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r/Endo is a subreddit with 84k members. Its distinguishing qualities are that the community is large in size, and has high activity.
This community aims to support all people affected by and interested in endometriosis. We pride ourselves on being a friendly, inclusive place, where patients and loved ones alike can discuss thoughts and concerns, ask questions, and share information.
Please try to engage with others in an empathetic and supportive manner and remember that Endometriosis is an extremely varied disease and each patient has different circumstances, experiences and treatment options.
Popular Themes in r/Endo
#1
Pain & Anger
: "The relief rage of finding out you weren’t crazy."
18 posts
#2
Advice Requests
: "“If it were endometriosis, it would have absolutely shown up on your CT scan.”"
13 posts
Popular Topics in r/Endo
#1
Endo
: "Endometriosis is NOT an autoimmune disease. STOP CALLING IT ONE!!!"
108 posts
#2
Pain
: "I am in Menopause and my doctor says my Endo is "gone" and denies me Painkillers."
46 posts
#3
Surgery
: "pushing for lap to get a diagnosis, but terrified if i actually do the Surgery."
40 posts
#4
Diagnosis
: "pushing for lap to get a Diagnosis, but terrified if i actually do the surgery."
20 posts
#5
Laparoscopic
: "Finally taken seriously, and I was right my endo is back"
17 posts
#6
Laparoscopy
: "Lap revealed no Endo but stuck ovary in pelvic wall, feeling really down."
14 posts
#7
Symptoms
: "Bringing up Symptoms to obgyn tomorrow - too detailed, not detailed enough?"
9 posts
#8
Doctors
: "Feeling completely dismissed by Doctors — I know this is just the start, but I already feel defeated"
6 posts
#9
Hysterectomy
: "Who’s had a Hysterectomy and how’s life afterwards?"
5 posts
#10
Period
4 posts
Member Growth in r/Endo
Yearly
+16k members(24.3%)
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