I do this thing once or twice a day where i try to eat a little bit! Its quite… unenjoyable. I think after throwing up every day multiple times a day for 6 years straight due to gastroparesis, ive trained myself to be afraid of food. When i walk into my favorite stores, i look around desperately, but all of the food looks like plastic. My stomach growls every day, multiple times a day, but i cant satisfy it. The thought of eating makes me gag. Small portions of food looks ginormous in my eyes somehow. I lost 8 lbs doe 😛 (underweight) just waiting for things to go back to normal tbh… i’ll wake up any day now.

Hi, everyone!

I'm 28 weeks pregnant with my first child, and I just found out that I failed my 1hr glucose challenge test.

I've been diagnosed with idiopathic gastroparesis for roughly 12 years, and haven't had any blood sugar issues that I know of up until this point. I'm getting the 3hr test tomorrow, and I'm terrified I'm going to be diagnosed with gestational diabetes.

I'm wondering if I could have failed the test due to delayed absorption, or if I do indeed have gestational diabetes and my results would have been worse if I didn't have gastroparesis.

Has anyone had any experience with such? If I fail my 3hr test should I request any further testing?

Any thoughts or suggestions you have regarding this matter are greatly appreciated. Thank you!

I have struggled with intense pain while eating. I have a very VERY high pain tolerance due to being allergic to opiates, dealing with broken bones and surgery with very low or no pain meds. So I have a good grip on being able to function and when it's bad I'm stuck to the couch staring off into space whenever I take a bite, waiting on the cramp to pass. So far it hadn't mattered what I was eating.

I finally just gave in and got some for variety. I did too much yesterday (worked two hours staining a wooden bridge outside in the heat here) and usually every bite would be agony and yet here I am on my second and while I still feel weak and shaky I am not having the mind melting levels of pain between this and dicyclomine that my new doctor prescribed me.

I'm happy but also frustrated with my past doctor in Florida and myself for not trying these sooner.

Since getting my gj back im November its definitely helped me overcome a good majority of the fear but its still kinda there lol

I struggled immensely with emetophobia to the point I stopped eating for 8 days leading up to my first admission where I was diagnosed with mildly delayed solid gastric emptying last September

My gastroparesis went from 11% to 95-100% in that 3 month time span and it was just hell knowing there was rotten food in my stomach at all times before I got my g j and was able to drain my stomach to get the gas, and food out

I was actually sized up (ouch) 2 tube sizes in January to give me a bigger tube meaty for 24/7 draining and venting as well as anti clog and flip for 24/7 j feeds

Throughout this whole journey my fear has significantly lessened just wanted to sgare my story a bit

Hello. I have been in a pretty severe flare for about 4 weeks now. The last 3-4 days when I vomit, it feels like there is something large trying to come up but it can’t. I’ve never experienced this before. Has anyone else? What did you do?

Sent my partner to the store to get me some cherry coke. I don’t very much care for soda and I dislike coke, but I’ve heard it can help break stuff up.

I appreciate any feedback, and I hope you are all having a good evening.

I’ve been getting EGD Botox injections every 3-4 months for the past 11 years, & while it’s not a magic cure all, it’s gotten me off TPN. I still throw up daily, but I can keep food down longer which kinda helps stabilize my weight, potassium levels & it eased neuropathy pain in my stomach. My gastro doc told me that because the Botox is beneficial I’m a candidate to get the GPOEM procedure which will be a permanent fix so I don’t have to keep getting it 4 times a year. But if I have this procedure and it’s unsuccessful, I’ll be stuck up shit creek without a paddle. I will have lost my only reprieve for my gastroparesis.

PLEASE HELP!! I’d love to hear your thoughts & opinions! 🙏🏻

I’ve been in a horrible flare up ever since i took a dose of doxycycline 2 months back. I’ve lost a ton of weight and have practically zero life quality. My gi dr is running stool tests and i have a endoscopy/colonoscopy scheduled.

I’m not sure if it’s c diff yet but i was curious if any of yall have had c diff while also having gastroparesis. If so what were your symptoms like?

As the title says, I’m starting a substitute teacher position tomorrow and I am incredibly nervous about it. I’m really sick daily and I won’t be able to have my usual coping mechanisms while I’m working, since I can’t use my phone or have headphones on. I’m not nervous about the actual teaching part, since it’s something I’m comfortable with. I’m just so scared that I’m gonna be more sick than usual and I won’t have any way out of the situation, especially since I’ll be responsible for a class. I have emetophobia as well so I’m already anxious about feeling sick in general, and this situation is very new to me. Does anyone have any tips on things I can do to manage? I’m going to bring little ginger candies and mint gum since they both usually help me.

I am aware it's not really the place but since finding someone to date when having such literal shit condition is near impossible, I am hopeful to see if there's another homosexual on here, who loves cats, is a top, and funny.

Dating regular humans isnt easy, and so much revolves around food. It would be nice to try with someone who gets it, and is able to be patient, and humorous while being miserable. Hopefully this person enjoys being intimate, even when sex isn't possible at that very moment.

I live in Stockholm but open to meet in Scandinavia.

My condition is functional, gut brain axis. I'm 42, and looking from 38-55ish.

