Does anyone know the diet for gastroparesis?

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I was recently diagnosed with gastroparesis and would like to know specifically what type of diet I am supposed to be following and what foods I should stay away from?? Thank you.
There is no specific diet for gastroparesis as such. The trick is finding out what you can tolerate and what works for you. In general terms, GP diets need to be low fat and low fibre. If you include things like bread, pasta or rice, stick to the white varieties. If you eat meat, stick to lean cuts. That's if you're able to tolerate solid food... The other really important thing is to have small, frequent meals - aim for 6-8 a day.

If you're not tolerating any solid food, you can try blending regular meals - personally, the idea of this is pretty revolting to me, but you can make some pretty decent soups. There are also some good nutrition support drinks around - you can get the basic strength ones at the supermarket and the others.  (+ info)

Gastroparesis - Can I eat fiber in small portions and be okay?

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Fiber takes longer to digest, so it can be a nightmare for many people, and I've noticed that eating a lot of cereal and bread sometimes makes me feel very sick. Is it okay to eat fiber in small portions? Does it make a difference at all and is it safe if you have gastroparesis?

Thank you!
are you 100% sure it is gastroparesis and not celiac? How are you with other gluten products? Have you had proper testing or did you self diagnose? The tip off here is cereal and bread issues. You need to talk to your doctor about this and ask for a IGA and TTG. Celiac is common, and one of the most underdiagnosed diseases!
go here:
http://digestive.niddk.nih.gov/ddiseases/pubs/gastroparesis/

and for celiac:
http://www.celiac.com/  (+ info)

what is the best way to manage gastroparesis and stop the formation of bezoars ?

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My mother is suffering from this condition and is a type 2 diabetic and is 82. Any help would be appreciated in this matter.
gastroparesis is a form of autonomic diabetic neuropathy.
in our clinic we use alpha lipoic acid (Thiogamma), B vitamins metoclopramide  (+ info)

Does anyone have eating tips or ways to deal with gastroparesis?

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I just found out I have it and I'm drained and going nuts. I'm 22 years old if that helps.
First, and foremost, consult with your physician. In addition to the above suggestions, you might benefit from Reglan (generic name is Metoclopramide), which is a small pill/tablet taken before meals, which aides in treatment of gasteoporesis. I've been on this medication for many years (15 so far) -- I'm 43, and have been a Type-1 diabetic for over 34 years, and it has helped me out greatly. But, it's something my doctor prescribed, and the dietician agreed with. Professionals are often the best source for advice and assistance in treating any medical problem.  (+ info)

How would a doctor test for crohns disease and gastroparesis?

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Could either of them be detected in a basic blood test?
  (+ info)

What autoimmune disorder has celiacs, gastroparesis, cystitus, vulvadynia and sub clinical hypothyroidism?

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I have been diagnosed with all of these disorders and the doctors have't figured out what the main autoiimune disorder is that contains the above. Yes, fibromyalgia has been thrown out there, can anyone think of anything else to be tested for? I also have pelvic pain, hip pain, elbow pain, leg pain and headaches.
Autoimmunes as you list are all related to each other as they are HLA type conditions. If you have one, you are more likely to have others.

There does not need to be one primary autoimmune disorder.

Are you being strict with your gluten free diet (i.e. being wheat free as well) and have they started you on thyroxine yet?

Both those things will improve your gastroparesis and vulvadynia. Improving the vulvadynia will improve the cystitis.  (+ info)

Does anyone have or know of a person with gastroparesis?

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I have gastroparesis and I've had an endoscopy, gastric emptying test, bariatric scan, and many blood tests...I have taken Protonix and now have a prescription for Prilosec. I haven't tried it yet. What can I do? Does anyone have suggestions other than go by the diet?
Hi Mollie,

I have been living with gastroparesis for about a year now. Mine is pretty severe, to the point that I cannot tolerate any solid food without vomiting and have lost about 1/3 of my bodyweight.

Changing your diet is going to be necessary, at least in the short term. Soft food, low in fat, low in fibre. Things like soups, yoghurts, pasta and similar foods are best . Have you tried any of the medications that increase the motility of your stomach? These were no good for me because of side effects, but a lot of people use them with great success - the two main ones are domperidone and metaclopramide. Another possible option is botox injections into the pyloric sphincter (where food leaves your stomach). This has very mixed results, but I am actually going to be trying it next week.

It's probably easier for you to ask any questions you might have than for me to ramble on here, so if there is anything in particular that you want to know please feel free to email me :-)  (+ info)

Is medication the best way to reduce depression in gastroparesis patnties?

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My sister has this disease and has days when she sleeps all day, on and off. it seems like depression to me.
Depression and anxiety are very real possibilities for those that suffer from gastroparesis.A dietitian might suggest that you try to:

Eat smaller meals more frequently.
Eat low-fiber forms of high-fiber foods, such as well-cooked fruits and vegetables rather than raw fruits and vegetables.
Choose mostly low-fat foods, but if you can tolerate them, add small servings of fatty foods to your diet.
Avoid fibrous fruits and vegetables, such as oranges and broccoli, that are likely to cause bezoars.
If liquids are easier for you to ingest, try soups and pureed foods.
Drink water throughout each meal.
Try gentle exercise after you eat, such as going for a walk.
Some people with gastroparesis may be unable to tolerate any food or liquids. In these situations, doctors may recommend a feeding tube (jejunostomy tube) be placed in the small intestine. Ask your doctor what is the best way to reduce depression gastroparesis's sister.
Take care as always.  (+ info)

For those with gastroparesis, have you had botox injections and did they work?

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I have idopathic GP and was thinking of asking my GI specialist about botox.
Yes and yes  (+ info)

Has anyone had a gastrectomy for gastroparesis?

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I've read that 86% of patients who have had a gastrectomy for surgically caused gastroparesis (slow stomach emptying) have had relief of their symptoms. I'm looking for anyone who has any information on this and/or a doctor in northern Illinois who has done this. Thanks in advance for any help you can give.
Dear TYSMOOCH.......

Visit this site,
http://www.healthcommunities.com/statelist/states/state_Illinois.shtml

Hope it helps.  (+ info)

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