Huntington's Dance website is to help educate people as to what Huntington's Disease is as well as to help promote the documentary Chris Furbee is working on.
http://www.huntingtonsdance.org/
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Huntington's Dance Foundation
Chris Furbee
1259A●●●●● Ave.
Eme●●●lle , Ca., 94608
US
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Huntington's Dance Foundation
Chris Furbee
1259A●●●●● Ave.
Eme●●●lle , Ca., 94608
US
View this contact
Huntington's Dance Foundation
Chris Furbee
1259A●●●●● Ave.
Eme●●●lle , Ca., 94608
US
View this contact
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Huntingtons' Dance - Dedicated in helping educate people as to what Huntington's Disease | huntingtonsdance.org Reviews
https://huntingtonsdance.org
Huntington's Dance website is to help educate people as to what Huntington's Disease is as well as to help promote the documentary Chris Furbee is working on.
huntingtonsdance.org
Huntington's' Dance: Honors & Awards
http://www.huntingtonsdance.org/honors.html
Slamdance Jury Special Mention for Most Compelling Personal Journey. Second Annual San Francisco Celebration of Hope Dinner. Honorary Chairperson San Francisco Mayor Gavin Newsom and Huntington's Disease Society of America honored Chris Furbee along with Michelle Byers, Dr. Steven Finkbeiner MD., PhD. and Cesar Plata on August 28, 2008. HD Person Of The Year Award. Congratulations to Chris Furbee for being chosen as the recipient of the 2008. Joseph P. Roberson. Site produced by Gregory Wilker.
Huntingtons' Dance: Definition
http://www.huntingtonsdance.org/definition.html
Subscribe to our mailing list. Huntington Disease is an autosomal dominantly inherited neurodegenerative disease. The clinical features and age of onset are quite variable, but symptoms are most frequently detectable between 30-50 years of age. Site produced by Gregory Wilker.
Huntingtons' Dance: Links
http://www.huntingtonsdance.org/links.html
Subscribe to our mailing list. Official IMDb page for Chris' film,. HDSA is doing research into CoQ10. It is believed to delay or slow the progress of Huntington's. This is an online disscusion group on HD for caregivers; go to the Group button. A very informative site which has newsstorys about HD research and storys about HD people. Huntingtons Disease Advocasy Center. A very informative site by HD Familys, it also has many links to personal webpages. HDSA Northern California Chapter Website. Maybe ano...
Huntingtons' Dance: Memorial Page
http://www.huntingtonsdance.org/memorial
This page is to help keep the names of people who have lost their lives to Huntington's Disease. To add a name to this list please email me at info@huntingtonsdance.org. Site produced by Gregory Wilker.
Huntingtons' Dance: Projects
http://www.huntingtonsdance.org/projects.html
Is an 18- year chronicle of one man’s reckoning with a hereditary disease. Brutal and unforgiving, the diagnosis is always fatal. Finding a way to overcome is the only answer. The film premiered at SlamDance Jan. 2014. For more information about the film Click here. To send a gift check to HD. Send the check to:. 1259 #A Ocean Ave. Emeryville, CA 94608. Site produced by Gregory Wilker.
TOTAL PAGES IN THIS WEBSITE
7
At Risk for Huntington's Disease: January 2015
http://curehd.blogspot.com/2015_01_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. Fighting – and writing – to stay healthy: ten year. Police killing of man with Huntington’s disease sp. View my complete profile. Huntington's Disease Society of America. I tested positi...
At Risk for Huntington's Disease: February 2015
http://curehd.blogspot.com/2015_02_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. 8216;None of us are free until we are all free’: scien. 8216;Darkness replaced by hope and light’: taking stoc. Huntington’s disease patients ‘feel better’ after . HD Free with PGD!
At Risk for Huntington's Disease: June 2014
http://curehd.blogspot.com/2014_06_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. New California stem cell chief stresses speed and . Fear of onset: the inescapable reality of the Hunt. View my complete profile. Huntington's Disease Society of America. Dr Mills was in...
