lmperkins

Founder of CSO Emerita LLC. Board Member, Foundation for Sarcoidosis Research. Chief Science Officer Emerita, Melanoma Research Alliance.

[lmperkins @lmperkins]

@jkyllhyde @jamiearnoldWMBF @wmbfnews

[Mehdi Mirsaeidi @mmirsae]

Always a pleasure meeting my friends from @StopSarcoidosis! I truly admire and support all the great work they're doing for the sarcoidosis community. @ATS_Assemblies @atscommunity @TrichaShivas

[FSR @StopSarcoidosis]

As we pass the halfway mark of Sarcoidosis Awareness Month on Day 20, let's reflect on the progress we've made and the work that still lies ahead. Together, we can create positive change.
https://t.co/ePjGq4NXGG
#Sarcoidosis #SaySarcoidosis #StopSarcoidosis #PostinPurple

[JDL8 @JL8jdl]

#SarcoidosisAwarenessMonth #purplepower believe in ourselves despite the stumbling blocks in our way.Focus on the positive aspects.Appreciate what you have and don’t be afraid to ask for help @BrenDee85
@SarcoidosisofLI
@chastasfight @StopSarcoidosis @Sarcoid_Network @duffynyc

[FSR @StopSarcoidosis]

Join us as we lace up for a cause! This year, we're offering five slots for dedicated runners to join Team Rally for Sarcoidosis. Raise $3,500+ to make an impact and be part of our exclusive team!
Applications close April 15, 2024 #RallyForSarc #TCSNYCMarathon

[FSR @StopSarcoidosis]

Studies estimate that around 90% of patients with sarcoidosis experience lung involvement. Early detection & management are crucial for improving outcomes. Let's raise awareness to ensure timely diagnosis and treatment. #Sarcoidosis #SaySarcoidosis #StopSarcoidosis #PostinPurple

[FSR @StopSarcoidosis]

📅 Save the Dates for Sarcoidosis Awareness Month Events!
Check the website for updated events or additions: https://t.co/BhxFZkBQVw
Join us for a month filled with learning, connecting, and raising awareness of sarcoidosis! 🌟
#SaySarcoidosis #StopSarcoidosis #PostinPurple

[FSR @StopSarcoidosis]

Connecting with others who understand the challenges of living with sarcoidosis can provide invaluable support, guidance, and encouragement. Find Support: https://t.co/9lNqRds5CN #SarcoidosisAwareness #Day10 #SaySarcoidosis #StopSarcoidosis #PostinPurple

[FSR @StopSarcoidosis]

Knowledge is power! Throughout April, we'll be sharing facts and information about sarcoidosis to help raise awareness and support those living with this condition. #SaySarcoidosis #StopSarcoidosis #PostinPurple #SarcoidosisAwareness #KnowSarcoidosis

[FSR @StopSarcoidosis]

It's April 1st, and you know what that means - Sarcoidosis Awareness Month is officially here! Let's kick things off by saying Sarcoidosis loud and proud. Sarcoidosis: pronounced Sar-Coy-Doe-Sis. #SarcoidosisAwarenessMonth #SaySarcoidosis #StopSarcoidosis #SarcoidosisAwareness

[FSR @StopSarcoidosis]

It's Sarcoidosis Awareness Month!
While Sarcoidosis (SAR-COY-DOE-SIS) may be difficult to pronounce, living with it presents even greater challenges. “Say Sarcoidosis” reminds us of the importance of speaking up about this often-misunderstood condition.
https://t.co/5F5srNZy8g

[lmperkins @lmperkins]

@TheGoldenRatio4 The artwork I got from DALL-E of an english cream golden stealing toilet paper

[FSR @StopSarcoidosis]

What an incredible weekend. Started our morning hearing Dr. Dan Culver from the Cleveland Clinic, Founding Member of the FSR Global Sarcoidosis Clinic Alliance, an extraordinary opportunity and experience to hear from him on sarcoidosis manifestations. #LeadingtheWay #FSRGSCA

[FSR @StopSarcoidosis]

Today, Feb 29th, marks Rare Disease Day, a rare event on this leap year! 🦓 Let's unite to raise awareness for diseases like Sarcoidosis. 💜 Our FSR staff proudly show their stripes! #RareDiseaseDay #ShowYourStripes #SarcoidosisAwareness

[Melanoma Institute Australia @MelanomaAus]

"Massive congratulations to @ProfGLongMIA & @ProfRScolyerMIA on being named 2024 Australians of the Year. Your tireless work & this incredible national accolade will benefit all melanoma patients & the melanoma community immensely. Enjoy celebrating with your families.” MIA CEO Matthew Browne

[FSR @StopSarcoidosis]

FSR is proud to partner with @OSUWexMed for the 3rd Annual Cardiac Sarcoidosis Symposium on Feb 23, 2024. Register now to earn 3.75 AMA/PRA Category 1 CME Credits TM. Register here: https://t.co/HcqgT5cPzX

#sarcoidosis #sarctwitter #cardiac

[FSR @StopSarcoidosis]

We are thrilled to have FSR CEO, Mary McGowan present at the upcoming Rare Disease Summit 2024! Unite with the #raredisease community to create powerful partnerships, advance orphan therapeutics and deliver life-changing breakthroughs. Register: https://t.co/vzFIB4Y1J3

[FSR @StopSarcoidosis]

THANK YOU for OVER $95,000+ raised to support more research and patient support efforts in 2024!💜Together, we are making a difference, and together, we are building towards a future with better treatments, more patient support, and a cure for #sarcoidosis.

[FSR @StopSarcoidosis]

Thanks to your dedication, thousands worldwide have received education and support, propelling us closer to better treatments and a cure for #sarcoidosis. Our FINAL Year-End Match starts now through 12.31.23 ! Your support creates meaningful change: https://t.co/RuCr3wWXqP

[Sarcoidosis News @SarcoidosisNews]

The Foundation for Sarcoidosis Research granted $50,000 each for two U.S.-based projects into cardiac sarcoidosis, which affects the heart. https://t.co/W4wOaIJakJ