I am 28 Year old male and I have EDS ... - Ehlers-Danlos Sup...

Ehlers-Danlos Support UK

2,983 members940 posts

I am 28 Year old male and I have EDS (Ehlers-Danlos syndrome) Everyone tells me that I have a soft body like a female. Is it related to EDS?

Alcatraz profile image
4 Replies

Hi Everyone. Last year I found out that I have EDS. I had hypermobility since I was a kid but from Last 3-4 years I started noticing that my body especially my upper arms, chest and belly started getting softer by day. I know that soft, doughy, smooth and velvety skin is a symptom of EDS but my body softness resembles to a Female. Many people tell me that my body is soft like a woman and being a man, it kills me inside (no offense to all the ladies but I have been through a depression because of this). When I press my hand or chest, it feels like I am pressing some cotton.

Does this have to do anything with EDS? I read a lot about EDS but no where I found this as a symptom of EDS. Please help me. Please help me.

Written by
Alcatraz profile image
Alcatraz
To view profiles and participate in discussions please or .
Read more about...
4 Replies
Pessox profile image
Pessox

Go see a doctor man and try your best to put no mind to it, for it would be wasteful.

I have soft velvety skin, but not the way you describe it, have someone else test your skin perhaps and ask what they think?

Bek85 profile image
Bek85

Yes it’s one of the common features of EDs , most of us have unusually soft skin.

jeffsimon profile image
jeffsimon

I'm a male and have EDS and yes I have soft, doughy, smooth and velvety skin. I'm now 76 yrs old and have lived with it all my life. It's been inconvenient in terms of regular visits to the hospital over the years getting stiched-up for cuts which would be be fairly tolerated for people with normal skin. However generally I have had a normal life and no complaints from the ladies!

ribby profile image
ribby

Yes. People with EDS have soft velvety skin. I’ve been told mine is as well. Be proud of it. It’s one of the upsides of EDS.

Not what you're looking for?

You may also like...

Does this sound like MCAS

Hi there. I have a diagnosis of HSD but my specialist EDS physio and GP both now think it is...

vADS presentation vs hEDS, especially on darker skin tones

I am under investigation with NHS at the moment, at my request, given I think a lot of what I have...

Vitamin Deficiency/ Pernicious Anaemia : How Common Are They With EDS and What's The Best Treatment for Us ? Please Tell Me Your Experience

I have suffered with Vitamin D Deficiency and Anaemia many times in the last ten years. Gastric...

supportive sofa / chair

i have eds 3 and have been through so many chairs and sofas. none are supportive enough and give me...

Vaccine & EDS

Has anyone who's had the covid vaccine notice their EDS symptoms suddenly get worse after the...