Flu.
Doc said he had to do a test and it turned out I had Pseudo Membranous Colitis. This came from taking antibiotics but the treatment is more antibiotics. Was given Flagyl which sent me to the emergency room with an allergic reaction. Then I was given Vancomycin in the dose of 125 mg a day. This did not work so I was given 500 mg a day.
Three months down the road, I still have pain in the upper left quadrant, diarrhea, nausea and vomiting. Cannot eat or drink. I have been in and out of the hospital about four times this year. Mostly for dehydration. I lost seventy-one pounds in less than three months.
Last week in the hospital, I had all kinds of tests. They did not really find much. The C-Diff test is now negative so it is not the colitis. I was told Gastritis and Irritable Bowel. Find it hard to believe that is the cause of all of this and my family doctor thinks it is something else, too.
On Saturday when I came home from the hospital and walked in my front door, I immediately had a sore throat, tightness in the chest and an upset stomach. The diarrhea, nausea, vomiting, pain and fever (low grade at about 99.6) were all back. Back to going to the bathroom, three to ten times a day and throwing up all I try to eat or drink.
Now my family doctor (as I do) thinks I am allergic to something in my house so next week I see an allergist. He thinks it is my new puppy but I only have him for one month and I have been sick for three months.
I live in a very old mobile home which could have lead paint, asbestos, formaldehyde, mold, mildew or who knows what.
One doctor made a comment to me that since I can stand to lose more weight (I was huge at 380 lb a year and a half ago. Lost the first 50 lb with diet and exercise over a year's time but lost the rest in the past two and a half months with still 100 lb to lose to be at a proper weight.), they will just wait until I lost weight down to a normal size and then see what is wrong with me. My appointment with the gastroenterologist is not until May 30.
Also, I was told that it could possibly be Eosiniphilic Esophagitis because there are Eosiniphils in my blood work. What is that?
If anyone can help me to get better or at least to get fluids down so I don't have to go to the hospital again, I will be ever so grateful for the advice.
Thanks everyone!"

[Carissa-to Cindy]

Hi Cindy-

All the symptoms you describe (except for the diarrhea) sound like gastroparesis.  Gastroparesis results in severe nausea, vomiting, abdominal pain (due to food sitting in the stomach for so long)after eating or drinking. It can be a complication of diabetes, post-surgical, or idiopathic (Unknown)  In some idiopathic cases, it can be linked to a virus or flu. Usually people with gastroparesis have more of a problem with constipation than diarrhea because food moves through so slowly.  I have heard of people having diarrhea with gastroparesis though...usually if they also have IBS.  It does seem weird though that the symptoms seem to worsen when you walk into your home...that would not be an indication of gastroparesis.  It does sound like something in the home might be making you sick.  

Gastroparesis is diagnosed by having a gastric emptying test done.  For this test, you will eat a meal (usually eggs, sometimes something else) with radioatctive material in it.  Then you will lie under a camera for two hours (or at some places they will put you under it every fifteen minutes for two hours).  The camera will trace the food as it goes out of your stomach and into your intestines.  At the end of the test, the radiologist will determine what percentage of food was left in your stomach after two hours. If there is an abnormally high amount left, it would indicate that your stomach is emptying slowly and would be an indicator of gastroparesis.   If the test comes back positive, your doctor will probably also do an endoscopy and possibly other tests to make sure that there is not a blockage or obstruction.  If there is no blockage, or anything keeping the food from emptying, then you would probably have gastroparesis.

Given your symptoms, I would recommend having this test done.  I don't know about why you get worse at home, but if nothing else, this test would at least rule out the possibility of gastroparesis.  Good Luck.

[Nikki]

