Resources for a Family of Diseases
  MPA Patient ResourcesMPA Mesage Board and Online Support Group The MPA support group is an outlet for those interested in microscopic polyangiitis. It is an outlet to meet others with this rare disease and a place to share stories, offer support and encouragment.This group is not intended as a substitute for medical advice from a qualified health care professional. Each person should rely on his/her medical team for specific medical advice. Over 80% of patients with MPA have kidney involvement. The National Kidney Foundation's website is an excellent resource for learning more about kidney disease. Listing of VF Chapters, Support Groups or Area Contacts. Most of the Vasculitis Foundation's support groups are open to patients with any type of vasculitis.. The groups meet several times a year to discuss medical updates, ongoing research studies and to offer comfort and support to each other. Much can be learned at a meeting, whether it is a discussion among patients or features a medical professional or other expert. MPA patients are encouraged to contact VF chapter leaders in their area for further information.
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About Vasculitis: Our Online ResourcesMedical ConsultantsVF medical consultants provide advice by telephone or e-mail to physicians who treat patients with Vasculitis.
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About Vasculitis Foundation
The Vasculitis Foundation (VF) is the only international organization for patients with Vasculitis. Founded in 1986, VF provides patients and family members with practical information and coping strategies to live successfully with Vasculitis.
Mission: The Vasculitis Foundation supports and empowers patients through education, awareness and research. Learn more