#rarepov

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In its new #‎HardWord‬ campaign, the Scleroderma Foundation is raising awareness about the autoimmune disease, which has no cause or cure. Go to HardWord.org ‪to learn about scleroderma and how you can help. #Scleroderma #Sclerodermaawareness #Sclerodermaresearch #Sclerodermasupport #RareDisease #RarePOV #autoimmunedisease

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Self-described "MRI Artist" Eric Hudson is a #Sarcoidosis patient who creates art from his scans and X-rays. See his work at ericchudson.com. He writes, "If it is going to be around in my life from here on out, I am going to take this condition and turn it into something that I think is kinda amazing." #Sarcoidosis #RareDisease #RarePOV #RareDisorder #LungDisease #SarcoidosisAwareness #SarcoidosisResearch #Neurosarcoidosis #artist

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February 28, 2015 marks the eighth international Rare Disease Day coordinated by EURORDIS. On and around this day hundreds of patient organizations from more than 80 countries and regions worldwide are planning awareness-raising activities around the slogan Day-by-day, hand-in-hand.http://www.rarediseaseday.org/article/about-rare-disease-day #RareDisease #raredisorder #rarePOV #patients#RareDiseaseDay

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Patricia Lay-Dorsey, an artist, was diagnosed with chronic progressive multiple sclerosis, and documents her journey with the condition through a series of strikingly raw photographs. Read about her here in the Huffington Post: www.huffingtonpost.com/2014/07/28/patricia-lay-dorsey_n_5611147.html. #MultipleSclerosis #MultipleSclerosisAwareness #MultipleSclerosisResearch #epatient #RareDisease #RarePOV #raredisorder