#sclerodermasucks search results
For my mom& grandma #Scleroderma #SclerodermaSucks #SclerodermaWarriors I just supported World Scleroderma Day 2018 on @ThunderclapIt thndr.me/1GnbVM
Well this just screwed my mood. #sclerodermasucks
In Systemic Sclerosis Patients, Heart Stiffness May Predict Worse Prognosis, Study Says sclerodermanews.com/?p=18051 via
I've decided that I look like a drunk old lady when my joints are hurting from a flare. Not cool, scleroderma! 🤣 #sclerodermasucks
#SclerodermaSucks @CromwellCalabro is the strongest person I know. Mentally & physically tough as nails 💪🏼🙏🏼 ❤️@__Scleroderma__
@bobsagat Thanks for sharing your sister's story. #sclerodermasucks. I was diagnosed 10 years ago. I just rewatched it since it came out.(13 years before I was diagnosed) Thank you for being an advocate.
Vilolördag! Återhämtning och att ta det lugnt är ett måste för mig. Får tvinga mig själv att läsa bok och ligga på soffan. ❤️ Glöm inte att göra inget! . . #sclerodermasucks #eatclean… instagram.com/p/BqSSJ_JlnII/…
Can they bring my puppies to me in the hospital? #sclerodermawarrior #sclerodermasucks instagram.com/p/Bq77iDCAV_e/…
#Sclerodermasucks Love you so much Jen 💋❤
I saw my cardio doc today. 🙃 instagram.com/p/Cc8M6KvuU5N/…
Follow my #scleroderma page for updates #sclerodermasucks #sclerodermawarrior m.facebook.com/sclerosara/
Kära jultomten, fryser redan. Kan man få ett förskott på julklappen? #snöiseptember #åre #sclerodermasucks @ Åre, Sweden instagram.com/p/BoxEnCFhZNi/…
I'm raising money for Jason Wright Medical Expenses. Click to Donate: gf.me/u/3iikvr #GoFundMe #sclerodermasucks
I was asked if I am ‘independently wealthy’ earlier this week. Why? To qualify for a potentially life saving Stem Cell Transplant. My insurance, Medicare, doesn’t cover the procedure. #sclerodermasucks #medicare
#Sclerodermasucks Love you so much Jen 💋❤
I saw my cardio doc today. 🙃 instagram.com/p/Cc8M6KvuU5N/…
#SclerodermaSucks @CromwellCalabro is the strongest person I know. Mentally & physically tough as nails 💪🏼🙏🏼 ❤️@__Scleroderma__
Mayo diagnosed my rare disease and saved my life in doing so. #DiffuseScleroderma #AntiRNApolymerase3 #SclerodermaSucks
Amazing and promising news!🙌 Now do diffuse systemic scleroderma! #SclerodermaSucks #CureScleroderma #SclerodermaFoundation
#SclerodermaSucks because for the last 2 days I've been bedridden because my leg muscles are completely locked up. Pain scale 9 😭#scleroderma #scleroMama #Chronicallyill
I’ve been stuck in quarantine for 9 days with two teenagers. We aren’t sick but I have an autoimmune disease + a lung disease so I hit the terrible lottery for “vulnerable people”. Thank goodness I have lovely friends that have delivered groceries. #sclerodermasucks #coronasucks
Had some big plans today to work on a blog post. . . Woke up with a migraine and feeling like I could puke at the drop of a hat. Chronic illness sucks! Guess I’ll try for tomorrow. Night all! #scleroderma #sclerodermasucks #chronicillness #ChronicPain
Nothing like having a horrible flare and being in curled up in the fetal position and crying pain for three weeks and a doctor saying ‘oh maybe it’s just the flu’! #sclerodermasucks #ChronicPain #chronicillness
"Scleroderma back up, I see you there RA, immune system don't you try that w/ me!" #campdiasozo #sclerodermasucks
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