Join us at the #CTRareDiseaseForum on March 17, 2026, at The Jackson Laboratory in Farmington! We’re excited to connect with peers to discuss collaboration, data, and innovation in rare disease research. See you there!
www.rareLifesolutions.com
#rareLifeSolutions #RareDisease #ForUsItsPersonal

We're grateful for our family, friends, and the rare disease community that inspires us every day. rareLife solutions wishes you a Thanksgiving full of comfort, joy, and meaningful moments.
#HappyThanksgiving #WeKnowRare #CareAboutRare #RareDiseaseAwareness #ForUsItsPersonal

August is #SMAAwarenessMonth. rareLife supports everyone affected by spinal muscular atrophy (SMA)—a rare genetic disease that causes progressive muscle weakness but not limits on potential. Together, we advance awareness, research, and hope.
#ForUsItsPersonal #CareAboutRare #rareLifesolutions

May is EDS & HSD Awareness Month. Often invisible, these conditions need greater recognition and care.
At rareLife solutions, we know rare—and for us, it’s personal.

#MakeMayMatter #EDSAwareness #HSDAwareness #rareLifeSolutions #RareDiseaseAwareness #WeKnowRare #ForUsItsPersonal #CareAboutRare

Contact me at lwuerth@rarelifesolutions.com to connect and learn how we can make a difference in the lysosomal disease community and explore innovative solutions in lysosomal disease publications and scientific communications.
#WORLDSymposia #LysosomalDisease #RareDiseaseAwareness #ForUsItsPersonal

It's #WorldAmyloidosisDay2025!
Amyloidosis stems from abnormal protein buildup that can cause organ failure, affecting the heart, kidneys, liver, spleen, & nervous system.
At rareLife, we bridge science & patient stories to drive better outcomes. contactus@rarelifesolutions.com
#ForUsItsPersonal

Attending #ISMPPAcademy 2025 in Boston?
Join Hugh Bartlett, CMPP, Senior Director, Solutions Development at rareLife on November 14 for “Pharma–Agency Partnerships: Evolving Roles, Shared Goals.”
Connect with Hugh via Whova to chat about #RareDisease innovation!
#WeKnowRare #ForUsItsPersonal

September 30 is #RareCancerDay! rareLife solutions is proud to stand with @NORD_rare and the Rare Cancer Coalition to raise awareness and support for those impacted by rare cancers. Join the zebra herd: https://bit.ly/RCD-23
#RareDiseaseAwareness #WeKnowRare #ForUsItsPersonal

Rare disease is complex—and so are the people living it. At rareLife, we combine scientific expertise with a deep understanding of patients, caregivers, and communities to build solutions that improve outcomes and access.
Learn more at www.rarelifesolutions.com
#TestimonialTuesday #ForUsItsPersonal

Wishing our clients, friends, and colleagues a joyful holiday season. We celebrate the patients, advocates, and caregivers who inspire our work and look forward to delivering innovative solutions that make a difference in the year ahead.
#HappyHolidays #WeKnowRare #CareAboutRare #ForUsItsPersonal

rareLife solutions is heading to WODC USA 2026.
Hugh Bartlett will be in Boston June 9-11 connecting with innovators advancing rare disease research, drug development, and patient access. We know rare. We think rare. Let’s connect.
#WODC2026 #RareDisease #OrphanDrugs #WeKnowRare #ForUsItsPersonal

Rare disease is complex—and so are the people living it. At rareLife, we combine scientific expertise with a deep understanding of patients, caregivers, and communities to build solutions that improve outcomes and access. Learn more at www.rarelifesolutions.com #TestimonialTuesday #ForUsItsPersonal

On International #MPSAwarenessDay, we stand with individuals affected by mucopolysaccharidoses (MPS) and mucolipidoses (ML), rare lysosomal storage disorders associated with progressive multisystem disease. Awareness drives earlier diagnosis, research, and action.
#MLAwareness #ForUsItsPersonal

Contact me at lwuerth@rarelifesolutions.com to connect and learn how we can make a difference in the lysosomal disease community and explore innovative solutions in lysosomal disease publications and scientific communications.
#WORLDSymposia #LysosomalDisease #RareDiseaseAwareness #ForUsItsPersonal

Contact me at lwuerth@rarelifesolutions.com to connect and learn how we can make a difference in the lysosomal disease community and explore innovative solutions in lysosomal disease publications and scientific communications.
#WORLDSymposia #LysosomalDisease #RareDiseaseAwareness #ForUsItsPersonal

Contact me at lwuerth@rarelifesolutions.com to connect and learn how we can make a difference in the lysosomal disease community and explore innovative solutions in lysosomal disease publications and scientific communications.
#WORLDSymposia #LysosomalDisease #RareDiseaseAwareness #ForUsItsPersonal

August is SMA Awareness Month—a time to spotlight the strength, needs, and voices of the SMA community.
Learn how you can get involved or attend an event: https://loom.ly/-gGpEJs
Let’s raise awareness, amplify stories, and stand together.
#SMAawarenessmonth #WeKnowRare #ForUsItsPersonal