Gastroparisis diet?
Went to Mayo last week had 3 tests done. I'm in the normal ranges but right at the top end for each Gastric emptying study stomach and small intestin. Told to use a puree diet. I bought protein shakes, mashed potatoes and cream of wheat. What else is there to eat?
Interested in more discussions like this? Go to the Digestive Health Support Group.
sfagan74,
I can eat ground chicken and turkey. I also cook poultry in my slow cooker pot until is very tender. I also eat baked or broiled fish.
I do not eat whole nuts, instead I use almond, pistachio and walnut butters. These are good sources of protein.
I can only eat egg whites. I have problems digesting the yolk ( too much fat). I try to eat only 2 grams of fiber with a meal. I am lactose intolerant and I also have gluten sensitivity. Along with gastroparesis I have Cohn's, GERD, SIBO, hiatal hernia and diverticula. It is a constant struggle! Stay strong!
Now I found out my new insurance won't cover liquid medications even with y diagnosis. I'm so frustrated
Anyone ever have to do a GI psychology appointment?
When you are having a flare up your diet should be liquid. Once that has passed introduce thick liquids. There is a book ‘Living ( well!) with Gastroparesis by Crystal Zaborowski CHC. My book was published in 2011 so I’m sure there are later ones.
You should eat 6 small meals/day. When eating chew well until food is mashed potato consistency. Avoid a lot of fiber,spicey foods, foods that can cause ‘gas’ and many fresh vegetables.Once in the chronic stage you can try different foods to find the ones you can tolerate. No two people are alike. Carbs. are my best friend but I still have to watch the fiber. Oatmeal is good for you but it has a lot of fiber.
I was diagnosed after many emergency room visits and stays in the hospital with many tests in 2014. I still have ups and downs.
I hope I have helped you.
Regarding your medication not being covered by insurance, I would suggest you find out the manufacturer and see if they offer the medication at a lower price and/or sometimes for free depending on your financial status. Most, if not all companies have what they call an assistance program. Don't automatically think you would not qualify because you may be surprised. Of course, there is paperwork involved.
The psych appt is likely to help with any stress, poor sleep, etc due to gastroparesis (GP). Stress, lack of sleep can cause GP symptoms to worsen or flare up. Several studies have shown that "cognitive behavioral therapy" helped people suffering from IBS or Functional Dyspepsia so a lot of places are trying it with GP patients now.
Carbs too are my best friend. Like English muffins and some white breads. Meat eggs and ice cream are a few of my triggers right now
Hi, thanks for a quick response. Luckily I’m not a fan of pork or beef. When I did try it I knew I should stick with chicken. I have added sweet potatoes and so far no issues.Have you seen any nutritionalists.Finding a good one took awhile but the now she is very helpful.
I would like to ask you something but it’s sort of personal and I don’t know if you are a female.
Yes, stress can be a gigantic trigger. I thought when I retired that would end stress but it hasn’t.
Have any of you been prescribed Amitriptyline? I was started on it six months ago. It is classified as an antidepressant but is also being used for ‘nerve pain’ ?
I was on that for migraines but haven't been given it for this yet
Sure yes I'm female