CSU & Angiodema Support Group
Private
1 member
$4/month
Why I Started Living With CSU and Angiodema.
Unless you've experienced CSU, it can be difficult to explain just how much it can affect everyday life.
The unpredictability, the flare-ups, the discomfort and the uncertainty can be incredibly challenging.
And sometimes, all you really want is to speak to someone who understands.
That's why I've decided to create Living With CSU, a supportive online community bringing together people affected by this condition from all over the world.
Whether you're living with CSU yourself, caring for a child with the condition or supporting someone you love, I want you to know that there's a place for you here.
A place to share experiences, ask questions, find friendship and feel understood.
I'm not a medical professional. I'm someone living with CSU who believes that sharing experiences and supporting one another can make a real difference.
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I'm not a medical professional. I'm someone living with CSU who believes that sharing experiences & supporting one another can make a real difference