These are very explicit photos of Purpura (rash) and Necrosis. Please know that NOT all patients will experience these symptoms.
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A Small Bit of Change goes a long way to Change How People Live Everyday!
Join our Campaign! A SMALL BIT OF "CHANGE FOR CHANGE".
VASCULITIS RESEARCH! IMPROVING THE QUALITY OF LIVES OF THOSE WE LOVE!
Join us on our Journey of Discovery to Improve the Lives of those suffering from Vasculitis Symptoms. Let's find new ways to treat our patients and how about Finding an Early Diagnoses? People suffer for years and years never knowing why they are so ill. Let's get together and share a small bit of "Change for Change".
app.mobilecause.com
I'm fundraising for The Vasculitis Foundation. It's an amazing organization. Everybody please check out my campaign! Find out more and donate here: igfn.us/vf/Vasculitis
The Alliance for Cryoglobulinemia is here for YOU.
Do you have Cryoglobulinemia? Do you have Questions about how to live with this Rare Disease?
Would you like to meet others living with this disease? We have a support group with friends who will share their experiences and knowledge about Cryo.
Send a friend request to Marianne Vennitti or Eileen McDermott Propp and Say I want to join the support group.The Alliance for Cryoglobulinemia is here for YOU.
Do you have Cryoglobulinemia? Do you have Questions about how to live with this Rare Disease?
Would you like to meet others living with this disease? We have a support group with over 100 members.
Visit us at allianceforcryo.org Or send a friend request to Marianne Vennitti or Eileen Propp.
This is how you Pronounce our Rare Disease.
Image: Vasculitis Foundation » Cryoglobulinemia
images.google.com
Found on Google from vasculitisfoundation.org