periodicparalysisnetwork.com
Periodic Paralysis Network, Inc.The Periodic Paralysis Network, Inc. (PPNI) welcomes you to share in the open and free exchange of knowledge and ideas without pre-conditions.
http://www.periodicparalysisnetwork.com/
The Periodic Paralysis Network, Inc. (PPNI) welcomes you to share in the open and free exchange of knowledge and ideas without pre-conditions.
http://www.periodicparalysisnetwork.com/
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Periodic Paralysis Network, Inc. | periodicparalysisnetwork.com Reviews
https://periodicparalysisnetwork.com
The Periodic Paralysis Network, Inc. (PPNI) welcomes you to share in the open and free exchange of knowledge and ideas without pre-conditions.
Periodic Paralysis Network, Inc./Support
http://www.periodicparalysisnetwork.com/support.htm
PERIODIC PARALYSIS NETWORK, INC. Hope - Support - Education - Advocacy. Another of our popular features, offering support through the PPNI, is our Blog. We offer support for individuals, their family members, caregivers and medical professionals by offering an open site for anyone to visit and learn more about the many and multifaceted aspects of Periodic Paralysis. It is interactive and has a translator. We have two Facebook Pages, trying to bring awareness to others about Periodic Paralysis and by doin...
PPNI Books
http://www.periodicparalysisnetwork.com/books.htm
PERIODIC PARALYSIS NETWORK, INC. Hope - Support - Education - Advocacy. A Bill Of Rights For Periodic Paralysis Patients. Susan Q. Knittle-Hunter. The Periodic Paralysis Network A.S.E.A. Series: Volume One. Authored by Susan Q Knittle-Hunter. Authored with Calvin Hunter. Paperback Edition: $7.95 USD. Publication Date: Sep 18 2015. ISBN/EAN13: 151719623X / 9781517196233. Trim Size: 6 x 9. Color: Black and White. About The Periodic Paralysis Network. ASEA Series:Awareness Support Education Advocacy. Is a m...
Periodic Paralysis Network, Inc./Adocacy
http://www.periodicparalysisnetwork.com/advocacy.htm
PERIODIC PARALYSIS NETWORK, INC. Hope - Support - Education - Advocacy. They are a worldwide network of individuals and independent organizations working toward the improvement of quality and safety in healthcare. Some may wonder why this is a concern and why we feel it is necessary to advocate for the health and safety for people with Periodic Paralysis? We are also concerned with the archaic and potentially life-threatening practice by uninformed doctors of provoking an individual's symptoms and paraly...
Periodic Paralysis Network, Inc./Education
http://www.periodicparalysisnetwork.com/education.htm
PERIODIC PARALYSIS NETWORK, INC. Hope - Support - Education - Advocacy. Our largest 'classroom' is the 'Periodic Paralysis Network Support, Education and Advocacy Group.' ( https:/ www.facebook.com/groups/periodicparalysisnetworksupportgroup/. We have over 300 members and gain more each week from all over the world. Visit our PPN Members World Map at: http:/ www.multiplottr.com/? It is an open site and was designed to teach the world about Periodic Paralysis. Over 80 separate articles have been compi...
Periodic Paralysis Network, Inc.
http://www.periodicparalysisnetwork.com/index.htm
PERIODIC PARALYSIS NETWORK, INC. Hope - Support - Education - Advocacy. What Is Periodic Paralysis? What Is Periodic Paralysis Network, Inc? What Do We Do? The Website: Periodic Paralysis Network, Inc. The Blog: Living With Periodic Paralysis Blog. Three distinct discussion groups: Periodic Paralysis Network Support, Education and Advocacy Group. Periodic Paralysis Network Genealogy-Genetic Discussion Group. Periodic Paralysis Network Book Discussion Group. PPN Members World Map:. How To Use This Site.
TOTAL PAGES IN THIS WEBSITE
6
thestandingovationjourney.blogspot.com
I Could Use A Standing Ovation, Could You? The Journey of An Anxious Girl: January 2015
http://thestandingovationjourney.blogspot.com/2015_01_01_archive.html
I Could Use A Standing Ovation, Could You? The Journey of An Anxious Girl. Wednesday, January 28, 2015. Hope i heard an acronym for it once: Hold On Pain Ends. that's what i think of every time i hear the word hope. and i hope that the pains in my life really will end. 2 years ago a and i were at wal-mart shopping for plants. i found a lovely small palm tree that came with a rock in it that said 'hope.' i bought her and kept her name hope. The metaphor was not lost on me. i can't say i've ever lost h...
