We are committed to improving the lives of patients with rare diseases.

Coral Gables, FL
Joined October 2013
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Sending a HUGE thank you to Catalyst Pharmaceuticals (@catalystforrare) for being a GOLD SPONSOR. 💛 Thank you for playing a vital role in helping our charity connect and empower Canada's #Duchenne #musculardystrophy community. 2024 Family Forum: bit.ly/3vCNrDT
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A special thanks to Catalyst Pharmaceuticals, Inc. for sponsoring the Free to Breathe Chicago and Anywhere Walks! #LungCancerResearch #FreeToBreathe @CatalystForRare LCRF.org/chicago LCRF.org/anywhere
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Thank you @CatalystForRare for being an exhibiting partner! #SCLCSummit2024
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We are thrilled to announce the winner of the RARE Champion in Industry for the 2023 RARE Champions of Hope awards – the incredible Amy Grover! We look forward to recognizing you at the upcoming 2023 RARE Advocacy Summit! To learn more about Amy: go.globalgenes.org/TW-COH
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This #RareDiseaseDay we welcome @CatalystForRare to highlight their work in empowering patients to take an active role in their healthcare. $CPRX is focused on in-licensing, developing, and commercializing novel medicines for patients living with rare diseases. #NasdaqListed
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We are so honored to have joined our friends at @CatalystForRare for the @Nasdaq 🔔 ringing ceremony #RareDiseaseDay #CareAboutRare #RareDisease
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Timely diagnosis can slow progression The 1st sign of LEMS is often muscle weakness in the legs/lower body. Left untreated, LEMS may progress & affect muscles in other areas as well as the part of the nervous system that controls autonomic bodily functions lemsaware.com/what-to-expect
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Kyle & Sean both understand the value of selfless help, as both lean on others from time to time. November is #CaregiverAwarenessMonth and @2DDPodcast is partnering with @CatalystForRare to help serve the unsung heroes of healthcare through lemsaware.com/caregivers
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The #BioFL2022 Company of the Year award was presented to @CatalystForRare, a commercial-stage biotechnology company dedicated to making a meaningful difference in the lives of patients suffering from rare diseases. Congrats!
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Its #RareDiseaseDay! To spread awareness around #LEMS we have launched our new #LEMSaware Podcast! Tune-in now for our first episode featuring Price and Ashley, two #LEMS patients who will share how their journey led them to become advocates. lemsaware.com/podcasts
It’s #RareDiseaseDay! LEMS, MG, muscular dystrophy, and rare community awareness shone bright over Time Square this morning! #LEMSaware #MGstrong #RDD2021 @RareDiseases @GlobalGenes @MDAorg @MyastheniaOrg @ConquerMG @myastheniakc @CatalystForRare @Nasdaq
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Honored to have joined our advocacy partners this morning to ring the bell on @NASDAQ for #RareDiseaseDay in Time Square! Can you spot our Director, Foundation Alliance Membership Services @prk2? @RareDiseases @MDAorg @MyastheniaOrg @ConquerMG @myastheniakc @CatalystForRare
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.@CatalystForRare Co-Founder & CEO Patrick McEnany joins @JillMalandrino on @Nasdaq #TradeTalks to discuss making a meaningful impact in the lives of those suffering from rare diseases. #RareDiseaseDay $CPRX xitter.cf/i/broadcasts/1yoKMWqRy…
This #RareDiseaseDay and every day, @CatalystForRare empowers patients to take an active role in their health care. Using cutting-edge science, $CPRX develops and commercializes innovative therapies to improve the lives of patients with rare and ultra-rare diseases. 🧬
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“[If you’re navigating finding a LEMS diagnosis], you need to hang in there and keep being persistent. Be willing to do some educating with your healthcare provider, because a lot of times you're the first person that they've ever seen with #LEMS.” Sponsored by @CatalystForRare

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