For anyone told they have Gastroparesis, I feel it’s my duty to give my own experience so that should you have a similar experience you can avoid some of the time-wasting that I experienced and get help faster.

You may not have Gastroparesis.

Equally, if you are seriously sick and your symptoms are throwing up, intractable nausea and stomach pain, this may help you get a diagnosis.

In the days before the ‘gold-standard’ Gastroparesis test which is the Gastric-Emptying-Test (GET) doctors tended to rely upon an EGG of your stomach to measure your stomach waves/contractions. What an EGG does is tell the doctor how your stomach is performing not in terms of motility so much as spasms and waves.

Nowadays they talk more about motility and the bias is toward slow motility. This means when you go and get a Gastric-Emptying-Test (GET) they are biased toward thinking you have slowed down motility. Although women’s stomachs are much slower than men genetically, and although people are different in their emptying/rates of emptying, there is a bias toward thinking stomachs all empty the same way.

Because one size doesn’t fit all, it’s important to find out what your stomach is doing. It isn’t sufficient to be told ‘your stomach is emptying slowly’ as this is usually based upon a short test that doesn’t capture the duration of your stomach’s experience with food. The reason it’s important is because when you go into the ER with symptoms they will often only run a GET for ONE hour. They will tell you that if your stomach hasn’t emptied 50 percent it is emptying slowly. That isn’t true, a stomach can take up to 4 hours to empty and you also need to know if they are referring to the top portion of your stomach or are also taking into account your small intestine as that is part of the stomach in terms of function.

The best GET test is to ask for a full four-hour test, and for them to photograph your small intestine as well as your stomach. Only then can they definitively say that your stomach is slow emptying. If that is not done, question the diagnosis of delayed emptying. In this day and age of Diabetes, it is a common bias that people are more likely to have delayed emptying than fast emptying. (The reason the EGG is a less popular test is also because doctors cannot make as much money from that test as a GET).

Furthermore, it’s not as simple as ’emptying’ because the Cajal cells in your stomach are connected to your brain, they have 70 percent of the serotonin in your body. In a way, that ‘gut instinct’ is accurate, and as such, you ‘feel’ things via your stomach. If you are throwing up, feeling violently nauseous and dizzy and have severe IBS symptoms this can be from the mis-firing of your Cajal cells in your stomach, that are overreacting and telling your body not to digest or to over-fast digest your food. This often happens after exposure to a VIRUS.

Here’s the real problem. Typically the medications you will receive will be medications for moving your stomach (prokenetics) that have bad side-effects and will make you sicker if your stomach is moving too fast. If the biased assumption is your stomach is moving too slowly, (not emptying fast enough) then these prokenetics will speed your stomach up but if your stomach is moving too fast this will exacerbate your symptoms.

I saw three Gastroenterologists as well as some on call in the ER. The first Gastroenterologist ordered very expensive tests (Colonoscopy & Endoscopy) then accused me of being anorexic (I had lost over 20 pounds due to throwing up all the time 24/7) and said I had Candida. He prescribed heavy-duty antibiotics for a month, when I told him I would throw up the antibiotics he insulted me and said if men in Vietnam with their stomachs blown off, can swallow antibiotics I needed to.

I went to see a second Gastroenterologist having no faith in the first. She was better, she said about the Cajal cells and the mis-firing and believed it was caused by a virus. She gave me a 40% chance of getting better but said I needed to force myself to eat more and prescribed me prokenetics x 3 a day and anti-anxiety meds x 3 a day as treatment (you get very, very, very anxious when you feel this way because you are throwing up non-stop). I had taken prokenetics before in the ER and they did nothing or made me worse, I told her that but that was her treatment. I decided after reading about prokenetics and how they have irreversible side-effects that I would not be taking them x 3 a day as that was madness, likewise with the anti-anxiety medications as I knew how addictive they can be. At this time I had had a GET for one hour so did not have any proof of Gastroparesis or even slow-motility but this was assumed to be the case.

The third Gastroenterologist explained things differently.

