my gastroparesis diagnosis story: delayed gastric emptying

For today's video I am telling my #gastroparesis story also known as delayed gastric emptying! What is it, how I got diagnosed and more! #PICCline #pots
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[@mike0133]

Why this fucking disease affect so many young people? I am 20 years old guy suffering of gastroparesis... Why God? Why me?. I wish you all the best, it's not simple to live with this shit. I wish you the best again, you are so strong.

[@user-ox6rw2gl3z]

هل وجدت حل لخزل المعده ارجو الرد هل تحس في رخاوه في المعده

[@Reborn3.2.3]

You ain’t alone 🪬🩻keep up champ and consult with the doctors like a man and you’ll be cured trust my words and be in the process .

[@StrawberrryBlud]

I did the gastric emptying test, had to eat a pancake with the radioactive product in it, the test took about 4 hours indeed and showed that there was still around 80% left that wasn’t digested,made me awfully nauseous. Surprisingly I rarely end up vomiting (thank god for that) because I have terrible emetophobia 😅my nausea is the worst symptom and I feel full and bloated very quickly. I do still eat solid foods but the things I can tolerate are very limited and because of that I’ve been underweight for the past few years, suffering from exhaustion and having no energy at all. I recently found your channel and really enjoy watching your videos, they’re so helpful and really show what it’s like to deal with gastroparesis since I find a lot of people don’t understand what this condition is like. In my personal case most people always assume I have an eating disorder which is something completely different from gastroparesis. Thank you so much for sharing your experiences and raising awareness 🥰💚

[@love_gracie_joy]

I know that this comment is really late, but I’m in the process of trying to get a diagnosis. I also have POTS and seizures along with many mental health issues. Anyway, thank you so much for sharing your story! It’s really making me feel less alone. And I know I don’t have the official diagnosis yet, and I wouldn’t wish it upon anyone else ever, but your honest videos make me feel like I’m not alone! Never change! -Gracie

[@jennyebbrell3862]

I was diagnosed two weeks ago with moderate gaatroparesis, the last year has been horrendous for me.. some very dark days. So you should be so bloody proud of yourself for being strong and getting through every day xxxxx 💖💖💖

[@ChronicallyLindsay]

Sending so much love! It’s a tough battle but you are not alone! 💖💖💖

[@nkadimashiane]

Neurofeedback and biofeedback might be able to help if damage to the autonomic nervous system is in the brain, which is usually what happens. I would also recommend the Comra laser therapy to heal any tissue or nerve damage. If its due to diabetes you will have to control you blood sugars.

[@user-bx8go7cj6q]

You are so strong (really) and beautiful, this makeup indeed looks good on you. I really hope you will find a cure!hugs from Estonia

[@violetcountry]

I am very glad I have found you! YOU ARE SO STRONG!

[@ChronicallyLindsay]

Glad you found me too! ❤️ thank you so much ❤️

[@kirsxc]

thank you so much for helping raise awareness for our conditions💓 you’re so strong & positive despite it all!

[@ChronicallyLindsay]

Your comment just made my day thank youu ❤️❤️✨

[@kirsxc]

@@ChronicallyLindsay and your vid upload made mine hahah- you help give me the strength & encouragement to carry on honestly☺️💗

[@ChronicallyLindsay]

@@kirsxc so much love 💚✨ your never alone! ❤️

[@teresagould6987]

I don’t think I’ve worn makeup 💄 for a couple of years. God I must make an effort.. I do pain my nails when I can. People dint understand just showering is enough lol 😂 love your vlogs and I’m finally having to pay privately for my gastric emptying test. Big hugs and hope your having a better day. I got my family to put our Christmas 🎄 decorations up and it’s just lovely xxxx

[@DanniD]

I was going the mention eds but then you brought it up. It is more unknown over here and hard to get the diagnose. Good to hear it is not the case where you live.

[@jisunmudd9970]

Thank you for sharing your experience and solutions it is very helpful and comforting. 💓

[@alyssawssinging4039]

Hey been vomiting all night so much pain with my stomach I have gastroparesis also I hate this illness but thank u for making this video

[@Dulcimerist]

Mestinon (Pyridostigmine) is the medication that worked best for my gastroparesis and intestinal dysmotility. This inexpensive 75-year-old medication has been repurposed by cutting edge research facilities like Mayo Clinic to treat motility issues like gastroparesis, IBS-C, pseudo-obstruction, etc. It stimulates the vagus nerve (which regulates digestion) and reverses gastric muscle paralysis. It can also be prescribed to treat POTS and dysautonomia.

[@EvaAntonia1]

Wow just have to say I am impressed with that you are still so positive with all what you are dealing with... Sending hugs, love and strength ❤️ I never heard about this which is apparently a theme watching your videos but I like learning something new so😊

[@ChronicallyLindsay]

Thank you for your consistent support in watching my videos ❤️✨🙏🏼 sending hugs and love right back at ya ❤️

[@EvaAntonia1]

@@ChronicallyLindsay You're more than welcome

[@averyreese7158]

hey there! i’ve totally been like binging your channel and let me just say you are so so strong! i’ve been sick with mono since january and then because i was bedridden for so long i got diagnosed with POTS in april. I’ve been on Propranolol for about a month now and they also just started me on Fludrocortisone for my symptoms. Since January i haven’t been able to use the restroom without using medicines to help and i’ve been throwing up stomach acid and it’s just been so bad. I’m seeing a GI soon and i’m afraid i have gastroparesis. I’ve also had like severe dehydration for the past two months and horrible migraines, like when i went to the hospital they had to stick me 6 times for an iv because my veins kept collapsing. Before i got sick i had acid reflux, uncontrollable bowel syndrome, and lactose intolerance so to go from having issues like that to not being able to use the restroom at all is so crazy. Hopefully i can get a diagnosis soon the pain has been so unbearable. Good luck to you! I hope things get better!

