The following is a listing of various conferences of interest to many in the rare disease space, some of which Engage Health will participate in.
ENGAGE HEALTH to APPEAR at the WORLD ORPHAN DRUG CONGRESS USA 2019
On Wednesday, April 10, 2019, Engage Health will host a workshop on Identifying and Engaging Patients and Clinicians in the Rare Disease Space as part of the World Orphan Drug Congress. Anyone in the rare disease space who has ever needed to find patients with rare diseases or the clinicians who care for them, will benefit from attending!
A complete description of the workshop is below. In order to attend our workshop, you must purchase the three day pass (conference and workshop day) when you register for the World Orphan Drug Congress.
Identifying and Engaging Patients and Clinicians in the Rare Disease Space
Has the experience of searching for patients with rare diseases, or for the health care providers who care for them, caused you to feel like you were looking for the proverbial needle in a haystack? If so, then this workshop is for you!
Advancing therapies for rare diseases requires a strong community comprised of patients, patient organizations, pharmaceutical companies and health care providers. Introducing new patients to the rare disease community is challenging. To begin with, the path to diagnosis is difficult, somethings taking as long as 9 years, and often involving an average of 7.3 specialists1. Once diagnosed, some families join a patient organization. Others become advocates at the state and national level. Some turn their pain into action by founding patient organizations for diseases that have none. Patients and their families who engage in these activities become part of the small but mighty rare disease community.
When a new therapy or a clinical trial is available, patients who are already part of the rare disease community are relatively easy to reach. But what about the ones who do not know there is a rare disease community? What about those who know but do not seek out community involvement? What about those who are lost to expert follow up? Many patients and their families obtain a diagnosis, are told there is nothing to be done, and are sent home to be cared for by their local health care provider. How do we find these patients? How do we find the health care providers who are treating them? How do we reach them with potentially life-saving or life-improving therapies before it is too late?
Hosted by Engage Health, Inc., this three-hour workshop will introduce new tools to engage patients and clinicians at every stage of drug development. Together we can find those needles in that haystack and speed the development of life-improving and life-saving therapies. Together we can make a difference to the patients and families impacted by rare diseases.
1 Engel PA, Bagal S, Broback M, Boice N. PHYSICIAN AND PATIENT PERCEPTIONS REGARDING PHYSICIAN TRAINING IN RARE DISEASES : THE NEED FOR STRONGER EDUCATIONAL INITIATIVES FOR PHYSICIANS. J Rare Disord. 2013;1(2):1-15. http://www.journalofraredisorders.com/pub/IssuePDFs/Engel.pdf. Accessed December 13, 2018.
For additional information about the workshop click HERE. You may also contact Engage Health at 651-994-0510.
The World Orphan Drug Congress will place April 10–12, 2019 at the Gaylord National Harbor Hotel in Oxon Hill, MD.