Scleroderma Foundation to Host National Patient Education Conference in July
The Scleroderma Foundation’s Annual National Patient Education Conference is right around the corner. Scheduled for July 29 – 31 in New Orleans, La., the event is dedicated to patients who struggle with the chronic and autoimmune disease, as well as caregivers and loved ones.
At the conference, according to the Scleroderma Foundation, participants will get plenty of opportunities to learn how to cope with the emotional challenges of living with scleroderma; develop strategies for staying positive and motivated; meet people who want to take charge of scleroderma, their health, and their lives; build a support network, and talk with others who share similar experiences; and learn about current therapies from the medical community.
Highlights of the two-day event include more than 50 workshops, an array of exhibitors, panel discussions, and educational sessions led by renowned scleroderma investigators and health workers. Organizers believe participating patients will consequently discover ways to help to raise public awareness about scleroderma while establishing new friendships.
A special program tailored for younger patients, and siblings or children of patients, is also included.
For first time attendees and those who are unable to attend without financial help, the foundation has created a Conference Scholarship Program. While the deadline for applying for the scholarship has already closed, the organization is recommending that those who wish to attend should contact the group to discuss their personal situation.
The per-person cost of hosting the conference is more than $700, according to theScleroderma Foundation, but the organization has garnered help from numerous sponsors to defray participant costs. Leading sponsors include Actelion, Bayer, Reata Pharmaceuticals, Gilead, Genentech, and United Therapeutics Corporation.
Learn more about scleroderma here: http://bit.ly/learnscleroderma
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