periodicparalysis.blogspot.com
Periodic Paralysis - A Journey: Atypical Periodic Paralysis - Maybee Syndrome
http://periodicparalysis.blogspot.com/2014/06/atypical-periodic-paralysis-maybee.html
Periodic Paralysis - A Journey. My family has a rare variant of Hypokalemic Periodic Paralysis. It spans 6 known generations. Our variant is called Periodic Paralysis Plus. The mutation is currently unknown. Saturday, September 13, 2014. Atypical Periodic Paralysis - Maybee Syndrome. These are the features of Atypical Periodic Paralysis for my family. My family has been the the United States and Canada since the 1600's. My family tree is extensive which has allowed for many variants of the same disorder.
periodicparalysis.blogspot.com
Periodic Paralysis - A Journey: My True and Personal Story of Periodic Paralysis (why it sucks to be rare)
http://periodicparalysis.blogspot.com/2013/11/my-hkpp-story-at-least-beginning.html
Periodic Paralysis - A Journey. My family has a rare variant of Hypokalemic Periodic Paralysis. It spans 6 known generations. Our variant is called Periodic Paralysis Plus. The mutation is currently unknown. Thursday, April 21, 2016. My True and Personal Story of Periodic Paralysis (why it sucks to be rare). Rule 1: Choose your words carefully when visiting a doctor. After six month of counseling, my psychologist could find nothing wrong. He declared me mentally healthy and sent me on my way. Rule 2: Doc...
periodicparalysis.blogspot.com
Periodic Paralysis - A Journey: Hypokalemic Periodic Paralysis, GERD, Gastroparesis or POTS
http://periodicparalysis.blogspot.com/2012/04/hypokalemic-periodic-paralysis-and-gerd.html
Periodic Paralysis - A Journey. My family has a rare variant of Hypokalemic Periodic Paralysis. It spans 6 known generations. Our variant is called Periodic Paralysis Plus. The mutation is currently unknown. Thursday, October 09, 2014. Hypokalemic Periodic Paralysis, GERD, Gastroparesis or POTS. It is believed that this constellation of symptoms is related to a Hypokalemic Periodic Paralysis / Ehlers-Danlos Syndrome. And Treatment of gastroparesis. PPI-Related Hypomagnesemia: Putting it in Perspective.
periodicparalysis.blogspot.com
Periodic Paralysis - A Journey: Disability Services at Universities - Why they fail.
http://periodicparalysis.blogspot.com/2015/03/disability-services-at-universities-why.html
Periodic Paralysis - A Journey. My family has a rare variant of Hypokalemic Periodic Paralysis. It spans 6 known generations. Our variant is called Periodic Paralysis Plus. The mutation is currently unknown. Thursday, March 03, 2016. Disability Services at Universities - Why they fail. That is not an answer! Now I must call a number of different department heads. I spend hours on the phone trying to resolve these simple issues. Some of the issues have not been simple and have required daily phone...It is...
periodicparalysis.blogspot.com
Periodic Paralysis - A Journey: Doctors often misdiagnose zinc deficiency, unaware of impact of excess zinc
http://periodicparalysis.blogspot.com/2015/06/doctors-often-misdiagnose-zinc.html
Periodic Paralysis - A Journey. My family has a rare variant of Hypokalemic Periodic Paralysis. It spans 6 known generations. Our variant is called Periodic Paralysis Plus. The mutation is currently unknown. Monday, June 22, 2015. Doctors often misdiagnose zinc deficiency, unaware of impact of excess zinc. Quoted from Science Daily: June 19, 2015. Journal of Clinical Pathology. Too much zinc, taken in the form of dietary supplements, may disrupt copper uptake. In particular, they looked at the reasons fo...
livingwithperiodicparalysis.blogspot.com
Living with Periodic Paralysis: The Blog: September 2014
http://livingwithperiodicparalysis.blogspot.com/2014_09_01_archive.html
Living with Periodic Paralysis: The Blog. Monday, September 29, 2014. The Incorporation of Periodic Paralysis Network, Inc (PPNI). Today I wanted to share our big news and give a little bit of background information into our organization, which is now formally a corporation. I would like to share our story. I had to do it myself. The story of my diagnosis is long and involved, but Calvin, my husband, and I did manage to secure a diagnosis after unbelievable resistance and much work on our part. Http:/ li...
livingwithperiodicparalysis.blogspot.com
Living with Periodic Paralysis: The Blog: Periodic Paralysis and Depression
http://livingwithperiodicparalysis.blogspot.com/2015/06/periodic-paralysis-and-depression.html
Living with Periodic Paralysis: The Blog. Tuesday, June 16, 2015. Periodic Paralysis and Depression. One of our members asked about the possible connection between Periodic Paralysis and depression. This comes up occasionally, so I thought I would write a blog article about it. There are five possible answers or issues to consider about Periodic Paralysis and depression. We know that (low potassium) can/may create mental issues including depression (and possibly psychosis, hallucinations and delirium).
