does anyone notice that clothing socks shoes seams etc leave marks on your skin like they are too tight and fibromyalgia | MyFibroTeam

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Top 10 Search Results for "does anyone notice that clothing socks shoes seams etc leave marks on your skin like they are too tight"

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Does Anyone’s Skin Seem To Mark More Easily?
A MyFibroTeam Member asked a question 💭

Clothing marks, pressure marks from a watch, sleeping etc seem to remain a lot longer than ever before. This whole illness worries me at the moment 🤔

A MyFibroTeam Member

Not sure if this is what you meant but I know when I bruise now it takes forever for the mark to go away. I have had to tell people, " No, my husband is not beating up on me," due to the bruises… read more

Has Any One Had Cupping Done?? Did It Help?
A MyFibroTeam Member asked a question 💭
A MyFibroTeam Member

Yes, I've had it. And acupuncture both relaxes the trigger points.

Change In Clothing With Fibro
A MyFibroTeam Member asked a question 💭

Is it just me, but I used to love to wear my jeans, nowadays I want to be in pull up type of pants. I dont dress up like I used to, even make up is too much to put on.
Anyone else change like that?

A MyFibroTeam Member

Yes I can't stand my jeans just want loose clothing

Anything That Helps With Clohtes Being Painful?
A MyFibroTeam Member asked a question 💭

Clothes hurt. SO bad. My biggest problem is my underarms and seams on shirts. I can only wear tank tops, hoodies, cardigans if they are loose enough. Anything else and im in tears within 20 minutes. Had anyone found anything that helps with that? Things like occupational therapy brushes?

A MyFibroTeam Member

I often have to change clothes because they become too painful. What feels ok one day will cause immense pain the next. It is always an experiment to see what will be tolerated on any day… read more

Peripheral Neuropathy
A MyFibroTeam Member asked a question 💭

Does anyone have peripheral neuropathy in their lower legs & feet without diabetes? I'd love to know your symptoms and experience as I think I've developed it too 😕

A MyFibroTeam Member

@A MyFibroTeam Member "Alpha Lipoic Acid 600mg" My friend's naturopath has her taking 600 mg three times a day. I hate that you and I and others are dealing with this and hope for some answers and… read more

What Type Of Shoes Do You Wear. ?
A MyFibroTeam Member asked a question 💭

I used to almost always wear high heel shoes. Shoot, i used to be able to jog in them if needed. As fibro grew on my i wore heels less and less. Now im down to slippers. I am wondering what type of shoes do you wear? Am i the only one weird and will heals ever be on my shoe list again ?

A MyFibroTeam Member

I find that my Hey Dudes are the most comfortable to wear. Heydude.com

Specific Area Flare Ups
A MyFibroTeam Member asked a question 💭

I have recently had a very painful flare up centered in my foot. It often happens that my flare ups are centered in specific areas. Is this common for others as well?

A MyFibroTeam Member

Fibro used to do that to me but because of arthritis and whatever they said was pseudo gout? Plus stupidity getting a knee replacement by an incompetent, . Fibro now
Hangs mostly in the knees and also… read more

FEET AND SHOE ISSUES
A MyFibroTeam Member asked a question 💭

im having issues with my feet, in flat shoes they swell and my calves cramp. when im in high heel or wedge shoes my feet and calves are fine, however i cant walk around in high heels especially on the farm. lol anybody got the same issues? i do have a high instep.

A MyFibroTeam Member

Hi, I have never been comfortable wearing shoes with heels. The only shoes I can wear are running shoes & I have orthotics in them.

Small Tender Lumps?
A MyFibroTeam Member asked a question 💭

Small tender lumps pea size on upper right leg and left side of abdomen. I've had an abdominal CT Scan that came back clear. I can feel two on the left side of my stomach and two on my upper right inner leg. My PCP says I'm just a "lumpy person" and they are cysts. Ive had two doctors look and they dont seem concerned as they don't change in size. They never go away though?

A MyFibroTeam Member

I have them on my hips and it tangles and itches at night. The only thing that eases it is Lidocaine patches

Does Anyone Else Here Have Hyperhydrosis? (a Sweating Condition)
A MyFibroTeam Member asked a question 💭

I have had Hyperhydrosis since I was a teenager, my hands and feet will just randomly sweat bad! It is so embarrassing at times. It isn't every day, but believe it or not, it happens more when I am cold (in winter) and in the Summer it rarely happens at all! I just found out a few years ago from my doctor that it's a real condition with a name. He said there is a surgery for it where they go in through your lungs to do something, I forget exactly what. But, if surgery works then the sweating… read more

A MyFibroTeam Member

Yep I do