Connect with others who understand.

  • Learn from expert-reviewed resources
  • Real advice from people who’ve been there
  • People who understand what you’re going through
Sign Up Log In
Powered By
Real members of MyFibroTeam 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 MyFibroTeam Member asked a question 💭
Brandon, WI

I get a rash in the summer around my ankles and behind my knees that looks like I am bleeding out but then turns an orange brown color. It is only on my legs and only in those areas. The doctors tell me it is from the sun cuz of my diseases. I am wondering if anyone else gets this and could it be something more?

February 24, 2016
 · 
Reactions

Answer Summary

Members shared their varied experiences with sun-related rashes, with many describing similar symptoms including welts, hives, heat rash, and... Read more

Members shared their varied experiences with sun-related rashes, with many describing similar symptoms including welts, hives, heat rash, and discoloration on their legs, arms, and other areas, often accompanied by itching, pain, migraines, and heat sensitivity. Several members recommended seeing a dermatologist for proper diagnosis and mentioned treatments that have helped them, including cortisone cream, Atarax, antifungal medications like Lamisil, cornstarch for sweat-related irritation, and Selsun Blue for fungal issues. A recurring theme was the complex interplay between autoimmune conditions like fibromyalgia, Celiac disease, and lupus with sun sensitivity, with members encouraging the original poster to advocate for specialist care while sharing practical strategies like staying cool, using sun protection, managing vitamin D deficiency with supplements, and treating symptoms promptly before they worsen.

A MyFibroTeam Member

I heard all this until going to mayo......they suggested cutting back on gluten but not eliminating it...it has made a huge difference.

February 28, 2016
A MyFibroTeam Member

I bruise so much I haven't noticed any rashes. Hope your doctor can help... Gentle hugs xoxo

February 27, 2016
A MyFibroTeam Member

Well, my Skin doctor said that mine was a form of psoriasis. It is exacerbated by the sun and the heat of the summer. I too have issues with absorbing vitamin D3 and I've been on supplements from my Dr. Yall, are in my thoughts and prayers. Here's hoping and praying that we all get the answers we seek and the relief that we need.

February 26, 2016
A MyFibroTeam Member

That kind of rash can indicate an autoimmune illness, among other things. If your doctor is trustworthy, I wouldn't bother getting a second
Opinion. If he isn't you might consider it just to be sure

February 24, 2016
A MyFibroTeam Member

I have heard of this. You wil think me olfasion but . Sometimes heat and mixtures of what you are putti g into your body and sweating out is just not a good mixture. Dust your self lightly with corn starch when you see it starting and stay in acooler area. For anyone who sees red bumps or white little spots try a little selson blur on those area like lotion after a shower. It works.

April 7, 2016

Related Questions

View All
A MyFibroTeam Member asked a question 💭
Eindhoven, NL

A MyFibroTeam Member asked a question 💭
Greenville, NC

A MyFibroTeam Member asked a question 💭
Pietermaritzburg, ZA