#sclerodermaawareness نتائج البحث
Morphea vs systemic scleroderma! Morphea = thickened, waxy skin patches (rarely affects organs, outlook usually excellent). Systemic = can be limited or diffuse + may involve lungs, heart + gut. Knowing the difference = earlier care + better outcomes. #SclerodermaAwareness
June is #sclerodermaawareness month. #Scleroderma is a debilitating, incurable and progressive disease. I’m raising awareness so we can fight this and one day find a cure! I’m in my 5th year now.
June is #SclerodermaAwareness Month. 💙 Scleroderma, also known as systemic sclerosis, is a group of rare diseases that involve the hardening and tightening of the skin. It may also cause problems in the blood vessels, internal organs, and digestive tract.
Walking for my dear friend Debbi, battling scleroderma. Support her fight by donating or joining us at the Scleroderma Foundation's Stepping Out walk. 💙 #SclerodermaAwareness #MidAtlanticChapter @SFDV1 @scleroderma national.scleroderma.org/site/TR/Steppi…
Scleroderma Awareness Month is a time to speak up and raise awareness for the scleroderma community. Scleroderma affects hundreds of thousands across the United States, and there is evidence that it affects the African American community more severely. #SclerodermaAwareness
🌏Today is World Scleroderma Day! ⭐ Let's raise awareness about this autoimmune disease 👉Your support fan make a difference in improving lives and advancing research 🌻 #SclerodermaAwareness #ResearchMatters @JOVREUM @EMEUNET @AEEsclerodermia @SEReumatologia
Our first charity stream is done & I’m overwhelmed with gratitude 💙 Thank you for lurking, chatting, sharing stories, & donating. We’ve unlocked the Palia Hide N Seek event! 🎉 Let’s keep the love going all month long #HauntedHeartsForHope #SclerodermaAwareness #CharityStream
Day 4 of Haunted Hearts for Hope is live! 💙 We’re back in @playPalia doing some cozy decorating and continuing our charity fundraiser for the National Scleroderma Foundation. Come hang out, support, or just vibe! 🧡 🔴 twitch.tv/saelysss #SclerodermaAwareness #Palia
June is Scleroderma Awareness Month, wear teal for Tom Tyler! #TomTyler #scleroderma #sclerodermaawareness #Junesclerodermaawarenessmonth #sclerodermawarrior
🌍 En el Día Mundial de la Esclerodermia, nos unimos para arrojar luz sobre esta enfermedad 💪🏻 Recordamos la valentía de pacientes, familias y profesionales de salud en su lucha diaria. ¡Su fortaleza nos inspira! #DME2024 #WSD2024 #SclerodermaAwareness #Bloomwithscleroderma
La esclerodermia también afecta a los hombres– conozca los signos, como la hinchazón de los dedos y el engrosamiento de la piel, y busque atención medica temprano #SclerodermaAwareness #MensHealthMonth
*June 29 is World Scleroderma Day!* Scleroderma is a chronic connective tissue disease generally classified as one of the autoimmune rheumatic diseases which is caused by excess collagen production. . . . #chronicillness #scleroderma #sclerodermaawareness #WorldSclerodermaDay
June is Scleroderma Awareness Month! Demi shares her experience with this rare disease during our "Living with Interstitial Lung Disease" webinar. Click the link to learn more about Scleroderma-associated interstitial lung disease. 💙 on.lung.org/4aVShuB #SclerodermaAwareness
Want to get under someone’s skin? Then tighten your pores and use Organ Mapping Antibody Panel-22 for skin developed by #_hubmap researchers Dr. Fiona Ginty, Liz McDonough, Christine Surrette @GEResearch to make this skin-tillating Cell DIVE image! #SclerodermaAwareness
Day 3 of charity fundraising is complete and we’re now at $705 raised!💙 So grateful for the Haunted Hotties who continue to show up, share their stories, and support this cause so close to my heart. You are everything.🤟 #HauntedHeartsForHope #SclerodermaAwareness #autoimmune
Going live for a cozy Palia cooking party! 🥘✨ We’re also fundraising for The National Scleroderma Foundation 💙 Come chill, cook, and support a cause close to my heart: 🔗 tilt.fyi/crhOQmgvcX 📺 twitch.tv/SaeLysss #SclerodermaAwareness #Palia #CharityStream
Tips to get over winter blues! #SclerodermaWarriors #SclerodermaIndia #SclerodermaAwareness #emotionalhealth #mentalwellbeing
