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r/lupus is a subreddit with 43k 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
: "Is it possible to get re-used to the sun?"
20 posts
#2
Pain & Anger
: "Lost my younger sister to Lupus at age 23, 3 months after diagnosis. Feel like I let her down."
14 posts
Popular Topics in r/lupus
#1
Lupus
: "Federal funding cuts for Lupus research"
36 posts
#2
Symptoms
: "Tired of flares and Symptoms with normal blood work"
20 posts
#3
Flare
: "When anyone asks me what a ‘Flare’ is:"
8 posts
#4
Diagnosis
: "Change in Diagnosis"
8 posts
#5
Pain
: "AAAAHHHHIAmInSoMuchPainAAAAAAHHHHH"
7 posts
#6
Fatigue
: "How do you enjoy vacation and fight through the Fatigue? 😔"
7 posts
#7
Plaquenil
: "Does anyone else take the Plaquenil all at once?"
6 posts
#8
Diagnosed
: "I was Diagnosed today"
4 posts
#9
Rash
: "Malar Rash?"
4 posts
#10
Sun
: "Is it possible to get re-used to the Sun?"
3 posts
Member Growth in r/lupus
Yearly
+10k members(29.8%)
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