Patient Comments: Gastroparesis - Diagnosis

How was your gastroparesis diagnosed?

Comment from: Tina, 65-74 Female (Caregiver) Published: May 21

Hi, my name is Tina, Now I have it but my mother does and she is 74 years old. She suffers so bad and she only had it for only 2 months. And she have so many other health problems alone with it. She get so frustrated and I try to keep her spirits up to the best of my ability, and it'd hard seeing her suffer every day. I've been her caregiver for 5 years and it's been stressful, so anyone going through this my prayers. and my mother's go out to you.

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Comment from: 33 years old, 25-34 Female (Patient) Published: March 19

I was diagnosed with Diabetic Gastroparesis just 3 days ago. I had been having stomach pain, always feeling full, vomiting constantly, and recently lost over 30 pounds in just a few weeks for almost a year before my family doctor referred me to my Digestive doctor. Although I was just diagnosed with this disease I have been living with it for over a year now and it is very frustrating and hard to live with. I also feel for others like myself because I know how hard it is to live with this disease.

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Comment from: sick 2mystomach, 55-64 Male (Patient) Published: August 03

Heidi, I am so sorry you are going through this. I am old enough to be your father and have been battling gastroparesis for 12 years. Whatever doctor told you it was emotional problem is a horse's behind. It seems too many docs do that when they're stuck for an answer. The problem is the vagus nerve is severely damaged and therefore your stomach does not produce contractions to aid in digestion and move food along to the duodenum. I suggest you find another gastroenterologist to see if he's able inject Botox into the muscle of the pyloric sphincter.

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Comment from: smilesallday, 35-44 Female (Patient) Published: August 08

Gastroparesis is the worst thing in the world. Oh my, I have been in pain for days and had gone to the hospital and they said, 'chronic abdominal pain'. So I went to my gastroenterologist and he says there is no cure; really! I've changed my diet, and it seems ever since they did the upper endoscopy I'm in worse pain every day and finally I'm getting an appointment for pain management, yes, that's where they sent me! My stomach gets so big as if I was pregnant approximately 9 months and the pains feel like contractions, no one that has not had gastroparesis can imagine the pain I go through on a daily basis.

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Comment from: AmyYo, 35-44 Female (Patient) Published: July 28

I have gastroparesis. I always had stomach issues, but I'm guessing, with diabetes for 34 years and taking poor care of myself, this is what happened.

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Comment from: Thomas, 19-24 Male (Patient) Published: October 15

I developed gastroparesis in 2001 when I was 11 and finally diagnosed with an endoscopy in 2007.

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Comment from: Chefchristina11, 35-44 Female (Patient) Published: May 23

I have had severe abdominal pain for about five years. The doctors ran every test and they all came back normal. They put me on pain medication and Reglan for the nausea. The pain meds helped a little bit, but I throw up anything I try to eat. I just found out that I will no longer get my pain medication because the doctor doesn't think there's anything wrong with me. I have been diagnosed with gastroparesis. I don't know what to do. I have a 2 year old and it's hard to take care of him when I can barely get out of bed. I wish I could eat and not throw up. I just don't eat at all – my stomach swells so much, I look like I'm 9 months pregnant (which I'm not.) For years, nobody believed that I have severe pain and thought I was just a drug addict. I don't know what to do. The pain is more than I can bear. Now they want to take away the one thing that helped a little (my medication). I can't take this much longer. And to find that there's no cure – I can't live the rest of my life like this.

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Comment from: ChrisC, 45-54 Female (Caregiver) Published: March 25

My wife has had gastroparesis for more than 20 years. She has tried all options, including a pacemaker and more medications. Finally, she had most of her stomach removed. She can only eat a few things and most of them make her sick. The only medication that seems to help her is Ativan and the doctors keep taking her off of it. It seems like we can't get doctors to listen to us. Now I'm watching her starve before my eyes. I feel so frustrated.

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Gastroparesis - Describe Your Experience Question: Please describe your experience with gastroparesis.
Gastroparesis - Possible Causes Question: What do you believe was the cause of your gastroparesis?
Gastroparesis - Symptoms Question: What symptoms do you experience with your gastroparesis?
Gastroparesis - Treatment Question: What kinds of treatment, including diet and medication, have you tried for gastroparesis?

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