This is how all doctors and people who have never had Nutcracker syndrome explain the symptoms. It is a lot worse that how it is described. The lack of proper blood flow causes a domino effect of symptoms and complications in the body. It causes pelvic congestive syndrome which on it's own is very painful then combine that with menstrual pain then multiply it by 100. Since the blood is not flowing properly it also cause tachycardia in some people and in others it causes POTS. Due to the irregularities, it also causes adrenaline overflow so it's a constant fight or flight horrible feeling. Then comes the chronic fatigue how can it not when the body is in constant pain and fight or flight mode. Oh, it doesn't stop there, more often than not the compression doesn't stop with the left renal vein, but the intestine is also compressed (SMAS) causing havoc on the intestines and digestive system. This then causes the stomach to paralyze (gastroparesis) causing one to be nauseous all the time, vomit and or not be able to eat for days at a time. Then you're so malnourished, fatigued and with brain fog that when you seek help from the doctors, they gaslight you and tell you it's all in your head. This phenomenal is real and is way more serious than what doctors are making it out to be.
Yup! Then there’s the possibility of dying from Hemorrhage if you have surgery. Been struggling with this since 2021. My entire left side feels like stab wounds that never heal. I found out i have it a whole year later because my Doctor said my MRI results were normal even though i knew something was wrong with my body. It's Torture. Physically and Mentally.
@@mamiiswiing429Hello to both of you, I do have the syndrome, they discovered it 3 years ago! And I am scared. Have you already got the surgery? I plan to do ot next year.
had a 13yo with lt varicocele today, was thinking about nutcracker syndrome, wish i had watched this video earlier today, would of been a bit out of our scope but if positive would have definitely thrown it in.
I had the choice to have a surgery but didn’t take it when I was 17 I was in so much pain I was like if they open me I’m going to be in more pain for weeks.
Je suis porteuse du nutcracker mais en France 15 ans d'errance nous sommes 600 femmes à en souffrir et que 3 chirurgiens qu'il l'opére mais n'y connaît rien nous sommes abandonner et en souffrance
Hey 👋 nutcracker phenomenon is the anatomy without symptoms does not require treatment. Nutcracker syndrome can be treated conservatively if is not causing to many issues. If the symptoms worsen they can put a stent in the left renal vein or do surgery to reposition the left renal vein..
@@SonographicTendencies is it difficult to reposition the renal vein or is open surgery stent best ? I just got diagnosed yesterday with NCS. My main issues are on the right (pelvic and buttock) but somehow NCS was noticed on my Venogram with contrast. Please advice I am scared too to develop DVT. Thank you
@@bsisthebs77207 Sorry to hear this. Are you saying you had your renal vein repositioned but it didn't work ? Or you went straight for stent ? This is all new to me. Sorry if I sound stupid.
Sonographic Tendencies According to the translation on the Medicosis Perfectionalis channel, you can protect yourself from surgery. You need to gain weight for fat to appear between the veins and loosen them. What do you think is it possible? Because I have just been diagnosed with this syndrome.
@@SonographicTendencies At this point, I am very thin. I weigh 68 kg with a height of 181 cm. So I don't know what would be a better choice for trying to gain weight 5-7 kg or surgery. Perhaps it would be worth a try, as it is said that most people with this problem are slim people who do not have adequate body fat between these arteries.
Приятель у меня такая же проблема, мой рост 177 см , вес 63 кг. Я тоже как ты думаю что это связано с тем что у меня нету жира! Сейчас я пытаюсь набрать вес и пью протеины и кушаю много
Hello, my name is Osama Ayoub. I had many examinations and passed 9 doctors to diagnose my condition. Only one doctor was known. I was diagnosed with mesenteric syndrome, and I underwent an operation. A month after the operation, my condition worsened until I vomited food and could not bear the pain. Doctors hurt me a lot, and I no longer have hope. Help me. I want a decent life to live.
@@smokeycity_youngin_9012 there's a FB group just search Renal Nutcracker and join! There's so many people to relate too and a long list of experience doctors who offer many options to help solve this issue! But yes, all my doctor's act like I'm making up something
This is how all doctors and people who have never had Nutcracker syndrome explain the symptoms. It is a lot worse that how it is described. The lack of proper blood flow causes a domino effect of symptoms and complications in the body. It causes pelvic congestive syndrome which on it's own is very painful then combine that with menstrual pain then multiply it by 100. Since the blood is not flowing properly it also cause tachycardia in some people and in others it causes POTS. Due to the irregularities, it also causes adrenaline overflow so it's a constant fight or flight horrible feeling. Then comes the chronic fatigue how can it not when the body is in constant pain and fight or flight mode. Oh, it doesn't stop there, more often than not the compression doesn't stop with the left renal vein, but the intestine is also compressed (SMAS) causing havoc on the intestines and digestive system. This then causes the stomach to paralyze (gastroparesis) causing one to be nauseous all the time, vomit and or not be able to eat for days at a time. Then you're so malnourished, fatigued and with brain fog that when you seek help from the doctors, they gaslight you and tell you it's all in your head. This phenomenal is real and is way more serious than what doctors are making it out to be.
