National Organization for Rare Disorders (NORD) (@RareDiseases) header
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#NORD has been the voice of the U.S. #RareDisease community for 40+ years strong. Official U.S. sponsor of #RareDiseaseDay. On Bluesky at @ https://nitter.cf/t.co/D7PIT4k0Py

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Joined October 2009
Hey #Montana residents: Join NORD this Monday, Nov. 9 at 4:30 p.m. MT for a virtual Rare Action Coalition information meeting on #RareDisease policy priorities in your state! Learn what's coming and how you can help. RSVP: bit.ly/4sQ9rnS
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25 runners. 26 #RareDisease community partners. More than $200,000 raised so far. Our hearts are full after the 2026 #NYCMarathon ❤️ This year, Team #RunningForRare was the largest in our history. Thank you to @NYCMarathon, @NYRR, and everyone who donated and cheered us on. You can still make a difference for people with #RareDiseases by reading our runners’ stories and supporting their fundraisers here: bit.ly/46IcZy0
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This #PulmonaryHypertension Awareness Month, learn about #PulmonaryArterialHypertension, a rare condition causing high blood pressure in the arteries of the lungs that can be difficult to recognize because early symptoms resemble other conditions. Watch the full 6-minute video: youtube.com/watch?v=iIzY0Xpj… #PHAwarenessMonth #Pulmonology #Cardiology #PAH
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Caring for patients with #NF1-associated plexiform neurofibromas can be complex, especially during the transition to adult care. Explore strategies for patient selection, adverse event management, and care coordination in this free, on-demand #CME program from NORD and @medliveofficial: bit.ly/4iwZo3D #MedicalEducation #MedEd #neurofibromatosis
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Run #Boston. Run for Rare. 🏃‍♀️💙 Applications are open for the 2027 #BostonMarathon with NORD #RunningForRare! Only 5 competitive team spots. Fundraise, advocate, and run with purpose. Apply by Nov. 1: runningforrare.org/events/ Boston is just the beginning! In 2027, run with NORD at @LAMarathon, @LondonMarathon, @grandmasmara, @tokyo42195_org, or @runcolfax. Every mile tells a story. Make yours one that moves the #RareDisease community forward.
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Join @ASGCTherapy for Breakthroughs in Cell and #GeneTherapy, Nov. 12–13 in Nashville or online. Cell and gene therapy is advancing rapidly, bringing new opportunities and challenges. Explore #CNS advances, targeted delivery, and manufacturing successes while connecting with experts across the #CGT field. Register today: bit.ly/asgct-breakthroughs
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A federal court sided with 25 states and D.C., striking down an added test for medically frail individuals under new #Medicaid work rules. The court also barred the federal government from penalizing those states for implementation errors or delays for six months. #NORD is monitoring the ruling and will continue our work to protect coverage for the #RareDisease community. Read the court order: storage.courtlistener.com/re… #StayCovered #HR1 #WorkRequirements
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Here are 2 ways your experience can build greater understanding of life with #POLG. Complete the POLG survey THIS WEEK by October 31: survey.alchemer.com/s3/89508… Then, join @mitoaction for the POLG Externally-led Patient-Focused Drug Development #ELPFDD Meeting on November 17, 10 a.m. ET. Register here: buff.ly/hgIWQuA #MitochondrialDisease
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Pam Gavin, President and CEO of the National Organization for Rare Disorders (#NORD), spoke on behalf of #RareDisease advocates at today’s @FDA Public Meeting on the Rare Disease Framework Initiative hosted by @ReaganUdall, offering strategic direction, partnership, and encouragement for the FDA’s efforts. We heard a few common themes rise up from the public comments about the importance of the patient voice, clarity and consistency, and ensuring the evidence requested by #FDA is reasonable and appropriate. These echoed this week's conversations at the #NORDSummit, and we're committed to addressing them together with urgency.