He looked at my symptoms and said that I could not have Gastroparesis because you would not have daily diarrhea with Gastroparesis as literally your system shuts down. I didn’t have early satiety, (feeling full quickly) although I found it hard/impossible to eat because of the 24/7 nausea. I threw up but not all the time, and I didn’t feel worse after eating (but I didn’t necessarily feel better either). Based upon symptoms he ordered an EGG rather than subjecting me to more radiation and because he felt it gave a more accurate picture. The EGG was quick, safe and painless. The results showed I had fast gastric arrhythmia.

What gastric arrhythmia means is when the rhythm of your stomach which usually is in three waves, gets disrupted, and causes extreme symptoms like 24/7 horrific nausea and throwing up. If you have diarrhea that’s a really clear sign your system is ‘dumping’ IE going too fast, and you develop a host of issues including bacteria over-growth etc. This doctor said prokenetics would worsen gastric arrhythmia of any kind but especially if you are too fast. He prescribed a Tricyclic Antidepressant at a hugely lowered dose (typical dose 300mg, he gave me 10mg) as they work on smoothing the muscles in your stomach, which slow the spasms and in time, re-set your system.

It is worth noting, gastric arrhythmia is unique in that it tends to feel a lot like arrhythmia of the heart, as the stomach is not far from your heart. You cannot tell that you are not having heart arrhythmia, which is why I said I felt I was the first time I went to the ER. Typically you will have very bad anxiety which is caused by the feeling of constant arrhythmia coupled with nausea and all the other symptoms. This is not your mind it’s actually your stomach! Heart patients with severe arrhythmia often experience crippling anxiety due to how they feel physically, the same is true with gastric arrhythmia but it is less well known so often doctors will assume you are suffering from some type of anxiety disorder until the results come back.

My doctor told me 90 percent of his patients got over gastric arrhythmia. But the key is proper diagnosis. I read online about many people who had gone through months of suffering before being properly diagnosed. It doesn’t help that when you do searches, Gastroparesis comes up a lot and many times, with cases that are not true Gastroparesis. It is worthwhile noting that Gastroparesis really means a stomach that doesn’t move. If you are going to the toilet, if you are able to eat something every day, your stomach is moving.

People with true Gastroparesis get big balls of undigested food trapped and sometimes they throw them up or have to have surgery to remove them. People with true Gastroparesis can’t eat but a few bites of food without being full. Gastroparesis is considered incurable, which isn’t true as if it is caused by a virus it often will go with time, but you wouldn’t know that from searching even reputable places online (the Mayo Clinic and many others say it is incurable and you have to ‘manage symptoms’ and the only way you find things about it being curable is when you add ‘viral Gastroparesis’ then there are many articles about remission and cure).

If you have Gastroparesis you can be cured with time. But if you have some of these symptoms and not all of them it is quite possible you do not have Gastroparesis and your doctor(s) are being lazy by using Gastroparesis as an umbrella term. When you don’t know anything and you are sick and scared it is very easy to just follow what you are being told and get really bad and inaccurate care.

If I had known about gastric arrhythmia and/or the nuances behind gastric motility problems, and why they are caused, I would have had a lot more hope and targeted treatment from the start, I may even be better now. But instead I spent a ton of money and fretted and worried and was so sick for months, before I was even correctly diagnosed. Now I am taking the right meds and I am hoping that they will cure me but I also know I have spent many months in agony which could have been dealt with better.

To help others, I want to make this clear. There is bad information out there, much of it negative, when you are sick you can really lose your mind reading the conflicting and negative information out there, so I’m trying to put out some that will help anyone who is experiencing these things.

IF you get sick like I did and you experience extreme chronic debilitating nausea, if you are throwing up, if you have diarrhea or get really bad IBS symptoms out of the blue, first things first get checked for common viruses like Epstein Barr, Shingles and NORO. If you come back as having a virus OR you experienced viral symptoms prior to experiencing these symptoms, chances are a virus caused this. It basically kicks your body into overreacting and like an autoimmune disorder, you develop some type of motility issue in your stomach almost overnight.

This is very different from developing it because of an autonomic issue or post-surgery or if you have Diabetes. Even in those cases, sometimes it can be cured but there is more of a physical reason for why it happened and it is not usually as rapid onset. Knowing why it started is important.