Yup! Then there’s the possibility of dying from Hemorrhage if you have surgery. Been struggling with this since 2021. My entire left side feels like stab wounds that never heal.
I found out i have it a whole year later because my Doctor said my MRI results were normal even though i knew something was wrong with my body. It's Torture. Physically and Mentally.
@@mamiiswiing429Hello to both of you, I do have the syndrome, they discovered it 3 years ago! And I am scared. Have you already got the surgery? I plan to do ot next year.
had a 13yo with lt varicocele today, was thinking about nutcracker syndrome, wish i had watched this video earlier today, would of been a bit out of our scope but if positive would have definitely thrown it in.
Superb video 👏👏 and thank you so much for such a nice explanation 👍. Its definitely helpful 😊
I had the choice to have a surgery but didn’t take it when I was 17 I was in so much pain I was like if they open me I’m going to be in more pain for weeks.
How do you cope with pain? this is unbearable
how are you doing these days?
Je suis porteuse du nutcracker mais en France 15 ans d'errance nous sommes 600 femmes à en souffrir et que 3 chirurgiens qu'il l'opére mais n'y connaît rien nous sommes abandonner et en souffrance
Very nice presentation ,thank you dear sir
Awesome! Thank you!
You’re welcome!!
항상 잘보고 잘 듣고 있어요 감사해요 ❤
great video. thank you.
I just had a DUS and that came back negative for nutcracker but i am not so sure. Do you mind if i send you my images to confirm?
Is there a way to cure NCS on its own or reverse it? I read sometimes it can cure itself on its own. I have NCS , just found out and I'm scared.
Hey 👋 nutcracker phenomenon is the anatomy without symptoms does not require treatment. Nutcracker syndrome can be treated conservatively if is not causing to many issues. If the symptoms worsen they can put a stent in the left renal vein or do surgery to reposition the left renal vein..
@@SonographicTendencies is it difficult to reposition the renal vein or is open surgery stent best ? I just got diagnosed yesterday with NCS. My main issues are on the right (pelvic and buttock) but somehow NCS was noticed on my Venogram with contrast. Please advice I am scared too to develop DVT. Thank you
@@1969strangelove it was a difficult procedure and I still ended up needing a Stent but it's different for everyone.
@@bsisthebs77207 Sorry to hear this. Are you saying you had your renal vein repositioned but it didn't work ? Or you went straight for stent ? This is all new to me. Sorry if I sound stupid.
@@1969strangelove we went for repositioning first.
Sonographic Tendencies
According to the translation on the Medicosis Perfectionalis channel, you can protect yourself from surgery. You need to gain weight for fat to appear between the veins and loosen them. What do you think is it possible? Because I have just been diagnosed with this syndrome.
Perhaps but then you’d have extra fat and all the potential metabolic issues that may bring…
@@SonographicTendencies
At this point, I am very thin. I weigh 68 kg with a height of 181 cm. So I don't know what would be a better choice for trying to gain weight 5-7 kg or surgery. Perhaps it would be worth a try, as it is said that most people with this problem are slim people who do not have adequate body fat between these arteries.
Приятель у меня такая же проблема, мой рост 177 см , вес 63 кг. Я тоже как ты думаю что это связано с тем что у меня нету жира! Сейчас я пытаюсь набрать вес и пью протеины и кушаю много
@@gis177 is it going better for you a month later? im thinking of doing the same thing
Have you ever thought that compression could be caused by a hernia?
Great job
Thank you
Is it not possible to have it in the right kidney?:)
cuz the aorta at the nuttcracker angle blocks part of the flow to the left kidney and not to the right one, not a dr.
Great stuff, very helpful
So happy i found this thanks beo
thanks
În romana se poate?
what is the cause of hematuria ?
The renal venous hypertension causes rupture of the small veins in the collecting system
Hello, my name is Osama Ayoub. I had many examinations and passed 9 doctors to diagnose my condition. Only one doctor was known. I was diagnosed with mesenteric syndrome, and I underwent an operation. A month after the operation, my condition worsened until I vomited food and could not bear the pain. Doctors hurt me a lot, and I no longer have hope. Help me. I want a decent life to live.
i hope youre doing better
@@youar33y3 No🥹
This is what I'm afraid of.
Аlthough it’s already hard for me to eat😢
👍👍👍👍👍
I wish you can do a tutorial on how you creat your ilustration .
Great video that question comes out in the RVT state exam yeeeeee.
Just found out I have this today. Smfh
I recently found out too! How is yours going? Are you doing OK?
@@Thefroggang101 being that it's very rare for a male an doctors here act like it's some alien diseases. Not too peachy
@@smokeycity_youngin_9012 there's a FB group just search Renal Nutcracker and join! There's so many people to relate too and a long list of experience doctors who offer many options to help solve this issue!
But yes, all my doctor's act like I'm making up something
How was your condition treated?
I got the same condition lmao