Amanda Dillard(@AmandaDGNN) 's Twitter Profile Photo

US overdose deaths decline slightly in 2023, CDC reports nessMonth nessWeek [Video] The CDC released data indicating a modest decrease in fatal overdoses in the… dlvr.it/T6xfNq

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Behind the Mystery(@btmcaresforrare) 's Twitter Profile Photo

April is month, a feeling that does not go unnoticed in the Community , where waiting for answers, uncertainties, and feeling invisible is common.

We see your strength and advocate for the battles unseen. 💙

April is #StressAwareness month, a feeling that does not go unnoticed in the #RareDiseaseCommunity, where waiting for answers, uncertainties, and feeling invisible is common.

We see your strength and advocate for the battles unseen. 💙 

#BehindTheMystery #RareDisease
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Adriana Simpson(@AdrianaSGNN) 's Twitter Profile Photo

Rebecca Alexander Recalls Progressive Vision and Hearing Loss Since Age 12 [Video] Rebecca Alexander New York City-based psychotherapist and sister of Weekend Today co-host… dlvr.it/T6zxzZ

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Behind the Mystery(@btmcaresforrare) 's Twitter Profile Photo

During , we highlight the importance of mental health within the .🧠 🧬

Refer to our guide, 'Navigating Your Rare Disease,' for psychological support, stress management, and more

Link in our bio. 🔗

During #BrainAwarenessWeek, we highlight the importance of mental health within the #rarediseasecommunity.🧠 🧬

Refer to our guide, 'Navigating Your Rare Disease,' for psychological support, stress management, and more

Link in our bio. 🔗

#BehindTheMystery #RareDisease
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Behind the Mystery(@btmcaresforrare) 's Twitter Profile Photo

Additional testing is often necessary, as many rare disease symptoms may not be revealed in a standard blood test.
To all the rare disease warriors undergoing testing: Share your advice in the comments below. 💪💙

Additional testing is often necessary, as many rare disease symptoms may not be revealed in a standard blood test. 
To all the rare disease warriors undergoing testing: Share your advice in the comments below. 💪💙 
#BehindTheMystery #RareDiseaseWarriors #RareDiseaseCommunity
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Adriana Simpson(@AdrianaSGNN) 's Twitter Profile Photo

Louisiana Teen Diagnosed with Rare Cancer in His Testicle [Video] When Ronal Salvador found a lump on his testicle at age 17, he knew something was wrong. He was diagnosed with a rare form… dlvr.it/T70D1m

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Behind the Mystery(@btmcaresforrare) 's Twitter Profile Photo

: 95% of rare diseases lack FDA-approved treatment.
400 million affected by rare diseases, yet gaining treatment approval proves exceptionally challenging.
Together as a Community , we can make a difference! 💙

#RareFactFriday: 95% of rare diseases lack FDA-approved treatment.
400 million affected by rare diseases, yet gaining treatment approval proves exceptionally challenging.
Together as a #RareDiseaseCommunity, we can make a difference! 💙
#BehindTheMystery #FDAapproval #RareDisease
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Behind the Mystery(@btmcaresforrare) 's Twitter Profile Photo

This holiday season, we appreciate your invaluable support for the rare disease community. Here's to a bright year ahead, filled with ongoing collaboration, good health, and shared triumphs. 💙 🦓 🎄

This holiday season, we appreciate your invaluable support for the rare disease community. Here's to a bright year ahead, filled with ongoing collaboration, good health, and shared triumphs.  💙 🦓  🎄
#BehindTheMystery #RareDiseaseCommunity #RareDiseaseAwareness #MerryChristmas
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Behind the Mystery(@btmcaresforrare) 's Twitter Profile Photo

Here's to a bright year ahead and a continued mission of going behind the mystery, sharing inspiring stories, and expanding our rare community. 💙 🦓

Awareness Community

Here's to a bright year ahead and a continued mission of going behind the mystery, sharing inspiring stories, and expanding our rare community. 💙 🦓 

#BehindTheMystery #YearInReview #RareDisease #RareDiseaseAwareness #RareDiseaseCommunity
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Rare Disease Clinical Trial Network, Ireland(@rare_trial) 's Twitter Profile Photo

👥 Today, we're amplifying the voices of those often unheard in research.📷 Meet Jackie, a powerful host for ! He speaks from his journey with his son, who has Arthrogryposis Multiplex Congenita (AMC).

👥 Today, we're amplifying the voices of those often unheard in research.📷 Meet Jackie, a powerful host for #TakeoverTuesday! He speaks from his journey with his son, who has Arthrogryposis Multiplex Congenita (AMC). #ICTD #RareDiseaseCommunity
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