flares/symptoms off RA? If so, it may not be the sun, but rather the heat. Some people with RA really thrive in the heat, feeling it makes them feel better. Others find that being too warm makes them feel worse. that's why some people find heat packs really useful for RA symptoms, while others find ice packs more useful.
If you find that your symptoms get worse when you are out on sunny days that are not warm, you may want to talk to your doctor about it. There are a number of autoimmune diseases that are similar to RA and some of them, e.g., lupus, do experience a worsening of symptoms when you're in the sun. This does not mean that I think you have lupus, just that it's something you should definitely mention to your rheumatologist.
Good luck! Please keep us posted on what happens?
Leslie Rott, one of RAHealthCentral's writers, has both RA and lupus. I'd suggest you send her a message - she might be able to tell you more. She's away from home for the holidays, so may not get to you for a week or two, but I'll let send her the URL for your question. I'm sure she'll get in touch as soon as she can.
Please keep us posted.
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Ice is always better for my hot spots. I have been diagnosed with scleroderma, narcolepsy, and ra. Adding lupus to the mix would not surprise me. My rhuematologist told me that it was possible but I have never heard of anyone with ra having that problem too. He ordered more bloodwork so we will see what it says in a few weeks. In the meantime, he upped my mtx and prednisone. Thanks for the quick answer and I will update when I find out if something new has shown up.