Huntingtons Disease || My struggles & experience
Leanne Delong Leanne Delong
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 Published On Jun 16, 2016

I have finally posted a personal story regarding Huntingtons Disease, which currently has no cure. I discuss genetic testing, having a family and early emotional and cognitive symptoms of the disease.
Please share this and help raise awareness about the disease.

MORE INFO: http://www.huntingtonsociety.ca

ENROLL PROGRAM: https://www.enroll-hd.org/

Edmonton HD Chapter: https://www.facebook.com/Huntington-S...

*100 % OF FUNDS RAISED WILL GO DIRECTLY TO THE HUNTINGTON SOCIETY OF CANADA*


BACKSTORY:
I have decided to raise money for the Huntingtons Disease Society of Canada, by completing insane challenges, pushing my body to its limits and also spread awareness about the disease through this campaign over the next several months.

On this channel you will find weekly updates on how the campaign is going, videos of completed challenges and even personal stories about the disease, how my family is affected, how my life is and plenty more!

CAMPAIGN LINK: https://www.gofundme.com/hdchallenge

Quick Fact video on Huntingtons:    • The Dancing Disease, called Huntingtons  

HD Society of Canada: http://www.huntingtonsociety.ca

FIND ME:
Twitter:   / leannedelong  
Tumblr:   / leannedelong  
Instagram:   / leanne_delong  
Snapchat: ReviewFools

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