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!
Mom goes to the oncologist tomorrow... I hope that we learn something new... something about what is going on and what the next steps are... it makes me anxious... maybe no news is better than the news that we may get... or maybe there will be some hope... I don't know...
This waiting crap sucks.
Posted by
TallGal
at
9:20 PM
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