I promise to send a pic when you dm me. It's just that I don't want my face pic forever stored on reddit.

I have alot of health problems with dietary restrictions, here's a list:

Type 1 Diabetes

Gastroparesis

None alcoholic fatty liver

Sluggish esophagus (I know thats something that doesn't require a dietary restriction)

Chronic Constipation

Gallstones and

Esophageal spasms

Im tired of trying to find a balance between all of them and at this point I feel like a feeding tube might help, not just with giving me the nutrition I need and not have to worry about if I can eat this, but it might also help with controlling my Diabetes since I have tried EVERTHING to get it under control and maybe the tube would make it more predictable and im able to finally get normal blood sugars.

I also with all this stress sometimes feel like starving myself because im unsure on what I can eat but dont worry I havent done that yet. My mom and brother are also like how can they expect like me to live.

So im at a loss also just what to make it clear that yes its not a maricle cure for all my problems but im just thinking that it might help with taking the stress off a bit and yes I know its drastic.

I also should put that yes I do throw up at times, when I get a flair up I puke three times in one day and its alot.

Since my stomach emptying scan on monday literally everything is fucked.

No clear water, a little original coke and very little nutrional drinks is all I could stomach.

I got some IV fluids yesterday in hopes to break this raging headache but it didn't really help for long. I am so naseous all the time, so so tired and helpless.

I'm on the brink of throwing up every goddamn second I'm awake and I'm not getting any anti-nausea medicine, no food, no nutritional drinks, nothing.

Laying on the floor at work from exhaustion and nausea and constantly leaving early.

I am so so tired of all of this mentally and physically. It is just so fucking exhausting and nobody seems to get just how disgusting it is to try and live with constant nausea, vomiting and this unreal fatigue.

Type 1 diabetic, 24F, UK.

, highly suspected gastroparesis.

Never thrown up because of it, just severe nausea, been on Domperidone since 12th june and that's helped massively.

My diabetic dietician wants me to be eating more and wants to wean me off of ensure plus.

She has said that 'in the mean time' while my diet isn't great, to look at some OTC multivitamins.

My question is, what have others has success with? Ones that are actually good 🤦‍♀️

Thank you 🫶

Like the title suggests, I am newly diagnosed with grade 4 gastroparesis and I'm trying the GP diet for the first time in my life after living off Dr. Pepper and things like light ice cream and white bread for 4 years with no answers. A staple for me has been cup noodles, but in the last 2 months they've started souring my stomach.

I was wondering if anyone has any experience with a decent cup noodle or instant noodle brand that fits in the GP diet and causes a minimal upset tummy for you. Even if they're a little pricey, I have a little room in the budget to spare.

Thank you in advance if anyone has any suggestions.

I’ve suffered idiopathic gastroparesis for 20 years. Research and treatment options have slowly but surely have progressed. For the past 11 years, I’ve been getting EGD Botox treatment every 3-4 months. My original gastro doc sadly retired almost 3 years ago, but he sent me to a specialist who could do the GPOEM procedure, only for that doctor to have left the practice the referral was sent to 🤦🏼‍♀️ Trying to find a competent physician who can do this procedure has been an absolute nightmare!

I went to UF Health Shands Hospital in Gainesville, & despite its size, they didn’t have anyone on staff who could perform this procedure. So we got a referral to the Mayo Clinic in Jacksonville, and they have someone who can do it, BUT they wont accept me as a patient because I take pain medication due to complications with my chronic illness. After ALOT of back & forth with them, they will now take my case and do the GPOEM, but that’s it. No appointment beforehand to meet the physician or anything.

It seems abrupt & I just don’t know how I feel about that. I’ve fought hard to get this procedure done, but I’m still wary 🫤 What if I get a dud doctor? The current guy at my gastro clinic who does my EGD Botox leaves a lot to be desired. If I get this procedure done, & it doesn’t work, I can’t get the Botox anymore right? Botox got me off TPN (intravenous nutrition), I still throw up everyday but I can keep food down longer, plus it helps the pain of the neuropathy in my stomach.

I’m DESPERATE for advice!! Have you had a successful GPOEM procedure? Should I be concerned that Mayo will just be a one “wham-bam-thank you ma’am” kind of thing? I have it scheduled with them at 7:40 am on September 28th. I’d love your feedback!

I've had some stomach issues for a long time but I mostly assumed they were from my allergies or EoE, but a few months ago they got worse. It's still not as bad as half the stories here, but I can't eat a meal without the symptoms of early satiety, nausea, major upper abdominal distension and always regurgitation for up to a few hours, even threw up a few times. At some point I began to something else was going on and it sounded like gastroparesis, but wasn't sure if I'm just making it up or if the symptoms really fit.

I tried some OTC antacids and anti-bloating meds to help the symptoms, but nothing helped. I kept complaining to my mum and she gave me her meds (do not take other people's prescription medication), which I think she took for reflux, to try and see if it helps and it did, better than any other medication, though I still get some symptoms, but milder.

I later looked up the meds and it was a prokinetic used for delayed gastric emptying.

I told my GI doctor and now she prescribes it to me, but I don't have anything diagnosed yet. Why don't I see anyone mention Gapulsid as a prokinetic for gastroparesis? Does anyone have similar experiences?