9p Minus Network retweeted
Congress is currently debating a vital piece of legislatioN: the 21st Century Cures Act #CuresNOW globalgenes.org/raredaily/ev… @EveryLifeOrg
@Jill_the_Pill , spread the word!!! teapaw.org/RareDiseases/status/77…
6 #researchgrants are available for the study of #rarediseases. Retweet. Spread the word. bit.ly/2bJRdi9
9p Minus Network retweeted
Social media has really changed how we connect with families with rare and genetic conditions
huffingtonpost.com/rachel-en… – at Sydney, New South Wales
9p Minus Network retweeted
10 people talk about what it’s actually like living with illness and disability bzfd.it/1NpNBS5
9p Minus Network retweeted
In honor of friends & family living w/autism. thewhatevermom.com/2016/04/0… #WorldAutismAwarenessDay #autismawareness
9p Minus Network retweeted
29 February: A rare day for Rare Disease Day. Join us in making the voice of rare diseases heard today! thndr.me/QxLkNL
9p Minus Network retweeted
.@IAmLaurenMiller says caregiving is much more than a 40 hr./wk job. It's 24/7. wb.md/1S6H52Q #EndAlz
amp.twimg.com/v/31ba752c-d9f…
9p Minus Network retweeted
Chat with the experts on rare diseases today at 2:00 pm ET using #NIHChat!
9p Minus Network retweeted
Women&girls with #disability must have equal participation in leadership & employment. More: owl.li/YrDF2





























