Teacher Survey: Raise Rare Disease Awareness IndoUSrare invites you to share your insights on rare diseases in India. Your input can drive awareness and better resources. 👉 Participate now: https://buff.ly/4feGTvP 🔗 Learn more: https://buff.ly/4fhvCef #RareDiseases #TeacherAwareness #EducationForChange #IndoUSrare
Indo US Organization for Rare Diseases (IndoUSrare)’s Post
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Digital & Social Strategy for Healthcare | Social Listening | Influencer Engagement Strategy | Consultant. Obsessed with AI but not the robots taking over part....
Be aware to spread awareness. Disease awareness months shed light on various diseases. Understanding these sentiments and insights can significantly impact future awareness efforts. #sociallistening #digitalintervention #supportawareness #diseaseawareness
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Connect to specialists for your Myositis with Know Rare. Know Rare has helped many people living with rare diseases connect to rare disease specialists and may be able to help you too. 💛💙 🔗 Send us a DM or visit https://lnkd.in/gUnYtHsb to learn more. — #myositis #chronicillnessawareness #myositisawareness #myositiswarriors #myositislife #myositissupport #myositiswarrior #raredisease #rarediseaseawareness #chronicpainawareness #rarediseases #KnowRare
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Connect to specialists for your Myositis with Know Rare. Know Rare has helped many people living with rare diseases connect to rare disease specialists and may be able to help you too. 💛💙 🔗 Send us a DM or visit https://lnkd.in/gWKVKnFS to learn more. — #myositis #chronicillnessawareness #myositisawareness #myositiswarriors #myositislife #myositissupport #myositiswarrior #raredisease #rarediseaseawareness #chronicpainawareness #rarediseases #KnowRare
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Know More About Your Options Living with Myositis Know Rare has helped many people living with rare diseases connect to rare disease specialists and may be able to help you too. 💛💙 🔗 Send us a DM or visit https://lnkd.in/ggvcBrSx — #myositis #chronicillnessawareness #myositisawareness #myositiswarriors #myositislife #myositissupport #myositiswarrior #raredisease #rarediseaseawareness #chronicpainawareness #rarediseases #KnowRare
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Carmen Rene invites you to celebrate #WorldLymphedemaDay on March 6 to educate the world about lymphedema, lipedema, and lymphatic disease. We encourage you to be creative with your celebration. It can be live or virtual, simple or elaborate. The goal is to use your voice to express the change you want to see in the world—a world where lymphatic diseases are a global priority. Get involved at linktr.ee/lymphaticnet #lymphedema #lipedema #lipedemaawareness #lymphaticdiseases #lymphoedema #linfedema #lymfoedeem #lymphoedème #lymphödem #linfoedema #lymfedeema #lymfødem #lifewithlymphedema #livingwithlymphedema #lymphedemawarrior #lymphedemaawareness #chronicdisease
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Connect to specialists for your Myositis with Know Rare. Know Rare has helped many people living with rare diseases connect to rare disease specialists and may be able to help you too. 💛💙 🔗 Send us a DM or visit https://lnkd.in/gUnYtHsb to learn more. — #myositis #chronicillnessawareness #myositisawareness #myositiswarriors #myositislife #myositissupport #myositiswarrior #raredisease #rarediseaseawareness #chronicpainawareness #rarediseases #KnowRare
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Globally, the rates of autoimmune disease cases are rising by between 3-9% each year. This is #AutoimmuneDiseaseAwarenessMonth, check out SWHR’s Autoimmune Policy Agenda to read about the #legislative steps necessary for improving #autoimmune care and #research: https://ow.ly/552w50QP8Jh #SWHRtalksAutoimmune
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Psoriasis is NOT contagious but awareness is. To start off #PsoriasisActionMonth let's get the facts straight. ⬇️ You don't have to take on psoriatic diseases alone; we are here to help. Find out more about psoriasis with the latest news, treatment updates, and more: https://lnkd.in/gCA7K-Au
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Being a doctor entails not only being a storehouse of medical knowledge needed to formulate a diagnosis and treat your patients, but it also entails raising awareness and informing- in my case about skin diseases- with the goal of building a supporting community. A friend of mine suffers from psoriasis. The first plaques appeared around a year ago on their elbows and ankles. To this day plaques have spread to other visible parts of their body. During their holidays people commented on how they should avoid wearing shorts and try to cover their skin lesions instead. Some people even said to avoid going camping, as the «rash» might be contagious. What this incident made me realize is that there is still a lot of work to be done regarding raising awareness and transferring knowledge regarding skin diseases in general and psoriasis in particular. People tend to fear what they cannot explain and understand. This is a prime example of how detrimental lack of information can be. Information can prevent discrimination, and stigmatization and lessen the psychological burden patients carry. 125 million people worldwide — 2 to 3% of the total population — have psoriasis according to the World Psoriasis Day consortium. #Dermatology #Psoriasis #ThisIsPsoriasis #PsoriasisActionMonth
Psoriasis is NOT contagious but awareness is. To start off #PsoriasisActionMonth let's get the facts straight. ⬇️ You don't have to take on psoriatic diseases alone; we are here to help. Find out more about psoriasis with the latest news, treatment updates, and more: https://lnkd.in/gCA7K-Au
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