I hate how google and web md classify DS as a "post surgery" problem. People like me who have never had any gastric surgery can still get this via IBS C turning into IBS D
Wow.. that feeling when within 1hour you find the diagnosis that atleast 5 different hospitals haven't been able to figure out in 3months, for my sister with excruciating pains.. Thank you for the video. I really think this is it..
The MRI gastric emptying study didn’t detect my dumping syndrome. I had to do a second study where they take hourly pictures to find it. Make sure you get the better study done, as it is more powerful in detecting abnormalities!
I alway remember a patient state the dumping syndrome she experienced in 2009 was from ruptured silicone implants. I thought this was absurd. I complained of dumping like syndromes post explantation and prior to my explantation June 2013 in Kelowna. We will never know the effects of the various implants and devices we place in our bodies. That's not really the crux of this comment. I noted last week, yes last week, that I had an Xray indicating lunacy/fracture of the L1 in June 2014 when I was seeing a hematologist and GI specialist at the same time and neither knew of this fracture. Fast tract 2020: dumping like syndromes continue to prevail coupled with pelvic/GI pain, weight loss and a diagnosis of severe osteoporosis and bilateral sacral fractures in the last 2 months here in Calgary. Yes, I had to relocate to Calgary to learn that I have sacral fractures and osteoporosis and I considered myself a physically fit and health 58 year old female. Drinking water triggers a dumping like sensation and I wake up feeling nauseous after a calm and uneventful sleep. There is a relationship between gut health and skeletal health--no doubt about it. It is offensive to listen to healthcare providers question my mental well being. Women are also more likely to undergo pelvic medical procedures such as ablations, tubal ligations, salpingectomy, D & Cs and are often labeled as "hysterical" and considered unreliable historians obsessed with their elimination systems when presenting with pelvic and abdominal pain. Seeking healthcare as been redundant and torturous just as my colon has been described in numerous medical reports over the course of several years. I enjoyed this very informative UA-cam. My diabetic mother may provide a clue to my health concerns. Thank you
I have neuropathy, which I also believe caused the damage to the vagal nerve. This all started in September 2017. I literally feel the neuropathy intensifying about 10 minutes after ingesting foods...but only foods containing folate and vitamin K. The more the vitamin, the worse and longer duration the symptoms. I started developing multiple symptoms since September 2017. 30 now in total.They tried me on multiple heart medications to control tachycardia and other arrhythmias and they all caused horribly painful reactions. Because of the neuropathy, I can literally feel when a food or drug hits my bloodstream. It always starts in my left foot first. I gave up trying meds because of the pain they caused. I still have trouble consuming foods with K and folate. Not only the neuropathy, but if I consume too much of either, my balance is horrible and I feel very 'odd', brain-wise. If I avoid them totally, the neuropathy goes away, totally. But I've already lost 40+ lbs since September. Much more and I'm pretty much done for. Those vitamins are about in every single food known. The only thing I can come up with is that I was on carbamazepine during all of this. Every symptom I have is listed under adverse reactions for that medication. Every heart medication I was tried on is known to react with that medication, causing increased plasma levels. I stopped taking it on December 15, and though it hasn't gotten any worse since then, it still hasn't gotten much better either. The carbamazepine has a half life of about 35 hours. They tested it at 2 weeks and it hadn't budged from two weeks before. They tested it again at fours weeks and it was at
I got a tif with a hh repair. I had and have severe bloating both pre and post op. 3 months after my surgeries I noticed I would get extremely lightheaded with blurry vision and migraine like symptoms for hours after I ate. 7 months later and it still happens everyday, i have no idea whats going on so im looking stuff up on my own. My doctors seem to treat me like a head case rather than try to genuinely help me. Turns out I have dysphagia or esophageal dysmotility based on a manometry, so i have no clue what part that plays. I also did get a gastric emptying test done due to bloat and constipation and it seemed to be normal, if anything it was on the slower side. So im genuinely lost here, just sharing my story incase somone else unfortunate as me can know they aren't alone
@@arupdebbarma4420 you had these surgeries and have the same issues? Im still not better unfortunately, but im seeing a new doctor that does tif and hh repair for another opinion tomorrow
I was just diagnosed with this, however, I have NO history of stomach surgery or peptic ulcer disease. What else can cause this to a relatively heathy 64 year old male with no history of digestive problems?
