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YPAHD | Young People Affected by Huntington DiseaseYoung People Affected by Huntington Disease
http://www.ypahd.ca/
Young People Affected by Huntington Disease
http://www.ypahd.ca/
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YPAHD | Young People Affected by Huntington Disease | ypahd.ca Reviews
https://ypahd.ca
Young People Affected by Huntington Disease
ypahd.ca
Teens | YPAHD
http://ypahd.ca/teens
Living at Risk for HD. On May 17, 2013 in Teens. 50% Chance of Inheriting HD. On May 17, 2013 in Teens. On May 17, 2013 in Teens. Searching for Characteristics of HD. On May 17, 2013 in Teens. Living Life While at Risk. On May 17, 2013 in Teens. On May 17, 2013 in Teens. Being at risk, causes a lot of worries and concerns for young people. So it is important that young people at risk are supported by those around them. As a family, the best way to cope with Huntington’s disease is to discus...Learning ab...
Mentorship Program | YPAHD
http://ypahd.ca/mentorship-program
The HSC is proud to have a mentorship program to offer it’s youth. Our mentors are required to go through training and are knowledagble about HD and also privacy, confidentiality and safety of the mentees. If you or anyone you know would like more information about becoming a mentee please contact Erin Stephen, Mentorship Coordinator at mentorship@huntingtonsociety.ca. Or toll free 1.855.253.0215. Like Us on Facebook!
Calendar | YPAHD
http://ypahd.ca/calendar
November 19 28, 2014. It’s election time and we are asking all of you to submit your nominations for the executive positions no later than November 19, 2014. If you would like to put your name forward, or nominate someone for a position, please send your nomination to Devin at dbonner@huntingtonsociety.ca. Elections will take place via email between November 19th and November 28th. First point of contact with HSC National Office. Familiar with all YPAHD activities. Time commitment: moderate to heavy.
YPAHD | Young People Affected by Huntington Disease
http://ypahd.ca/page/2
We provide a community and support network for young people affected by Huntington’s Disease. Ever wondered what you can do more to help someone with HD? It is important that young people at risk are supported by those around them. Testing is a personal choice a choice only you have the right to make. We provide a community and support network for young people affected by Huntington’s Disease. Ever wondered what you can do more to help someone with HD? Posted on Mar 14, 2015 in News. What is a Mentee?
News | YPAHD
http://ypahd.ca/category/news
Posted on May 20, 2015 in News. The HSC is proud to have a mentorship program to offer it’s youth. Our mentors are required to go through training and are knowledagble about HD and also privacy, confidentiality and safety of the mentees. If you or anyone you know would like more information about becoming a mentee please contact Erin Stephen, Mentorship Coordinator at mentorship@huntingtonsociety.ca. Or toll free 1.855.253.0215. Posted on Apr 25, 2015 in News. Posted on Mar 14, 2015 in News. Mentees are ...
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Link | Huntington's Disease News
http://www.newshd.net/link
Venerdì, aprile 21, 2017. Sign in / Join. Log into your account. FDA approves a new drug for symptoms of Huntington’s disease. FDA Approves Second Drug for Huntington Disease Symptom. New discovery is a step towards developing Huntington’s disease treatments before…. Affrontare il rischio genetico e proteggere la speranza. Stanford study identifies new biomarkers for Huntington’s disease. HD free with PGD. Predictive testing for HD. Independent Swedish HD Site. 8211; Information in Swedish about HD.
Huntington's Disease Youth Organization - Links
http://en.hdyo.org/eve/links
Sign up to save your choice. Sign in or join HDYO. A great site from a group of students at Stanford University, America. This site is full of information about Huntington’s disease, and some cool stuff for kids too. Teens. A site with lots of information on medical and research aspects of Huntington’s disease, along with a forum to ask questions. Teens. HD free with PGD. A nice site set up by a young woman to provide advice, information and support to those looking/going through PGD. Teens. The official...
Peterborough Chapter, Huntington Society of Canada
http://www.hdpeterborough.org/youth.html
Walk to cure HD. Young people often have special problems understanding and adjusting to life in a family that's touched by HD. The Huntington Society of Canada has created a special nation-wide "chapter" for young people where you can connect via social media and online to share experiences and find support. It's Young People Affected by Huntington Disease - YPAHD. Young people can head over to their web site and get started! LOTS OF FUN, too. Check out the great video "What is HD? August 19-22, 2016.
HD Organizations | HSC Southern Alberta Chapter
https://curehd.wordpress.com/organizations/hd-organizations
Health and Advocacy Organizations. HSC Southern Alberta Chapter. 124; Comments RSS. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 37 other followers. We are volunteers raising funds and awareness for a treatment and ultimately a cure for Huntington disease. While this promising research is ongoing, we try to improve the lives of families affected by HD. Check out our Wish List. We also work closely with HSC's Resource Centre Director. HDSA is a U...