Second, once you know this, if your symptoms are very severe it may be worthwhile having a Colonoscopy and Endoscopy because it can rule out other things with similar presentation. However, they are expensive so if you are not able to do this, or do not wish to, then ask for a four-hour gastric emptying test or an EGG to be performed. The latter may be harder to find as it is only found in selective Gastroenterology clinics whereas gastric emptying tests are done everywhere. Ideally if you can find someone who will do an EGG that’s going to give you more complete answers. You can google your city and gastric EGG.

Third, find a good Gastroenterologist. Google ‘good gastroenterologists’ or ‘stomach motility gastroenterologists’ in your city. How I found my good one was by finding that there was a Gastroenterology Research Center in my city and I asked to see the head of it. Even if they are not in your insurance you can request they be or you can pay out of network costs which are more but are usually partially covered by insurance. Call them and try to get an appointment ASAP if you say that you are throwing up and unable to keep food down they usually will take it seriously and see you quickly.

Fourth. When you go to see them take all your information with you and say that you suspect you may have a motility issue but you are not sure if it is too fast or too slow. If they ‘assume’ it’s slow, question that, and ensure your symptoms fit slow before accepting that diagnosis (if you have diarrhea it stands to reason your system isn’t slow!). Take someone with you who is a thinker, so that they can be your advocate. I have felt so sick I couldn’t think straight and having someone else there, helps when your brain turns to mush. Write everything down.

I pieced some of the puzzle together myself. I was proactive in finding a doctor I felt was decent. I tried even though I have been so sick at times I couldn’t even get up from all fours on the floor. Sometimes a doctor will have a piece of the puzzle like my second Gastroenterolgist, but they will still do something ass-backwards like prescribe prokenetic drugs (that cause your stomach to speed up) without thinking through whether this is logical and right.

The hardest part is many of the anti-nausea medications don’t actually help with the nausea, (I’ve yet to figure out why) but especially those with prokenetic properties if your stomach is too fast. In which your doctor should prescribe something that will slow it down but typical antispasmodics don’t treat the problem they just force your stomach to slow, so you want to ensure your doctor is considering a less invasive approach such as very, very low dose tricyclics. At that dose they have none of the harmful effects of tricyclic antidepressants and do not work as antidepressants but just help smooth the spasm and speed of your stomach. My doctor said it may take a while for them to work to reset your system, if I had known about them from the get-go I may be over this by now so as soon as you can, get on them.

I’ve been told I will heal. At times I find that impossible to believe this because I have been so sick for so long it seems like a cruel dream to imagine being well. But I hold onto hope because it’s what I have. And I feel lucky to have it. If someone had told me what I am writing here, I would have avoided a lot of pain and suffering. So I’m passing this on in the hope that even if one person is saved some of the suffering of bad diagnosis and bad medicine, it’s worth it.

If you have anyone you know going through something like this, show them this and if I can help them I will. It’s been the worst thing I have ever experienced and you do think you are losing your mind after months and months of it, but with the RIGHT treatment there is hope and we must hold onto that.

28 Replies to “For anyone told they have Gastroparesis read this”

  1. Perfect and very clear! Thank you! It shows as much as we think we know, we often know so little. Helping one another heal with posts like this is wonderful and important for all of us to do!

  2. “Every day, a new beginning”. You already know how I feel about all of this. I’m happy you’re informing others. This is helpful and pertinent in today’s healthcare world. *big hugs*

  3. You will heal because you’re already getting there. Doctors don’t know everything, but some of them have a problem with accepting that.

  4. Thanks for this informative post, Candice. Will save it for future reference. There are a lot of doctors who need to be re-educated about stomach disorders (and there are so many). You’ve done more research than probably most of them.
    Hoping you’re on the way to true healing and relief now. That day will come. It must! ๐Ÿ’•

  5. As you know, I read this on FaceBook. I can only repeat that it is so well said, and that I am pleased you had the strength to write it.

  6. I can also empathise with this impression that something is wrong but doctors just have no idea what, and are giving a diagnosis just for the sake of it.
    I have experienced it myself with my leg injury 4 years ago. I have experienced it through my child last fall. It is exhausting to have to fight against doctors who believe you’re crazy (one told us my child was not in pain, and that we needed to deescalate medical treatment. Seriously. As if HE knew better than my child what they felt! I will avoid seeing this doctor at all costs now).
    So glad you are seeing the end of the tunnel!

