Today is #EosinophilicDiseasesDay
One of the forms of Vasculitis is one of these diseases. To learn more listen to podcast episode 194 or click the link and read about it! Including insight from patients! https://t.co/Z9GPWvVy9G
#worldeosawareness#vasculitis
@NatRevRheumatol This is by FAR the best one I have read. I share it often with my community. It is much appreciated that it is the first that doesn't use fear and the need to end any ability to have children as the first thing it says patients need.
#vasculitis#vasculitisawarenessday
It is #VasculitisAwarenessDay
Remember... you may feel alone but there are THOUSANDS of us and you can find support here or on the Team Vasculitis Instagram page.
#VAM2023#Vasculitis
Rare Diseases are misdiagnosed 40%+ of the time.
Then #raredisease warriors are labeled "drug seekers" when they keep asking for help because they're getting the wrong treatment.
We need to do better.
#rarediseasetruth#chronicillness
Have you ever dealt with your Doctors dismissing symptoms + struggles because you have a #raredisease?
Suddenly you're not a whole person anymore. It's just about your disease. Share your #rarediseasetruth
There are 30 million #raredisease patients in the US. 95% of those do not have a single FDA approved medication for their disease. That's 28,500,000 people at minimum.
Stop using this as a "reason" to not use a medication. It's more complicated than that. #ableist
It's been almost a YEAR since the official launch of Team Vasculitis. I am SO grateful to the community and excited about what we're creating!!!
#chronicillness#patientadvocate#vasculitis