Ride4Gabe (@Ride4Gabe) header
Ride4Gabe (@Ride4Gabe) profile picture
Birmingham, Alabama
Joined April 2014
Photo by Ride4Gabe (@Ride4Gabe)Photo by Ride4Gabe (@Ride4Gabe)Photo by Ride4Gabe (@Ride4Gabe)Photo by Ride4Gabe (@Ride4Gabe)Photo by Ride4Gabe (@Ride4Gabe)Photo by Ride4Gabe (@Ride4Gabe)Photo by Ride4Gabe (@Ride4Gabe)Photo by Ride4Gabe (@Ride4Gabe)
Very proud of this story! Cross-country trip calls attention to huge price spike for muscular dystrophy drug #KCStar kansascity.com/news/local/ar…
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Cross-country trip calls attention to huge price spike for muscular dystrophy drug Read more here: kansascity.com/news/local/ar…
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Entering the first night of RAAM! Brian's pedaling strong for @Ride4Gabe at #RAAM2017 ride4gabe.com/single-post/20… #H4G #Ride4Gabe
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Hope for Gabe Foundation calls 11,599% Price Increase outrageous @RAAMraces #Ride4Gabe prn.to/2sXZsP2
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A win for #raredisease patients--> #CuresNow passed the House by a vote of 392-26! The Senate is expected to take up this version next week.
With #CuresNow, fewer barriers will stand in the way of research and development. spkrryan.us/2gucQUF
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Thank you @RepByrne u have been a hero for the #raredisease community. #AlabamaProud #voteyes nitter.gq/repbyrne/status/804078…
I've enjoyed getting to know Gabe and his family. We can't let an outdated approval process stand between him & a cure. #CuresNow
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In the coming days, the #Senate will consider the bipartisan 21st Century Cures, as well as a CR to keep the government funded. #CuresNow
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.@NIH advances knowledge of #rarediseases, as demonstrated by recent news. We support robust NIH funding ow.ly/Kuqb305gnku #CuresNow
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Gabe tells a reporter why #CuresNow must pass #Congress- Unedited Uncut Interview - #Ride4Gabe to #EndDuchenne - m.youtube.com/watch?v=dlljHG…
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#TBT to this summer's @Ride4Gabe, a great example of hard work on the #Path2Cures. Read the @hope4gabe story here >> bit.ly/2bgU3Km
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Gabe, supporters hope drug approval opens more doors | Shelby County Reporter shar.es/1xtXKr #CuresNow #Path2Cures
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Good things happening for one Shelby Co. family. @abc3340
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Meet Alexander-a great kid fighting Duchenne Muscular Dystrophy. Help by visiting walkingstrong.org/
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Sarepta Drug Critic Departs FDA, Raising Hope for Approval - TheStreet - Linkis.com linkis.com/MNh8u
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