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 😍😍😍😍😍😍
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
📢 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
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 💟