This is ME after toupet fundoplication. Thanks for making it easy to understand. I’ve tried some dietary modifications already and I’m still not the same on how I was before surgery. I wish I knew this was going to happen. I wouldn’t have gotten surgery if I knew dumping syndrome would be a thing. The surgery did fix my lpr but the dumping syndrome has disrupted my sleep latency and maintenance
@@Ladeliciadelinda I have surgery anterior fundoplication after two month my symtoms blur vision....lightedness,,heart racing,,, nausea,,,, I think I'm soon die
@@arupdebbarma4420 I never fully recovered until around a year. And I still had symptoms afterwards. The hardest time period is in the 1-4 month mark. It will get easier. Drink warm fluids and talk to your doctor
I have these exact symptoms...came on 4 months after duodenum stricture bypass surgery... Took a couple of months for the doctors to tell me what was going on. Bit frightening whilst in the supermarket and the heart racers. Anyway lifestyle changes for me...
Msg also causes this. glutamate from Msg attach glutamate receptors which trigger the Vagus nerve to trigger digestive nerves causing rapid gastric emptying . I developed an immune disease from it.
This stuff sucks. But yes in my case Sugary drinks aka coke really upsets my stomach. Also no matter what I eat I still get diarhea within an hour and lasts for hours. very watery. I need to get checked asap.
I hate how google and web md classify DS as a "post surgery" problem. People like me who have never had any gastric surgery can still get this via IBS C turning into IBS D
this is just like an IELTS listening test.
bro wtf😂!!
Wow.. that feeling when within 1hour you find the diagnosis that atleast 5 different hospitals haven't been able to figure out in 3months, for my sister with excruciating pains.. Thank you for the video. I really think this is it..
Have her get a gastric emptying study and google gastroparesis.
Me too. I just didn't understand the correlation between my palpitations and my eating. I was sick about doctors calling it anxiety.
The MRI gastric emptying study didn’t detect my dumping syndrome. I had to do a second study where they take hourly pictures to find it. Make sure you get the better study done, as it is more powerful in detecting abnormalities!
Great info, what also came to mind was histamine and fructose intolerance, mast cell activation and SIBO. All worth looking into in addition as well.
Made it really clear for me . Thanks guys for making life easy for the future doctor .
Very clear lecture. I understand why obeying instructions is so important for bariatric surgery patients.
this just saved my life
So helpful as a RNY patient!
YOU HAVE EXPLAINED IT VERY WELL
Thank you. Are there any differential diagnoses for pts w/no history of gastric surgery?
Awesome case, made it really clear for me.
Michael Jackson See
Thank you.. I will take my NCLEX soon this year ❤
I alway remember a patient state the dumping syndrome she experienced in 2009 was from ruptured silicone implants. I thought this was absurd. I complained of dumping like syndromes post explantation and prior to my explantation June 2013 in Kelowna. We will never know the effects of the various implants and devices we place in our bodies. That's not really the crux of this comment.
I noted last week, yes last week, that I had an Xray indicating lunacy/fracture of the L1 in June 2014 when I was seeing a hematologist and GI specialist at the same time and neither knew of this fracture. Fast tract 2020: dumping like syndromes continue to prevail coupled with pelvic/GI pain, weight loss and a diagnosis of severe osteoporosis and bilateral sacral fractures in the last 2 months here in Calgary.
Yes, I had to relocate to Calgary to learn that I have sacral fractures and osteoporosis and I considered myself a physically fit and health 58 year old female.
Drinking water triggers a dumping like sensation and I wake up feeling nauseous after a calm and uneventful sleep.
There is a relationship between gut health and skeletal health--no doubt about it. It is offensive to listen to healthcare providers question my mental well being.
Women are also more likely to undergo pelvic medical procedures such as ablations, tubal ligations, salpingectomy, D & Cs and are often labeled as "hysterical" and considered unreliable historians obsessed with their elimination systems when presenting with pelvic and abdominal pain.
Seeking healthcare as been redundant and torturous just as my colon has been described in numerous medical reports over the course of several years.
I enjoyed this very informative UA-cam. My diabetic mother may provide a clue to my health concerns.
