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r/lupus is a subreddit with 39k members. Its distinguishing qualities are that the community is large in size, and has high activity.
This is a space for those Living with Lupus to Connect, Share Experiences, Build Support, and Create Community. Those who have other autoimmune conditions or loved ones of those with Lupus are welcome, with the loving reminder that this forum is for Lupus patients first. Respect our needs as much as we do our best to respect yours.
Popular Themes in r/lupus
#1
Pain & Anger
: "I already suffer so much… no pasta??? "
83 posts
#2
Advice Requests
: "My diagnosis from my biopsy says that I have lupus nephritis stage 4, what's next for me?"
17 posts
#3
Solution Requests
: "Dating?"
11 posts
#4
Money Talk
: "For people who get the saphnelo infusion: How much is your copay with insurance?"
1 post
Popular Topics in r/lupus
#1
Lupus
: "“Lupus doesn’t cause…”"
53 posts
#2
Rash
: "New development with my Malar Rash"
8 posts
#3
Pain
: "Cervical spine/neck Pain"
8 posts
#4
Medication
: "First time Methotrexate "
6 posts
#5
Symptoms
: "I’m tired of having all the “rare” Symptoms."
6 posts
#6
Benlysta
: "Benlysta "
6 posts
#7
Flare
: "My PCP pushed me too far during a Flare"
6 posts
#8
Fatigue
: "Lupus doesn’t cause Fatigue?!?"
5 posts
#9
Diagnosis
: "I haven't 'accepted' my Diagnosis yet"
5 posts
#10
Hospital
: "I don’t know if I should go to the Hospital after my shift today"
4 posts
Member Growth in r/lupus
Daily
+18 members(0.0%)
Monthly
+832 members(2.2%)
Yearly
+6k members(17.6%)
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