These are very explicit photos of Purpura (rash) and Necrosis. Please know that NOT all patients will experience these symptoms.
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If you haven't read about the 2019 International Vasculitis Symposium here is the info.
Has anyone registered? I you are interested in attending please let me know and I will see if we can get it paid for you if you are not able to cover the expense
July 19-21, 2019
Hyatt-Regency
3200 E. 81st Street, Bloomington-Minneapolis
mscrmapp.clickdimensions.com/editor/previewversion?accountKey=aD70WfXxEEGEn7dYTDS4Q&version=4&typ...
CAN YOU POSSIBLY HAVE A RARE DISEASE IF YOU HAVEN'T FOUND A DIAGNOSES?
alsnewstoday.com/2019/05/15/rare-diseases-constitute-public-health-issue-ncats-director-warns/
Rare Diseases Constitute a ‘Public Health Issue,’ NCATS Director Warns
The healthcare system fails millions of Americans due to the "invisible" cost of treating rare diseases, a National Institutes of Health official says.
Who does the most for Vasculitis and us the patients living with Cryoglobulinemia? It's the Vasculitis Foundation. Check out this page!
Thank You, VF!
www.vasculitisfoundation.org/education/forms/cryoglobulinemia/?fbclid=IwAR1ipVmL5XFiq_KXMHsUx0x8T...
Vasculitis Foundation » Cryoglobulinemia
Cryoglobulinemia Swap out your current Facebook Profile Cover with image below! Help spread awareness about vasculitis on your social network by replacing your current Facebook Cover artwork with this...