#sclerodermaresearch نتائج البحث
“Scleroderma research is important to me because our lives would be drastically different without the progress made so far," says Tiffani P. (dx at age 18.) Read her full story: bit.ly/46Gn0v8 #sclerodermaresearch #scleroderma #SRFcure
Understanding a disease as complex as scleroderma requires collaboration. 🌐 Learn more about how the CONQUER Registry is transforming research and how you can get involved: bit.ly/3lLriy5 #SRFcure #sclerodermaresearch #scleroderma #CONQUER
Sisters Evie & Josie from the South Chapter recently sold lemonade and cookies at their "2 Ladies Lemonade Stand!" They raised $1,000 for #sclerodermaresearch in honor of their grandmother who had #scleroderma via National Scleroderma Foundation @scleroderma
Amazon has announced that they are discontinuing AmazonSmile on February 20, 2023. To everyone who prioritized the SRF while you shopped, thank you. You've helped us accelerate the pace of research—bringing us closer to finding a cure. #sayscleroderma #sclerodermaresearch
As we start the new year, join us in welcoming the newest member of the team! Meet Kate Ceredona, our Director of Philanthropy. Any questions, or want to say hi? Reach out to her at [email protected] or leave a note in the comments! #sclerodermaresearch
Consider donating to #SclerodermaResearch to find a cure. I was diagnosed with it in 2011. #RareDiseaseDay2024 #AutoimmuneAwareness
The first SRF eNews of 2023 is now online! Learn more about upcoming awareness campaigns in February, why one of our funded investigators thinks we're entering an exciting new era in #sclerodermaresearch, and more. Read now at conta.cc/3Y2TABF
🎥 Watch Kimberly (dx 2008) share why she believes that funding research is key to finding a cure. Join her in supporting the SRF Research Challenge by donating today. Donate today and bring us closer to a cure: bit.ly/40s2zzQ #SRFcure #scleroderma #sclerodermaresearch
🌟 Kicking off Day 2 of the 8th World Congress on Systemic Sclerosis with insightful sessions covering ILD, Heart issues, and Vascular concerns in SSc.. #Prague2024 #SclerodermaResearch #SScWorldCongress #WorldSclerodermaFoundation #MedicalCongress
🎬Exciting Expert Insights Series Alert!🎤In our episode meet Prof. @delgaldoFrances, @EUSTAR_org President that will provide us with a unique perspectives on the EUSTAR initiatives for young investigator. #Prague2024 #SclerodermaResearch youtu.be/FimPLgzSrMI?si…
If you're living with scleroderma, consider joining this study. The study focuses on an investigational product for diffuse cutaneous systemic sclerosis (dcSSc), a type of scleroderma. Read the full article here: sclerodermaaustralia.com.au/a-clinical-stu… . . #Scleroderma #SclerodermaResearch
It's New Years Eve, and we're excited to share a 1-day ONLY matching gift opportunity to close out the year. Inspired by your outpouring of support, a generous SRF Board member will match all gifts made today, up to $10,000: bit.ly/3Ngh1o1 #sclerodermaresearch
“I saw many specialists over the years and often felt dismissed,” Melissa, dx 2021, shares. “There were times I believed others thought I was over-exaggerating my symptoms and the way I felt." Read her full story: bit.ly/4jCXHzP #research #sclerodermaresearch
Our team was very well represented by @BeatrizHFe, who showcased her work at the 8th Systemic Sclerosis World Congress #SclerodermaResearch #SScWorldCongress
🎉 Today marks an exciting day for the medical community focused on scleroderma! We're witnessing the kickoff of the 8th World Congress on Systemic Sclerosis in Prague 🇨🇿. #Prague2024 #SclerodermaResearch #SScWorldCongress #WorldSclerodermaFoundation #MedicalCongress
🛰️Delving into the complexities of SSc, we're excited to present the first @GSK Satellite Symposium at the 8th World Congress on SSc🧬'New Paths, New Crossroads: Seeing into Systemic Sclerosis' explores the latest in SSc-ILD, addressing challenges #Prague2024 #SclerodermaResearch
🎓The 8th World Congress on SSc opens with a series of enlightening lectures. A pivotal question is addressed: Is it time to implement patient care through patient education? @carlochizzolini @maureenMayes @suefarrington D. Furst @yannickallanore #Prague2024 #SclerodermaResearch
We're proud to announce the Carolle & Lita PhD Scholarship for research into non-pharmacological scleroderma care. Congrats to Christabell Elbitar, our first recipient! Learn more here: sclerodermaaustralia.com.au/phd-scholarshi… #SclerodermaResearch #PhDScholarship
🌅 Good morning from the final day of the WSC! Today’s 'Breakfast Meet the Expert' session features prominent specialists discussing the latest in SSc treatment, vascular involvement, the significanc #Prague2024 #SclerodermaResearch #SScWorldCongress
Join us in rocking your wildest '80s attire for this year's Slow Walk for Scleroderma! We're raising funds for scleroderma research. 🔗Learn more: scleroderma-queensland.grassrootz.com/slow-walk-for-… . . . #Scleroderma #SclerodermaAwareness #SclerodermaResearch #DonateToday #Queensland
Understanding a disease as complex as scleroderma requires collaboration. 🌐 Learn more about how the CONQUER Registry is transforming research and how you can get involved: bit.ly/3lLriy5 #SRFcure #sclerodermaresearch #scleroderma #CONQUER
“Scleroderma research is important to me because our lives would be drastically different without the progress made so far," says Tiffani P. (dx at age 18.) Read her full story: bit.ly/46Gn0v8 #sclerodermaresearch #scleroderma #SRFcure