livingwithperiodicparalysis.blogspot.com
Living with Periodic Paralysis: The Blog: July 2015
http://livingwithperiodicparalysis.blogspot.com/2015_07_01_archive.html
Living with Periodic Paralysis: The Blog. Sunday, July 26, 2015. Bill of Rights for Periodic Paralysis Patients. Bill of Rights for Periodic Paralysis Patients. A ‘bill of rights’ may also be called a ‘charter of rights’ or a ‘declaration of rights.’. A doctor must have the best interest of the patient. A doctor’s treatment must be based on equality and fairness. A doctor must “do no harm”. A doctor’s treatment may be accepted or refused by the patient. A doctor must treat patients with dignity. Individu...
livingwithperiodicparalysis.blogspot.com
Living with Periodic Paralysis: The Blog: A New Drug For Periodic Paralysis? Helpful Or More Of The Same?
http://livingwithperiodicparalysis.blogspot.com/2015/08/a-new-drug-for-periodic-paralysis.html
Living with Periodic Paralysis: The Blog. Monday, August 10, 2015. A New Drug For Periodic Paralysis? Helpful Or More Of The Same? There is a big announcement in the world of Periodic Paralysis today! A drug has been approved by the FDA as the first drug to treat Periodic Paralysis. It is Dichlorphenamide also known as Keveyis. It is a carbonic anhydrase inhibitors (a. Dichlorphenamide, needs to be used with great care, just as the off-label drugs. Here is some more information about dichlorphenamide:.
TOTAL LINKS TO THIS WEBSITE
46
periodicparalysis.blogspot.com
Periodic Paralysis - A Journey
Periodic Paralysis - A Journey. My family has a rare variant of Hypokalemic Periodic Paralysis. It spans 6 known generations. Our variant is called Periodic Paralysis Plus. The mutation is currently unknown. Tuesday, June 23, 2015. Your Cell Phone Carrier Matters When You Have a Chronic Illness. Fastest Mobile Networks - PC magazine. Links to this post. Monday, June 22, 2015. Doctors often misdiagnose zinc deficiency, unaware of impact of excess zinc. Quoted from Science Daily: June 19, 2015. Doctors oft...
PeriodicParalysis.com is available at DomainMarket.com
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PPA - Welcome to the Periodic Paralysis Association
Diseases - Diagnosis and Management. Welcome to the Periodic Paralysis Association. Please attend the Periodic Paralysis Conference 2015. Oct 23-25 Orlando, Fl. Online PPA Auction to Benefit Conference 2015. Please see tab on left for all information. Oin our NEW discussion forum. To do so, please register as. NEW MEMBER or RE-REGISTER. Using the MEMBERSHIP link to your left). WATCH VIDEO ABOUT THE PPA. CLICK HERE for Article on Hypokalemic Periodic Paralysis. We welcome you to the PPA and will do our be...
periodicparalysis.wordpress.com
My Journey. My Story | Periodic Paralysis in NZ
My Journey. My Story. Periodic Paralysis in NZ. Ash Cash funds booze and satellite tv. Hospital doctors around New Zealand are charging grieving families for cremation certificates and spending the proceeds on parties and Sky TV. Http:/ www.stuff.co.nz/national/health/7945363/DHB-doctors-use-cremation-fees-for-perks. Comments : Leave a Comment. Well it has been a while since I have posted, too long in fact. Thanks for reading,. Comments : 3 Comments. I just received an exciting letter from Ulm! After a b...
Periodic Paralysis Network, Inc.
PERIODIC PARALYSIS NETWORK, INC. Hope - Support - Education - Advocacy. What Is Periodic Paralysis? What Is Periodic Paralysis Network, Inc? What Do We Do? The Website: Periodic Paralysis Network, Inc. The Blog: Living With Periodic Paralysis Blog. Three distinct discussion groups: Periodic Paralysis Network Support, Education and Advocacy Group. Periodic Paralysis Network Genealogy-Genetic Discussion Group. Periodic Paralysis Network Book Discussion Group. PPN Members World Map:. How To Use This Site.
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Periodic Physics
Fourth Stage of Physics. Modern Physics insightfully solved difficulties that Classical Physics encountered. When applied to the entire universe. Modern Physics loses its magic. Standard Model of particle physics is also far from being satisfying. Indications that Modern Physics is a simplification of a more general theory. A proposal for that more general theory, the fourth stage of physics, is introduced here. Postulates Introduced by Periodic Physics. Flaws of Modern Physics. Part II: Macro Gravitation.
The Periodic Pilgrim | “For we have no permanent city here…”
8220;For we have no permanent city here…”. June 13, 2011. A new Hanout and Saudi Arabian coffee. The corner food/dollar grocery on 6. After a pleasant chat (1/2 in Arabic, even though Ethiopians speak Amharic. 8211; for you, good price ) with the man behind the bullet-proof window, I walked home with my milk and glasses. I had read about the smooth and strong cardomom-rich Saudi coffee in In the Land of Invisible Women: A Female Doctor’s Journey in the Saudi Kingdom. I looked up a few recipes:. This arti...
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