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Website: www.raiseforrare.ca

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National Organization for Rare Disorders Student Association 21.02.2021

Check out this teaser clip from NORDSA's Co-Presidents @magnus.stenlund and Jessica Wijesundera interviewing Marta Rode for RDD 2021! Full interview will be released on February 28.

National Organization for Rare Disorders Student Association 07.02.2021

Here you have the criteria for how the winners will be decided for these amazing prizes! If you haven't registered, what are you waiting for? Click on https://www.raiseforrare.ca/ to register #rarediseaseday #raredisease #raiseforrare #mitocanada #invisibleillness #chronicpain #rarediseases #rarediseaseawareness #disabilityawareness #hope #awareness #careforrare #rareisreal #mito #mitochondrialdiseases #chronicillnesswarrior #rare #invisibleillnessawareness #butyoudontlooksick #mitochondrial #savealife #geneticdisease #zebra #health #healthy

National Organization for Rare Disorders Student Association 24.01.2021

Gentle reminder to register for Raise For Rare now! Link in bio. DM us if you have any questions about the event. #rarediseaseday #raredisease #raiseforrare #mitocanada #invisibleillness #chronicpain #rarediseases #rarediseaseawareness #disabilityawareness #hope #awareness #careforrare #rareisreal #mito #mitochondrialdiseases #chronicillnesswarrior #rare #invisibleillnessawareness #butyoudontlooksick #mitochondrial #savealife #geneticdisease #zebra #health #healthy

National Organization for Rare Disorders Student Association 09.01.2021

Get fit while donating for a cause and also getting a chance to win for yourself. It doesn't get better than this! Hope you have registered for Raise For Rare. If not, it's not late! Go ahead and register on our website. You don't want to miss this amazing opportunity! #rarediseaseday #raredisease #raiseforrare #mitocanada #invisibleillness #chronicpain #rarediseases #rarediseaseawareness #disabilityawareness #hope #awareness #careforrare #rareisreal #mito #mitochondrialdiseases #chronicillnesswarrior #rare #invisibleillnessawareness #butyoudontlooksick #mitochondrial #savealife #geneticdisease #zebra #health #healthy

National Organization for Rare Disorders Student Association 21.12.2020

We are so thankful to all our sponsors for contributing in our efforts to help MitoCanada and the rare diseases community. Hurry, register for Raise For Rare if you haven't already! #rarediseaseday #raredisease #raiseforrare #mitocanada #invisibleillness #chronicpain #rarediseases #rarediseaseawareness #disabilityawareness #hope #awareness #careforrare #rareisreal #mito #mitochondrialdiseases #chronicillnesswarrior #rare #invisibleillnessawareness #butyoudontlooksick #mitochondrial #savealife #geneticdisease #zebra #health #healthy

National Organization for Rare Disorders Student Association 15.12.2020

Introducing our ambassador for our event, Raise For Rare: Cory Wallace Here's a bit about him: "Growing up in Jasper I launched my career as a professional mountain biker with Kona Bikes in 2011. Since that time I have chased races and adventures all over the World. The highlights have been Winning 3 straight World 24 HR Titles (Italy, Scotland, Brazil) and being a 2 x Canadian Marathon Champion. I hope to inspire more to get out there in the World to chase their dreams wit...hout holding back." Huge thanks to Cory for supporting us in this cause! Kudos to your achievements! Don't forget to register through our website! Link in bio. #rarediseaseday #raredisease #raiseforrare #mitocanada #invisibleillness #chronicpain #rarediseases #rarediseaseawareness #disabilityawareness #hope #awareness #careforrare #rareisreal #mito #mitochondrialdiseases #chronicillnesswarrior #rare #invisibleillnessawareness #butyoudontlooksick #mitochondrial #savealife #geneticdisease #zebra #health #healthy