🎥 Watch Kimberly (dx 2008) share why she believes that funding research is key to finding a cure. Join her in supporting the SRF Research Challenge by donating today. Donate today and bring us closer to a cure: bit.ly/40s2zzQ #SRFcure #scleroderma #sclerodermaresearch
“Scleroderma research is important to me because our lives would be drastically different without the progress made so far," says Tiffani P. (dx at age 18.) Read her full story: bit.ly/46Gn0v8 #sclerodermaresearch #scleroderma #SRFcure
Understanding a disease as complex as scleroderma requires collaboration. 🌐 Learn more about how the CONQUER Registry is transforming research and how you can get involved: bit.ly/3lLriy5 #SRFcure #sclerodermaresearch #scleroderma #CONQUER
Consider donating to #SclerodermaResearch to find a cure. I was diagnosed with it in 2011. #RareDiseaseDay2024 #AutoimmuneAwareness
Sisters Evie & Josie from the South Chapter recently sold lemonade and cookies at their "2 Ladies Lemonade Stand!" They raised $1,000 for #sclerodermaresearch in honor of their grandmother who had #scleroderma via National Scleroderma Foundation @scleroderma
Amazon has announced that they are discontinuing AmazonSmile on February 20, 2023. To everyone who prioritized the SRF while you shopped, thank you. You've helped us accelerate the pace of research—bringing us closer to finding a cure. #sayscleroderma #sclerodermaresearch
As we start the new year, join us in welcoming the newest member of the team! Meet Kate Ceredona, our Director of Philanthropy. Any questions, or want to say hi? Reach out to her at [email protected] or leave a note in the comments! #sclerodermaresearch
“I saw many specialists over the years and often felt dismissed,” Melissa, dx 2021, shares. “There were times I believed others thought I was over-exaggerating my symptoms and the way I felt." Read her full story: bit.ly/4jCXHzP #research #sclerodermaresearch
If you're living with scleroderma, consider joining this study. The study focuses on an investigational product for diffuse cutaneous systemic sclerosis (dcSSc), a type of scleroderma. Read the full article here: sclerodermaaustralia.com.au/a-clinical-stu… . . #Scleroderma #SclerodermaResearch
🌟 Kicking off Day 2 of the 8th World Congress on Systemic Sclerosis with insightful sessions covering ILD, Heart issues, and Vascular concerns in SSc.. #Prague2024 #SclerodermaResearch #SScWorldCongress #WorldSclerodermaFoundation #MedicalCongress
The first SRF eNews of 2023 is now online! Learn more about upcoming awareness campaigns in February, why one of our funded investigators thinks we're entering an exciting new era in #sclerodermaresearch, and more. Read now at conta.cc/3Y2TABF
Thanks to ongoing research and clinical trials, there's hope for better understanding and more effective treatments for people living with scleroderma!🌻 Check out our blog to read the full article: sclerodermavictoria.com.au/understanding-… . . . . #Scleroderma #SclerodermaResearch #HopeForACure
Our team was very well represented by @BeatrizHFe, who showcased her work at the 8th Systemic Sclerosis World Congress #SclerodermaResearch #SScWorldCongress
It's New Years Eve, and we're excited to share a 1-day ONLY matching gift opportunity to close out the year. Inspired by your outpouring of support, a generous SRF Board member will match all gifts made today, up to $10,000: bit.ly/3Ngh1o1 #sclerodermaresearch
Join us in rocking your wildest '80s attire for this year's Slow Walk for Scleroderma! We're raising funds for scleroderma research. 🔗Learn more: scleroderma-queensland.grassrootz.com/slow-walk-for-… . . . #Scleroderma #SclerodermaAwareness #SclerodermaResearch #DonateToday #Queensland
Scleroderma research starts with you. Learn more to find out if enrolling in the CONQUER registry is right for you! Learn more about how you can get involved with CONQUER: bit.ly/3lLriy5 #SclerodermaResearch #CONQUERRegistry #SRFcure #CONQUER
Check this out! Doctors Wendy Stevens and Laura Ross at St Vincent's Hospital Melbourne have been working on a special project to create a tool for measuring scleroderma! Check out our website to learn more: sclerodermaaustralia.com.au/asig-developme… . . . #Scleroderma #SclerodermaResearch #ASIG
🎉 Today marks an exciting day for the medical community focused on scleroderma! We're witnessing the kickoff of the 8th World Congress on Systemic Sclerosis in Prague 🇨🇿. #Prague2024 #SclerodermaResearch #SScWorldCongress #WorldSclerodermaFoundation #MedicalCongress
If you're living with scleroderma, you might want to consider joining this study. Read more details here: sclerodermaaustralia.com.au/a-clinical-stu… . . . . #Scleroderma #SclerodermaResearch #HopeForACure #ClinicalStudy #Awareness #Resources
DID YOU KNOW that scleroderma affects both sexes, but it is three to four times more common in women! Learn more about scleroderma here: ➡️sclerodermaaustralia.com.au/research/ . . . . #Scleroderma #SclerodermaAwareness #SclerodermaResearch #SclerodermaWarriors #SclerodermaStrong
We're proud to announce the Carolle & Lita PhD Scholarship for research into non-pharmacological scleroderma care. Congrats to Christabell Elbitar, our first recipient! Learn more here: sclerodermaaustralia.com.au/phd-scholarshi… #SclerodermaResearch #PhDScholarship
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