#sclerodermaawarenessmonth resultados de búsqueda
June is #SclerodermaAwarenessMonth treatment options used, such as chemotherapy. We NEED a cure and understanding of the cause to systemic sclerosis (scleroderma), NOW 🙏 #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds @RoyalFreeNHS
It's #SclerodermaAwarenessMonth, and everyone should know what this disease is and does. Dr. Lori Chung of Stanford University (and an SRF-Funded investigator) goes into detail about how common scleroderma complications. This is originally from an episode of #BehindTheMystery.
June #SclerodermaAwarenessMonth This infographic shows the different types and their similar symptoms. #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue
Thank you all for an INCREDIBLE #SclerodermaAwarenessMonth. Join us in giving a big shout out to another amazing effort—our collaborators at Scleroderma Outreach Northwest successfully made June the official #SclerodermaAwarenessMonth of Idaho! #SayScleroderma
As we wrap up June, let's raise awareness on World Scleroderma Day! Today, we stand in solidarity with those affected by scleroderma, spreading knowledge, support, and hope. #SclerodermaAwarenessMonth
Proud to celebrate #sclerodermaawarenessmonth by acknowledging the efforts of many #sclerodermawarriors for continuously educating the public, raising awareness, and supporting individuals affected by #autoimmunedisease.
For this last day of #SclerodermaAwarenessMonth, we talked to Ken, who created “Angel Applicant"—a documentary on his experiences with scleroderma. Read our full interview with Ken online at bit.ly/kens-story-srf #SayScleroderma
This month is all about Scleroderma Awareness Month, so let's raise awareness of the signs and symptoms. Please help us spread the word by sharing our animation video and keep the conversations going beyond #SclerodermaAwarenessMonth.
I was diagnosed with this disease in 2011 within about 2-3 months after returning from a deployment. I'm almost 12 years in ith it now. A crazy condition, but grateful to still be alive. It's been a journey. #SayScleroderma #SclerodermaAwarenessMonth
🌟 Happy World Scleroderma Day! Today and every day, Dermatology Times is raising awareness and advocating for early and advanced diagnosis and treatment options for patients with this rare autoimmune disease. #WorldSclerodermaDay2025 #SclerodermaAwarenessMonth #DermTwitter
#SclerodermaAwarenessMonth: Learn about this complex autoimmune disease – diagnosis, treatment, & research. linkedin.com/pulse/june-scl… #scleroderma #autoimmunedisease
June is #SclerodermaAwarenessMonth This Friday, June 7th we have @FeghaliLab of @ResearchMUSC joining us to discuss the impact of scleroderma beyond the skin. We’ve ALSO invited patient advocate Dr Kemper from @ClemsonUniv to join in! Register here:⬇️ zoom.us/WEBINAR/REGIST…
#SclerodermaAwarenessMonth is here. Join us and #SayScleroderma, so that everyone knows what this diseases is and does. Lack of awareness causes delays in treatments and diagnosis. But together, we can change this. Visit our website to learn more: srfcure.org/sayscleroderma
June is Scleroderma Awareness Month! Help us Raise the Flag for Scleroderma Awareness at 2 locations in Atlantic Canada. 💙 City Hall, St. John's NL at 11am 💙 Province House, Halifax, NS at 2pm #sclerodermaawarenessmonth
Stolen from a #scleroderma group I’m in. It’s #sclerodermaawarenessmonth and it is definitely one worth knowing. It’s a predominantly silent fight we have but we never give up
Scleroderma is a rare & often misunderstood autoimmune disease affecting the connective tissues in the body. It causes thickening & hardening of the skin & internal organs, as well as joint pain & fatigue. We'e helping raise awareness for this disease. #SclerodermaAwarenessMonth
There's still time to sign up for our #SclerodermaAwarenessMonth event "Collaborating for a Cure," the SRF Patient Forum on June 6th at 9:00 am PDT/12:00 pm EDT! Register now at bit.ly/collab4cure23R… #SayScleroderma
July is #SclerodermaAwarenessMonth! Take a moment to read this blog post by Patient Advocate/Public Speaker, Amy Gietzen: morethanlupus.com/post/my-journe… #scleroderma #autoimmune #chronicillness #awareness
#SclerodermaAwarenessMonth #Research offers #HOPE @NIHRresearch @NIHRtakepart rdn.nihr.ac.uk/news/rare-dise… #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #ConnectiveTissue #BePartOfResearch
