Heat/sun Intolerance And Fibro? | MyFibroTeam

Connect with others who understand.

sign up Log in
Resources
About MyFibroTeam
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.
Heat/sun Intolerance And Fibro?
A MyFibroTeam Member asked a question 💭

For about a year now, whenever I go out into the sun for more than an hour at a time, I feel incredibly sick once I get out of the sun, and it lasts for either a few hours, or a few days after. Sometimes, it feels like my skin is burning, but there’s no actual sunburn there
I’ve tried to research this, but not much has come up. I was wondering if anyone else has gone through this, and if it is a symptom of fibromyalgia
I recently had my blood work done, too, where they checked for lupus and… read more

posted August 7, 2018
View reactions
A MyFibroTeam Member

Are you taking any meds that make you sensitive?

posted August 8, 2018
A MyFibroTeam Member

It's a side effect of your meds. I have four meds that make me sensitive to the sun. I wear a hat and sunglasses. It allows you to be in the sun more often.

posted August 9, 2018
A MyFibroTeam Member

Yes for years now I have not been able to be in the sun. I was told it was because of all the medications I take. Also my skin, face, head seems to be hot for days after sun exposure. The thing I do to prevent a full on episode of migraine, nausea, dizziness, burning eyes, is to cool down my body as quickly as I can even with just a cold face cloth. keep the face cloth on my neck. drink lots of water and maybe just lie down if I feel too nauseous. This year I have developed massive body sweating from slight exertion or from becoming nervous. They say Botox will help with that?

posted August 8, 2018
A MyFibroTeam Member

Hey all im the same. The more im expose to sun, heat or light im screwed over. Im photophobic which means wearing sunglasses everywhere even at night and light intolerant is there assumption. But there is a rarer condition that a specialist can do. Brain fog stopping me remembering the name atm. They test your urine but do not expose it to any light and immediately wrap it in foil. Im in australia and it is considered unusual here but does that not just some up almost every fibro symptom. I always say to my gp when things are divided up into percentages go through the under 5% options and the answer will be there. So much faster.

posted August 8, 2018
A MyFibroTeam Member

I have the burning skin from time to time and it’s called allodynia as Nallewoh said. I used to have it constantly, but now I only get it occasionally. Removing sugar from my diet helped this symptom. I use stevia in place of sugar and follow the paleo diet. I have my medicinal cannabis card and the cannabis creams help with this symptom as well. Just google fibromyalgia and allodynia.

posted August 7, 2018

Related content

View All
Doctor In Los Angeles
A MyFibroTeam Member asked a question 💭
Fibro Flare From Too Much Sun
A MyFibroTeam Member asked a question 💭
I Am Suffering With Fibromyalgia And Under Active Thyroid Taking 300mg Thyroxin Any Suggestions??
A MyFibroTeam Member asked a question 💭
Continue with Facebook
Continue with Google
Lock Icon Your privacy is our priority. By continuing, you accept our Terms of use, and our Health Data and Privacy policies.
Already a Member? Log in