RareKC is driving innovation in the diagnosis, care and treatment of rare diseases by connecting and inspiring our Kansas City community

Kansas City
Joined October 2015
As patients and advocates, we must turn our pain and challenges into opportunities and change…. #sicklecellmidwest #FocusForward #BioNexusKC #RareKC
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Great DEI & Health equity discussion at @ChildrensMercy Research Institute with Juny Simpson of @genentech - "it's a big problem, you've just got to jump in" "start, learn, iterate, scale" - with @RareKC @RARE_X_ @CHCofWyCo @BioNexusKC
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#SaveTheDate 1/26/2023 This #Collaborate2Cure series will feature national & regional rare disease speakers. It is designed to stimulate collaboration to solve challenges facing patients, families, & caregivers impacted by rare diseases. collaborate2cure.org w/ @RareKC
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We had a great time at @BioNexusKC's annual event - Focus Forward. The night brought together over 500 leaders to celebrate #healthcare #innovation in #kansascity. Thanks for having us, @BioNexusKC. We are grateful for the opportunity to sponsor such an impactful night!
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We just registered for #RareAcrossAmerica2022 🎉 Join us in advocating on behalf of the #KansasCity #rare community 📢
Attention rare disease advocates, #RareAcrossAmerica2022 registration is open! - Make an impact in your district - Share your rare disease story - Meet other rare disease advocates When? August 8th to August 19th, 2022 To learn more and register visit rareacrossamerica.org
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TOMORROW: Our friends at The Rare Disease Diversity Coalition are hosting The Global Impact of Sickle-Cell Disease: Who is at Risk? How is it Managed? What’s Next? Taking place via YouTube from 1pm-2pm EST.youtube.com/watch?v=8E4DEIPR…
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We are proud to share a report from our friends @RARE_X_ entitled, "The Power of Being Counted." This report discovered that there are as many as 10,867 rare diseases, rather than the oft-reported previous estimate of 5,000-8,000. #raredisease #research rare-x.org/case
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Calling all #rare Artists 🎨🧑‍🎨 Our friends @EveryLifeOrg are now accepting submissions for the Rare Artist Annual Contest until July 13th! To learn more or to submit your artwork visit RareArtist.org
Lysosomal Storage Disorder (LSD) Community 🔊 We invite you to join us and @KUmedcenter for our Rare Disease Educational Meeting: Building Patient Education & Advocacy Pathways in LSDs on July 30th. Register for this half-day, virtual event: eventbrite.com/e/rare-diseas…
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Join us as we discuss disease management, mental health, advocacy, and so much more. Community Check In calls Saturdays at 1 PM. Email the Association for the details. #sicklecellmidwest # communitycheckin #StrongerTogether
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RareKC is proud to support @KCRising and their vision of regional prosperity and opportunity for all in #KC. We were honored to represent the #RARE community in #KC at the #HorizonKC 2022 event today. 💙
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According to @ojrarediseases, 82% of those with a rare disease reported having anxiety and stress on a daily basis. @KansasFT, @kulifespan & LEND at @KUMedCenter are offering a free film screening on May 25th, "Just Like You Anxiety & Depression." conta.cc/38UP8ka
Join a community listening session to share your experiences with #rare and complex health conditions and inform research at @ResearchCM. 🗣️✍️ Learn more at: redcap.link/ListeningSession….
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Join us (virtually) on Capitol Hill for the May 2022 Congressional Caucus Briefing on May 25th at 2 pm EST to discuss community priorities for the Prescription Drug User Fee Act (PDUFA) Reauthorization.🗣⚖️ To register – click the link below. everylifefoundation.salsalab…
RareKC Community❗️ Register for a family account through @SeeInMe_Inc using the code "Individual100" to get a FREE Instant Connector. 💙 seeinme.com/#home
Visit our friends at @_AbilityKC on April 27th for their Spring Wheelchair Wash! 🧼 Stop by and let their volunteer washers and the fine folks from @GoNumotion tighten and adjust your wheelchair. To register: WWW.ABILITYKC.ORG/WHEELCHAIR…
Join the @RareAdvocates for the March Monthly Webinar tomorrow @ 9 am PT/12 pm ET. ⚖️ Once a month RDLA convenes to discuss legislation and developments that affect the rare disease community. To register and see the full agenda visit: bit.ly/36kUt3a
The #RAREis Scholarship Application is now open! 📣 @HorizonNews and @EveryLifeOrg will be granting 53 young adults with rare diseases a one-time scholarship of $5,000 to pursue their dreams through education. Apply below ⬇️ everylifefoundation.org/rare…
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