Anyone out there with Ehler's Danlos syndrome?

[dobermom21]

Would love to connect with others dealing with this disorder, and compare notes on what has helped you - and what hasn't.

I have the hypermobility type, and it's rare to even meet a doctor that's familiar with it.

 

[YoYoFat]

Yup, I have it.

 

[WholesomeApril]

Yes me 💗

 

[WholesomeApril]

Biggest tip is keep strong 💪

 

[deleted.user.16]

I have it ✋

My joints have been extra achy since losing 20 lbs on Reta (they didn't used to lol). Just bought some glucosamine and fish oil yesterday, hope they will do something.

 

[dobermom21]

Would love to connect with others dealing with this disorder, and compare notes on what has helped you - and what hasn't.

I have the hypermobility type, and it's rare to even meet a doctor that's familiar with it.

I just made a new post about this topic in the public square for anyone interested in a peptide/eds community.

Resources and discussion related to peptides and Ehler's Danlos syndrome. https://glp1forum.com/threads/resou...to-peptides-and-ehlers-danlos-syndrome.13764/

And this is a new Discord server for this purpose. https://discord.gg/49X7t9HGq