Top Tweets for #IgnoreNoMoreACTNow
It's the LAST CHANCE to take help us close the gap and take the ACTe Now! patient survey for Black Americans with #sarcoidosis: https://t.co/zsAax7yNhm
#IgnoreNoMoreACTNow #RepresentationMatters #Equity #RareDisease #clinicaltrial
#BlackAmericans are 2.5x more likely to have #sarcoidosis than White Americans & have a mortality rate 12x higher. Help us close the gap. ACTe Now by taking this patient survey https://t.co/JE579tz0qB #IgnoreNoMoreACTNow #ClinicalTrials #Research #Equity #RareDisease #BlackHealth
To close the gap, we must increase representation of #BlackAmericans in #clinicaltrials & #research. The time to ACTe is Now! Learn about your options & how you can help improve care for #sarcoidosis patients. Step 1: Take the survey: https://t.co/zsAax7zl6U
#IgnoreNoMoreACTNow
.@LivProof is proud to partner with @StopSarcoidosis for the #IgnoreNoMoreACTNow Campaign to Advance Clinical Trials for #Equity in #Sarcoidosis.
Learn how you can support and share your stories here https://t.co/WfUOKr4Bc3
#RepresentationMatters #RareDisease
I am proud to support @stopsarcoidosis for the #IgnoreNoMoreACTNow Campaign to Advance Clinical Trials for #Equity in #Sarcoidosis. Click to learn more https://t.co/H74nxbdz2c #ClinicalTrials #Research #RepresentationMatters #RareDisease
https://t.co/wPoTkQ2XD5
How much do you know about #clinicaltrials? There are more #sarcoidosis trials than ever before, so the time to LEARN is now. Share your experience and knowledge by taking this survey. https://t.co/40hhx8bTOy #IgnoreNoMoreACTNow #RepresentationMatters #Equity #RareDisease
Join @Stopsarcoidosis's #IgnoreNoMoreACTNow campaign to help increase representation of Black #sarcoidosis patients in #clinicaltrials. Complete the #patient survey before 11/30! Learn more: https://t.co/ztxeh0cNrI
Join @Stopsarcoidosis's #IgnoreNoMoreACTNow campaign to help increase representation of Black #sarcoidosis patients in #clinicaltrials. Complete the #patient survey before 11/30! Learn more: https://t.co/ztxeh0cNrI
#BlackAmericans are 2.5x more likely to have #sarcoidosis than White Americans & have a mortality rate 12x higher. Help us close the gap by taking this patient survey: https://t.co/zsAax7yNhm
#IgnoreNoMoreACTNow #ClinicalTrials #Research #Equity #RareDisease #BlackHealth
Increasing representation of #BlackAmericans in #clinicaltrials & #research will lead to more effective treatments & equitable outcomes for all #sarcoidosis patients. Take the patient survey: https://t.co/zsAax7zl6U
#IgnoreNoMoreACTNow #Equity #RareDisease
Increasing representation of #BlackAmericans in #clinicaltrials & #research will lead to more effective treatments and equitable outcomes for all #sarcoidosis patients. Take the first step. Complete FSR’s survey. https://t.co/19hlVAOdFf #IgnoreNoMoreACTNow #Equity #RareDisease
How much do you know about #clinicaltrials? There are more #sarcoidosis trials than ever before, so the time to LEARN is now. Share your experience and knowledge by taking this survey. https://t.co/40hhx8bTOy #IgnoreNoMoreACTNow #RepresentationMatters #Equity #RareDisease
Mary McGowan, FSR CEO discusses Five Things We Must Do to Improve the US Healthcare System, physician shortages, and how she
got involved with the sarcoidosis community.
Read now: https://t.co/ZB2Cl2eBA9
#sarcoidosis #raredisease #actnow #ignorenomoreactnow #healthdisparities
Black Americans are 2.5x more likely to have #sarcoidosis than White Americans and have a mortality rate 12x higher. Help us close the gap. ACTe Now! Take the patient survey: https://t.co/zsAax7yNhm
#IgnoreNoMoreACTNow #RepresentationMatters #Equity #RareDisease #clinicaltrial
Increasing representation of #BlackAmericans in #clinicaltrials & research will lead to more effective treatments & equitable outcomes for all #sarcoidosis patients. Share your stories via FSR’s survey. https://t.co/eepoecUFkl @StopSarcoidosis
#IgnoreNoMoreACTNow #RareDisease
We are proud to partner with @StopSarcoidosis the #IgnoreNoMoreACTNow Campaign to Advance Clinical Trials for #Equity in #Sarcoidosis. Learn how you can support and share your experience here https://t.co/60j3Gl7Sn7 #ClinicalTrials #Research #RepresentationMatters #RareDisease
How much do you know about clinical trials? There are more #sarcoidosis trials than ever before, so the time to LEARN is now.
Share your experience and knowledge by taking this survey: https://t.co/zsAax7yNhm
#IgnoreNoMoreACTNow #RepresentationMatters #Equity #sarctwitter
Increasing representation of #BlackAmericans in #clinicaltrials & #research will lead to more effective treatments and equitable outcomes for all #sarcoidosis patients. Take the first step. Complete FSR’s survey. https://t.co/U0G46zbta7 #IgnoreNoMoreACTNow #Equity #RareDisease
How much do you know about #clinicaltrials? There are more #sarcoidosis trials than ever before, so the time to LEARN is now. Share your experience and knowledge by taking this survey. https://t.co/40hhx8blZ0 #IgnoreNoMoreACTNow #RepresentationMatters #Equity #RareDisease
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