At last, something to help our patients with PG! There is a new, non-profit Patient and Family Advisory Council for PG and the kickoff meetings will take place on October 1 and October 7. This is a resource for practitioners, as well. Any provider or caregiver is welcome to join.
This is a major milestone for patients living with PG!
Flier- Strengthening Voices through Patient and Family Advisory Councils
Additional Resources:
- Try This! A Clinical Scoring Tool to Diagnose Pyoderma Gangrenosum (Since You Can’t Trust a Biopsy) – Caroline Fife M.D.
- Pyoderma Gangrenosum and the International PyGaTe Registry – Guest Blog by Dr. Alex G. Ortega-Loayza – Caroline Fife M.D.
- A Case of Pyoderma Gangrenosum Successfully Treated with Vilobelimab (the COVID Antibody) – Caroline Fife M.D.
- At Last! Hope for Patients with Pyoderma Gangrenosum! Share This Information About a Clinical Trial. – Caroline Fife M.D.
- Pyoderma Gangrenosum, PASH, and Playing the Odds – Caroline Fife M.D.
- The Many Faces of Pyoderma Gangrenosum – This is Not a Pressure Injury – Caroline Fife M.D.
- Hidden in Plain Sight: Pyoderma Gangrenosum – Caroline Fife M.D.
- Pyoderma Gangrenosum (PG) Hiding in Plain Sight – Caroline Fife M.D.
- Pyoderma Gangrenosum (PG): Not So Rare, and When in Doubt, Take a History. – Caroline Fife M.D.
- A New Review Article on Pyoderma Grangrenosum by Dr. Alex Loayza! – Caroline Fife M.D.
- Here’s my Presentation on using PARACELSUS to Diagnose Pyoderma Without a biopsy! – Caroline Fife M.D.
- The Many Faces of Pyoderma Grangrenosum – a Leg Ulcer Present for a Year – Caroline Fife M.D.
