Category Archives: Blog

Remembering Gillian MacLean

The GFPD is heartbroken to report the sudden passing of Gillian MacLean, who worked with...

GFPD Awarded RARE Impact Innovation Grant for Pilot Study

      We are very happy to announce that we have been awarded a...

GFPD/STAIR Collaboration Invites Patient Input in Research

Among medical professionals, rare diseases like Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder (PBD-ZSD) are challenging to...

Retinal Gene Therapy Trial Underway at McGill University

Our dedicated researchers worked hard over the holidays, making great progress on the PBD-ZSD retinal...

Your End of Year Gift Can Make Research a Reality

Season’s Greetings from the Global Foundation for Peroxisomal Disorders!   We are wrapping up a...

GFPD Fall 2016 Newsletter

The GFPD’s Fall 2016 Newsletter features stories about all the work our families and supporters...

Developing a Game Plan for School: One Parent’s Experience with the IEP Process

This month, I had the pleasure of interviewing my sister, Kelly Dauer-Hubschmitt. Her four-year old...

My experience attending the 2016 Deafblind Symposium

“How was your conference?” It’s a question many people have asked me. Others have no...

September is Leukodystrophy Disease Awareness Month! What Do You Know About It?

What is Leukodystrophy? Leukodystrophy causes the myelin, or “white matter,” of the brain to progressively...

Family. Research. Hope.

October 5th marks the sixth birthday of the Global Foundation for Peroxisomal Disorders. In just...