[@ChronicallyLindsay]

Hope my videos have been helpful to you and help you feel less alone! Wishing you the best of luck on your health journey!! I hope you start to get some answers and treatments that help you soon ❤️

[@Dulcimerist]

Sorry your have all of that. I have POTS and gastroparesis due to having hypermobile type Ehlers Danlos syndrome. Sometimes beta blockers like Propranolol can aggravate gastroparesis, so keep an eye out for that. (Calcium channel blockers are much worse for gastroparesis, so avoid those.) Mayo Clinic has pioneered Pyridostigmine as a repurposed treatment option for gastroparesis, and it's also been pioneered by the dysautonomia research center at Vanderbilt to treat POTS. This has been a miracle for treating both of those issues in me.

[@elenaaaa2035]

You are so strong❣️

[@ChronicallyLindsay]

Thank youu ❤️✨🥰

[@josiecallahan2712]

I really love your video and it is great that you are working to inform the public on such an uncommon disease. However, I feel it would be beneficial to keep your chronic illness videos focused almost completely on your experience (i.e. keep the information from webMD, wikipedia, etc.) to minimum. Lots of these sites list general symptoms which can be misleading and even cause some to attempt to self diagnose. This goes for the discussions of medications as well. If you feel it is absolutely necessary to include some of this information, you should also stress to your audience the importance of consulting with physicians. That being said keep up these great videos to spread awareness and tell your story!

[@ChronicallyLindsay]

Thank you for your comment and constructive criticism!! I appreciate your point of view, and I definitely see where you are coming from! I usually include a disclaimer of some sort about self diagnosing and consulting with doctors but brain fog is a thing and I forgot in this video, talked a little about this in my description though! Will keep that in mind for future videos ❤️✨ lots of love!

[@5p674]

You are mind-blowingly cute and smart!

[@ChronicallyLindsay]

Awe thank you!!

[@jessiewhittred1806]

I might have this coz after and before food I’m sick and bloating

[@peacefrog2357]

Was halitosis a symptom? Like I eat something the day be4 and the next day I’m still burping with the smell of the food I ate. Like I feel heavy for awhile after I eat something heavy

[@tdunkley001]

Do chew and spit. That’s what I do. I have Gastroparesis as well and I have a G-tube to.

[@khadijaibrar9558]

Im 15 and 3 months ago my paerants bought burgers and I couldn't Evan eat half of the burger I didn't know why so I thought I probably just ate already too much. but after that day I eat less then I used to . I ate less because I feel full and if I eat more I feel like I'm forcing my self to eat . When I make my self eat a whole burger I feel really sick and bloated . After that in the morning I would still feel a bit sick and I wouldn't feel hungry and I would loose my apatite whereas before I would always wake up feeling hungry and excited for breakfast. Also I get this weird feeling that goes up my thought and it feels like an air bubble I don't know what this is or if this is normal but does anyone know what this is cause I'm a bit worried so I decided to search my symptoms

[@simplysweet0016]

I am just wondering if people who have GP if they are on disability?

[@jisunmudd9970]

Does nutritional drinks help?

[@JuanitaClarkGarcia]

That's what's I'm wondering

[@marym6733]

this might be a weird question but did you ever get stomach spasms/twitching? x

[@sabrinacoleman8399]

Medical Supply/TPN Organization btw Ilysm 🥰🥰🥰 You can message me if you need someone to talk to about chronic illness or if you just want to vent

[@ChronicallyLindsay]

Adding it to my filming list!! Thank you so much, same goes for you! Only a message away if you ever need to vent ❤️❤️✨ so much love 🥰

[@donnaclemow5061]

I have Gastroparisis since 2023

[@Anjalisharma-sw3xj]

Please pray for me i have same symptoms 😔😔😔

[@IdkIdk-gw3qo]

i also have same symptoms and i live in india koi bhi doctors ne help nhi kri meri aiims m bhi dikhwa diya just waiting to die i guess:(

[@mohamedninja85]

You so Amazing lindsay stay staff you Heath 💘💘💘💘😘

[@nancyhagan3673]

Do most pots people gave intentional issues?

[@summerlea1026]

Do you have Ehlers Danlos Syndrome ? X

[@caredfor3422]

Did you gain or loose weight. Did you have vitamin d and B12 defeciency?

[@faith_over_fear8896]

What kind of watch is that?

[@MammaLubUSA]

🙏❤️❤️🇺🇸

[@mohamedninja85]

You always so Beautiful ❤️❤️❤️❤️❤️

[@ChronicallyLindsay]

Thank you!! ✨❤️