WE AS A COMMUNITY should have a voice so the things we need are researched and that's where groups like the Vasculitis Foundation could increase how they support us exponentially by INCLUDING us.
Your thoughts. Your journey. We, as a community, need to know your truth. No matter how THEY see it. From onset due to vaccination. To sexism and ableism from our medical staff. To medical gaslighting and on and on. I have stories, and many of you have shared stories with me, that your medical staff have treated you with ableist bias and dismissiveness AND THEN grandstand on the fact that because they are medical staff they can't be ableist.
WHAT!?
So my fellow patient - participate here. TOGETHER we have power and we will make a difference. Right now, we're just getting started but I have BIG plans.
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