We are a student organization at Northeastern University that aims to increase awareness for rare diseases and provide support to those in need.

Joined October 2017
7 Photos and videos
This week we welcomed Mike Miller of the Huntington’s Disease Society of America! Thank you to everyone who came to our first speaker event of the semester! instagram.com/p/B7_sF0xAWre/…

RARE Northeastern retweeted
Out now! Download the official poster for #RareDiseaseDay 2020 now available via rarediseaseday.org/downloads. Share it today to show your support for the rare disease community!
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Marking our return to Twitter with an important PSA: We’re at Curry Crossroads today until 6pm selling insomnia cookies! 🍪🍪🍪
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Update: THIS FUNDRAISER WILL BE MOVED to a later date due to an unforeseen cookie emergency!
First General Meeting - mailchi.mp/e86e02c6a262/rare…

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RARE Northeastern retweeted
Your patient experience is your expertise and the role of the FDA Patient Representative® is an equal part of the important equation. Learn more about the FDA Patient Representative Program® youtu.be/F4yxgzGVRXg
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RARE Northeastern retweeted
The Power of Public Awareness & #SocialMedia Exemplified - Rarest of Blood Found Following Unprecedented Global Search theepochtimes.com/donor-foun… #IoT #ITRTG #IT #advocacy #SciComm #MedEd #tech #blood #technology #awareness #BigData #RareDisease #inspiration #hematology #cancer
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RARE Northeastern retweeted
Did you know that your organisation can support Rare Disease Day 2019 by becoming a friend today? >> rarediseaseday.org/become-a-… #RareDiseaseDay #ShowYourRare
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RARE Northeastern retweeted
#OpenEnrollment ends on Saturday, December 15. Learn more about this critical time in choosing a 2019 #healthinsurance plan in webinar recording from #NORD policy department here: ow.ly/71c450jUPoX

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Join RareNeu at @NUafterHOURS tonight for a free musical performance by TEGA. All proceeds will be going to @SCDAAorg to support sickle cell disease! Succulent fundraiser at 7, concert at 8 🎤🎼🎉
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RARE Northeastern retweeted
Patient Affairs Staff works closely with #FDA medical product centers to find ways to include your voice as patients, caregivers, and advocates. #NORDSummit go.usa.gov/xPXQD
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RARE Northeastern retweeted
Did you know.... The average #raredisease patient waits four years before receiving a correct diagnosis. That's why we call it 'diagnostic odyssey'.
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RARE Northeastern retweeted
About 80% of #RareDiseases have a genetic cause. Learn about basic #genetics in our Genetics 101 infographic! raremark.com/articles/geneti…
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RARE Northeastern retweeted
What is Stiff Person Syndrome? Despite being rare there are many sites where you can get information. ispub.com/IJN/7/ @lizblows @DrPas84Ele #stiffpersonsyndrome #sps #oneinamillion #tinman #raredisease

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RARE Northeastern retweeted
Retweet for #WednesdayWisdom: 30 Million Americans are living with #rarediseases and more than half of those individuals are children.
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We had a great time hearing from the Executive Director of @targetcancer this week! #rarecancers #rareresearch #raredisease
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Our members celebrated Rare Disease Day the best way we know how - spreading awareness to other students! #RareDiseaseDay #PatientDriven
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We’ll be tabling with these adorable Valentine’s Day succulents to raise awareness for @1p36DSA tomorrow in Curry Table #1B 10am-4pm, and Wednesday 12-6pm!
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