About Periodic Paralysis International
Periodic Paralysis International and Our Mission
Periodic Paralysis International is a registered not-for-profit company based in Alberta, Canada, but we serve patients and physicians world-wide. Our organization is run entirely by volunteers. Our purpose is to disseminate timely, medically accurate and useful information, to provide supportive services, and to conduct and encourage research which enhances the quality of life for people with skeletal ion channelopathies, i.e. the periodic paralyses.
Our Medical Advisory Council
The physicians and scientists who serve on Periodic Paralysis International's Medical Advisory Council are without question among the world's foremost authorities on the periodic paralyses and the cardiac, cognitive and physical issues which come with them. We are honored that they share with us and our members the gifts of their time, experience and knowledge. Read about the members of our Medical Advisory Council
Periodic Paralysis International Website, the HKPP Listserv and associated forums subscribe to HONcode Principles, including principles of confidentiality. Confidentiality of data relating to patients and visitors to this website is respected. Read our commitment to your privacy
The Periodic Paralysis International website is the official website of Periodic Paralysis International and the HKPP Listserv. The HKPP Listserv is an on-line group which has provided medically accurate, up-to-date information and peer support to patients with periodic paralysis, their families, caregivers and medical professionals since 1997. Read our HonCode information
Trust it or Trash it?
Trust It or Trash It is a tool from the Genetic Alliance to help you think critically about the quality of health information (including websites, handouts, booklets, etc.). Click on Who said it? When did they say it? and How did they know? to guide you through the process.
The seed of Periodic Paralysis International was planted in mid-1995 with an e-mail between Deb Cavel-Greant and one other patient with hypokalemic periodic paralysis. One by one, patients found Deb's page on HypoKPP, which was part of her genealogy site. Read our history