This is a subreddit preview page. If you have a GummySearch account, please add this Subreddit to your audience to view the full analysis features there.
r/eds
19k members
r/eds is a subreddit with 19k members. Its distinguishing qualities are that the community is large in size, and has high activity.
Ehlers Danlos Syndrome (EDS) is a underdiagnosed connective tissue disorder characterized by a genetic fault in collagen. It manifests as hypermobile joints and affects every organ system because we’re all made of connective tissue! We welcome all EDS subtypes, hypermobility spectrum disorder, Loeys Dietz, unnamed genetic disorders that present like EDS, self-diagnosed & suspected zebras. || || || Crowdsourced medical care saves lives. We welcome medical advice!
Popular Themes in r/eds
#1
Pain & Anger
: "GOT SCAMMED BY ZEBRASPLINTS"
6 posts
#2
Advice Requests
: "tested positive for vEDS. i’m so confused."
6 posts
Popular Topics in r/eds
#1
Eds
: "Eds is a nightmare"
33 posts
#2
Pain
: "Has anyone figured out out the cause of their Pain when sitting?"
22 posts
#3
Diagnosis
: "Got a diagnoses finally, and and turned work into art therapy!"
7 posts
#4
Skin
5 posts
#5
Symptoms
: "Why do so many geneticists seem to have a distain for hEDS referral patients?"
5 posts
#6
Doctor
: "I had a good Doctors visit !!!"
4 posts
#7
Eds
: "tested positive for vEds. i’m so confused."
4 posts
#8
Joint Pain
: "Does your Joint Pain worsen before/during menstruation?"
4 posts
#9
Ribs
: "Rib Concerns"
4 posts
#10
Cellulite
: "Cellulite and itching?"
4 posts
Member Growth in r/eds
Yearly
+8k members(68.1%)
Similar Subreddits to r/eds
r/cfs
61k members
23.6% / yr
r/ChronicIllness
85k members
22.2% / yr
r/ChronicPain
133k members
23.2% / yr
r/covidlonghaulers
70k members
20.7% / yr
r/CrohnsDisease
72k members
18.8% / yr
r/Endo
82k members
25.4% / yr
r/endometriosis
101k members
40.1% / yr
r/Fibromyalgia
90k members
24.7% / yr
r/POTS
92k members
57.1% / yr
r/Sciatica
48k members
39.9% / yr