My endo caused my ureter to be adhered to my pelvic wall. I'm so incredibly grateful that i found a great surgeon and i credit him for saving my right kidney.
this made me cry, thank you so much for posting.. you put a lot into perspective of the symptoms I've been experiencing with my endometriosis diagnosis I received recently, I can't believe my doctor never told me this information and it's really disappointing that there's such a lack of education out there, God bless you
thank you very much for your video! I lost my right kidney due to endometriosis. I visited three gynecologists before the third one, in shock, diagnosed a grade 4 kidney blockage. By then, the kidney was beyond saving.
thankyou so much for talking about the fact that it doesnt just effect the gynaecological organs! as someone who had bowel and had to have kidney surgery because of endo and adenomyosis im so glad someone is actually raising the awareness!
I had surgery for endometriosis 40 years ago, after 6 months I was pregnant and I had 2 daughters in a period of 3 years. Never again had issues or pain the only problem is my incontinence had many test but they never mention that could be due to the endometriosis, but I will talk to my doctor about it. Thank you so much for informing us about it.
I think I have ureter endometriosis. I have severe endometriosis and have had a hysterectomy as they thought it was ovarian cancer. Im going in on 3rd January to have major bowel surgery as my cervix is stuck to my bowel. They couldn't remove it when I had the hysterectomy. My endo specialist said its so rare to get endo on the ureter it's definately not that but I now have ckd and a failing kidney. Your videos really do help thankyou x
Hi I have an appointment with an endo specialist in May as whenever I’m due on or on my period I suffer with the worst kidney pain, my bladder also get a really bad a week before I’m due and again while I’m on, I’ve been waiting since 2021 for this appointment, I was seen before and diagnosed with Adenomyosis but they wouldn’t check for endo unless I had a hysterectomy but because this kidney pain has got so bad my GP referred me back, is this a typical symptom of kidney or bladder endo, I have always had a bad bladder since a child and I had regular Botox injections in my bladder under a urologist
I am almost certain that I have this. I have left sided kidney/flank pain on my back on day 21 (always day 21, when it happens) of my cycle and have been experiencing this since 2011 or so. It does not happen every month and has been doing better since I have been eating ketogenic, but last month it came back with a vengeance. :( I have been to the ER so many times.
My endo caused my ureter to be adhered to my pelvic wall. I'm so incredibly grateful that i found a great surgeon and i credit him for saving my right kidney.
this made me cry, thank you so much for posting.. you put a lot into perspective of the symptoms I've been experiencing with my endometriosis diagnosis I received recently, I can't believe my doctor never told me this information and it's really disappointing that there's such a lack of education out there, God bless you
thank you very much for your video! I lost my right kidney due to endometriosis. I visited three gynecologists before the third one, in shock, diagnosed a grade 4 kidney blockage. By then, the kidney was beyond saving.
thankyou so much for talking about the fact that it doesnt just effect the gynaecological organs! as someone who had bowel and had to have kidney surgery because of endo and adenomyosis im so glad someone is actually raising the awareness!
I had surgery for endometriosis 40 years ago, after 6 months I was pregnant and I had 2 daughters in a period of 3 years.
Never again had issues or pain the only problem is my incontinence had many test but they never mention that could be due to the endometriosis, but I will talk to my doctor about it.
Thank you so much for informing us about it.
I think I have ureter endometriosis. I have severe endometriosis and have had a hysterectomy as they thought it was ovarian cancer. Im going in on 3rd January to have major bowel surgery as my cervix is stuck to my bowel. They couldn't remove it when I had the hysterectomy. My endo specialist said its so rare to get endo on the ureter it's definately not that but I now have ckd and a failing kidney. Your videos really do help thankyou x
My daughter has had trouble with her liver since she was young all from overload of hormones.
Hi I have an appointment with an endo specialist in May as whenever I’m due on or on my period I suffer with the worst kidney pain, my bladder also get a really bad a week before I’m due and again while I’m on, I’ve been waiting since 2021 for this appointment, I was seen before and diagnosed with Adenomyosis but they wouldn’t check for endo unless I had a hysterectomy but because this kidney pain has got so bad my GP referred me back, is this a typical symptom of kidney or bladder endo, I have always had a bad bladder since a child and I had regular Botox injections in my bladder under a urologist
Loving your channel ❤❤
I am almost certain that I have this. I have left sided kidney/flank pain on my back on day 21 (always day 21, when it happens) of my cycle and have been experiencing this since 2011 or so. It does not happen every month and has been doing better since I have been eating ketogenic, but last month it came back with a vengeance. :( I have been to the ER so many times.