My situation doesn't sound as severe as others and my sympathy goes out to everyone. I have been diagnosed with gastroparesis. My symptoms started about a month after I had a viral infection which caused my throat to feel tight due to the blisters in it. My left arm felt numb & I felt a tightness in my chest. I went to an urgent care facility & had an EKG(normal) &  a GI cocktail which didn't offer any relief. My family doc put me on tylenol (arm pain)& 30mg Prevacid. Driving home from a  stressful day at work, I felt an increased pressure in my chest(to the point where I didn't want my seatbelt or bra touching my chest) & I felt like passing out. I went to an urgent care facility where I had another EKG & GI cocktail. Still no relief. My family doc ordered an upper GI(normal.) She then decidied some anxiety must be involved (stressful job & getting married soon) & gave me Klonopin so I could relax & sleep at night (when my symptoms were worse.) At the 1 month follow up visit she referred me to a GI doc & did an upper chest xray. The following day I had another episode (again driving in the car, tightness in chest & left arm & feeling like passing out.) It was during office hours, I went to see my doc who did another EKG (normal like the chest xray.) She then ordered an ECHO (ultrasound of my heart) which was normal & gave me Serzone for anxiety. My GI doc ordered a gastroscopy & gastric emptying study. The gastroscopy showed mild irritaiton of the esophagus & the gastric emptying showed delayed. He diagnosed me with gastroparesis which was causing acid reflux & gave me Propulsid & upped the Prevacid to 2xday. He advised me to eat low fiber/fat diet w/ no dairy fat or raw fruits/vegs. I had a bad reaction to Propulsid & switched to Reglan. This helped but he was concerned about long term use & swithced me to liquid emycin. Which seemed to help. Then more chest, arm & shoulder pains (left side). Drs office sent me to ER where ultrasound of gallbladder came back ok. Then they referred me to cardiologist where I had another normal EKG. My GI doc then ordered a stress test for heart (normal) & HIDA scan on gallbladder (normal.) I have had good & bad periods since. My ob wanted a 2nd opinion before I tried getting pregnant. The new GI doc wanted me to go off emycin & repeat gastric emptying in 3 wks. I felt bad going totally off so took only 1xday instead of 4xday with none 2 days prior to test. Two more almost passing out episodes while driving where attributed to side effect of anxiety med Serzone (drop in blood pressure) & dosage reduced which helped. Last Friday my gastric emptying test was rescheduled to following Tuesday. Going off the emycin, I have noticed I do not have a bm everyday like I use to on it. Yesterday (Saturday), I had some of the ususal tightness in chest, shoulder & arm which I attributed to going off emycin. It got worse when I walked on treadmill but thought that was b/c I already did not feel 100%. Then driving I had another episode but much worse & called 911. They took me to ER & I had another EKG (normal). The ER doc was able to pull stress test and HIDA scan results.  He believes the attacks (though on the left side & not on right as most people have) are from gallbladder.  HIDA scan was actually borderline abnormal (emptied 33% with 35% up being normal.)  He gave me pain medicine for arm, sholder, chest & now back.  No relief.  GI cocktal. No relief. So a stronger pain med. No relief. So then he gave me nitroglycerin (even though he did not think it was my heart - normal tests, 31 years old, no family history.) All I could feel then was heart pounding & not sure if pain went away.  Then more pain medicine & everything else is fuzzy. He talked with my GI doc & a surgeon & they think I should have my gallbladder removed. I am a little hesitant to under go surgery if they cannot say definitely it is the gallbladder that causes these attacks & not the gastroparesis, acid reflux or esophageal spasms. I am at a loss & just hope they figure it out soon. These episodes are scary. Sorry my story is so long but I wanted to include as many details as possible to see if anyone else has had a similar experience. Thank you for letting me share my experience.

[Carissa-to Nikki]

Weird...

Gastroparesis causes nausea, vomiting, abdominal pain (on left side from food sitting so long, usually in the stomach),
early satiety after eating, and bloating.
It does not cause a weird pain in your chest...at least I have never heard of that.  That can be caused from acid
reflux though because I have had it since my reflux got worse.  I actually feel food food getting trapped in my
throat and chest on the rare occasion it doesn't completely come back out (almost like vomiting). I have never had pain
in my arm or shoulder because of gastroparesis...the only reason I have pain there is because of some nerve damage that
was done during a major surgery four years ago.  Your symptoms don't sound typical of gastroparesis.  What was your emptying
percentage? Do you know?  It may be a mild case, but I would say that there is something else going on.  I don't know
if it's the gallbladder or not, but I would say if your symptoms don't completely match up, that I would have other
things checked out before you go to the extreme of having surgery...since there is no solid evidence that is the problem.]
Do you also have those symptoms I listed above of gastroparesis?  Have you tried taking Prilosec?  I've heard it's better
than Prevacid.  It's worth a shot.  Other than that, I don't really know what to tell you.  I've never had (or heard of)
those symptoms being caused by gastroparesis.  Good luck.

