Gastroparesis info
Hi, ya'll. I've been away for awhile and currently 3 yrs out of chemo and so far ned! But I wanted to let you know what has been happening to me in case there are others here that have chronic nausea and vomiting ever since going through cancer treatment.
Throughout my chemotherapy I suffered with bad nausea and vomiting and none of the medications helped to stop it. Then after I finished chemo, the vomiting and nausea persisted. I would have good days and then the symptoms would return. I also had bad diarrhea about 8 months out from chemo and for 3-4 months wrongly diagnosed with colititis, diverticulitis and had two-7 day hospital stays before they could determine I had cdiff bacterial infection. I fired my GI Doc and got another one, which was the best decision. Anyways, I also had my gallbladder removed because during the workup for this, they found my gallbladder was non-functioning. Through all this, my nausea and vomiting persisted. My new Gi Doc was so much better than the first. At first I continued with diarrhea also, so he suspected I was lactose intolerant and ordered the test which was positive in the last part of the test. I cut out all lactose and still nausea, vomiting persisted, but the diarrhea slowly subsided through the next year and was replaced with constipation. After several ct scans, xrays, blood work, etc, he finally sent me for a gastric emptying study. I failed miserably and it showed that it took my stomach 20 hours to empty after eating. I finally had the answer for all the nausea and vomiting: Gastroparesis, which is literally paralysis of the stomach. they tried me on different medications to improve the motility of my stomach but nothing worked and they were affecting my blood pressure so he sent me to have a Gastric Electrical Stimulator surgically implanted in August of last year. This is like a heart pacemaker but the leads are attached to the stomach to make it contract. Until last month, this pretty much controlled my symptoms but then the nausea/vomiting and this time, epigastric and chest pain, reared its ugly head. I was admitted from the ER and after and EGD scope, I was diagnosed with duodenitis, gastrititis, esophagitis and a hiatus hernia. They adjusted my pacemaker, told me to take prilosec with every meal and sent me home. The nausea and vomiting has persisted bad. I've had the pacemaker readjusted 3 more times and currently still having bad symptoms. My work and boss were great through the cancer treatment and through all this. I missed alot of work and when symptoms are like this, I can only work if I've been fasting the night prior. I go in til around 11am and then have to go home and eat. I spend the rest of the day on phenergan to keep food and drink down. This past monday, I learned my boss was going to let me go because my job needs a fulltime person in the position it do. I broke down and filed for disability. now my boss is willing to work with me on a trial basis to continue to work only in the mornings. But I no longer have my percieved job security. My finances are in jeapordy and hubby and I are trying to adjust to life with me having a drastic cut in pay. We are not making enough to cover our living expenses. I saw my gi doc yesterday and he is going to do everything he can to help wtih getting disability but I know its a long hard fight to get it.
They tell me I have Idiopathic Gastroparesis and it could have been caused by the chemotherapy, mastectomy, gall bladder surgery, abdominal migraines or a virus. Something damaged the vagus nerve leading to the stomach. I suspect it was from mastectomy or chemo since I had no problems until I had those.
sorry this is so long, but I wanted to let ya'll know in case someone is having unexplained nausea and vomiting ever since your cancer treatment. It took my doctors over 2 years to properly diagnose me. If you are experiencing this. (symptoms tend to by cyclic and have periods of no symptoms,to months of bad symptoms) please have your doctor check for this. Have them order a gastric emptying test. this will show how long it takes for your stomach to digest food.
Oh, I ended up not being lactose intolerant. Becuase of the gastroparesis, the last part of the test was positive because the lactose drink sat in my stomach and went bad during the test.
I dont' know why life dealt me with this, but If my relating my experience can help another, than maybe THAT is the reason.
Take care ya'll,
Deb
Comments
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I'm so sorry to hear of all your issues. Mine are not as severe but I can definetly say I've got some stomach issues since chemo. I'm on prontonix and recently zantac, I've tried a number of drugs and combo's to see what works. The dr's keep saying it will get better but so far I've seen no improvement. I hope you can get some relief and answers soon and thanks for posting.
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The simple solution for this condition is a medication called domperidone. Gastroparesis is a symptom of Parkinson's which I have.
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I am sorry you have to go through this difficult times, I can feel you and hoping things will get better soon. I share the same problem, my cancer was found out because of severe abdominal pain, my dr. thought it was gallbladder infection, he requested an abdomen ultrasound and found out I have tumor in my liver. The same day I had an emergency request for CT SCAN and confirmed that it was cancer and they found a lession in my bones as well. Everything happened so fast and after few days they confirmed that it was a breast cancer stage 4.
I was referred to an ONCO and I still complain about my abdominal pain, she said it could be something else because tumor in liver would not have cause the pain. I was requested to have endoscopy and doctor found out I have moderate gastritis and they had a biopsy for some tissue which turned out that I have bacteria in my stomach. I was told to take the antibiotics but still having second thought because it might have an effect on my CHEMO.....I was thinking to take it after my last 2 cycle which will end in JULY. Not sure of my decision, but ONCO told me it is safe to take the antibiotics.....I will think about it because I dont want to mix up any meds while on CHEMO. I hope that you feel better soon and thank you for sharing your story.
Jenifer
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My husband has it too due to a metabolic muscular dystrophy. Glutamine helps him. I wish you well and feel sorry for what you are going through right now. My prayers and thoughts to you.
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Jennyboog-hope they help with your gi problems, and find the answers to make u feel better.
bluedahlia-Hi. I wish it were that simple for me. I've been on Reglan, protonix, Zofran, and some other meds I can't recall the names. Reglan made me so sick and my blood pressure went to 190/110 so they had to take me off of it. I still had some nausea/vomiting while on it too. I;'ve read that Domperidone is restricted in the us. So I don't think I've tried it. I also have cut down on what I eat. I will only eat chicken, fish, bread, hard cheeses, mayo, eggs,potatoes. I've tried plain cheeseburger with nothing but the meat, cheese, bun, but very seldom. Nothing fried ever. I also been eating a handful of Almonds. Most of the time the only drink I can tolerate is sipping on a soda. Water makes me sick to my stomach faster than anything. I do take phenergan and that lessens the symptoms. I do not eat without it. I still get queazy and it makes me very tired and sleepy., I've found a yahoo group for people with this and so many of them dont' have much relief or still get the cyclic symptoms no matter what they've done. Most of the documentation I've read on the net says that all the medications and surgical procedures have a limited success rate. Some patient's do good and others it doesn't help. I've heard of botulinem injections too with limited success. Anyways, hope your doing good.
Sweetangel-so sorry that your going through stage IV cancer. I pray you feel better very soon. thanks for sharing your story, too.
Voraciousreader-I'll have to talk to my doctor about Glutamine. Sorry to hear your husband suffers with this. I don't wish it on anybody.
Take care,
Deb
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