Poop Live, Bowel Endometriosis and You
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- čas přidán 5. 07. 2021
- An in-depth conversation with Indian Centre for Endometriosis's Dr Abhishek Mangeshikar all about poop and bowel endometriosis. IBS is so often confused for bowel endometriosis and in this video you can learn why, you can understand poop shape and explore all things belly pain and endometriosis. Dr Sallie Sarrel, a pelvic physical therapist and Co-Founder of The Endometriosis Summit hosts.
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I am so excited to watch this!
Can bowel endo cause inflammation to show on the colonoscopy where the endometriosis is?
Wow I think I finally know what's wrong with me.
Well crap! This explains me so well!
I always had super soft during my periods. Entering menopause and i poop rocks
I wish I had access to see you.
Is there a difference between pain with bowel movement and pain after bowel movement? I get pelvic pain during ovulation days about 10 minutes after I have a bowel movement that last for about 15-20 ‘minutes
Hi 👋 great info thanks 🙏 🤗I live in NJ/ NYC area . Can you please kindly refer me to a specialist surgeon for bowel , bladder endometriosis. Thank you 🙏
What is the name of the herbal supplement/anti-fungal that you mentioned for SIBO?
Is one of symptoms of these lesions, besides pain with bowel motions, labour type pain?
I have pain on both sides of my lower sides of the back that take my breath away.....and it goes on for ages.....my dad rubs my back to try to calm down the nerves.
I find I get pain when any stools are sitting in the transverse colon or gas.
If the stool stays there, it causes immense burning pain....close to vomiting.
I've had this pain for 25 yrs since my first laparoscopy.
I've always felt that something was missed.
I also get vaginal zaps on and off, especially after squatting or doing some lifting.
I'm wondering if it's adhesions or disease.
My bowel pain can start after eating.....I had awful bloating that caused anorexia and nausea for many years to the point I thought I would die.....I went on the FODMAP diet and it's changed my life for the best.
Please advise what to do.
I live in New Zealand and our surgeons are not very expert.
I did have stage 4 endo and adenomyosis, so I have no ovaries or uterus.....but after physio and toileting techniques and diet.....im still having immense pain.
My descending bowel is fine, it's the transverse colon or higher that needs looking at.
I feel for you, i can say having had endometriosis that the pain felt like \i was giving birth! the pain would come and go like contractions, and each time the pain hit it would be worse than the last one, I used to pass out, having took to many pain relief that didn't really relieve it, it took five years to get the proper diaonosise they kept telling me I had IBS years later i was still in agony after many operations to remove it then lasered, i had it on my bladder and pelvic wall, my bowels were very much affected as well, years later i had most of the symptoms they have discussed in this video, I had a hysterectomy around 8 years ago and 7 months after i had the hysterectomy They discovered i had Several internal abscesses, all extended from one huge one on my colon.
Since then I have stomach pain after eating, burping constantly pain in abdomon, bowel movements are different throughout the day, sometimes like cow pats.
Yet the bowel surgeons and the Gynocologists never once mentioned my bowels problems could be related to having endometriosis?
Now i have had an hysterectomy the gynocologists don't want nothing to do with me as I have no womb or ovories. Sorry about the spelling mistakes.
What the doctors don't inform us of, is the scar tissue that occurs after each operation, which can also cause pain after surgery.
And I was given HRT after the hysterectomy I did not take it as I had found out that if their was any endometriosis cists that had been missed, the HRT would help the endometriosis to grow.
I have lost a lot of weight and cant seem to put it back on, I have had three bouts of abdominal pain lasting two weeks leaving me bed ridden and in extreme pain.
I think its the endometriosis yet no one listens, no one in the medical professions every listens.
11 comments not many, yet no one has had a reply, says a lot.
@@nikkibaxter5550 There aren't enough expert surgeons in 2022.
We are 20 yrs behind where we need to be.
Because endometriosis is so misunderstood and so painful it will take years for drs and surgeons to really be of help to us.
They must do a year's education of the pelvic anatomy, including nerves and organs like the ureters.
My surgeon butchered me....went in like I'm gonna cut this stuff out, without any thought of nerves and possible entrapment.
So we suffer in isolation hoping that some day, we will have a surgeon experienced enough to improve our quality of life.
I've spent too long in my bedroom, in tears begging to die.
It's completely unfair.
@@nikkibaxter5550 I'm so sorry you are still suffering
@@jomassey4207 Hi Jo i am so sorry to hear you went through that, I now others who were also butchered and who was left with horrendous scars on their body, due to other medical issues, these surgeons have no empathy no emotions they don't care about the individual they i think just see us as a body to mess with!
I was diagnosed with endometriosis in 1994, they know full well that women all over the world are suffering this affliction, they know full well how it affects us, I sometimes think that they are playing ignorant for a reason, like to stop us from reproducing?
I was not able to have children, even though i do like you said feel like i was giving birth but without the baby at the end.
I have even thought on what the actual cause of the endometriosis could be?
Seeing as they keep saying thy don't know how the cells of the lining of the womb get out of the womb and into the other areas of the body?
One i thought could be the blood, is the cells from the lining womb being carried through the blood? as blood flows through all areas of the body?
Then after more years passed and many many strange things happening to me, I have another thought on how the lining may be getting distributed to the other organs and areas of the body.
This may sound ridiculas and a little "way out there" but!
Say something was happening to us that we were unaware of?
If your were to some how take out a fetus out of a womb via the stomach that would surely leave drops of the lining of the cell wall the fetus was attatched to in other places outside the womb.
This is going to sound crazy but here goes.
I have had several encounters with what people call greys, tall blonds, Nordics type beings, (fallen angels? Aliens? Demons?) and lights in the sky, that began to happen in 1992 have had marks left on my body after these experiences, small red triangles where my naval is, and below on top of my public hair line.
As well as other areas of my body.
And dreams of them doing things to my stomach, which gave me a lot of pain.
I say it started in 1992 yet i had many weird experiences as a child so it may have been happening to me as a small child to?
People men and women all over the world are having similar experiences, and women claim to have been impregnated and then had the fetus removed from their womb taking it out from the stomach area.
So that is why i am thinking there is something else going on here.
That would make sense of how the endometriosis gets out of the womb, i once asked the Gyno if i had a hole in my womb? As I couldn't understand how the cells got out of the womb when gravity pulls everything downwards, the lining of the womb creates blood that comes down and out, so i couldn't understand how it could get into and onto organs much higher up and outside the womb?
It would be interesting to find out how many of these women who have experienced this type of phenomena also suffer from endometriosis?
I also thought it could be due to the pill, but I suffered pain when i began my period and that's why they put me on the pill, which wrecked my joints by the way.
If it's hereditary then why is it not looked into like all the other hereditary dis-eases?
I am so sorry you are to, i not having any womb or anything am not having that pain on a weekly or fortnightly basis which i am thankful for, and I am in more of a peaceful state of mind which helps, and having done my own research into the medical institutions have a better understanding of what is best for my body, and it's not their Pharmacia drugs, which they test on us.
And which do not improve our situation, but give us more issues to deal with.
To have a healthy self it seems we need to heal-thy-self.
Another thing I thought that caused me to have endometriosis is having had an abusive upbringing I switched of my femimine side, and took on a male persona, became "one of the lads" as a form of protection, i think thought that could have been a possible cause, having shut down the femine aspect of my true being had shut down the workings of my female organs?
Have you pondered on the possible cause?
Can this cause yellow stool?
I think I have this! I burp 20 times a day from water. Or absolutely nothing. But they say it's ibs and Gerd 😮
IBS and endo go hand and hand.