Jenica Leo (@JLLeo8) profile picture
Joined July 2012
Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)Photo by Jenica Leo (@JLLeo8)
Thank you to @RepAuchincloss for co-sponsoring the PASTEUR Act! We had a great meeting with Legislative Aide Hailey Reed, talking about the urgency of bacterial resistant antibiotics. #cfadvocacy @CFF_MassRI @CF_Foundation
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Jenica Leo retweeted
Until It’s Done — that means we celebrate this amazing news today, and we’re back to work tomorrow. Until everyone with #cysticfibrosis has a highly effective modulator. Until “CF” stands for “Cure Found.” #UntilItsDone #CFadvocacy
Today, the U.S. FDA approved the triple-combination modulator elexacaftor/ivacaftor/tezacaftor (Trikafta™) for people with #cysticfibrosis 12 years and older who have at least one F508del mutation. on.cff.org/31vq0a9
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Friends, for nearly 15 years you have been loving on our girl in so many ways ... you have joined us as walkers, cyclers, hikers, runners, prayers, concert-goers, and check writers. And… instagram.com/p/B35f2ItBdTnW…
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"We’ve always encouraged Ellie to dream big--college, career, family, travel, and more. With all the exciting advances that have resulted from so much research, we’re more confident than ever that Ellie will make her dreams a reality." -Jonathan Leo, parent to a child with CF
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Thank you so much to Nikki Hurt at the office of ⁦@SenMarkey⁩ for taking the time to talk with us about the specialized care and concerns patients with cystic fibrosis require and face every day! #CFadvocacy @CF_Foundation ⁦@CFF_MassRI⁩
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Thank you Drea Shropshire from the office ⁦⁦@RepMcGovern⁩ for taking the time to talk with us about the specialized care and concerns patients with cystic fibrosis require and face every day. #CFadvocacy ⁦@CF_Foundation⁩ ⁦@CFF_MassRI⁩
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Wonderful meeting with ⁦@RepJoeKennedy⁩ talking about the specialized care and concerns patients with cystic fibrosis require and face every day. #CFadvocacy ⁦@CF_Foundation⁩ ⁦@CFF_MassRI⁩
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Look for Ellie at the end telling part of this great story ... @CF_Foundation #CureCF #65Roses
The term #65Roses has been used by kids of all ages to describe #cysticfibrosis. But, making it easier to say doesn't make CF easier to live with. On 65 Roses Day, you can help change that by joining the 65 Roses Club. 🌹 on.cff.org/65RosesClub
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Ellie couldn’t stop talking about how sweet and adorable (and funny) all the kids were! 💜💜💜
Tomorrow is PURPLE DAY!! 💜 Today we got to meet ELLIE!!! We spent our gym class with her and even got her autograph!!! These firsties were SO excited! Thanks Ellie! #NPScelebrity #NPSpride #littleschoolbigheart
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I could not love our Norton schools more!! 💜💜💜
My students and I had the great honor of hanging out with Ellie this morning!! She was an amazing guest and she taught us so much! #cfawareness #littleschoolbigheart #purpleday2019 @catherineluke49 @jcteachfirsties @MrsLyonsNPS @FalveyFriends @JLLeo8 @JerushaBjork
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Thank you @TranslateBio for a wonderful lunch and for all you do for our community! #CureCF #cffmari
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Abby Leo and Billboard award winning artist, Krisanthi Pappas are hosting a concert to benefit cystic fibrosis research ... only 50 tickets left!
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"Yankee Stadium will shatter eardrums it'll be so loud."
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Jenica Leo retweeted
We're here for #Brocktober.
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Jenica Leo retweeted
CLINCHED ✔️✔️✔️
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ICYMI 👀
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It’s commonly understood by those who closely associate with me; that my inclination is leaning toward and to directly utilize methods such as this in my style of communication. “I do this” – at Braintree, MA
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Honored to be inducted into @Athletics Inaugural Hall of Fame Class with Rickey, Reggie, Rollie, Stew, Catfish and Charlie O.
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