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NORD's policy leaders appreciated the opportunity to have candid discussions on key #FDA modernization initiatives with the directors of each @FDA center both onstage and offstage at the 2026 #NORDSummit. Pictured here with the Director of the Center for Drug Evaluation and Research (#CDER) Dr. Mike Davis (center right) is #NORD EVP of Government Affairs Kathryn Lowell (center left), VP of Federal & Global Public Policy Mike Beard (right), and Policy Analyst Sarah Royka (left). @FDADrugs #RareDisease
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Advances in precision #oncology are creating new opportunities for people living with rare #cancer, but access to biomarker testing remains uneven in many states. Yesterday's #NORDSummit panel on Closing the Gap in Precision Oncology with @ACSCAN, @ChildrensNatl, and NJ Senator Troy Singleton (@Troy4NJ7) explored the policy solutions and patient advocacy needed to expand equitable access to testing. #HealthEquity #biomarkers
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Changes to #Medicaid are coming fast. Work requirements and accompanying eligibility questions, like the two-part test, are first. #NORDSummit panelist Dr. Heather Saunders of @KFF says the impact could be felt hardest in #rural areas. NORD has an FAQ and recommended policies for state agencies to ensure #RareDisease patients retain coverage: rarediseases.org/medicaid-wo…
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In our #NORDSummit panel, Closing the Access Gap in Precision Oncology, our panelists highlighted the power that #biomarker testing has for #cancer patients and how too many people lack access to it. The science is already here, the problem is affordability and access. NJ State Senator @Troy4NJ7 explained how #NewJersey passed a law requiring #HealthInsurance coverage for biomarker testing. This must be a #HealthEquity model for other states to follow, and about half of states so far have. Thank you to our panelists from @ChildrensNatl, @ACSCAN and moderator Jim Palma of @TargetCancer
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National Organization for Rare Disorders (NORD) retweeted
Modernizing FDA's review process starts with listening. Acting Commissioner Kyle Diamantas joined @RareDiseases at the #NORDSummit Monday to discuss how patient voices are central to building a fit-for-purpose framework for #RareDisease therapies.
Acting @FDA Commissioner Kyle Diamantas, @FDA_KyleD, sat down for a fireside chat with #NORD President and CEO Pam Gavin to kick off the 2026 #NORDSummit, where he shared that the #FDA is committed to modernizing its review process and is relying on #RareDisease patient voices to help shape its fit-for-purpose regulatory framework. We appreciated the opportunity to break down what that will entail, and we're excited to be a partner in this crucial, timely mission.
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During our 2026 #NORDSummit FDA Rare Disease Regulatory Roundtable, moderator Amy Comstock Rick asked the Directors of #FDA CDER, CBER, and CDRH: Where can patient voices make the most difference? Center for Devices and Radiological Health (#CDRH): Identifying unmet needs, prototyping #MedicalDevices, involving patients in design of clinical trials to maximize participation and efficacy, gauging product quality once released Center for Biologics Evaluation and Research (#CBER): Risk-benefit analysis of #GeneTherapy, defining acceptable outcomes and meaningful clinical endpoints Center for Drug Evaluation and Research (#CDER): Patient-focused drug development meetings help explain which symptoms needs to be treated and which do not
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We're sharing today's full, hour-long #NORDSummit conversation between the CEOs of #NORD, @BioMarin, @JazzPharma, and @OtsukaUS, moderated by @CNBC Cures host @BeckyQuick, so that the entire rare disease community can hear their urgent insights about the next decade of #RareDisease research and care. Watch it now: youtube.com/watch?v=UDf3BPnG…
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We had the honor of presenting Mark Skinner with a Lifetime Achievement #RareImpactAward at today's #NORDSummit in D.C. When Mark was born, #hemophilia had no approved treatments. Today, huge progress has been made thanks to Mark's decades of leadership as a #BleedingDisorder advocate nationally and internationally. Mark has also championed patient-centered outcomes research, which is critical for rare diseases. Today, he serves on NORD's Board of Directors. Join us in congratulating Mark on this well-deserved award for his lifetime of dedication to the #RareDisease community! Learn more at rareimpact.org.
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During a #NORDSummit panel on moving "Beyond One Disease at a Time: The Future of Individualized Genetic Therapies," Apriligen CEO @Nicholas_Vita had insightful words for #pharma investors: "What #healthcare investors should be asking is, how do I generate the best risk-adjusted return? And you can't do it anywhere else the way you can in #RareDisease. And that's the argument we should be making with investors, because when you have the regulators giving you tailwinds that have never existed before, when you have the scientific community coming up with innovation like they never have before." #Investment #GeneTherapy
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We were proud to present a 2026 NORD #RareImpactAward for Youth Leadership to Paridhi Tyagi live at the #NORDSummit in D.C.! Paridhi founded a #genetics club at her high school through NORD #StudentsForRare, raised awareness in her town on #RareDiseaseDay, and collaborated with @GirlScouts to host workshops where she taught #GirlScouts about inclusion and acceptance of people with #RareDiseases and the science of genetics through DNA extraction and modeling. Learn more at rareimpact.org.
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