We are sorry you need us

but glad you found us

Members of the PSN-Network

The Polyarteritis Nodosa Support Network 2012 (PSN) is a not-for-profit organization with more than 700 members world-wide. Patients, caregivers, physicians, research specialists provide invaluable education and support through a mailing list, live chat sessions, and other web resources.

Thank you for visiting the PAN Support Network 2012 web site. I hope you find everything you need to understand PAN and you discover resources to make the best possible decisions about your care.

Edward Becker
PAN Support Network 2012
Pittsburgh, PA USA
eob50 [at] consolidated [dot] net
PAN Support Network 2012

Learn how and why the PAN Network was created.

Terms of use:

This web site is intended only as a means of learning more about PAN and getting support from other PAN/ autoimmune diseases patients. The information provided on this site, any advice from other people on this site, and the links provided are not intended to replace your current medical care or current course of treatment.

NOTE: The content of this website or any information to which this site is linked cannot replace your doctor's care. The PAN Support Web Site is merely a resource; another tool to use to help you understand PAN or autoimmune diseases. Do not make any changes to your current course of treatment without your doctor's knowledge.
  • PSN cannot guarantee the accuracy of the information that you find in any of the websites to which this site is linked.
  • PSN cannot guarantee the accuracy in any information shared by other PAN patients or anyone with assumed knowledge of the disease. Discuss any information that could have an influence on your illness with your doctor or health care professional.
  • PSN is not liable for any course of action undertaken from information on this website without your doctor's knowledge.
  • Do not make any changes in your course of treatment unless you first consult your doctor.

    The PAN Support Network 2012
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    the terms of use]