[Nikki]

Carissa,
Thanks for responding. My gastric emptying was delayed with T 1/2
greater than 120 minutes. I don't exactly know what that means but the nurse told me I did not pass any of the 1/2 egg sandwich in 2 hours. I have not had any nausea or vomiting and advised my doc of such. Early satiety - I just assumed I rarely got hungry and felt full because I ate too much and never mentioned it to a doctor until after the gastric emptying study. I have not tried Prilosac b/c my HMO won't cover it - just Prevacid. My GI doc says the tight pressure in my chest and numb arm are from acid reflux resulting from the gastroparesis but I've never had the acid taste which I am told is common with GERD.  He also cannot explain the passing out sensation I have had on occassion. I did feel better before I went off of the emycin. Hopefully the second gastric emptying study will help.  Thanks again for your time and input.  My best to you and everyone else.

[Jeannine.......Hi Monica]

To all.....

It has been my experience that if you eliminate all fibre from
fruit and veggies and you have to many carbohydrates you may be setting yourself up for feeling worse.Its good to try to have some protien with a carb and to have "some" veggies/fruit even if you have to put them in the blender or have really small amounts through the day.If you can't handle fresh raw veggies
try frozen and smash 'em up.

Jeannine

[Debbi]

I was so fascinated by the number of people who suffer with gastroparesis.  I have diabetic gastroparesis.  I have been diabetic for 34 years and developed this disorder 6 years ago.  I had surgery on my hands and developed a complication called neuropathy.  There are a couple of kinds. One is where you can't feel anything, like in your feet(that is why there are so many foot and leg amputations.)  Some diabetics can't feel if they have a soar.  The other kind is PAINFUL neuropathy which is what I got after my hand surgery.  I became suicidal in the hospital because they could not control my pain.  After 8 weeks, I was put on liquid morpheine.  It took my system 2 years to get used to it.  During that entire time, my gastroparesis was getting worse and worse.  My husband became very frustrated, not believing there was nothing any one could do. I have all the nasty symtoms.  Throwing up is second nature to me. Because I am diabetic, my nutritional needs are very specific, but I can not take care of them.  My doctor just mentioned las week about the stomache stimulator for gastroparesis.  I will try ANYTHING.  I am so sorry that so many people have this, but am grateful to know that mine is not so out of the ordinary.  Thanks for this forum  Deb Ritter - Minneapolis

[cindi]

Two and a half years ago I started with frequent "stomach flu" symptoms.  I figured my resistance was low and I just kept getting the stomach flu.  One July day, before leaving for a trip, I was so sick and so determined to go on vacation, that I literally ate Tums, Gatorade and dry Cheerios for a day until the pains and vomiting went away.  Then I made an appointment with a Gastroenterologist who did an endoscopy on me.  He found an ulcer on my esophagus and diagnosed me with GERD.  Two years later, I continued to complain that my stomach always felt full and that Prilosec (which I was taking because my insurance would not pay for Prevacid) was not working.  He wrote a letter and switched me to Prevacid and told me that the pains I was having were "all in my head."  I went to a new Gastroenterologist (A WONDERFUL PHYSICIAN) who sent me for a gastric emptying scan.  I was found to have gastroparesis (my stomach only works at about 45% capacity).  I am currently taking Propulsid 20mg. three times a day and doing well(but worried because it will soon be taken off of the market).  There aren't many options left except maybe Reglan--------and that's a drug I'm really afraid of.  I sure hope that find a way to control this problem soon--without such severe side effects.

[Philip1815]

Hi! I have posted a few times in the past. Recently my gastroparesis/GERD (non diabetic) is worse. I get totally full from eating 1/2 banana even. I'm 41. Should I ask my gastro guy about domperidone (? sp) in that does it help this? Every time I eat anything, I end up burping it back up. This is raising havoc on my esophagus and emotions. I am now living on gatorade and vanilla yogurt, which also leaves me feeling full. I take prilosec 20 mg in the morning, Axid in the evening. Nothing seems to help. I can't take Reglan, it makes me feel nuts!!
HELP!!! Does anyone know of studies/good gastroparesis doctor in the So. NH/Boston, MA area?? Thanks. Kim

[Bud]

I experience upset stomach close to diarhea at different part of days with different foods. I've been to a GI but he said everything is fine. He sent me to a psychologist and I checked out fine. What could I possibly do?

[Jeannine.......Hi Monica]

There is a web site that you may want to check out:

www.dailyfutures.com/gastro.html

It has information,internet links, alternative medicine info. and helpful ideas re gastroparesis.

Jeannine