Angela Degrassi

397 posts

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Angela Degrassi

Angela Degrassi

@AngelaDegrassi

Katılım Mayıs 2022
36 Takip Edilen18 Takipçiler
Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
We’re proud to launch the HEROES Toolkit: a free, first-of-its-kind resource created with and for salon professionals to help clients living with scalp and skin conditions like psoriasis feel seen, supported, and empowered. Click the link in bio to explore the toolkit and learn how you can be a HERO: bit.ly/HEROES_Toolkit #HEROESToolkit #PsoriasisAwareness #SkincareSupport #ChronicIllnessAwareness #GHLF #CreakyJoints #BeautyWithEmpathy
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Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
We want to hear from you. If you’re living with RA, AS, axSpA, PsA, or GCA, your feedback could help improve doctor visits for everyone. Take our short 2-minute survey (click the link to share your experience. You’ll be entered to win one of three $100 gift cards.) Don't wait! The survey closes Sunday, April 27th. research.net/r/2CRFZX3?SV_I… #CreakyJoints #RheumatoidArthritis #AnkylosingSpondylitis #PsoriaticArthritis #GiantCellArteritis #AxialSpondyloarthritis #ChronicIllness #PatientVoices #Rheumatology
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Angela Degrassi retweetledi
Shelley Fritz
Shelley Fritz@shelley_fritz1·
Living with psoriasis? We want to hear from you! Help shape care, research, and support by sharing your experiences. 💸Paid opportunity 🗣️Your voice, your impact 👉 Take the short survey to see if you're eligible: research.net/r/52H5KKQ?SV_I…] #Psoriasis #PatientAdvocacy
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Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
What are the options for Sjögren’s? At CreakyJoints, we are committed to connecting you with opportunities to participate in clinical research that has the potential to improve treatment outcomes in the future. The DAFFODIL trial is evaluating an investigational medicine for adults with Sjögren’s disease. See if you may qualify here: SjogrensDiseaseResearch.com/GHLF
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Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
This #CCAwarenessWeek, @keyla_ire highlights the misconceptions people face, the hidden struggles of living with IBD, and the individuality of every patient's journey.
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Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
“Advocating for yourself is practicing advocating for others” Rachael Eckles, lawyer and bioethicist suggests starting to advocate by using your voice to speak up for what you need. #AdvocacyInAction
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Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
Today is a great day to discover the latest research on #AxSpA #lupus #OA #PsA #RA Sjögren's and more! What are you interested in learning about? #ACR24
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Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
#ACR24 study looked at giant cell arteritis (GCA) in Medicare fee-for-service and found that prevalence: ⬆️Rises with age (highest in 85+) ⬆️Is ~2x higher in females ⬆️Is highest in White persons ⬇️Is lowest in Asian persons @abbVie @DrPeterMerkel cdmcd.co/zE64yY
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Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
Are you satisfied with your rheumatoid arthritis control? 🤔 A new #ACR24 study reveals: 🩺 73% of 26,377 patients are satisfied, but 57.5% of those not 'very satisfied' want med changes. 🩺 Top concerns: fear new meds won’t work & thinking current meds are 'good enough.' @venkyshilpa1 @GHLF_Kelly acrabstracts.org/abstract/explo…
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Angela Degrassi retweetledi
Looms4Lupus
Looms4Lupus@Looms4Lupus·
Thank you to the @GHLForg for inviting us to the Clinical Trials Talks Podcast. We’re excited to collaborate & share @JuanaMataa & @estelamata's experiences as patient & caregiver. Our goal is to inspire & empower minority communities affected by autoimmune diseases like lupus.
CreakyJoints.org@CreakyJoints

Ran into the amazing #MataSisters at #ACR24! 💜✨ Always inspired by @Looms4Lupus & @estelamata and Juana Mata. Stay tuned for their episode on our Clinical Trials Talks podcast — dropping soon! 🎙️🔥 #Lupus #ClinicalTrials ghlf.org/patient-educat…

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Angela Degrassi retweetledi
CreakyJoints.org
CreakyJoints.org@CreakyJoints·
Do you have fatigue or pain from #lupus (SLE) even on your "good" days? New #ACR24 research showed that 24% of lupus patients experience moderate to severe symptoms even on their "good" days, which greatly impacts quality of life. acrabstracts.org/abstract/impac…
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