When Doctors Don't Have the Answers: Posthypoxic Myoclonus

Lance Adams Syndrome

Paula B


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Joined Apr 28 2012
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FEMALE
Vancouver, BC
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When Doctors Don't Have the Answers Posthypoxic Myoclonus

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3 Comments

Reply JoAnne Davis
11:27 PM on January 17, 2013 
Hi Paula, My name is JoAnne and my husband has Lance Adams syndrome. If you would like to contact me my email is [email protected]
Looking forward to hearing from you.
Reply Tammi hale
4:17 PM on July 21, 2012 
Hi Paula. My husband also suffers from post anoxic action myoclonus. Would love to chat via email if you are open to it. [email protected] Thanks!
Reply Paula B
8:45 AM on June 16, 2012 
I have been diagnosed with posthypoxic myoclonus since March 2011 after a cardiac arrest resulting from an asthma attack. to learn more about me please contact me by email @ [email protected] or find me on facebook. My name is Paula Bednjak and I am from BC, Canada. I am very interested in talking to someone else with posthypoxic myoclonus. We could help eachother out I think! =)