Meet the couple behind this project.

Jay and Cath have just been married for a month and were enjoying their new life as husband and wife. Jay has been in the software industry as a seasoned software/mobile developer while Cath was at the peak of her career as a Product Manager when she was struck with GBS in Feb 2011. 

At the early stage of their married life, their vows were immediately put to test. Suddenly, all their plans came crashing down. They fought this battle hand in hand, together with their families and many friends. Through GBS, they became stronger. They vowed to give support and help those affected with the same condition.   

This website is their first project and a start of their mission to reach out and make a difference.  Cath documented her journey with GBS in a blog called Life On Detour.

About GBS|CIDP Foundation International

The Foundation began over 30 years ago as a support group for patients & families impacted by Guillain‐Barré syndrome, chronic inflammatory demyelinating polyneuropathy (CIDP) or any of the variants that exist. Since then, our commitment has been to provide support to those affected by these disorders so that every patient obtains an early diagnosis, proper treatment & the opportunity for a full recovery.

Read more about them here.