NADZIEJA DLA HD Choroba Huntingtona
http://nadziejadlahd.blogspot.com/2010/06/inspirujace-biografie-dr-nancy-wexler-i.html
NADZIEJA DLA HD Choroba Huntingtona. Wirtualna grupa wsparcia dla ludzi młodych dotkniętych chorobą Huntingtona. Choroba Huntingtona jest dziedziczną chorobą mózgu. Powoduje, że chory traci kontrolę nad ruchami własnego ciała. Stopniowo prowadzi do utraty zdolności do samodzielnego życia. Dotknięty nią człowiek nie jest w stanie samodzielnie chodzić, mówić ani nawet przełykać. Dotychczas jeszcze nie wynaleziono na nią lekarstwa. Środa, 2 czerwca 2010. DR NANCY WEXLER i dzieło jej życia. Fundacja dra Wexl...
NADZIEJA DLA HD Choroba Huntingtona: 03/19/10
http://nadziejadlahd.blogspot.com/2010_03_19_archive.html
NADZIEJA DLA HD Choroba Huntingtona. Wirtualna grupa wsparcia dla ludzi młodych dotkniętych chorobą Huntingtona. Choroba Huntingtona jest dziedziczną chorobą mózgu. Powoduje, że chory traci kontrolę nad ruchami własnego ciała. Stopniowo prowadzi do utraty zdolności do samodzielnego życia. Dotknięty nią człowiek nie jest w stanie samodzielnie chodzić, mówić ani nawet przełykać. Dotychczas jeszcze nie wynaleziono na nią lekarstwa. Piątek, 19 marca 2010. Podaj Dalej, komu dać 1%". Maile kierujcie na adres:.
NADZIEJA DLA HD Choroba Huntingtona: ważne rozmowy
http://nadziejadlahd.blogspot.com/2009/10/wazne-rozmowy.html
NADZIEJA DLA HD Choroba Huntingtona. Wirtualna grupa wsparcia dla ludzi młodych dotkniętych chorobą Huntingtona. Choroba Huntingtona jest dziedziczną chorobą mózgu. Powoduje, że chory traci kontrolę nad ruchami własnego ciała. Stopniowo prowadzi do utraty zdolności do samodzielnego życia. Dotknięty nią człowiek nie jest w stanie samodzielnie chodzić, mówić ani nawet przełykać. Dotychczas jeszcze nie wynaleziono na nią lekarstwa. Czwartek, 15 października 2009. O tym, czego doświadczam, czym teraz żyję.
NADZIEJA DLA HD Choroba Huntingtona: 50/50?...
http://nadziejadlahd.blogspot.com/2009/10/5050_29.html
NADZIEJA DLA HD Choroba Huntingtona. Wirtualna grupa wsparcia dla ludzi młodych dotkniętych chorobą Huntingtona. Choroba Huntingtona jest dziedziczną chorobą mózgu. Powoduje, że chory traci kontrolę nad ruchami własnego ciała. Stopniowo prowadzi do utraty zdolności do samodzielnego życia. Dotknięty nią człowiek nie jest w stanie samodzielnie chodzić, mówić ani nawet przełykać. Dotychczas jeszcze nie wynaleziono na nią lekarstwa. Czwartek, 29 października 2009. 50/50 - to mój stan ducha. Przez kilka lat o...
NADZIEJA DLA HD Choroba Huntingtona: 06/02/10
http://nadziejadlahd.blogspot.com/2010_06_02_archive.html
NADZIEJA DLA HD Choroba Huntingtona. Wirtualna grupa wsparcia dla ludzi młodych dotkniętych chorobą Huntingtona. Choroba Huntingtona jest dziedziczną chorobą mózgu. Powoduje, że chory traci kontrolę nad ruchami własnego ciała. Stopniowo prowadzi do utraty zdolności do samodzielnego życia. Dotknięty nią człowiek nie jest w stanie samodzielnie chodzić, mówić ani nawet przełykać. Dotychczas jeszcze nie wynaleziono na nią lekarstwa. Środa, 2 czerwca 2010. DR NANCY WEXLER i dzieło jej życia. Fundacja dra Wexl...
NADZIEJA DLA HD Choroba Huntingtona: 10/12/09
http://nadziejadlahd.blogspot.com/2009_10_12_archive.html
NADZIEJA DLA HD Choroba Huntingtona. Wirtualna grupa wsparcia dla ludzi młodych dotkniętych chorobą Huntingtona. Choroba Huntingtona jest dziedziczną chorobą mózgu. Powoduje, że chory traci kontrolę nad ruchami własnego ciała. Stopniowo prowadzi do utraty zdolności do samodzielnego życia. Dotknięty nią człowiek nie jest w stanie samodzielnie chodzić, mówić ani nawet przełykać. Dotychczas jeszcze nie wynaleziono na nią lekarstwa. Poniedziałek, 12 października 2009. Z czym kojarzy Ci się HD? Przez kilka la...
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YPAHD | Young People Affected by Huntington Disease
We provide a community and support network for young people affected by Huntington’s Disease. Ever wondered what you can do more to help someone with HD? It is important that young people at risk are supported by those around them. Testing is a personal choice a choice only you have the right to make. We provide a community and support network for young people affected by Huntington’s Disease. Ever wondered what you can do more to help someone with HD? Posted on May 20, 2015 in News. This is a great oppo...
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