Rare In Common @RareInCommon
MANY VOICES. ONE MISSION. A user-generated short-film about the inspiring people in the rare disease community — Rare in Common. rareincommon.com Cambridge, MA Joined February 2015-
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Bella, pictured here with her service dog and loving companion, George, was diagnosed with Morquio A syndrome as a little girl. “I grew up with it, so I don’t know what it’s like to not have it.” Read more about Bella and her journey at Facesofrare.com #FacesOfRare
Diane lived through questions and mysterious symptoms for decades and now she has dedicated herself to helping others to avoid the uncertainty she faced for so much of her life. Now diagnosed with familial chylomicronemia syndrome. Learn more at facesofrare.com #ActionFCS
Christian recognizes the importance of seeing past the label of a rare disease and encourages others to do the same. “Rare diseases shouldn’t really define who people are." Read about Christian’s story with hemophilia A at FacesOfRare.com #FacesOfRare
Arista shares a lot with her twin sister, Arielle, including a diagnosis of hereditary angioedema (HAE). She remains positive: “I think the best part of the journey is having each other.” Hear more about Arista’s and Arielle’s stories. At FacesofRare.com #FacesOfRare
Francesca has overcome a lot in the face of and in spite of a diagnosis of familial partial lipodystrophy (FPLD). Her advice to others in the same shoes? Remember that you are truly unique–1 out of millions!–and that’s special. Read more at facesofrare.com #FacesOfRare
Did you make it to Boston City Hall Plaza on Rare Disease Day? If you missed it, don’t worry. You can still meet these incredible people who face rare diseases every day. Read their stories on facesofrare.com. #FacesOfRare
Learn more about our #FacesofRare campaign, including last night’s event at @CityHallBoston and about patient Arista Lee via @BostonGlobe bit.ly/2NDGOGW
It’s Rare Disease Day! Today we celebrate the brave people who face rare diseases every single day. Visit City Hall Plaza today starting at 6:00 to meet all the #FacesOfRare!
Tomorrow is the big day! Can you tell Francesca has been looking forward to Rare Disease Day? Read her story at facesofrare.com and come visit us at Boston City Hall Plaza at 6:00 PM tomorrow! #FacesOfRare
Have plans for Thursday (2/28)? You should! Come check out an initiative in honor of Rare Disease Day at Boston City Hall Plaza at 6:00 PM. Want to learn more? Check out our new LIVE site at facesofrare.com. Link in profile. #FacesOfRare
Christian poses for the Rare Disease Day photoshoot. Want to learn more about his story? Check it out at facesofrare.com AND come see the big event at Boston City Hall Plaza on Thursday, February 28. The fun starts at 6:00! #FacesOfRare #RDD
Check out Bella and George! We had so much fun capturing their pictures and story. The #FacesOfRare website is launching next week. Get ready to be inspired! And join us at Boston City Hall Plaza at 6:00 on 2/28.
Amazing photoshoot. Amazing day. Here, Diane poses for the camera. Something truly special is coming for #RDD. Will you be joining us and Diane at City Hall Plaza on Thursday, February 28 at 6:00 PM? #FacesOfRare
#TBT to Arista behind the scenes at the shoot. Join us to see what all the fuss is about at Boston City Hall Plaza on Thursday, February 28 at 6:00 PM! #RDD #FacesOfRare
Rare Disease Day is celebrated on the last day of February each year. Why? Because February 29 is RARE! This year it’s being celebrated on February 28 and something big is coming. Come check it out! #FacesOfRare
Nous sommes heureux d'annoncer que #RareInCommon est maintenant disponible avec des sous-titres en Français! bit.ly/2pC0IZi
We are happy to announce that #RareInCommon will now be available with French subtitles! @RareInCommon bit.ly/2pC0IZi
We are happy to announce that #RareInCommon will now be available with French subtitles! bit.ly/2pC0IZi
Nous sommes heureux d'annoncer que #RareInCommon est maintenant disponible avec des sous-titres en Français! bit.ly/2pC0IZi
¡Estamos muy emocionados en anunciar que #RareInCommon estará disponible con subtítulos en español! @RareInCommon bit.ly/RICspn
Effie Parks @OnceUponAGene
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Cambridge Rare Diseas... @camraredisease
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NWRareCoalition @nw_rare
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Brookfield House Pare... @BrookfieldAssoc
40 Followers 481 Following Brookfield Association is the Parent/Teachers Association for Brookfield House Special school which is part of the Lime Academy Hornbeam. Est November 1975
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8675309 @linlin8
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Somatic Cell Genome E... @somaticediting
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Joanne Hatchett @sjhatch_joanne
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MANZI Ndamukunze @MNdamukunze
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Andréa Soares @dedeaas
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Michelle @JePensePlus
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Rarity Life @raritylifemag
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Clement Chow @ClementYChow
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Kristen C. Duncan @kristencreed76
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Neighbourhood Pharmac... @pharmacy_CAN
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SoniyaFit @SoniyaFit
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National Organization... @RareDiseases
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EveryLife Foundation @EveryLifeOrg
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Global Genes @GlobalGenes
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Genetic Counselors @GeneticCouns
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Stephanie Fischer @RarePOV
7K Followers 5K Following #Raredisease patient advocate & #stroke survivor.🦓 Member of @PARareDisease. Opinions are my own.
RDLA @RareAdvocates
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CORD @raredisorders
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SXSW @sxsw
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urddad-foundation @TerenceHoey
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AHC Foundation @AHCkids
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R.M.C. Inc @RMCAwareness
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751 Followers 714 Following Groundbreaking documentary on the hidden healthcare epidemic about millions who live without answers to their debilitating illnesses.
Harmony 4 Hope @harmonize4hope
1K Followers 952 Following Leading Nonprofit Mobilizing Community & Raising Funds 4 Rare Disease through the Universal Power of Music & Storytelling. We Tweet #RareStorytellers
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22K Followers 2K Following NHS England's Genomics Education Programme. Providing knowledge, skills and experience in #genomics #NHSgms #genomes100K #NHS #GenomicsConversation
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577 Followers 301 Following I'm a mum of 2 beautiful boys... Fighting to raise awareness of Duchenne Muscular Dystrophy, which my youngest son Aidan has... Please help me in this fight....
Harvard Health @HarvardHealth
2.4M Followers 790 Following Knowledge is the best medicine. Providing you with trustworthy health information from the halls of @Harvardmed and world-famous affiliated hospitals.
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Duchenne Foundation @DMDfoundation
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2K Followers 3K Following Conquer a rare skeletal disease. Congenital fusion of cervical spine. Organs, nerves, muscles. 🗝 Research | Educate | Empower | Advocate #Genetic #Neuro #Pain
AMA @AmerMedicalAssn
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jackie @jackie_frank
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Melissa VanHouten @melissarvh
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ros reines @RosReines
16K Followers 1K Following Author, journalist and award-winning content writer. My novel A Tabloid Tale, will be out next. Instagram @rosreines
PhRMA @PhRMA
80K Followers 52 Following Representing America’s biopharma & biotech companies. Shaping policy so science thrives & patients benefit.
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Rare Point of View @RarelyYours
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Rare Diseases South A... @rarediseasessa
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Putting RDPF! @PuttingRDPF
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