Happy May 1st, all! This month we recognize both Lupus Awareness and Myositis Awareness month-2 of the autoimmune diseases we are working to treat. #lupus awareness #lupus #LupusAwarenessMonth #myositis #myositis awarenessmonth #myositis awareness

Thank you to Peter Frampton​ for bringing awareness to #IBM and the #Myositis community!

#inclusionbodymyositis #myositisawareness #philadelphia #psgdonors

Peter Frampton's Performance-Ending Muscle Disorder medpagetoday.com/blogs/celebrit…

Register for this years nationwide Neuromuscular Symposium! Taking place May 3rd and 4th! Sharing the latest in research, knowledge translation, new treatments, best practices and advanced technologies.

To learn more and regsiter, follow this link: ow.ly/NGlA50h4TfP

Though #PolymyalgiaRheumatica (PMR) is the second most common rheumatic disease in the United States, it only has a diagnosis rate of about 50%.

Last day at the Myositis Patient Conference!! Having a blast meeting everyone! #myositis #myositis awareness #polymyositis #dermatomyositis #ivig #biotekremedys #myositis conference @ DoubleTree by Hilton Bloomington… instagram.com/p/B2HYFush2V0/…

#MyositisAwareness is important to me because I had symptoms for 8 yrs before a dr. said #myositis .

#Inclusionbodymyositis stands out by aggregation of protein waste products such as B-amyloid, tau, TDP43 etc., reminiscent of neurodegenerative diseases.
⬇️ Congophilic inclusions lighting up in a muscle fiber
#RareDisease #pathology #MedEd #neurotwitter #myositisawareness

Watch this video of me made about one year ago, living with Dermatomyositis 👉 youtu.be/1Qnw_N_s96I
#MyositisAwareness #dermatology #dermatologia #rheumatology #dermatomyositis #raredisease #upstateny

The treatment and cost burden for Inclusion body myositis
#MyositisAwareness #inclusionbodymyositis
#myositisresearcher

You hear the thundering of hoofbeats and you know a heard of horses is headed your way. Yet somewhere in that herd, a zebra is running too.
Physicians may encounter some conditions less frequently than Feb29th-Rare Disease Day
#rarediseaseday#myositisawareness#careabouttherare

Come see #Keeogo and #MartinJarry who is living with #myositis at the Nationwide Neuromuscular Symposium in Quebec City, on May 3rd and May 4th #MyositisAwareness twitter.com/MD_Canada/stat…

May is #myositis awareness month. I made this pic to do my part (or at least help people know how to say it.) Out of 1 million people, fewer than 10 are diagnosed w/ the #autoimmune disease that attacks & destroys its own muscle tissue. I am one of them. #myositis awareness

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Quite rightly for #MyositisAwareness month of May, we are flat out with pushing for research money via grant applications, updating our approvals and planning for upcoming projects. It's hectic, but an exciting time for Myositis research!

What a perfect day for an exercise session on Myositis / IBM in Poole! Excited to work with a great group! #MyositisAwareness #IBMAwareness #HereForYou Exercise Works! University Hospital Southampton 💙 Muscular Dystrophy UK

Alagille syndrome (ALGS) is a complex condition with symptoms that can vary greatly from one person to the next. If you’re feeling overwhelmed with what comes next after a diagnosis, here are the first four steps we recommend. themighty.com/topic/rare-dis…

The Myositis Association so excited to honor virginia ladd at the AARDA luncheon @AARDATweets #AutoImmuneDisease #myositis #myositis awareness #myTMA

May—Myositis Awareness Month—presents a month-long opportunity for advocates to inform the public about this rare disease to elevate the needs for more research & gain a keener understanding of it.
#MyositisAwareness #SimplifyingComplexCare #SpecialtyPharmacy

May is Myositis Awareness Month. Myositis means muscle inflammation, and can be caused by infection, injury, certain medicines, exercise, and chronic disease. It take 3.5 years on average to diagnosis Myositis. #Myositis Awareness #Myositis The Myositis Association

How many people suffer from sporadic Inclusion body Myositis? #myositisawareness #inclusionbodymyositis #myositisresearcher

#LupusAwarenessMonth and #MyositisAwareness Month are both in May

Last Day of the Nationwide #Neuromuscular Symposium with Muscular Dystrophy Canada - Martin is sharing his story about how the #Keeogo helped him regain his #mobility

#MuscularDystrophyAwareness
#MobilityAwareness
#MyositisAwareness

Inclusion body Myositis, where does the name come from? #myositisawareness #myositisresearcher #AcademicTwitter #inclusionbodymyositis

This survey is being done to understand how myositis affects other aspects of life such as your emotional and mental well-being and that of your caregiver. Please share and spare a few minutes bit.ly/3vC8S56 #myositis #myositis awareness #caregivers Myositis Support and Understanding (MSU)