Last Updated on Oct 26, 2018

Support Groups

1. Health Network – Allergies and Immunity Support Group – Vasculitis

2. ExperienceProject – I have Microscopic Polyangiitis

3. Inspire – Autoimmune Diseases Support Group

4. Yahoo Groups - MPAvasculitis - Microscopic Polyangiitis Support

5. Vasculitis Foundation

6. Voice4Vasculitis


  1. Harrison’s Principles of Internal Medicine 17th Edition.
  2. Stephen K. Frankel, Eugene J. Sullivan, Kevin K. Brown. Vasculitis: Wegener granulomatosis, Churg-Strauss syndrome, microscopic polyangiitis, polyarteritis nodosa, and Takayasu arteritis. Crit Care Clin 18 (2002) 855– 879.


rosemary85 Friday, October 28, 2011

I would like to connect with others that have this disease. What treatments have you tried, what has helped, what type of specialist do you see, etc. I have had this disease for a very long time but it has only been recently that a biopsy of my kidney was done and this disease diagnosed. I currently see a nephrologist, am on cellcept...had 4 infusions of rituxan. What symptoms do you have? Rosemary85

Concernedwife Monday, November 14, 2011

My husband was diagnosed [after several hospitalizations with undiagnosed symptoms..high potassium, etc.] in May 2011. His kidneys have not responded to treatments. He is on dialysis. No doctors in our area are skilled in treatment. He developed infections requiring hospitalization when trying cytoxin. He is trying to be approved for rituxan. Did it help? He is fatigued, and he is in pain in his back and legs.

rosemary85 Sunday, December 18, 2011

The rituxan I had in August is helping in reducing some of the can see improvement over the course of a year after the treatment. I take cellcept, did the 4 treatments [infusions] of rituxan and on prednisone. I live in N. Idaho...where are you from?

warrior128 Friday, September 20, 2013

my husband has this disease, he has been on cytoxin, white blood cell count bottomed out twice. We are trying to get approved for rituxan, could you tell me about your experience with rituxan? Thank you sandy

ennairam_23 Thursday, February 3, 2011

A very informative article! Autoimmune diseases such as this significantly affects one's life. I hope that diseases such as this one will have a cure in the near future so that suffering will be alleviated.

WhiteDove600 Wednesday, June 13, 2012

I was diagnosed with MPA in 2007. I was given cyclosphomide, prednisone and other toxic medicine that threw the illness into remission. Eventually the toxic drugs were replaced with milder ones and in the Spring of 2010 I was gradually taken off the drugs. I take raprinil, not so much for blood pressure control, but more to protect my kidneys that took a hit back in 2007 before I was diagnosed. Prior to the attack I had survived two battles with breast cancer, but the pain of MPA made the cancer seem like a walk in the park. They say that I am still in remission, and for a while I forgot and worked in the garden breaking concrete, planting trees, moving furniture around and this after working full-time 5 days a week. Then recently, I noticed the rash on my ankles, inflamed sinuses, fatigue going up the stairs, dropping things, losing my balance. It happens when I get tired and then I remember, MPA is still in the background.

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