We’re looking for scleroderma patients to join our blood donor program. Your donation could help advance scientific understanding and lead to better treatments for others living with the condition. Learn more: hubs.la/Q03JFXxH0 #SclerodermaAwareness #DonateBlood
JOIN US for our October #VirtualEducationSession with guest speaker A/Prof Amanda Saracino! WHEN: Saturday, 11 October at 10:30 AM AEST WHERE: Online via Google Meet TOPIC: Morphoea Management COST: It's FREE! Register here: eventbrite.com.au/e/morphoea-man…? #SclerodermaAwareness
💙 Don’t miss this chance to connect directly with the researchers shaping the future of scleroderma care and treatment. 🎟️ Tickets are $35 | Register now through the link in our bio! #Scleroderma #SclerodermaAwareness #HardWordHarderDisease #Autoimmune
We’re looking for scleroderma patients to join our blood donor program.Your donation could help advance scientific understanding and lead to better treatments for others living with the condition. Learn more: hubs.ly/Q03JLrS70 #SclerodermaAwareness #DonateBlood
Morphea vs systemic scleroderma! Morphea = thickened, waxy skin patches (rarely affects organs, outlook usually excellent). Systemic = can be limited or diffuse + may involve lungs, heart + gut. Knowing the difference = earlier care + better outcomes. #SclerodermaAwareness
✨ Join us Oct 25 in Burnaby for the SABC 41st AGM & Conference! A full day of learning, research updates & community. 🎟️ Tickets $35. 👉 Register now through the link in our bio! #Scleroderma #SclerodermaAwareness #HardWordHarderDisease #Autoimmune
Join us for our September #VirtualEducationSession with guest speaker #RossSottile! TOPIC: Scleroderma and Workspace Exposure WHEN: Saturday, 13th September at 10:30 AM AEST WHERE: Via Google Meet COST: It's FREE! Register today! eventbrite.com/e/scleroderma-… . . #SclerodermaAwareness
JOIN US for our September #VirtualEducationSession with guest speaker Ross Sottile! TOPIC: #Scleroderma and Workspace Exposure WHEN: Saturday, 13th September at 10:30 AM AEST WHERE: Online via Google Meet COST: It's FREE! ➡️eventbrite.com/e/scleroderma-… #SclerodermaAwareness
We’re looking for scleroderma patients to join our blood donor program.Your donation could help advance scientific understanding and lead to better treatments for others living with the condition. Learn more: hubs.ly/Q03zyYRV0 #SclerodermaAwareness #DonateBlood
Who gets scleroderma? - Anyone can -Women 3–4x more likely -Most often 40–60, but can appear at any age (even in kids) -All ethnicities (less common in African & Polynesian backgrounds) -It’s not inherited and rarely affects more than one family member. #SclerodermaAwareness
What’s really going on with #scleroderma? It’s not just a skin issue - it affects the immune system, blood vessels & organs. Thickening & hardening happen from too much collagen. Learn more here: sclerodermaaustralia.com.au/wp-content/upl… #SclerodermaAwareness
This graphic holds the names of every incredible haunted hottie who donated — thank you for sharing your kindness, your stories, and your hearts. Here’s to making sure no one feels alone in their battles. 🤟 #HauntedHotties #StrongerTogether #SclerodermaAwareness
Living with scleroderma means enduring the lows—but also finding strength in the ‘moments in between.’ Silvia Petrozza shares what keeps her rising — via @healthing_ca #SclerodermaAwareness #ChronicIllness #Resilience #HealthCanada #PatientVoices healthing.ca/rare-diseases/…
healthing.ca
Living with scleroderma: Appreciating the ‘moments in between’ to find strength
Living with scleroderma: Appreciating the ‘moments in between’ to find strength
Living with scleroderma means enduring the lows—but also finding strength in the ‘moments in between.’ Silvia Petrozza shares what keeps her rising — via @healthing_ca #SclerodermaAwareness #ChronicIllness #Resilience #HealthCanada #PatientVoices healthing.ca/rare-diseases/…
healthing.ca
Living with scleroderma: Appreciating the ‘moments in between’ to find strength
Living with scleroderma: Appreciating the ‘moments in between’ to find strength
