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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I was diagnosed with GCA at your age and had a biopsy and it came up negative. The doctor gave me prednisone for the swelling in my temple and it went away, so I forgot about it, but then it showed up for real at 72. Doctors say it was just a coincidence and it couldn't have been GCA and wasn't possible, but I think it was very weird.
Thanks for that insight, gives me some hope that this will settle down and I can live a normal life for another 20- 30 years.
The heaviness in my arms, upper chest, neck and shoulders started on Prednisone and continue on Hydrocortisone. My endocrinologist and cardiologist say it is muscle myopathy. They say I will feel better once I am off steroids. At the rate I am going in terms of tapering the steroids, I have no idea when this will happen.
Thanks so much for this information. I have been treated for PMR for five years. Tapering doses of prednisone up and down, multiple flare ups. I was down to 2mg, having pain but able to manage with the help of acetaminophen. Stress seems to aggravate it, so during the holidays and extreme cold recently was not surprised that I hurt more. I started getting dull headaches in my right, then left temple, along with stiff and painful jaw, new right neck pain and horrible shoulder and neck stiffness and pain. I never get headaches, several new symptoms for me. Called rheumatologist who told me to come in for a steroid injection. I did, but his nurse gave me the shot and I never saw my doctor. I went on an overnight trip the next day and the following morning woke with slightly blurred vision. Headaches continued. I ended up in the ER, and was diagnosed with temporal arteritis based on symptoms, elevated sed rate and negative for bleed head CT. Gave me 60mg oral prednisone and a script for 60 mg daily in 3 - 20mg doses. F/U with rheumatologist next week. My mom had this, but not PMR. Vision is good today after 1 dose, as are the headaches. Bracing myself for the side effects.
The same thing for me. As I am tapering off the steroids I have noticed that the heaviness in my chest, shoulders and arms have gotten better. As good as steroids are that is how bad they are.
Hi @marmak, I'm so glad you caught the GCA fast. I had symptoms of GCA a few months before diagnosis, and PMR maybe 9 months before that. After biopsy was positive for GCA, I started on prednisone 40 mg, tapering down by 5 mg every two weeks. It went pretty well. I only had to go back up to the previous dosage once when tapering. I've been off prednisone a few months now. I have odd pains here and there, but am much better than what I was.
My worst side effect while on the high dosage of prednisone was insomnia. My appetite returned as I'd been anorexic with PMR and GCA, but I watched what I ate. I also have osteoporosis, but that started before the prednisone.
I wish you the best. My mother-in-law was diagnosed with GCA in her 80s and lived to be nearly 100.
What a terrific outcome. High dose prednisone causes hypertension in me, so I've been watching my BP which is now about 30 points higher than normal. Was on a taper for my pmr which I've had almost 6 years now. Tolerated a good deal of pain in my quest to get off it. May have been unrealistic. Am currently having no pain and loving it.
Yes, it's wonderful to be pain free.
I wonder I'd anybody who took methotrexate ended with continuous hiccups and burping after every meal.
This has gone on for about 5 months after only 8 weeks on MTX. I stopped the drug but the hiccups and burps contined. Any comments?
Any update?