
sclerodermacan
Scleroderma Canada
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HARD WORD. HARDER DISEASE. raising public awareness one tiktok at a time!
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Sanique C from Ontario, Canada lives with a rare, autoimmune disease called Scleroderma. This his her #MySclerodermaStory 🌻 For more information on scleroderma, please visit scleroderma.ca
#Scleroderma #RareDisease #Autoimmune #AutoimmuneDisease #SclerodermaWarrior #SclerodermaAwareness #SclerodermaAwarenessMonth #HardWordHarderDisease
#Scleroderma #RareDisease #Autoimmune #AutoimmuneDisease #SclerodermaWarrior #SclerodermaAwareness #SclerodermaAwarenessMonth #HardWordHarderDisease
Did you know that June is Scleroderma Awareness Month? We Make a Move for Scleroderma to raise awareness and have a chance to get together and connect with the community.
Get started at MakeAMoveCanada.ca!
#MAM4Scleroderma #MakeAMove2023 #Scleroderma #RareDisease #SclerodermaAwareness #Research #Canada #HealthCanada
Get started at MakeAMoveCanada.ca!
#MAM4Scleroderma #MakeAMove2023 #Scleroderma #RareDisease #SclerodermaAwareness #Research #Canada #HealthCanada
Scleroderma is in @hello_canada_mag for “The Skin You’re In” campaign 🎉
This campaign focuses on ones physical and mental health when living with a rare disease, so this was a perfect opportunity for scleroderma to get more awareness out there! If you’re not sure where to start and want to get involved, join us for our Make a Move Events throughout June!
#scleroderma #hardwordharderdisease #raredisease #hellocanada #magazine #article #awareness #sclerodermaawareness #MAM4Scleroderma
This campaign focuses on ones physical and mental health when living with a rare disease, so this was a perfect opportunity for scleroderma to get more awareness out there! If you’re not sure where to start and want to get involved, join us for our Make a Move Events throughout June!
#scleroderma #hardwordharderdisease #raredisease #hellocanada #magazine #article #awareness #sclerodermaawareness #MAM4Scleroderma
Make a Move is coming to #LondonOntario this Saturday, June 3 at Gibbons Park! London’s own Mayor Morgan encourages everyone to come out, spread awareness and make a move for scleroderma!
Visit MakeAMoveCanada.ca for more info and registration, we can’t wait to see you there!
#LondonOn #LondonOntarioCanada #MAM4Scleroderma #MakeAMove2023 #scleroderma #hardwordharderdisease #thingstodoinontario #todoontario #raredisease #sclerodermaawareness #autoimmunedisease
Visit MakeAMoveCanada.ca for more info and registration, we can’t wait to see you there!
#LondonOn #LondonOntarioCanada #MAM4Scleroderma #MakeAMove2023 #scleroderma #hardwordharderdisease #thingstodoinontario #todoontario #raredisease #sclerodermaawareness #autoimmunedisease
It’s time to Make a Move for Scleroderma and we’re inviting you, your friends, loved ones or even your medical team to join us at one of our 13 in-person celebration events!
Can’t join in person? No worries, you can join us virtually throughout May and June and make a move from the comfort of your own home!
There are so many ways to make a move and show your support and we can’t wait to see how you #MAM4Scleroderma
#MakeAMove2023 #Scleroderma #Canada #Ontario #AtlanticCanada #Alberta #RareDisease
Can’t join in person? No worries, you can join us virtually throughout May and June and make a move from the comfort of your own home!
There are so many ways to make a move and show your support and we can’t wait to see how you #MAM4Scleroderma
#MakeAMove2023 #Scleroderma #Canada #Ontario #AtlanticCanada #Alberta #RareDisease
It’s crucial to have a good support system when you’re living with a rare disease like scleroderma.
Silvia’s family makes a move with her everyday to support her AND to help raise scleroderma awareness. How will you make your move?
#MAM4Scleroderma #MakeAMove2023 #Scleroderma #HardWordHarderDisease #SclerodermaAwareness #Canada #CDNHealth #RareDisease #autoimmunedisease
Silvia’s family makes a move with her everyday to support her AND to help raise scleroderma awareness. How will you make your move?
#MAM4Scleroderma #MakeAMove2023 #Scleroderma #HardWordHarderDisease #SclerodermaAwareness #Canada #CDNHealth #RareDisease #autoimmunedisease