Ride4Gabe retweeted
Very proud of this story! Cross-country trip calls attention to huge price spike for muscular dystrophy drug #KCStar
kansascity.com/news/local/ar…
Cross-country trip calls attention to huge price spike for muscular dystrophy drug
Read more here: kansascity.com/news/local/ar…
Ride4Gabe retweeted
Entering the first night of RAAM! Brian's pedaling strong for @Ride4Gabe at #RAAM2017 ride4gabe.com/single-post/20… #H4G #Ride4Gabe
Hope for Gabe Foundation calls 11,599% Price Increase outrageous @RAAMraces #Ride4Gabe prn.to/2sXZsP2
Ride4Gabe retweeted
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.
Thank you @SpeakerRyan for supporting #CuresNow to end #raredisease nitter.gq/speakerryan/status/804…
With #CuresNow, fewer barriers will stand in the way of research and development. spkrryan.us/2gucQUF
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 We can't let an outdated approval process stand between him & a cure.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
Ride4Gabe retweeted
.@NIH advances knowledge of #rarediseases, as demonstrated by recent news. We support robust NIH funding ow.ly/Kuqb305gnku #CuresNow
Gabe tells a reporter why #CuresNow must pass #Congress- Unedited Uncut Interview - #Ride4Gabe to #EndDuchenne - m.youtube.com/watch?v=dlljHG…
Ride4Gabe retweeted
#TBT to this summer's @Ride4Gabe, a great example of hard work on the #Path2Cures. Read the @hope4gabe story here >> bit.ly/2bgU3Km
Ride4Gabe retweeted
Gabe, supporters hope drug approval opens more doors | Shelby County Reporter shar.es/1xtXKr #CuresNow #Path2Cures
Ride4Gabe retweeted
Here is why we need #CuresNow for the acceleration of follow-on treatments. #endDuchenne #historymade2day nitter.gq/abc3340/status/7780807…
"we started fighting immediately" Shelby Co. family now closer to Duchenne treatment abc3340.com/news/local/we-st…
Ride4Gabe retweeted
Meet Alexander-a great kid fighting Duchenne Muscular Dystrophy. Help by visiting walkingstrong.org/
Sarepta Drug Critic Departs FDA, Raising Hope for Approval - TheStreet - Linkis.com linkis.com/MNh8u
















