This blog was created and designed to educate the world about Periodic Paralysis a rare, inherited, hard to diagnose, debilitating and cruel mineral metabolic disorder. I have two variants of this condition and my life is filled with constant challenges as I attempt to manage my symptoms to stay alive. My husband and I are co-founders of the Periodic Paralysis Network, Inc. This blog is an extension of our educational and support network at www.periodicparalysisnetworkinc.com .
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Tuesday, February 28, 2017
Wednesday, February 8, 2017
Best Way to Share Awareness of Periodic Paralysis With Others
Hello All,
Yesterday was Periodic Paralysis World Awareness Day. One of the best ways we can make people and doctors aware of the various forms of Periodic Paralysis is to share our latest book with them. I wrote it for this very reason. The first two books were written to help you understand PP and manage your symptoms...to "be the best you can be" and to be able to get a diagnosis. The 'Bill of Rights' book is to help to empower you as you deal with the medical professionals in your life...to know your rights as they try to take them away from you or intimidate you. The fourth and final book "What Is Periodic Paralysis?: A Book Like No Other" was written to share with all of those people in your life who need to know about and understand PP and how it affects you. It was designed to be personalized by you...there are places for you to fill in your own information if you want to share it...how it affects you personally (This is also the way the Workbook was designed).
"What Is Periodic Paralysis?: A Book Like No Other" can be purchased at CreateSpace:
https://www.createspace.com/5809100
or
Amazon.com:
https://www.amazon.com/Susan-Q-Knittle-Hunter/e/B00HVEBSSQ/ref=dp_byline_cont_pop_book_1
Proceeds from the book...a few dollars each...goes back into our organization....to help run our organization and to purchase books for those who cannot afford them or passing them along to doctors, etc...for awareness and education.
Until Later....
Yesterday was Periodic Paralysis World Awareness Day. One of the best ways we can make people and doctors aware of the various forms of Periodic Paralysis is to share our latest book with them. I wrote it for this very reason. The first two books were written to help you understand PP and manage your symptoms...to "be the best you can be" and to be able to get a diagnosis. The 'Bill of Rights' book is to help to empower you as you deal with the medical professionals in your life...to know your rights as they try to take them away from you or intimidate you. The fourth and final book "What Is Periodic Paralysis?: A Book Like No Other" was written to share with all of those people in your life who need to know about and understand PP and how it affects you. It was designed to be personalized by you...there are places for you to fill in your own information if you want to share it...how it affects you personally (This is also the way the Workbook was designed).
"What Is Periodic Paralysis?: A Book Like No Other" can be purchased at CreateSpace:
https://www.createspace.com/5809100
or
Amazon.com:
https://www.amazon.com/Susan-Q-Knittle-Hunter/e/B00HVEBSSQ/ref=dp_byline_cont_pop_book_1
Proceeds from the book...a few dollars each...goes back into our organization....to help run our organization and to purchase books for those who cannot afford them or passing them along to doctors, etc...for awareness and education.
Until Later....
Tuesday, February 7, 2017
PPN Sixth Anniversary of Providing HOPE!!!!
Today is the Sixth Anniversary of providing HOPE to those with Periodic Paralysis through our Periodic Paralysis Network. It is also 'Periodic Paralysis World Awareness Day'... Six years ago today I (Susan Q. Knittle-Hunter, PPN Managing Director) got my Andersen-Tawil Diagnosis after nearly being killed by my doctors. It took me over 50 years...so a day of celebration!!!!
The following is a list of our services and features which have been developed for providing HOPE through AWARENESS, SUPPORT, EDUCATION and ADVOCACY, using all natural methods:
The following is a list of our services and features which have been developed for providing HOPE through AWARENESS, SUPPORT, EDUCATION and ADVOCACY, using all natural methods:
PPN Website: www.periodicparalysisnetwork.com
PPN Books:
"Living With Periodic Paralysis: The Mystery Unraveled"
https://www.createspace.com/4111713
"The Periodic Paralysis Guide And Workbook: Be The Best You Can Be Naturally"
https://www.createspace.com/4326356
Video about this Guide and Workbook: https://www.facebook.com/sqkhunter/videos/10153659957417014/
"A Bill Of Rights For Periodic Paralysis Patients"
https://www.createspace.com/5705192
"What Is Periodic Paralysis?: A Disease Like No Other"
https://www.createspace.com/5809100
Our books are also found on
Amazon.com:
https://www.amazon.com/Susan-Q-Knittle-Hunter/e/B00HVEBSSQ/ref=dp_byline_cont_pop_book_1
and
our PPN website:
http://www.periodicparalysisnetwork.com/books.htm
PPN Blog: http://livingwithperiodicparalysis.blogspot.com/
PPN Book Discussion Group:
https://www.facebook.com/groups/periodicparalysisnetwork/
PPN Genealogy Discussion Group:
https://www.facebook.com/groups/580168915344191/
PPNI Genetics Discussion and Research Group:
https://www.facebook.com/groups/1574048096186578/
The PPN Learning Center and Workshop:
https://www.facebook.com/groups/1416848568618404/
Periodic Paralysis Caregivers:
https://www.facebook.com/groups/366386850151623/
PP and Co-existing Conditions:
https://www.facebook.com/groups/145866829183840/
PP Buddies (Support when in an emergency)
https://www.facebook.com/groups/173361553092830/
PPN Website Facebook Page:
https://www.facebook.com/PeriodicParalysisNetwork
PPN Author's Page:
https://www.facebook.com/SusanQKnittleHunterauthor
Email: periodicparalysisnetwork@gmail.com
GoFundMe: http://www.gofundme.com/ftnr50
Bravelets: https://www.bravelets.com/bravepage/alone-in-the-dark-periodic-paralysis
Video about Periodic Paralysis: https://www.youtube.com/watch?v=YSRVOkdFRQc
Twitter: https://twitter.com/NetPeriodic
Periodic Paralysis World Awareness Day Page:
https://www.facebook.com/PPAwarenessDay/
Please check out our PPN Members World Map:
http://www.multiplottr.com/?map_id=55083
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 © 2017 Periodic Paralysis Network