Think I have Giant Cell Arteritis (or GCA)
I’ve been having pain on the left side temple starting last Monday every night around 9pm. Taking ibuprofen at bedtime in order to sleep. I sent my Rheumy a note thru the portal for guidance but she was off Friday . What alarmed me was the symptoms started at 6pm on Friday and worse. So I went into a google overdrive, long story short, I self medicated with 30mg of prednisone given i take 6mg every morning for PMR. The pain went away within an hour. I have a long standing appt with my Rheumy on Monday so I’ll continue with the 30mg additional prednisone until then. Don’t like taking the addition prednisone but the thought of possible blindness made the decision to self medicate until Monday was easy.
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Susan
I think I have already responded I want to address and it may help for anyone else with GCA. I found a neurologist researched and spent two hours with me looking at scans and info on GCA. I found an article going back years which I have a copy of about a man who went deaf for two days. The only hint of GCA was a high ESR. He was given doses of 60 mg of prednisone and within 48 hours his hearing came back. So when we are told it only happens to the large vessels this is not true because the small veins going into the ear had giant cell arteritis. Had he not been given prednisone immediately he would have been deaf permanently. My situation relates to my tongue which was paralyzed as a result of GCA because in 2015 my doctors had no idea that my curled tongue could be a result of GCA. Honestly I’m not sure if They could have done any more than what they did except to keep me on a higher dose a little longer. Who knows.
You're welcome. By the way, GCA is a vision threatening form of vasculitis (Cecil and Goldman's Textbook of Medicine). Glad you're on prednisone now.
I was surprised to be given a general anesthetic for my temporal artery biopsy. It went well without any pain. The Rheumatologist asked me what side of my head most of my symptoms were on, and the surgeon did one biopsy on that side. Sometimes people have both sides done. Good luck@SusanEllen66!
Yes, last night I paid attention to how I felt when I put my head on the pillow on the “bad” side. Sure enough, my scalp started to hurt, the pain in my face returned.
So, there it is…
I’m so bummed about this not only for me, but for my son. Both his father and I are plagued with Vasculitis. His dad has PMR. I have PAN in addition to the new GCA. Hopefully, there isn’t a genetic problem for him.
Every day is an adventure for sure!
Thanks for sharing your information!
Very long story for another time I’m afraid. Take care and treat it like GCA. If 60 doesn’t work you might need 80.
The prednisone should be helping, @SusanEllen66. How long have you been taking it?
Friday morning so that’s 3 days.
I’m taking things day by day.
I think sometimes it takes a few days to kick in. Take care.
Listen Susan. GCA is not the end of the world. Take your prednisone and see if you can get on Actemra. After symptoms are gone and you have enough prednisone in your body, Actemra will help you reduce quickly. It brings down the inflammation and so ESR and CRP come down. I started before it was approved for GCA and I was part of the trials so I didn’t pay for it. I’m still on 7 mg of prednisone for my adrenals. Good luck. Ps. If the biopsy is negative so was mine but I was treated for GCA and I’m still here at 80.
Thank you! I’m very glad you are doing well.
Not one test, of any kind, has shown any evidence for GCA. Nothing. MRI, CT with contrast, blood work (no inflammation). Zero. So, hopefully a biopsy will help me feel less like I’m pretending or something…
I already have another form of Vasculitis. It’s a very rare one (30/1,000,000). Diagnosed with that in 2015.
So, yea me…I’m almost 73, and blessed every day!
I’m not making a little of GCA. when I originally had head pain and a ESR of 85 this was it. Went from Florida to Mayo in Minnesota. They couldn’t tell me anything else. Did the cat scan And found out I was allergic to the dye but nothing else showed up. It was difficult not having a diagnosis but I became accustomed to it.
Which other autoimmune disease do you have? I have PMR and Raynauds hence Florida instead of NJ.