Morphea vs systemic scleroderma! Morphea = thickened, waxy skin patches (rarely affects organs, outlook usually excellent). Systemic = can be limited or diffuse + may involve lungs, heart + gut. Knowing the difference = earlier care + better outcomes. #SclerodermaAwareness
Walking for my dear friend Debbi, battling scleroderma. Support her fight by donating or joining us at the Scleroderma Foundation's Stepping Out walk. 💙 #SclerodermaAwareness #MidAtlanticChapter @SFDV1 @scleroderma national.scleroderma.org/site/TR/Steppi…
La esclerodermia también afecta a los hombres– conozca los signos, como la hinchazón de los dedos y el engrosamiento de la piel, y busque atención medica temprano #SclerodermaAwareness #MensHealthMonth
An estimated 300,000 Americans have #scleroderma, a chronic #autoimmunedisease that can affect more than just your skin. ➡️ Learn more: cle.clinic/4babrN5 #SclerodermaAwareness
It's Scleroderma Awareness Month! Each individual's experience with Scleroderma is unique and different which is why every journey matters. 🌟 @scleroderma @WeAreSRUK @Worldsclerofnd @ScleroAus #scleroderma #systemicsclerosis #sclerodermaawareness #everyjourneymatters
June is Scleroderma Awareness Month, wear teal for Tom Tyler! #TomTyler #scleroderma #sclerodermaawareness #Junesclerodermaawarenessmonth #sclerodermawarrior
Early diagnosis of symptoms and seeking medical attention promptly can make a significant difference in treatment outcomes. For any signs, consult our Skin specialists: kailashhealthcare.com #scleroderma #SclerodermaAwareness #skindisease #EarlyDiagnosisMatters…
June is #sclerodermaawareness month. #Scleroderma is a debilitating, incurable and progressive disease. I’m raising awareness so we can fight this and one day find a cure! I’m in my 5th year now.
Our first charity stream is done & I’m overwhelmed with gratitude 💙 Thank you for lurking, chatting, sharing stories, & donating. We’ve unlocked the Palia Hide N Seek event! 🎉 Let’s keep the love going all month long #HauntedHeartsForHope #SclerodermaAwareness #CharityStream
#sclerodermaawareness #findthecure #worktogether #TraditionalMedicine #naturalpathicmedicine #holisticmedicine #complementaryalternativemed #herbalmedicine #peace #love
🌍 En el Día Mundial de la Esclerodermia, nos unimos para arrojar luz sobre esta enfermedad 💪🏻 Recordamos la valentía de pacientes, familias y profesionales de salud en su lucha diaria. ¡Su fortaleza nos inspira! #DME2024 #WSD2024 #SclerodermaAwareness #Bloomwithscleroderma
JOIN US for our September #VirtualEducationSession with guest speaker Ross Sottile! TOPIC: #Scleroderma and Workspace Exposure WHEN: Saturday, 13th September at 10:30 AM AEST WHERE: Online via Google Meet COST: It's FREE! ➡️eventbrite.com/e/scleroderma-… #SclerodermaAwareness
Want to get under someone’s skin? Then tighten your pores and use Organ Mapping Antibody Panel-22 for skin developed by #_hubmap researchers Dr. Fiona Ginty, Liz McDonough, Christine Surrette @GEResearch to make this skin-tillating Cell DIVE image! #SclerodermaAwareness
Scleroderma affects men too—learn the signs, such as swelling or puffiness of the fingers, and skin thickening, seek early care. #SclerodermaAwareness #MensHealthMonth
June is National Scleroderma Awareness Month - thinking of Tom Tyler all month. #TomTyler #NationalSclerodermaAwarenessMonth #SclerodermaAwareness #sclerodermawarrior #scleroderma
Day 3 of charity fundraising is complete and we’re now at $705 raised!💙 So grateful for the Haunted Hotties who continue to show up, share their stories, and support this cause so close to my heart. You are everything.🤟 #HauntedHeartsForHope #SclerodermaAwareness #autoimmune
🚀 ¡Avance en la investigación de #esclerodermia! La SRF lanza CONQUEST, un ensayo único en reumatología que prueba múltiples tratamientos a la vez. Un paso hacia terapias que cambien vidas. 💙 #SclerodermaAwareness #InnovaciónEnSalud #EnfermedadesCrónicas
June is #SclerodermaAwareness Month. 💙 Scleroderma, also known as systemic sclerosis, is a group of rare diseases that involve the hardening and tightening of the skin. It may also cause problems in the blood vessels, internal organs, and digestive tract.
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