Corbin
GBS | CIDP Foundation International, President

Corbin was a successful engineer, avid traveler, and regular gym-goer—until debilitating CIDP symptoms changed everything. Despite going years without a diagnosis and with doctors predicting he wouldn’t survive, he pushed through with the help of his faith, family, and optimistic outlook. 

Currently, he serves as president of the GBS | CIDP Foundation International with a deep commitment to the CIDP community. Corbin is now a business consultant and founder of his own company.  

Cindy
GBS | CIDP Foundation International, Volunteer

Once an active and ambitious student pursuing dual master’s degrees, Cindy had to change her life drastically when she was diagnosed with a severe CIDP variant. This condition took away much of her independence, leaving her reliant on her parents as caregivers.

Although she faced initial mental health challenges, Cindy reframed her perspective, focusing on positivity and discovering a passion for helping others. Today, Cindy serves as a social worker at a local California nonprofit and participates in organizations dedicated to supporting the disabled community.

Dr. Jeffrey Allen
GBS | CIDP Foundation International, Board of Directors

Dr. Jeffrey Allen, associate professor in the Department of Neurology at the University of Minnesota, offers insight into CIDP diagnosis, treatment, and what the future holds. Serving on the GBS | CIDP Foundation International Advisory Board, he is also the primary investigator for the foundation’s patient registry.