Introducing mApIt, the AI-Powered Strategic Medical Publications Insights Tool from rareLife solutions. Transform months of publication landscape research into minutes to develop actionable insights and build smarter, market-responsive publication strategies.
#mApIt #rareLifeSolutions #WeKnowRare

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

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

Great science deserves great storytelling. At rareLife, we design strategic, rare-customized slide decks that turn complex data into clear, compelling narratives. Because for us, it’s personal.
Learn more: www.rarelifesolutions.com
#MedicalAffairs #RareDisease #WeKnowRare #MedPubs #SciComms

Medical affairs success starts with strategy. rareLife brings expertise in rare diseases and proven experience facilitating strategic workshops that move ideas into action. Let’s partner to shape what’s next.
Learn more: contactus@rarelifesolutions.com
#WeKnowRare #MedPubs #SciComms

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

Today is #WorldHPPDay!
#Hypophosphatasia is a rare genetic disorder that weakens bones and teeth, leading to deformities, fractures, premature tooth loss, and pain.
At rareLife, we bridge science and patient stories to drive better outcomes.
Learn more: www.rarelifesolutions.com
#WeKnowRare

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

Today, on #InternationalZebraDay, we stand with the rare-disease community—patients, families, caregivers, and advocates whose resilience inspires everything we do. Every zebra has a unique pattern. Every rare-disease story deserves to be seen, heard, and understood. #RareDisease #WeKnowRare

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

On #WorldSanfilippoDay we honor those affected by Sanfilippo syndrome—a rare disease known as childhood Alzheimer’s where a genetic defect leads to buildup of toxins in the brain & early death. rareLife is dedicated to advancing treatments & improving outcomes for the rare community.
#WeKnowRare

Meet Michele Kinrade, Senior Medical Writer at rareLife solutions.
Her rare superpower is purpose-driven passion, inspired by her daughter’s rare disease journey. She keeps teams focused on patient-centered priorities, bringing empathy and purpose to every project.
#rareLifeTeamSpotlight #WeKnowRare

May is Prader-Willi Syndrome (PWS) Awareness Month. PWS is a rare genetic disorder marked by hyperphagia and complex developmental and hormonal challenges. At rareLife, we know that behind every diagnosis is a community driving change.

#PraderWilliSyndrome #PWSAwareness #RareDisease #WeKnowRare

We think rare. We live rare. We are rare med comms.
With expertise across 65+ rare & oncology indications, we unite strategy, science & storytelling to improve drug development—for industry & families.
We’re creatives, caregivers, scientists & patients—connected by purpose.
#WeKnowRare #MedCommsDay

Today we celebrate #MedComms Day and the power of medical communications to advance science and amplify rare disease voices.
At rareLife solutions, we know rare. We think rare. And we are proud to help turn complex science into meaningful impact.
#MedComms #RareDisease #WeKnowRare #ISMPP #rareLife

rareLife solutions is heading to ISPOR 2026. Laura will be onsite Mon, 5/18, and Tues, 5/19, connecting with innovators advancing evidence, access, and patient-centered research in rare disease. At rareLife, we know rare. We think rare. Let’s connect.
#ISPOR2026 #HEOR #rareLifesolutions #WeKnowRare

At rareLife solutions, we are proud to stand with patients, families, and caregivers worldwide—putting patients at the center of everything we do as we advance rare disease research and support access to innovative treatments. #RareDiseaseDay #ShowYourStripes #WeKnowRare #RareDisease #RareIsPersonal

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