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 💭
Liverpool, UK

Does anyone sweat but your skin feels cold when it happends my clothes are wet and it's embarrassing

July 3, 2016
 · 
Reactions

Answer Summary

Members shared their experiences with excessive sweating and cold skin, with many describing soaking wet clothes, hair, and faces that leave... Read more

Members shared their experiences with excessive sweating and cold skin, with many describing soaking wet clothes, hair, and faces that leave them feeling embarrassed in public, especially while shopping or eating out. Several members noted that their sweating worsened after developing fibromyalgia or chronic pain conditions, with some linking it to medications like Cymbalta or morphine, while others identified triggers such as sensory overload from bright lights and strong smells in stores, physical exertion, heat, or certain foods like milk. A recurring theme was the emotional toll of this symptom, including the shame of constantly wiping down in front of others and the frustration of losing the ability to do everyday activities, paired with practical coping strategies like carrying cold washcloths in purses or using stronger deodorants.

A MyFibroTeam Member

OMGOSH yes. Before Fibromyalgia I never sweat, even during the 98 degree days of summer. Niw I can function without sweating, any physical movement what so ever sweat goes to running. Now that it is Summer if the temperature is over 85 this chick doesn't go outside. The heat simply drains what little energy completely. My family just doesn't seem to understand how going out in the heat affects me physically, especially my husband.

July 4, 2016
A MyFibroTeam Member

Yes I sweat a lot of the time and hate it!! It is so embarrassing when your hair is soakend wet and everyone else is frozen. Another embarrassment we have to put up with!

July 4, 2016
A MyFibroTeam Member

I don't think it has to do with medication. But I do think medication that causing sweating can make it worse or more often. All the meds for fibro I have seen that have a side effect of sweating, just simply say sweating.
But if you look at the site below with a very detailed list of possible fibro symptoms, under general at the top is 'extreme sweating' that is the only place I have ever seen the word extreme with it. And mine is extreme and often not associated with heat. I think a lot of times mine is associated with sensory overload because when it is at it's worst I am usually in a store where I have fluorescent lights, perfumes, colognes, lotions and noises all affecting me at once. I also have a tendency to sweat after a shower, but I am very fatigued at that time. I also have very bad night sweats sometimes. My shopping sweats are the worst though. By the time I leave my head is usually soaked and my hair is dripping and my face is red and I feel like everyone is watching me.
Most of the time I carry a cold wet washcloth in a ziplock bag in my purse when I am shopping. I will also have a dry one as well.
https://www.verywell.com/fibromyalgia-symptoms-...

July 3, 2016
A MyFibroTeam Member

I sweat ita horrible I just wish for my old life back

July 4, 2016
A MyFibroTeam Member

Yes! @A MyFibroTeam Member, I have the same thing! If I'm in a store too long I get hot and red and sweaty. I feel like everybody thinks I'm trying to steal stuff, I'm sweating so much. This is why I wear make up, I can't stand being tomato red, sweating my face off. It's so beyond embarrassing. I think sensory overload is a possibility for me, I've never thought of it that way! Thanks for the insight!

July 4, 2016

Related Questions

View All
A MyFibroTeam Member asked a question 💭
Georgiana, AL

A MyFibroTeam Member asked a question 💭
Tauranga, NZ