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Real members of MyLupusTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
A MyLupusTeam Member asked a question 💭
Moncton, NB

I was wondering if sun exposure could cause this.

August 16, 2025
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A MyLupusTeam Member

Hi Willow2044! Even thought the answer is AI generated, it's pretty accurate. I know it sounds like a lot, especially if it's not something you did pre-Lupus. Biggest thing for me, 50+ Sunscreen. Talk with you Rheumatologist if you have one about your specific "must dos" in the sun & if there any you might be able to get away with not always using like the umbrella. Blessing and keep fighting Willow! Always here to talk or listen💜

August 16, 2025
MyLupusTeam

Yes, sun exposure can definitely cause redness and swelling in people with lupus. About 75% of people with lupus are photosensitive, meaning they have increased sensitivity to ultraviolet light. This can trigger symptoms that look and feel like a sunburn, even with minimal sun exposure.

Common sun-related symptoms include
• Show Full Answer

Yes, sun exposure can definitely cause redness and swelling in people with lupus. About 75% of people with lupus are photosensitive, meaning they have increased sensitivity to ultraviolet light. This can trigger symptoms that look and feel like a sunburn, even with minimal sun exposure.

Common sun-related symptoms include:
• Bright red or purple skin patches
• Skin rashes that resemble sunburn
• Swelling and inflammation
• Fatigue and weakness
• Joint pain To protect yourself from sun-related symptoms:
• Wear broad-spectrum sunscreen with SPF 50 or higher
• Use protective clothing like long sleeves and hats
• Carry an umbrella on sunny days
• Stay in shaded areas when possible
• Be aware that even artificial lighting can trigger reactions

Remember that sun exposure can trigger broader lupus flares beyond just skin symptoms, so sun protection is essential for managing your condition.

August 16, 2025
A MyLupusTeam Member

Yes, there is, but their specialty is pulmonary not rheumatic.

August 18, 2025
A MyLupusTeam Member

Sheesh! I hate to hear this, Willow! Is there a university medical center nearby where you can see a rheumatologist? That's worth exploring, as they are often more knowledgeable about our uncommon disease.

August 18, 2025
A MyLupusTeam Member

I see my GP next Thursday to see how my rheumatology appointment went (I complained to him the rheumatologist is blaming any findings on being too fat ( I am around 15 pounds overweight). My latest CRP was 60. The ER doctor I went to on Thursday because my face was swelling so much and so painful, did tests and said it was autoimmune. She said the CRP of 60 is never because of a person’s weight. For precautionary measures she tests for infection, but it came out negative. She gave me a name of a more thorough rheumatologist, so I might ask my GP for the referral to see him. One more chance. I was told I have lupus and APS by a hematologist, but the rheumatologist I see doesn’t like her and won’t acknowledge it - but I am on medications though for lupus and APS.

August 16, 2025

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