2023 MSU and #MyositisLIFE Sponsors
Learn more about our sponsors
Empowering Myositis Sponsors
argenx
argenx is a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases. Partnering with leading academic researchers through its Immunology Innovation Program (IIP), argenx aims to translate immunology breakthroughs into a world-class portfolio of novel antibody-based medicines. argenx developed and is commercializing the first-and-only approved neonatal Fc receptor (FcRn) blocker in the U.S. and Japan. The Company is evaluating product candidates in multiple serious autoimmune diseases and advancing several early stage experimental medicines within a number of therapeutic franchises. For more information, visit argenx and follow us on LinkedIn, Twitter, and Instagram.
IndeeLift
Steve Powell, founder of IndeeLift sought out the help of several inclusion body myositis patients, IBMer’s, to adapt the residential lift to meet the needs of Myositis patients, now lifting to a standing position.
Steve says, “IndeeLift is becoming larger and more successful by living with the philosophy people count! All of our efforts are being aimed at achieving the greatest good for the greatest number in all that we do! Consequently, IndeeLift is partnering with Myositis Support and Understanding and the Myositis Community and as such, Myositis will be the primary recipient of IndeeLift corporate giving efforts for the foreseeable future! Together we can really make a difference in the day-to-day lives in this community, while also enabling the research that may one day lead to the real goal of slowing or curing IBM and ultimately Myositis.”
To learn more about the new HLF, how it can help you regain and maintain your independence, and IndeeLift’s plans to help the Myositis Community, visit the MSU Indeelift Program page.
Sponsorship opportunities are available
MSU is instrumental in improving the lives of people living with myositis (idiopathic inflammatory myopathies), a group of rare, complicated autoimmune muscle, skin, and often multi-organ diseases, through education, support, awareness, advocacy, access to research, and need-based financial assistance.
We are a fast-growing patient-led 501(c)(3) nonprofit organization with the experience needed to support and advocate for myositis patients and caregivers. Myositis affects the whole person and every aspect of their life. Understanding this disease isn’t limited to symptoms, we push for the inclusion of the patient voice in research and clinical care, and we work to empower the community to acknowledge patients and caregivers as equals – a part of a team – in their healthcare management.
We provide more than support. We continually work hard as an all-volunteer organization providing patient-centered programs and services and building unique and meaningful partnerships in the rare disease community. Technology is a driving force in our continued growth and success; educating, supporting, and connecting patients, caregivers, and family members with one another, and with doctors, researchers, clinical trials, partners, and patient-first focused providers.
Sponsorships include both our comprehensive myositis website, Understandingmyositis.org, and our #MyositisLIFE program and website; giving a voice to patients and caregivers.
#MyositisLIFE is our newest program with a dedicated interactive community-based website, and it provides a solution to a missing piece in awareness and research; the patient voice.