  7. Love and strength to you, dear Candice! I know how it is to fight the medical system for proper and timely diagnoses. I’m so glad you have found someone who is working with you in finding the right meds and approach. I hope with time you see relief and full health. But, as you, I also know that letting go of expectations is the only way to survive the bumpy rollercoaster of chronic illness. One day at a time! <3

  8. This was so educational. It will help many. I wish I had had it years ago to read. So many doctors are just straight up cruel ego maniac and forget there is a suffering person . As if you WANTED to throw up the antibiotics. I’m so sorry you have gone through this. Throwing up is so vulnerable and can bring up so much else emotionally especially not having answers, being mistreated during the process of trying to find out and the endless tests.
    I’m thinking about you and I’m so sorry you are going through this!!!!

  9. So sorry to read about you suffering like this!

    (I also had some of these symptoms, but (mercifully) very little nausea.
    Having lost 56 pounds in 5 months it turned out that I was wasting away with malnutrition
    because my pancreas has stopped working.
    One needs powerful enzymes, with each meal, to break down food, or it just goes straight through.)

    I hope your condition has improved.

    Thank you for the informative post.

  10. Oh dear Ken I’m sorry. At least the pancreas can be fixed I pray you’re feeling much improved. I am doing better I regained the weight it’s a battle still but I’m definitely doing better thanks so much for caring, as you know illness can be very lonely and I’m very grateful for your compassion. I wish you continued improved health ๐Ÿ’“

  11. Unfortunately I didn’t put the weight back on, and remain very unwell.

    None of my illnesses seem curable. (Shall spare you the list!)
    I have been feeling so bad that my main hope, at present, is just living a few more years, while managing to get past creative work online.
    Wish I could spend more time at WordPress and make friends, but struggle in even producing one post per week (hence views are really low).

    Thank you for your kindness.

  12. Ken, I can’t say I understand. I know part of the struggle, but if you remain sick that’s much worse than my experience which I thought was bad but I know many, many people have it worse. I am a believer in answers. I saw three doctors who were totally wrong before finding one who was excellent. The guy I see is the head of the Gastro research center for the whole of the US – I wonder if it would be worthwhile for you to see someone like that or someone at the Mayo? Only because there are radical differences in what someone says versus someone else and for all you know what you have had treatment wise thus far, isn’t helping or even the right treatment. I don’t know if this is true but if i can help in any way perhaps in finding a place or person for you to go, this may help somewhat. I also believe diet, stress, adequate hydration and exercise can help but of course if you are really sick that’s not always possible. I would like to help so if I can do anything at all please email me meanwhile please know you are in my prayers for somehow a recovery. There was a time I did not think I would get well at all and I gave up – I am not completely well but I am better – I have to hope the same could happen to you.

  13. Apologies for the delay in response.

    I think a big difficulty is that my 31 years suffering M.E./CFS (since 1987)
    (constant pain, exhaustion, mood swings, over-sensitivities (to light, sound, etc.))
    has worn me down so much I can hardly cope with additional health problems.

    Having brain fog, it’s hard to even remember them all:
    IBS, insomnia, anxiety, depression, PTSD (childhood abuse/violence), stress, TMJ, migraine, herpes, kidney stones, pancreatic insufficiency, and chronic vertigo…

    At present, I feel too broken to be fixed, but appreciate your kindness.

    On a positive note: seeing your lovely icon on my blog was a highlight of the week.
    (And I hope you visit again.)

    Am looking forward to reading more of your work.

    Best wishes from Ken

  14. I was on a prokinetic for years and I recovered. Please donโ€™t go around saying they have โ€œirreversible side effectsโ€. People have an incredible ability to heal, which youโ€™re clearly not aware of.

  15. Dear Anna thank you so much for reading this. I have learned so much since this so if I can ever help you please let me know. I wished someone were there to help me when I was first going through this so I try to help others. I am here if you need any help seriously please reach out we are stronger if we help each other and I know how awful it can be xo

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