Just because you can’t see Dys (dis)

Doesn’t mean it doesn’t exist!

Incase you haven’t seen them already. I had to share these breathtaking images posted by Dysautonomia International when they hosted an awareness campaign at Niagara Falls, Ontario Canada. The falls were lit up turquoise in recognition & honor of Dysautonomia awareness month 😍😍😍😍😍😍

سبحان الله

And then to enlighten you further, why awareness is such a big deal!!! Have a look at the image below with a caption that celebrates the differences regarding knowledge of Dysautonomia between the years – 2012 – 2019 🤩

Where our community was…

Where our community is at present 🎉

And where we can be in the future 🔮

Continue striving towards that vision

6|15

📢 Turn the 6 year delayed diagnosis period into 15 minutes

Can the educational changes between that period, be made any clearer?!

A statement by 17 year old @chronicallyshelby

(POTS is a comorbid condition of Dysautonomia & will be explained at greater length in the upcoming chapters. God-willing)

These 2 introductory chapters have been updated. They contain some important Dysautonomia facts. Kindly read through if possible

https://kayborninmay.wordpress.com/2017/11/16/you-do-not-see/

https://kayborninmay.wordpress.com/2017/11/19/watch-dys-movie-episode/

Some of our supporters put up these graphics 👇

It’s one simple gesture that truly means the world to us. In a country and province where we’re fighting endlessly for literally every part of our lives… Its heartwarming, life saving, & life changing for Dys battle to be seen & recognized 💙💙💙

Support keeps our fighting spirit alive 💟