Anyone out there with Ehler's Danlos syndrome?

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dobermom21

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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 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 said:
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. [archived internal link]

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