Anyone dealing with ANCA GPA Vasculitis?

Posted by melodyanne @melodyanne, Jul 25 11:55am

Newly diagnosed in November, 2024, I am looking for people fighting this same disease to connect with.

Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.

Profile picture for daze @daze

My 55 year old son has ANCA. I am sorry for you and your family. Sending prayers

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Thank you for the prayers. Hope your son's was caught in its early stages, before organ damage. Do you know if his is GPA, MPA, or EGPA? I have learned more than I ever wanted to know these last 8 months about ANCA. I am ANCA GPA PR3. Best to your son.

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Profile picture for melodyanne @melodyanne

How fortunate for you! Blessings! I have been on a battery of meds (prednisone included) but this devil is being rather stubborn! Prayers appreciated.

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@melodyanne I’m sorry you are having to continue to fight this Vasculitis.

I am praying for your complete healing.

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I have had GPA (formerly known as Wegener's granulomatosis) for twenty years. I worked in an old building that had a lot of asbestos and three of us came down with GPA. It took me several years to get diagnosed and I had to almost die to get a correct diagnosis. With treatment and lot of rehab I survived and after a couple years reached my new "normal level of functioning" and had to seriously downsize my life style. But the near death experience and one serious relapse caused by covid vaccination, have give me a great appreciation of the miracle of still being alive 16 years after my diagnosis. If you are lucky enough to get properly diagnosed early so you can avoid the most serious body damage, one can have a pretty good active life. Many people even attain a drug free remission. I still need 10 mg of prednisone and occasional RTX infusions to control my GPA.
I was active on a forum for years with other people with PGA that I found very helpful. It may have ended due to large decline in members and activity as people switched to various Facebook groups for support.

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Profile picture for zatff @zatff

I have had GPA (formerly known as Wegener's granulomatosis) for twenty years. I worked in an old building that had a lot of asbestos and three of us came down with GPA. It took me several years to get diagnosed and I had to almost die to get a correct diagnosis. With treatment and lot of rehab I survived and after a couple years reached my new "normal level of functioning" and had to seriously downsize my life style. But the near death experience and one serious relapse caused by covid vaccination, have give me a great appreciation of the miracle of still being alive 16 years after my diagnosis. If you are lucky enough to get properly diagnosed early so you can avoid the most serious body damage, one can have a pretty good active life. Many people even attain a drug free remission. I still need 10 mg of prednisone and occasional RTX infusions to control my GPA.
I was active on a forum for years with other people with PGA that I found very helpful. It may have ended due to large decline in members and activity as people switched to various Facebook groups for support.

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@zatff Welcome to Mayo Clinic Connect! Sounds like you had a rough time getting here! This is a wonderful, caring group of people. You’ll be a great addition.
May I ask if you have a particular question you wish to ask? And, can you tell me how you found MCC?

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