Tuesday, December 18, 2012 KelliB asks

Q: Hi, is it common for the sun to trigger flares or worsen symptoms? Even with preventive measures, I am always worse after being in the sun.

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Answers (3)
Lene Andersen, Health Guide
12/20/12 1:36pm

 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?

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12/20/12 2:08pm

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.

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Lene Andersen, Health Guide
12/20/12 10:30pm

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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Leslie Rott, Health Guide
12/21/12 10:28am
Kelli, I'm not a doctor, but what you describe sounds like lupus-related photosensitivity. Do you have a problem with fluorescent lights, as well? In either case, I was diagnosed with both lupus and RA, which is rare yes, so if you want to discuss this further, let me know. Reply
12/21/12 12:34pm

I would enjoy talking with you but I will wait until after the holidays. I won't see my rhuematologist until Feb.5 and it might be something besides lupus. Either way, I will contact you in January. Have a great holiday season.

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1/ 3/13 1:00pm

I feel better in the sun than during cold and sunless days. Although, with the meds that I take, I am light sensitive and can feel headachy.

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By KelliB— Last Modified: 01/04/13, First Published: 12/18/12