Happy #WorldSclerodermaDay 🥳 #SclerodermaAwarenessMonth Research offers #HOPE rdn.nihr.ac.uk/news/rare-dise… #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #BePartOfResearch
PAH is a serious, potentially fatal condition, often silent at first. That’s why annual screening is vital. PHA Europe supports early detection, timely care, and better lives for those affected.💪 #PHAEurope #WorldSclerodermaDay #SclerodermaAwarenessMonth #PAH #raredisease
June is National Scleroderma Awareness Month. More than 300,000 Americans live with some type of scleroderma. The face of scleroderma includes people of all ages, genders, and backgrounds. Learn more via @TheIowaClinic iowaclinic.com/specialties/rh… #SclerodermaAwarenessMonth
🌟 Happy World Scleroderma Day! Today and every day, Dermatology Times is raising awareness and advocating for early and advanced diagnosis and treatment options for patients with this rare autoimmune disease. #WorldSclerodermaDay2025 #SclerodermaAwarenessMonth #DermTwitter
Happy #WorldSclerodermaDay 🌻 #SclerodermaAwarenessMonth 'Living with a rare disease without a cure, is most character building that's for sure'. #Research offers #HOPE #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #BePartOfResearch #NoCure
June is #SclerodermaAwarenessMonth 💙 This autoimmune disease affects skin & organs. Let’s spread awareness & promote early diagnosis! 🩺 #Scleroderma #AutoimmuneDisease #MPLCares #HealthAwareness #JuneAwareness #mpllabs 💙
Is your skin trying to tell you something? Unusual changes in your hands or joints, or discomfort while eating, might be more than just routine signs of aging. #SclerodermaAwarenessmonth #Sclerodermaawareness #Raredisease #chronicillness #KnowTheSigns #CNCHospitals
June #SclerodermaAwarenessMonth MEDICAL RESEARCH. Research offers HOPE. Hope that improved treatments, better understanding and ultimately a cure. #SclerodermaFreeWorld #RaynaudsFreeWorld #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #BePartOfResearch
June is National Scleroderma Awareness Month. More than 300,000 Americans live with some type of scleroderma. The face of scleroderma includes people of all ages, genders, and backgrounds. Learn more via @ClevelandClinic my.clevelandclinic.org/health/disease… #SclerodermaAwarenessMonth
June #SclerodermaAwarenessMonth PERSONAL EXPERIENCE SURVIVAL GUIDE #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue
Awareness opens the door to understanding — and understanding drives progress. 💚 #SclerodermaAwarenessMonth #RareDiseaseAwareness #HealthcareLeadership #CompassionateCare #BobbieStoneInternational
June #SclerodermaAwarenessMonth sclerodactyly hands and the subsequent #disability. Stiff, fragile fingers covered by tight skin blog.raynaudsscleroderma.co.uk/2018/05/sclero… #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure
June #SclerodermaAwarenessMonth ORAL / DENTAL Infographic blog.raynaudsscleroderma.co.uk/2018/11/the-sc… #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue
#SclerodermaAwarenessMonth TELANGIECTASIA Infographic Symptoms, Treatment Options. blog.raynaudsscleroderma.co.uk/2018/05/telang… #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue
June is #SclerodermaAwarenessMonth 🧬 This study shows that children with autoimmune rheumatic diseases including #scleroderma had comparable cellular responses to the COVID-19 vaccine as healthy peers, despite reduced antibody levels. 📖 bit.ly/3XSCZ61 #Immunology
June #SclerodermaAwarenessMonth FATIGUE / EXHAUSTION Infographic blog.raynaudsscleroderma.co.uk/2017/05/fatigu… #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue #TiredAllTheTime
#SclerodermaAwarenessMonth 🌻MOBILITY Infographic #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue #arthritis
June is #SclerodermaAwarenessMonth! ❄️ Cold weather worsens symptoms like Raynaud’s & joint pain. Join our #SnuggleUp campaign - host a cosy event or donate to help fund scleroderma nurses. Let’s warm hearts & lives this winter! sclerodermavictoria.com.au/snuggle-up-for… #SupportTheCause
June is #SclerodermaAwarenessMonth treatment options used, such as chemotherapy. We NEED a cure and understanding of the cause to systemic sclerosis (scleroderma), NOW 🙏 #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds @RoyalFreeNHS
Proud to celebrate #sclerodermaawarenessmonth by acknowledging the efforts of many #sclerodermawarriors for continuously educating the public, raising awareness, and supporting individuals affected by #autoimmunedisease.
