A New Hope for Treatment-Resistant Multiple Myeloma: CellCentric Advances InoPd into Pivotal Clinical Testing
- April 7, 2026
Gilead Ends Midstage HIV Study as FDA Clinical Hold Continues
Can We Fix This Broken Heart? – Part 1
Draft Guidance from FDA Introduces Important Changes to Drug Development for Rare Diseases
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Bohring-Optiz Syndrome (BOS) is a rare genetic disorder that impacts growth and development, often associated with feeding difficulties, developmental delays, and distinct physical characteristics. While uncommon, it has a profound impact on individuals and families within the BOS community.
Observed annually on April 6th, Bohring-Optiz Syndrome Awareness Day is dedicated to increasing understanding, supporting affected families, and advancing research. By raising awareness, we help foster greater recognition, compassion, and process toward improved care and outcomes.
Share your rare disease journey and inspire others here: bit.ly/4dV7gru
#bohring-OptizSyndrome #BOSAwarenessDay #PatientWorthy
Throughout the week, Patient Worthy is highlighting HIV with educational content aimed at raising awareness and fostering greater understanding in our community.
We’ll be sharing information on our socials and patientworthy.com to educate, empower, and support those affected.
If you'd like to share your story with HIV, click here: bit.ly/4dV7gru
#HumanImmunodeficiencyVirus #HIV #HIVAwareness #ShareYourStory #PatientWorthy
April 5th is Barth Syndrome Awareness Day - a time to shine a light on a rare genetic condition that affects the heart, muscles, and immune system. Barth Syndrome may be a little known, but for those living with it, the challenges are very real. Raising Awareness helps drive research, early diagnosis, and support for families who need it most.
Every voice matters. By learning, sharing, and advocating, we can help create a future where rare diseases like this are better understood and treated. #barthsyndromeawareness #geneticdisorders #PatientWorthy
