We at the Periodic Paralysis Network are now providing HOPE,
SUPPORT, EDUCATION and ADVOCACY to over 725 members worldwide!!!
The following are the services and features of our PPN
forum:
PPN Website: www.periodicparalysisnetwork.com PPN Support
Group: https://www.facebook.com/groups/periodicparalysisnetworksupportgroup/
PPN Books:
"Living With Periodic Paralysis: The Mystery
Unraveled"
"The Periodic Paralysis Guide And Workbook: Be The Best
You Can Be Naturally"
Video about this Guide and Workbook: https://www.facebook.com/sqkhunter/videos/10153659957417014/
"A Bill Of Rights For Periodic Paralysis Patients"
"What Is Periodic Paralysis?: A Disease Like No
Other"
Our books are found on
Amazon.com: https://www.amazon.com/Susan-Q-Knittle-Hunter/e/B00HVEBSSQ/ref=dp_byline_cont_pop_book_1
PPN Blog:
We have over 140 blog articles written about all aspects of
Periodic Paralysis.The Blog was created to provide information to all of our
members, as well as, family members, friends and medical professionals who want
to know more about Periodic Paralysis.
PPN Book Discussion Group:
We have a discussion board to discuss specifically the
issues and aspects of Periodic Paralysis found in our books.
PPN Genealogy Discussion Group:
This group was designed for discussion and research into the
genealogy of those families with Periodic Paralysis in the hopes of finding
links and perhaps a new way to get a diagnosis.
PPNI Genetics Discussion and Research Group:
The Periodic Paralysis Network Inc. (PPNI) Genetics
Discussion and Research Group is designed for discussion and research into the
genetics of the many forms of Periodic Paralysis.
The PPN Learning Center and Workshop:
We have web cam or live video group sessions periodically
for education, support and discussion. Please watch for announcements and
invitations to RSVP.
Periodic Paralysis Caregivers:
The Periodic Paralysis Caregiver Group is designed to assist
the caregivers of those individuals with Periodic Paralysis. This could include
parents, children, siblings, friends, grandparents or anyone else who is
responsible to care for anyone who has any form of Periodic Paralysis. This
group is an extension of the Periodic Paralysis Support Group.
PP and Co-existing Conditions:
This group is designed for those who have Periodic Paralysis
and other co-existing conditions. The PPN Support, Education and Advocacy Group
is geared for discussions about Periodic Paralysis only.
PP Buddies (Support when in an emergency)
This 'PP Buddies Group' is designed for members of the PPN
Support, Education and Advocacy Group. Anyone can join who may need help or
assistance in the ER or in an emergency and anyone who would like to 'buddy
with' or help them at those times. We do not want to see anyone who is
frightened or new to PP, have to go through these experiences alone. Using IM,
Chat, Skype or exchanging phone numbers ahead of time may be helpful.
PPN Website Facebook Page:
Our PPN Facebook Page is designed to share more general
information and articles related to Periodic Paralysis, Chronic Illness and
Invisible Illness. It is also designed to share with family members and friends
to provide them with a better understanding about PP, chronic and invisible
illness.
PPN Author's Page:
Fun posts shared relating to writing and reading books.
Video about Periodic Paralysis:
https://www.youtube.com/watch?v=YSRVOkdFRQc
Twitter: https://twitter.com/NetPeriodic
(I am not good at Twitter..let me know if you would like to
help with this.)
Periodic Paralysis World Awareness Day Page:
This page was created to bring awareness to the world about
Periodic Paralysis. We have declared and observe 'Periodic Paralysis World
Awareness Day' February 7th each year!
Please check out our PPN Members World Map:
Let us know if you want to be added to our map!
Thank you all for your support
Calvin Hunter and Susan Q. Knittle-Hunter
Co-Founders, Co-Creators, Co-Managers
Periodic Paralysis Network, Inc.
Sequim, Washington U.S.A.
All rights reserved. copyright © 2013 Periodic Paralysis
Network
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