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Indeed.(especial para @liliantrigo)

Help us spread awareness so less people have to suffer from something without knowing what it is!

Don't be reckless.

Ah! You look so good! Yep, these kind words can leave you feeling bummed out for some reason. Somehow, they invalidate the pain and we feel like they dont believe its really all that bad.This little button is a way to create awareness for ALL the people who are out there who live with an invisible illness or invisible pain (like a back condition.) Thank you for being a part of creating more understanding about invisible illness.

"Do you or a loved ones suffer from: … You may have dysautonomia-P.O.T.S. (Postural Orthostatic Tachycardia Syndrome)" | Dysautonomia-POTS – Awareness & Support – Say No2Pots

Dysautonomia is not RARE, it is rarely known. More people have Dysautonomia than MS, Lupus, most cancers (except breast and prostate), and many other diseases that are well known. Promote Dysautonomia Awareness!

Dysautonomia Spread the word....

I don't mean to dismiss your desire to be helpful, it's just that I've heard every "helpful" suggestion from the 1001 people who said it already. EDS Ehlers-Danlos awareness is something I never get tired of hearing about!