For the first time in more than a decade, new NTM treatment guidelines have been published. These guidelines were issued by
@atscommunity
@EuroRespSoc
@ESCMID
&
@IDSAInfo
to improve patient care and health outcomes.
We are thrilled to sponsor the
@GlobalGenes
RARE Patient Advocacy Summit; the largest gathering of
#raredisease
stakeholders in the world. We value the opportunity to engage with the community and are excited for what’s in store over the next few days!
#2019GGSUMMIT
Today we celebrate
#InsmedDay
! Each year on this date we reflect on our commitment to the
#NewJersey
biopharmaceutical community and celebrate our wonderful team with a well-deserved day off work.
Today marks the first annual
#WorldBronchiectasisDay
. We're proud to work alongside the global lung health community to support patients around the world. You can learn more about this day and access bronchiectasis resources here:
Today marks
#WorldLungDay
. We're proud to work alongside the global lung health community to support patients around the world. You can learn more about our work here:
Thank you,
@S2S_Org
, for your dedication to developing inclusive and diverse workplaces. Earlier this
#BlackHistoryMonth
, we launched our new employee resource group, BEING (Black Employees at Insmed Networking Group), as part of our commitment to prioritizing DE&I efforts.
As we celebrate
#BlackHistoryMonth
, we want to highlight the recent launch of BEING - Black Employees of Insmed Networking Group. We look forward to seeing the important work they will do in advancing Diversity & Inclusion efforts
@Insmed
and in the biopharmaceutical industry!
Bronchiectasis is a lung disease that can be triggered by a variety of conditions including autoimmune disease,
#COPD
, and even Crohn’s disease. Follow
@LungAssociation
to stay up to date on lung disease facts and resources.
“It can also be quite shocking to have a diagnosis of a condition you have never heard of or have little information about.” This article by
@MagdaIbrahim
on
#raredisease
is a must read for everyone!
This year, in honor of
#RareDiseaseDay
, we are showing how we’re
#ReframingRare
. Watch as Jessica from our research department describes how she is changing the status quo for the
#raredisease
community.
November is Chronic Obstructive Pulmonary Disease (COPD) Awareness Month. Did you know that people with COPD are 16 times more likely to get NTM lung disease? Learn more: .
#LaceUpforLungs
#COPDAwarenessMonth
This
#NewYearsDay
, we look forward to another year of continuing our mission to transform the lives of patients living with serious and
#rarediseases
.
Did you know that approximately 50% of people with
#bronchiectasis
may also have
#NTM
lung disease and not even know it? Learn the signs of NTM and speak with your doctor about getting tested if you are experiencing symptoms.
We know that living with a
#raredisease
can often mean spending considerable time at doctors’ offices. That’s why we are grateful for the part that Health Centers play in providing support to patients. Learn more about
#NHCW21
: .
#ValueCHCs
Our Global Day of Good activities are underway! As part of one of our New Jersey projects, employees are volunteering at Bound Brook High School, leading career readiness workshops and site beautification projects.
#CountUsIn
Thank you
@BioNJ_Org
for inviting our CMO, Martina Flammer, to participate in today’s Rapid Fire Research Showcase. We’re proud to be contributing to new research in the fight against COVID-19.
We are working hard to develop scientific
#innovations
as we strive to serve overlooked, underserved, and difficult-to-treat conditions, such as non-CF
#bronchiectasis
.
Find out more about what’s in store at Insmed:
It’s that time of year again! The month of February means dedicated time to celebrate the rare disease community. Although this year our activities will be virtual, we have no doubt that this
@rarediseaseday
will be a meaningful one for our community.
#ShowYourColors
Do you have
#NTMlungdisease
? Rare diseases can often contribute to feelings of loneliness and isolation – check out these resources to stay
#connected
with others:
Earlier this year we had the pleasure of welcoming Amy Leitman, Director of Policy & Research
@NTMinfo
to our Insmed Knowledge Now Sessions. She discussed the work the organization is doing in support of patients with
#NTMlungdisease
.
#TBT
It was a pleasure speaking yesterday at the Insmed Knowledge Now Sessions. Our Director of Policy and Research Amy Leitman discussed the work we are doing in support of patients with
#NTM
#lungdisease
. Thank you for having us, Insmed!
