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r/lupus is a subreddit with 44k 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
Advice Requests
: "I just got diagnosed with lupus my doctor started yelling and didn't explain anything. I would love any explanation about Anything I should know or any advice."
9 posts
#2
Pain & Anger
: "Sometimes the pain is just too much"
3 posts
Popular Topics in r/lupus
#1
Lupus
: "Federal funding cuts for Lupus research"
36 posts
#2
Symptoms
: "Is it normal that I didn't notice UV Symptoms last year but I do this year?"
20 posts
#3
Flare
: "How long did it take to recover from your first Flare?"
8 posts
#4
Diagnosis
: "Help how to support my boyfriend with his recent Diagnosis"
8 posts
#5
Pain
: "Sometimes the Pain is just too much"
7 posts
#6
Fatigue
: "I can't remember the last time I was this tired"
7 posts
#7
Plaquenil
6 posts
#8
Diagnosed
: "What was your experience like getting Diagnosed?"
4 posts
#9
Rash
4 posts
#10
Sun
3 posts
Member Growth in r/lupus
Yearly
+11k members(31.7%)
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