It’s also one of the most common as approximately 1 in every 100 Canadians has been diagnosed with it. There is so much that is still unknown about this neurological disease. If anything it’s made me a stronger person. It’s something that has definitely changed my life, with some added bumps in the road, but hasn’t hindered me from living. If you know me, you know I was diagnosed with epilepsy in my 20’s. This is a cause near and dear to my heart, that I feel I could support more. 🖤 282 💬 10 During this Season of Giving I’ll be donating a portion of my commission from every deal I do as of December until the end of March, to Epilepsy Research. #aneurysmawareness #aneurysmsurvivor #shareyourstory #brainaneurysm #brainaneurysmsurvivor #brain #brainhealth #brokenbrain #braininjuryawareness #braininjury Have a story about how your life has been impacted by brain aneurysms? Reach out today! Read her full story now by clicking the link in our bio. Tag all of your friends ‘UNLIMITED ENTRIES ALLOWED’ - each separate comment with a tagged friend counts as an entry⠀īonus ‘REPOST’ to your story for another 3 entries to win or share to your page and tag for 10 entries! Susan wrote a memoir “Where There is Breath, There is Life.” Published by #Adelaide Press, 2018 and is giving away 2 books! In this blog, Susan Davis shares the story of her wife, who suffered a twice ruptured brain aneurysm in 2008. We at The Bee Foundation appreciate the opportunities we have to speak with other people whose lives have been impacted by brain aneurysms. Brain aneurysms are a devastating disease that impact the lives of many.
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