Adjusting to life with temporal arteritis
Would like to hear from people that have gone thru or going thru temporal artritis. I am now going on my 5 month after being diagnosed. It is getting better but very slowly. Is this normal?
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@kimh. I was really scared too, when I was told I had to have a biopsy of my temporal artery! It wasn't one bit painful. My artery was so inflamed that the surgeon said to his nurse during the procedure, "Look how big it is!" He told me he knew without getting a biopsy report that it was GCA because the inflammation was so obvious. He confirmed that I had GCA right after the surgery. Don't worry about this minor procedure, Kim. You'll do fine! Warmest wishes, Laurie
@kimh . Hahaha, don't worry, they won't go near your brain! I'm going to start calling you Nervous Nellie. 😂 That's what my 3 sons call me when I'm stewing too much about something. You're going to be fine! I hope all this info has put some of your fears to rest. Thinking of you. Take care.
Good to know. Mine come and go, so maybe migraines are coming back.
hahhaha....you brought a smile to my morning! BTW, I have three sons as well!
@kimh, but check with your doctor!
Oh absolutely. He's keeping a close eye on me. I'm very lucky to have the 'team' that I do!
@kimh. That's GREAT to know, Kim!
I am interested in following discussions of Giant Cell Arteritis. Unfortunately, I have it but still have my vision.
Hello @mariannj , you will notice that I have moved your post into an existing discussion on Temporal Arteritis as a way to connect you to information and members in this discussion.
@mariannj Welcome. May I ask how long you have had GCA and what treatment you’ve received? Do you take any prednisone?
I have a different autoimmune disease but I find that we all learn from each other. Strength in numbers!