← Return to My Journey with Polyarteritis Nodosa (PAN)
DiscussionMy Journey with Polyarteritis Nodosa (PAN)
Autoimmune Diseases | Last Active: Mar 28, 2022 | Replies (19)Comment receiving replies
Replies to "Hi Susan, how have you been?I also was diagnosed with PAN with a biopsy. My symptoms..."
@brookraven I”m glad you found Mayo Connect and hope you’ll find some of the help, advice, and tips that you’re looking for. PAN is a serious autoimmune disease and needs prompt treatment. I included a link to The Vasculitis Foundation. My sister, who has some form of vasculitis, highly recommends this group for information. Her vasculitis mostly impacted her kidneys, leaving her in chronic renal failure. I suggest that you listen to your rheumatologist and start medication or get a 2nd opinion.
https://www.vasculitisfoundation.org/education/forms/polyarteritis-nodosa/#:~:text=or%20muscle%20tissue.-,Treatment,such%20as%20methotrexate%20or%20azathioprine.
What do you hope to learn from your bloodwork?
Oh finally, a fellow PAN-ite!!
You are the first person with PAN I have ever been in contact with…
Aren’t we special! lol
PAN is serious stuff. I hope you have a rheumatologist who is familiar with this disease because it can be life threatening.
In my opinion, you are experiencing the effects of inflammation. I believe that you should consider taking prednisone. It can put the evil PAN in its place for awhile and prevent it from destroying your organs or nerves. Very important.
Most doctors know nothing about PAN. I have had to teach mine…
Please be careful with this situation. Keep me posted on your journey.
Susan