I suffer from endo and one they didnt mention is one of the ones i suffer from and its endometriosis has attached to my kidneys causing me to go into kidney failure anytime i got my monthly visitor. Just wanted you to know that there is one other place they havent documented and i dont know why but in my situation I almost died 2 times due to this tissue being attached to my kidneys, Good luck ladies who can understand my pain and even those who cant.
@flavacreations hiya i can understand your pain i have endo on one of my kidneys. endometriosis was found on all my reproductive organs, my kidney, my urethra and my bladder, i had extensive surgery in march, one of the down falls of it being on my kidney is i have to have my blood pressure taken and my red blood cells counted every 6 months to prevent kidney failure. i take medication for pain relief and to keep the disease at bay as best they can. am very lucky tho it doesnt affect me daily
I just had a ct scan to diagnose painful soft tissue mass, found during ultrasound, located in my right rectus muscle,. Turns out it looks like endo...I was diagnosed with endo when i was 24 years old...lost left ovary and left tube to the disease.....many lapro scopic surgeries and 4 c-sections has caused it to migrate to rectus muscle...has anyone else heard of this happening?
THANK YOU SO much for this video. PLEASE make another explaining the crazy-long list-of symptoms/detailed!! i think a lot of us would find relief from this.<3 -18 year old female.
In 2011 I received many emails about organs not listed on the video causing monthly symptoms due to hormonal bleeding. Many have nose bleeds, but most letters are from women with catamenial hemoptysis, coughing up blood monthly. Physicians are more aware than ever before in the history of this disease about the destruction it can cause and more women are being diagnosed with proper treatment being rendered. But we still have a long way to go and there is currently no cure.
my girlfriend has endo, it plays a big toll on her life, i try to be there as much as i can but its hard, shes always in pain, crying, depressed, not sleeping and moody, i wish i could do something to help
...when shes crying in my arms and i ask if i can help...all she says is "please take the pain away..."
i dont think endo only effects the person in question but everyone around them...
She is lucky to have such an understanding boyfriend! Being supportive and learning about the disease is one of the best things you can do. Having an endo specialist excise all endo makes a huge difference in pain levels. Many of us also find that eliminating meat, dairy, and gluten from our diets, as well as going organic and eliminating all artificial foods really helps. Good luck and feel better! XO
Losing your job to it, unable to work again, money problems, doctors and psychiatrist bills, and the devastating news that you will never have children. My husband and I are devastated. Sorry-Bad day today
what about the navel? i have it there
anyone else?
ChynnaDoll2 10 months ago
i have endometriosis to and i am in unbearable pain every day ty for posting this video
leahcrow1 2 years ago
i have endo to and i am in unbearable pain everyday it never goes away and i hate endo it sucks i want my life back i had before endo
leahcrow1 2 years ago
I suffer from endo and one they didnt mention is one of the ones i suffer from and its endometriosis has attached to my kidneys causing me to go into kidney failure anytime i got my monthly visitor. Just wanted you to know that there is one other place they havent documented and i dont know why but in my situation I almost died 2 times due to this tissue being attached to my kidneys, Good luck ladies who can understand my pain and even those who cant.
flavacreations 2 years ago
@flavacreations hiya i can understand your pain i have endo on one of my kidneys. endometriosis was found on all my reproductive organs, my kidney, my urethra and my bladder, i had extensive surgery in march, one of the down falls of it being on my kidney is i have to have my blood pressure taken and my red blood cells counted every 6 months to prevent kidney failure. i take medication for pain relief and to keep the disease at bay as best they can. am very lucky tho it doesnt affect me daily
stacygallagher 7 months ago
I just had a ct scan to diagnose painful soft tissue mass, found during ultrasound, located in my right rectus muscle,. Turns out it looks like endo...I was diagnosed with endo when i was 24 years old...lost left ovary and left tube to the disease.....many lapro scopic surgeries and 4 c-sections has caused it to migrate to rectus muscle...has anyone else heard of this happening?
ijjklj 2 years ago
THANK YOU SO much for this video. PLEASE make another explaining the crazy-long list-of symptoms/detailed!! i think a lot of us would find relief from this.<3 -18 year old female.
hacsince91 2 years ago
Thank you all for the great comments and wonderful emails of support.
Glynis D. Wallace DMD,
Author: Living With Lung and Colon Endometriosis: Catamenial Pneumothorax
Yatanell 3 years ago
In 2011 I received many emails about organs not listed on the video causing monthly symptoms due to hormonal bleeding. Many have nose bleeds, but most letters are from women with catamenial hemoptysis, coughing up blood monthly. Physicians are more aware than ever before in the history of this disease about the destruction it can cause and more women are being diagnosed with proper treatment being rendered. But we still have a long way to go and there is currently no cure.
Yatanell 2 months ago
Thank you for this video!!
I have endo..it hurts!!
Medicluvstrauma 3 years ago
I Have This Too. =(
SlayNKitti 4 years ago
:( I hate having this!
mommy2aidenc 4 years ago
my girlfriend has endo, it plays a big toll on her life, i try to be there as much as i can but its hard, shes always in pain, crying, depressed, not sleeping and moody, i wish i could do something to help
...when shes crying in my arms and i ask if i can help...all she says is "please take the pain away..."
i dont think endo only effects the person in question but everyone around them...
any advice for me to hlep both her and i?
blitzer26 4 years ago
She is lucky to have such an understanding boyfriend! Being supportive and learning about the disease is one of the best things you can do. Having an endo specialist excise all endo makes a huge difference in pain levels. Many of us also find that eliminating meat, dairy, and gluten from our diets, as well as going organic and eliminating all artificial foods really helps. Good luck and feel better! XO
shoegirl1111 3 years ago
I have Endometriosis,is hard to live with it.
surgeries,hormones,pain and painkillers ,depression,gastro problems..
to know theres no cure only TREATMENTS is too sad!! wish to keep contact
thank you
pacificyellowmermaid 4 years ago
Losing your job to it, unable to work again, money problems, doctors and psychiatrist bills, and the devastating news that you will never have children. My husband and I are devastated. Sorry-Bad day today
thebitteryellowpill 3 years ago
thank you!
frog0830 4 years ago
thanks
A123nto 4 years ago