Thank you
I have neuropathy, which I also believe caused the damage to the vagal nerve. This all started in September 2017. I literally feel the neuropathy intensifying about 10 minutes after ingesting foods...but only foods containing folate and vitamin K. The more the vitamin, the worse and longer duration the symptoms. I started developing multiple symptoms since September 2017. 30 now in total.They tried me on multiple heart medications to control tachycardia and other arrhythmias and they all caused horribly painful reactions. Because of the neuropathy, I can literally feel when a food or drug hits my bloodstream. It always starts in my left foot first. I gave up trying meds because of the pain they caused. I still have trouble consuming foods with K and folate. Not only the neuropathy, but if I consume too much of either, my balance is horrible and I feel very 'odd', brain-wise. If I avoid them totally, the neuropathy goes away, totally. But I've already lost 40+ lbs since September. Much more and I'm pretty much done for. Those vitamins are about in every single food known. The only thing I can come up with is that I was on carbamazepine during all of this. Every symptom I have is listed under adverse reactions for that medication. Every heart medication I was tried on is known to react with that medication, causing increased plasma levels. I stopped taking it on December 15, and though it hasn't gotten any worse since then, it still hasn't gotten much better either. The carbamazepine has a half life of about 35 hours. They tested it at 2 weeks and it hadn't budged from two weeks before. They tested it again at fours weeks and it was at
Brian French did you ever find any help?
Did u find any solutions
How are you now
I got a tif with a hh repair. I had and have severe bloating both pre and post op. 3 months after my surgeries I noticed I would get extremely lightheaded with blurry vision and migraine like symptoms for hours after I ate.
7 months later and it still happens everyday, i have no idea whats going on so im looking stuff up on my own. My doctors seem to treat me like a head case rather than try to genuinely help me.
Turns out I have dysphagia or esophageal dysmotility based on a manometry, so i have no clue what part that plays.
I also did get a gastric emptying test done due to bloat and constipation and it seemed to be normal, if anything it was on the slower side.
So im genuinely lost here, just sharing my story incase somone else unfortunate as me can know they aren't alone
How are you now ????
Helo are you ok
My problem same i can't see proper
@@arupdebbarma4420 you had these surgeries and have the same issues? Im still not better unfortunately, but im seeing a new doctor that does tif and hh repair for another opinion tomorrow
@@oOTheMastaOo240 I had anterior fundoplication
Now my condition not well
I soon die 😭😭😭
I was just diagnosed with this, however, I have NO history of stomach surgery or peptic ulcer disease.
What else can cause this to a relatively heathy 64 year old male with no history of digestive problems?
thank you
nice presentation
I was just diagnosed with this today
sorry to hear that buddy. Good thing you listened to this video. Now you know what to do
Wat test u made pls rpy
This is ME after toupet fundoplication. Thanks for making it easy to understand. I’ve tried some dietary modifications already and I’m still not the same on how I was before surgery. I wish I knew this was going to happen. I wouldn’t have gotten surgery if I knew dumping syndrome would be a thing. The surgery did fix my lpr but the dumping syndrome has disrupted my sleep latency and maintenance
How are you now
@@arupdebbarma4420 dumping syndrome is a little better but still there! Thank you for asking
@@Ladeliciadelinda I have surgery anterior fundoplication after two month my symtoms blur vision....lightedness,,heart racing,,, nausea,,,,
I think I'm soon die
@@arupdebbarma4420 I never fully recovered until around a year. And I still had symptoms afterwards. The hardest time period is in the 1-4 month mark. It will get easier. Drink warm fluids and talk to your doctor
Same dumping syndrome after fundoplication it cause vagus nerve damage? Plz reply
I have these exact symptoms...came on 4 months after duodenum stricture bypass surgery... Took a couple of months for the doctors to tell me what was going on. Bit frightening whilst in the supermarket and the heart racers. Anyway lifestyle changes for me...
Outstanding ✋❤️
Thanks! Good explanation and friendly voices :-)
that was so easy. thank u so much☺
excellant talk
very helpful. thanks
Poor diet and lack of exercise is the main cause of this type of issue it seems. Most people who develope this are overweight or obese.
Msg also causes this. glutamate from Msg attach glutamate receptors which trigger the Vagus nerve to trigger digestive nerves causing rapid gastric emptying . I developed an immune disease from it.
Hi, do you have any source for your info?
Thanks
What immune disease?
Восстанавливается ли вагус со временем? Слышал, что после ваготомии часто возвразаеься выработка излишнего сока, значит и нерв заростает?
Los nervios frénico que estructura inervan?
Thank u soo Much❤❤❤
So i was fucked before nissan and after im still fucked. Doesnt seem like a fair trade off
It's "Nissen Fundoplication though"..
Can we get it without surgery
i love it
This stuff sucks. But yes in my case Sugary drinks aka coke really upsets my stomach. Also no matter what I eat I still get diarhea within an hour and lasts for hours. very watery. I need to get checked asap.
Idaho Storm Chasers yeah me to its sucks big time
Yes you do. I pray that things are better for you now in Jesus name.
very nice...:-)
En Español porfavor🤦🇦🇷💌💃
❤❤👏👏👏
Thank you