Showing posts with label testing. Show all posts
Showing posts with label testing. Show all posts
Thursday, February 09, 2012

The quandary of denial in the Huntington’s disease community (Part I)

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The natural human tendency toward denial presents one of the biggest obstacles to strengthening the Huntington’s disease movement, including...
10 comments:
Sunday, December 18, 2011

Kate's untested baby (Huntington’s disease and abortion – Part II)

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Kate Sandbulte, a 20-year-old woman who lives in Iowa, long lived life to the fullest. Her mother, Tara Hansen, recalled that Kate was “was ...
8 comments:
Friday, October 21, 2011

Huntington’s disease and the financial jitters

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As I’ve written before, living with the deadly gene for Huntington’s disease is like a high-wire act . Fearful that HD’s terrible symptoms c...
Friday, September 02, 2011

One Man's Story: Entering the Light

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(At the invitation of the Huntington’s Disease Society of America [HDSA], I wrote this article for the September 2011 issue of the HDSA su...
1 comment:
Monday, March 14, 2011

A cascade of emotions about Huntington’s disease

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The world will remember Friday, March 11, 2011, as the day that a devastating earthquake and tsunami overwhelmed Japan and triggered a poten...
2 comments:
Monday, October 11, 2010

Losing control, seeking connections

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As a person who is gene-positive for Huntington’s disease, I have steadily stepped up my involvement in the cause to stop it. My commitment ...
1 comment: