SclerodermaAwareness
@__Scleroderma__
Scleroderma is a Rare Autoimmune Disease. There is no cure.
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Looking for gift ideas for #scleroderma warriors this season? The Autoimmune Slayer (and Scleroderma Society of Ontario board member) has cushions, shirts, hoodies and more! Shop her website at theautoimmuneslayer.com/collections/me…
Kierra (dx 2020) looks to research as her best hope for a better future. “#Scleroderma research is so very important to me because literally my life depends on it,” Kierra says. Will you help Kierra & all with scleroderma by supporting research? Give now: bit.ly/3Pao2X9
Join Silvia at this year's National Scleroderma Conference on September 16 & 17 in Niagara Falls, Ontario! Watch this video to find out why she enjoys attending this incredible event. 💙 Learn more and register at sclerodermaconference.ca
To know #scleroderma is to make people with scleroderma feel seen and understood. During #SclerodermaAwarenessMonth, @IAMQUEENLATIFAH shares her experience as a scleroderma caregiver and offers advice for others facing the disease. bit.ly/3QhYGXL
Help us raise funds to reach our fundraising goal. All money raised directly supports ongoing advocacy, education and research. Want to make a difference? Donate at bit.ly/3x7EPBw.
June 29th is World Scleroderma Day, this is a day to recognize the courage of everyone affected by scleroderma. Let’s use this day as an opportunity to join together and support each other. For more information about Scleroderma: scleroderma.ca
Interstitial lung disease is associated with scleroderma, and is a frequent source of symptoms in patients. On this day in 1940, Swiss painter Paul Klee died. He had scleroderma and his artwork was widely influenced by his experience with the condition. #WorldSclerodermaDay
June 29 is a day to recognize those who live with #scleroderma. Cheers to all the warriors, you are so strong and nothing can stop you. But for us, every day is #SclerodermaAwarenessDay, We will keep continuing spreading the #Awareness across all groups #sclerodemaindia
For #WorldSclerodermaDay, we’re celebrating the voices of those living with #Scleroderma and looking to raise awareness of this rare disease. We cannot wait to #BloomWithScleroderma with @FScleroderma and with the #Scleroderma community! 🌻
✨ This #WorldSclerodermaDay is also about recognising the difference. When it comes to #scleroderma, no two patients are alike and no two experiences are the same. Only a holistic approach to care can give patients the support they need. Join us as we demand change! #FESCA
Join us on June 29th for a Facebook Live broadcast (facebook.com/SSCanada/) approximately 15 minutes before 10pm EST for the illumination of #NiagaraFalls in blue for #WorldSclerodermaDay.
June is Scleroderma Awareness Month. Here, in a song written for her father who suffers from this disease, is @Ileenlauramusic newest video. Check out Fight Left In Me (Official Music Video) youtu.be/1Dawpn89YEE via @YouTube
youtube.com
YouTube
Fight Left In Me (Official Music Video)
It's #WorldSclerodermaDay! 🌎 Today, we celebrate scleroderma warriors who fight #scleroderma every day. You can celebrate by making a donation at hardword.ca/donate, sharing this post, and educating yourself on what #scleroderma is. Together, we can find a cure! 💙
Today is world scleroderma Day Scleroderma was first diagnosed year 1754 in Indonesia Systematic sclerosis otherwise known as scleroderma It's a chronic and Rare disease which flip dreams and change lives. Living with this disease has changed me a lot
#WorldSclerodermaDay If you need to find a local event in your area, check out the website below. sclerodermavictoria.com.au/events/ #Scleroderma #SclerodermaVictoria
Tonight the #CNTower will be lit blue for #WorldSclerodermaDay / Ce soir la #TourCN sera illuminée en bleu pour la Journée mondiale de la sclérodermie @scleroderma_sso
#BobSaget worked tirelessly to raise awareness and funding for us. @JohnMayer, thank you for designing a hoodie with the SRF to keep Bob's memory and his enduring fight for a #scleroderma cure alive. Proceeds benefit our work to fund research for a cure represent.com/srf
Like many chronic & incurable diseases, #scleroderma can cause psychological stress and #depression. Patients often feel alone and there's no doubt the pandemic has made it more difficult. Family, friends, and support groups are vital - we are here for each other. #BellLetsTalk
Registration is officially OPEN for @SclerodermaCAN's Trivia Night! Visit: sclerodermaontario.akaraisin.com/ui/Scleroderma… to register today!
We invite you to join us for an informational discussion June 21, 1pm Mountain/3pm EST/4pm Atlantic. Special guests @TheGeneratorCa will share tips to reach more people on social during #SclerodermaAwarenessMonth. Register and submit Questions in advance 👉 [email protected]
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