Top Tweets for #FastForwardForRARE
Our hearts are warmed by this @people article featuring the Ouimet family. It was an honor to help this family of incredible advocates share their story during #FastForwardforRare. Read about their generosity in helping others with #primaryhyperoxaluria: https://t.co/cGoRpOJnvK
Tomorrow! Join the #FastForwardForRARE Practice Your Pitch webinar in partnership with @SmithSolve
Receive tips to share your story & leave with the confidence to advance legislation during #RareDC2021 https://t.co/fPo1amH8nx
Thank you to our sponsor @IpsenUS for their support!
If you are registered for #RareDC2021, join the #FastForwardForRARE Practice Your Pitch webinar on July 8, hosted by the RDLA in partnership with @SmithSolve. Receive tips to share your story & leave with the confidence to advance legislation. https://t.co/fPo1amYJf5
We just had a great. @RareAdvocates @SmithSolve #fastforwardforrare practice your pitch webinar for #rareacrossamerica2021 The #raredisease community is awesome and just so kind and forthcoming! Thank you to everyone who attended and shared your story! #rarediseaseweek
Thanks @rareadvocates sign up #fastforwardforrare webinar to learn how to best share your story and legislative ask to your congressmen and senators! #rareacrossamerica2021 @SmithSolve
Meet @SwapnaSpeaks a #RareAcrossAmerica2021 Advocate and one of our coaches who will help you share your story with legislators.
Sign up for the #FastForwardforRare webinar on Feb. 24th to receive personalized coaching! https://t.co/prcA6Upqrg @SmithSolve
Meet @SwapnaSpeaks a #RareAcrossAmerica2021 Advocate and one of our coaches who will help you share your story with legislators.
Sign up for the #FastForwardforRare webinar on Feb. 24th to receive personalized coaching! https://t.co/prcA6Upqrg @SmithSolve
#ICYMI, last week #FastForwardforRARE coaches from SmithSolve and @RareAdvocates led a virtual workshop to help #raredisease advocates share their stories during #RareAcrossAmerica.
To learn more about how you can participate in events like this, visit https://t.co/cW59WSPEso.
That's a wrap!
Today, #RareAcrossAmerica advocates geared up for their meetings with Members of Congress by practicing their pitches! @SmithSolve #FastForwardforRare
(To participate in the webinar, first make sure you register for Rare Across America, then register for the webinar).
To register for #RareAcrossAmerica visit: https://t.co/k8XS9vNgZ7
To register for the #FastForwardforRARE webinar visit: https://t.co/s2MpOvKtS2
Tomorrow is the last day to register for RARE Across America! When you do, you can enroll in the #FastForwardforRARE webinar on July 23 at 3:00 pm ET. You'll receive tips and coaching from @SmithSolve and @RareAdvocates to help you impactfully share your story and inspire action.
Tomorrow is the last day to register for #RareAcrossAmerica You can enroll in the #FastForwardforRARE webinar to receive tips and coaching from the @SmithSolve and #RDLA teams to help you share your story with Members of Congress. https://t.co/kiS8VSziuK
Tomorrow is the last day to register for RARE Across America! When you do, you can enroll in the #FastForwardforRARE webinar on July 23 at 3:00 pm ET. You'll receive tips and coaching from @SmithSolve and @RareAdvocates to help you impactfully share your story and inspire action.
Are you a #rare advocate interested in sharing your story? Register for Rare Across America and the #FastForwardforRARE webinar on Tues., July 21. You’ll receive tips and coaching to help you share your story with members of Congress and inspire action. https://t.co/8CzBBAdonL
Interested? Register for Rare Across America to enroll in the #FastForwardforRARE webinar on Tuesday, July 21, 2020 at 3:00 pm and learn how to share an impactful story with Members of Congress.
As the world pauses for #COVID19, it's more important than ever to raise awareness and push for new legislation and continued investment in #RareDisease research. Check out our new blog post as we reflect back on Rare Disease Week with #FastForwardforRARE. https://t.co/nqrN7jpEbK
#RareDisease @RareAdvocates: '1/2 Are you a #RareDisease advocate interested in sharing your story? Register for Rare Across America to enroll in the #FastForwardforRARE webinar on Tuesday, July 21, 2020 at 3:00 p.m. ET…, see more https://t.co/Mmf1eHDOeE
2/2 (To participate in the webinar, first make sure you register for Rare Across America, then register for the webinar).
To register for #RareAcrossAmerica visit: https://t.co/k8XS9vNgZ7
To register for the #FastForwardforRARE webinar visit: https://t.co/s2MpOvKtS2
1/2 Are you a #RareDisease advocate interested in sharing your story? Register for Rare Across America to enroll in the #FastForwardforRARE webinar on Tuesday, July 21, 2020 at 3:00 p.m. ET.
We're very excited to be partnering with @SmithSolve for #FastForwardforRARE Make sure you visit https://t.co/DVoeKZw6iR 👇
@SmithSolve and @RareAdvocates are proud to announce the launch of the #FastForwardforRARE website! Listen to advocates share their powerful stories and join the movement by visiting https://t.co/TLnIeHZ4jg. #RareDisease
@SmithSolve and @RareAdvocates are proud to announce the launch of the #FastForwardforRARE website! Listen to advocates share their powerful stories and join the movement by visiting https://t.co/TLnIeHZ4jg. #RareDisease
Thank you to everyone who visited #FastForwardforRARE during #RareDC2020! We were honored to help so many of you hone your storytelling skills to inspire legislators to take action and make a difference for families living with #RareDiseases!
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