Some videos for you too!
Click on the links for some videos of the storm...
this one makes me laugh because I have no idea what I was saying...
This one is just crazy windy
This blog began as a way for me to record my journey with PVNS, its struggles as well as many moments of success.The posts have slowly been moving away from PVNS as has my life, but PVNS(pigmented villonodular synovitis) is still a part of my life....I hope others can read my experiences and feel less isolated. My surgery was July 17th 2007, and the posts after that date include pics of the incisions/scars. Best of luck to other PVNS patients/survivors!
Posted by TallGal at 6:24 PM
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