At Risk for Huntington's Disease: March 2015
http://curehd.blogspot.com/2015_03_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. The precious participation of the Huntington’s dis. View my complete profile. Huntington's Disease Society of America. Huntington's Disease Drug Works. HDSA Orange County (CA) Affiliate.
At Risk for Huntington's Disease: August 2014
http://curehd.blogspot.com/2014_08_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. News flash: Isis and Roche hope to start Huntingto. Bidding farewell to CoQ10: a long-studied suppleme. Making the threat of Huntington’s disease ‘small s. View my complete profile.
At Risk for Huntington's Disease: January 2014
http://curehd.blogspot.com/2014_01_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. Riding the advocacy revolution: stem cell activist. Game-changers in the fight against disease: a repo. View my complete profile. Huntington's Disease Society of America. Starting with A...
At Risk for Huntington's Disease: March 2014
http://curehd.blogspot.com/2014_03_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. What’s in a name? How Huntington’s disease gene ca. 8216;It’s really getting real’: payoffs in the effort . View my complete profile. Huntington's Disease Society of America. On the DNA ...
At Risk for Huntington's Disease: October 2014
http://curehd.blogspot.com/2014_10_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. Another major supplement, creatine, proven ineffec. View my complete profile. Huntington's Disease Society of America. Huntington's Disease Drug Works. HDSA Orange County (CA) Affiliate.
At Risk for Huntington's Disease: February 2014
http://curehd.blogspot.com/2014_02_01_archive.html
At Risk for Huntington's Disease. HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. Accentuating the positive: Olympic medalist Sarah . To take, or not to take, unproven supplements in t. My ongoing search for the meaning. View my complete profile. HD Free with PGD!
TOTAL LINKS TO THIS WEBSITE
30
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Chris Furbee's Blog
Wednesday, January 24, 2007. Posted by Chris Furbee at 3:17 PM. Monday, November 13, 2006. Well the NYT's has finally decided to run an article on me or at least about my film. I know I should be writing more in this blog so people can keep up with what's going on with me and my film all I can do is say that I will try. I hope you are well. Posted by Chris Furbee at 4:53 PM. Sunday, April 02, 2006. Posted by Chris Furbee at 4:04 PM. Emeryville, California, United States. View my complete profile.
Huntingtons' Dance - Dedicated in helping educate people as to what Huntington's Disease
As the days unfolded, Chris realized that Rosemary was in complete denial of her condition. With few resources organized, Chris had to find ways to provide critical medical care for his mother who not only resented his help and felt he was meddling in her life but who also felt there was nothing wrong with her. Site produced by Gregory Wilker.
huntingtonsdisease-laxplayer212.blogspot.com
Huntington's disease
Saturday, April 13, 2013. Saturday, March 7, 2009. Sources used for these blogs. Huntington's Disease." Medicine Net. Feb. 2009 http:/ www.medicinenet.com/huntington disease/article.htm. Prevalence and Incidence of Huntington's Disease." Wrong Diagnosis. Feb. 2009 http:/ www.wrongdiagnosis.com/h/huntingtons disease/prevalence.htm. Huntington's Diseaes." Mayo Clinic. Feb. 2009 http:/ www.mayoclinic.com/health/huntingtons-disease/DS00401/DSECTION=symptoms. Monday, March 2, 2009. The Hereditary Disease Foun...
huntingtonsdisease.org
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HDA Blog – The blog of the Huntington's Disease Association England & Wales
The blog of the Huntington's Disease Association England and Wales. Welcome to the blog of the Huntington’s Disease Association England and Wales. New posts will be coming soon…. HDA England & Wales. January 24, 2016. Visit hda.org.uk or click here. For more information about Huntington's Disease and how we can help. Proudly powered by WordPress.
Hereditary Neurological Disease Centre
Welcome to the Hereditary Neurological Disease Centre. The Hereditary Neurological Disease Centre (HNDC) is a 501 (c) (3) tax exempt organization. HNDC's mission is to provide diagnosis, disease management, and support services for individuals with Huntington Disease and their families. The Centre provides diagnosis and referral for persons with other hereditary neurological diseases. We offer diagnostic services, professional care, genetic testing, and patient advocacy. Jun 27, 2017. Jun 27, 2017. Appro...