We are thrilled to share that Insmed has been named the top company to work for in
@ScienceMagazine
’s 2021 Top Employers Survey! Thank you to all our employees for your passion and commitment to those we serve.
#PoweredByPurpose
#Rarediseases
are more common than you may think–they impact over 300 million people globally and deserve to have a platform in the public health conversation.
#NationalPublicHealthWeek
Tonight, we’re kicking off
#ATS2022
with a team dinner. I’m excited to be with our global colleagues as we get ready to engage with the respiratory community. – DW
Every day, our team members are driven by their dedication to the
#RareDisease
community. This year, we are proud to stand with the
#RareDiseaseDay
message: “Rare is many, rare is strong, rare is proud.”
#ReframeRare
#Insmed
We’re honored to be a finalist for the
#ScripAwards
2019 in the Best New Drug Award category for our NTM MAC lung disease treatment. Congrats to all of the nominees! We look forward to the
@PharmaScrip
ceremony on December 4th.
#PoweredByPurpose
Recently, we gathered at our HQ to learn more about bronchiectasis and show our support for the patient community. Together, we were proud to honor the first World Bronchiectasis Day, which took place last Friday.
#PoweredByPurpose
Did you know there is an active online community of people living with
#bronchiectasis
? Join now to connect with other patients, caregivers, and health care professionals. .
@COPDFoundation
#TBT
to earlier this year when we held our annual "Take Our Daughters & Sons to Work Day." We were delighted to welcome the next generation of
#champions
for the
#raredisease
community.
#RareLivesHere
Did you know that 1 in 10 Americans lives with a
#raredisease
? It’s important that people living with a rare disease, such as
#NTMlungdisease
, have a strong support system. Learn more about available resources:
#rarediseaseawareness
Did you know that the initial airway damage that leads to
#bronchiectasis
often begins in childhood? However, symptoms may not appear until months or even years after you have repeated lung infections. Learn more about the symptoms now:
Our dedication to patients is not just a company tagline. We put the
#patient
at the forefront of every decision we make. Take a look at how we include patients at every step.
#raredisease
#NTMlungdisease
Thank you
@atscommunity
for the opportunity to highlight our data and engage with researchers and physicians at
#ATS2022
! I had a great time sharing our team’s experience behind the scenes. We’re already looking forward to next year in Washington, D.C. – DW
Insmed’s culture is unique. If you enjoy challenging the
#statusquo
and working collaboratively, this might be your right next step. We are
#nowhiring
for an Executive Director of Commercial Effectiveness. See where your path could lead at
#Insmed
.
If you have a
#raredisease
or are a
#caregiver
to someone with a rare disease, you know that it can be an isolating experience. Finding a support community is important, and
@RareDiseases
has a database of patient organizations that can help. Check it out:
We look forward to being an exhibitor at this year’s virtual
@accpchest
Annual Meeting, which features live sessions on various lung conditions. Learn more:
#CHEST2020
If you suspect or have been diagnosed with
#NTMlungdisease
, there are doctors who specialize in lung disease trained to treat you. Learn more about available resources here:
Today, our CEO Will Lewis spoke at the
#NORDSUMMIT
about developing effective collaborations between
#patient
organizations and companies to advance the shared goal of improving lives of
#raredisease
patients. Thanks to
@RareDiseases
for organizing a great event!
This week, we're at the
@EuroRespSoc
International Congress and will be presenting data from one of our latest studies. We’ll also be at booth S.03 - come visit us!
#ERSCongress
I’m looking forward to meeting with colleagues & other professionals to learn the latest in respiratory science. Our team is starting the day with a pre-conference meeting. If you are at
#ATS2022
, be sure to visit Insmed at booth 1033. – DW
As we expand our presence in Japan, we are excited to launch —a new Japanese website that will provide local information about Insmed for our colleagues, candidates, and partners.
Today on
#RareDiseaseDay
, we’re honoring all those who work tirelessly to uncover answers & support each other along the way. Through each of our unique contributions, we’re painting a colorful picture of the future for patients living with rare diseases.
