Susan Schept

302 posts

Susan Schept

Susan Schept

@sschept1

Susan is a science writer and editor for the Cystic Fibrosis Foundation. My views are my own and do not reflect those of the Foundation.

Bethesda, MD Katılım Şubat 2016
185 Takip Edilen208 Takipçiler
Susan Schept
Susan Schept@sschept1·
Want to learn a new healthy recipe and spice up your meal rotation? Join us from 12-1 pm ET for a vegan cooking class where you will learn how to make a curry sweet potato stew. All proceeds benefit the Cystic Fibrosis Foundation: #IworkforCFF passion.cff.org/vegancookingcl…
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Susan Schept
Susan Schept@sschept1·
@repdonbeyer, as a constituent and someone deeply concerned for people with #cysticfibrosis, I’m calling on Congress to prioritize CF-related research and drug development by protecting the NIH and FDA. #CFadvocacy
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Susan Schept
Susan Schept@sschept1·
@markwarner, as a constituent and someone deeply concerned for people with #cysticfibrosis, I’m calling on Congress to prioritize CF-related research and drug development by protecting the NIH and FDA. #CFadvocacy
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Susan Schept
Susan Schept@sschept1·
@sentimkaine, as a constituent and someone deeply concerned for people with #cysticfibrosis, I’m calling on Congress to prioritize CF-related research and drug development by protecting the NIH and FDA. #CFadvocacy
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Susan Schept retweetledi
Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
Alyftrek, a new, once-a-day CFTR modulator for people with cystic fibrosis has been approved by the @US_FDA.
Cystic Fibrosis Foundation tweet media
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Susan Schept
Susan Schept@sschept1·
@NBCOlympics pls stop announcing results before you show the event!! Why watch if you already know what happens??
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Susan Schept
Susan Schept@sschept1·
May is Cystic Fibrosis Awareness Month! Did you know? There are approximately 1,000 new cases of cystic fibrosis diagnosed each year. #CFAwarenessMonth
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Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
We have invested more than $6.6 million in additional funding in Sionna Therapeutics to continue research into the development of potential new modulator therapies for people with #cysticfibrosis with an F508del mutation.
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Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
Phase 3 trial results were positive for the new vanzacaftor triple-combination modulator for people with CF, showing improvements in sweat chloride, though no improvement in lung function compared to Trikafta.
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Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
We’re investing up to $3M in ViaNautis, which is developing a non-viral mechanism that may address challenges in delivering a genetic therapy to the body. Genetic therapies have the potential to benefit all people with CF, regardless of their mutations. on.cff.org/46bPKcX
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Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
We are investing up to $9M in additional funds in Arcturus Therapeutics to test an mRNA therapy that could treat the underlying cause of #cysticfibrosis in all people with CF. An early-stage clinical trial in people with CF is planned for Q4 2023. on.cff.org/3RGghfb
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Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
The @US_FDA has approved Kalydeco for infants with cystic fibrosis ages 1-4 months who have certain mutations. Research indicates that early intervention with modulators can help slow or even prevent the irreversible progression of this disease. on.cff.org/3HE9AnO
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Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
The @US_FDA approved Trikafta for children with CF ages 2-5 years with at least one copy of the F508del mutation or one copy of certain mutations. With this approval, more than 900 children will have access to a CFTR modulator for the first time. cff.org/news/2023-04/t…
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Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
Thanks to advances in research and care, the proportion of adults with cystic fibrosis — at 62% — has surpassed that of children. While we’re encouraged by these trends, there is more to be done to meet the changing needs of the CF community.
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Ella Balasa
Ella Balasa@ellabalasa1·
A lively and thought provoking conversation about antimicrobial resistance on the @CDCFound’s Contagious Conversations podcast between myself, @DrJudyMonroe and @ThatMould. Thank you for inviting me as guest to share about the importance of spreading awareness!
CDC Foundation@CDCFound

Today: Join Dr. Meghan Perry, an infectious disease physician for @scotgovhealth & a senior clinical lecturer at @EdinburghUni, and @ellabalasa1, a patient advocate for cystic fibrosis, to discuss antimicrobial resistance on Contagious Conversations. cdcf.link/podcast

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Cystic Fibrosis Foundation
Cystic Fibrosis Foundation@CF_Foundation·
We’re excited to announce that we expanded our lab’s footprint, creating space for startup companies and industry scientists to work and learn alongside lab staff. By sharing our expertise, we will help speed up the development of new treatments. on.cff.org/3Fu4adj
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