#SclerodermaAwarenessMonth: Learn about this complex autoimmune disease – diagnosis, treatment, & research. linkedin.com/pulse/june-scl… #scleroderma #autoimmunedisease
June is #SclerodermaAwarenessMonth This Friday, June 7th we have @FeghaliLab of @ResearchMUSC joining us to discuss the impact of scleroderma beyond the skin. We’ve ALSO invited patient advocate Dr Kemper from @ClemsonUniv to join in! Register here:⬇️ zoom.us/WEBINAR/REGIST…
Thank you all for an INCREDIBLE #SclerodermaAwarenessMonth. Join us in giving a big shout out to another amazing effort—our collaborators at Scleroderma Outreach Northwest successfully made June the official #SclerodermaAwarenessMonth of Idaho! #SayScleroderma
#sclerodermaawarenessweek #SclerodermaAwarenessMonth #sclerodermawarrior #sclerodermaawareness #scleroderma #sclerodermafacts #SclerodermaSymptoms Visit & Join facebook.com/groups/ahodgep…
As we wrap up June, let's raise awareness on World Scleroderma Day! Today, we stand in solidarity with those affected by scleroderma, spreading knowledge, support, and hope. #SclerodermaAwarenessMonth
#SclerodermaAwarenessMonth is here. Join us and #SayScleroderma, so that everyone knows what this diseases is and does. Lack of awareness causes delays in treatments and diagnosis. But together, we can change this. Visit our website to learn more: srfcure.org/sayscleroderma
What is scleroderma? Learn about #scleroderma and the groundbreaking work happening at @UHN's Schroeder Arthritis Institute for #SclerodermaAwarenessMonth! ➜ bit.ly/3NT7OCK @SchroederInst @SindhuJohnson5 @UofT
🌟 Happy World Scleroderma Day! Today and every day, Dermatology Times is raising awareness and advocating for early and advanced diagnosis and treatment options for patients with this rare autoimmune disease. #WorldSclerodermaDay2025 #SclerodermaAwarenessMonth #DermTwitter
June is #SclerodermaAwarenessMonth, so we're sharing information to answer questions around what #scleroderma is, diagnosis, treatment and more. Click the link provided to learn all about scleroderma 👇 bit.ly/3qit2k9 #KnowScleroderma @WeAreSRUK
Esclerodermia significa "piel dura". Es una enfermedad autoinmune que causa inflamación y engrosamiento de la piel y otras partes del cuerpo. ¿Por qué ocurre? Eso y más en el enlace ow.ly/QnTW50SiMxS #SclerodermaAwarenessMonth
June is Scleroderma Awareness Month! Help us Raise the Flag for Scleroderma Awareness at 2 locations in Atlantic Canada. 💙 City Hall, St. John's NL at 11am 💙 Province House, Halifax, NS at 2pm #sclerodermaawarenessmonth
It's #SclerodermaAwarenessMonth! Let's shine a light on this rare autoimmune disease that affects thousands of people worldwide. It also been shown to have effects on the #GItract. Click the link below to learn more: iffgd.org/gi-disorders/s… #DigestiveHealthMatters #GITwitter
There's still time to sign up for our #SclerodermaAwarenessMonth event "Collaborating for a Cure," the SRF Patient Forum on June 6th at 9:00 am PDT/12:00 pm EDT! Register now at bit.ly/collab4cure23R… #SayScleroderma
Scleroderma Awareness Month Scleroderma is a rare autoimmune disease affecting the body's connective tissues. Raising awareness during this month can support research and treatment options for those affected. #UplandCA #HomeCare #SclerodermaAwarenessMonth
June is Scleroderma Awareness Month. Those familiar with Tom Tyler's life and career have probably heard about this rare auto-immune disease which eventually took his life at the young age of 50. scleroderma.org/scleroderma-aw… #scleroderma #sclerodermaawarenessmonth
Did you know that there is no known cause of Scleroderma? Scleroderma takes place when your immune system inflames your skin and other organs. Check out the symptoms of Scleroderma in this picture below! #georgiapca #SclerodermaAwarenessMonth
June #SclerodermaAwarenessMonth This infographic shows the different types and their similar symptoms. #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue
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