Happy
#MemorialDay
from all of us at Insmed. We’re using this day to reflect on the brave sacrifices of our fallen U.S. service members. We hope your day is filled with remembrance, along with time to connect with family & friends.
A dedication to
#patients
and improving their lives is at the center of everything we do!
#ICYMI
, earlier this year our CEO, Will Lewis, shared Insmed’s view on
#patientcentricity
.
This week we are at
#JPM2020
in
#SanFrancisco
! Our Chairman and CEO, Will Lewis, will be speaking about the progress at Insmed and what’s in store next. Tune in at 9AM on the 16th.
#PoweredByPurpose
Living with
#bronchiectasis
isn’t easy but hearing from other people experiencing this condition may help. Check out these patient stories from the
@lunguk
or contribute your own experience here: .
#DYK
on average, it takes 8 years to be correctly diagnosed with a
#raredisease
? People living with
#NTMlungdisease
are often told their symptoms are signs of other, more common conditions. Find out more:
Today is International Women in Engineering Day! At Insmed, we are committed to championing women in STEM roles. Learn more about our mission:
#INWED20
This week, we will be presenting at the
@accpchest
Annual Meeting. We’re excited to hear about the latest work in this space and catch up with some familiar faces.
#PoweredByPurpose
#CHEST2019
This week, we had the opportunity to take part in the
@RedCross
Holiday Mail for Heroes initiative, expressing our thanks to the men and women in the armed forces overseas.
#InsmedCares
While navigating your
#raredisease
journey, finding a support system can help. If you are living with pulmonary arterial hypertension, consider following
@PHAssociation
for resources, information, and community.
No matter who you are, you can be the change by advocating for progress for small patient populations every day. Consider following organizations like
@RareDiseases
,
@eurordis
, or
@LungAssociation
to get involved.
Over the next several days, our Head of US & General Manager, Drayton Wise, will be taking you behind the scenes of
#ATS2022
. Watch this space for live updates!
Did you know that Insmed supports medical and scientific
#research
carried out by scientists, clinicians, and organizations? Learn more about what we do
#PoweredByPurpose
Have you recently been diagnosed with
#NTMlungdisease
? You are not alone. Listen as a
#pulmonologist
and
#patient
discuss the important lifestyle changes you can make to help manage symptoms.
Today is
#WorldLungDay
. Caring for your lungs should be as important as caring for any other part of your body. Check out tips for ensuring you’re protected:
This month is Chronic Obstructive Pulmonary Disease Awareness Month. People living with
#NTM
are often misdiagnosed with
#COPD
. Check out some top tips for caring for your lungs:
#NTMLungDisease
#RareDisease
This month is National Minority Mental Health Awareness Month. Now more than ever, it is important for those living with
#rarediseases
to take care of their
#mentalhealth
. Learn more:
#TBT
to earlier this year when we welcomed Amy Leitman to our Insmed Knowledge Now Sessions. She discussed the work
@NTMinfo
is doing in support of patients with
#NTMlungdisease
.
It was a pleasure speaking yesterday at the Insmed Knowledge Now Sessions. Our Director of Policy and Research Amy Leitman discussed the work we are doing in support of patients with
#NTM
#lungdisease
. Thank you for having us, Insmed!
Being diagnosed with
#NTMlungdisease
can feel overwhelming, especially when it comes to what questions to ask your doctor. We’re here to help. Check out our resources, including a doctor discussion guide to start the conversation: .
Have you heard of bronchiectasis? This disease, which affects the
#respiratory
system, is on the rise in women and older individuals and may increase the risk of developing
#NTMLungDisease
. Learn more:
Did you know, on average, it takes 8 years to be correctly diagnosed with a
#raredisease
? People living with
#NTMlungdisease
are often told their symptoms are signs of other more common conditions. Find out more:
We are proud to work with
@ConnectforCOVID
to lend our iPads to local hospitals so that critically ill COVID-19 patients can see their families. Hundreds more devices are needed. Learn how you can share your devices at
We are looking forward to the
@Jefferies
Virtual Healthcare Conference. Our Chairman and CEO, Will Lewis, will be presenting tomorrow at 8:30 a.m. ET. Tune in for the live webcast: