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The secrets for Qualifying for Disability Benefits for Lupus You could be receiving disability benefits! FREE advice from a SuperLawyers rated attorney on what it takes to receive the financial assistance you deserve.

BREAKING NEWS for those suffering from the effects of Lupus!
Most are initially denied disability benefits but here's the thing:
You need to file an appeal!
A disability attorney with 30 years' experience tells how.
#LivingWithLupus #LupusWarrior #LupusAwareness
www.brrlaw.com/practice-are...

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#LupusAwareness

#LivingWithLupus

#ChronicIllness

#AutoimmuneWarrior

#LupusSupport

#HealthJourney

#InvisibleIllness

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#LupusAwareness

#LivingWithLupus

#ChronicIllness

#AutoimmuneWarrior

#LupusSupport

#HealthJourney

#InvisibleIllness

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#LupusAwareness

#LivingWithLupus

#ChronicIllness

#AutoimmuneWarrior

#LupusSupport

#HealthJourney

#InvisibleIllness

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#LupusAwareness

#LivingWithLupus

#ChronicIllness

#AutoimmuneWarrior

#LupusSupport

#HealthJourney

#InvisibleIllness

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Living With Lupus : When I’m Down Music Gets Me Through Many people ask me what helps me get through when I'm feeling down and that's music. Not many know that when I was a teenager, I was heavily into music.

Living With Lupus : When I'm Down Music Gets Me Through #livingwithlupus #music #lupus #lupusblog

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Transplant recipients and other immunocompromised people worry about measles exposure Transplant recipients and other immunocompromised people worry about measles exposure.

And people in my life since 2020 wonder why I've become a hermit, MIA introvert, disassociated. I was actually starting to venture out into public space a bit more and now this. #ImmuneCompromised #LivingWithLupus Thankful for my garden, small home, simple rural life.
barrie360.com/transplant-r...

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Steamy start to the day 🩵🧖🏽‍♀️

Just me and my @doterra.bsky.social

#livingwithlupus #iykyk #essestialoils

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#kaleidoscopefightinglupus #lupus #sle #spoonie #lupusfighter #lupuslife #spoonielife #lupuscommunity #invisibleillness #butyoudontlooksick #autoimmune #lupuswarrior #autoimmunedisease #weeklyinspiration #dailyinspiration #livingwithlupus #inspirationalquotestoliveby #lupusstrong #lupuswarriors

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Though ‘Grit’ isn’t on my fave list, it has a great reference to ‘having a (life) purpose’ through Jane Golden’s #lupus story (Ch.8)

Despite constant pain, her art activism shows how purpose (spirit of service) can transcend the here and now.

Lupus teaches us this, and much more #livingwithlupus

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Wild to me that lupus has been known since at least the 13th century but didn't have effective treatment until the 1950s. Even today there is a very short list of medications that work. I've exhausted most of them. #lupus #disability #medical #livingwithlupus

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I limped to bed today. I am so tired that my legs were shaking. I got online with my friends and laughed, saw @NursePatMacRN schooling folks and leading citizen science, and I am going to sleep happy. #LivingWithLupus is hard but it will not break my soul. I choose joy.

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