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!
I'm leaving tomorrow, to return home... How do I do that? How do I pack up my stuff, get in my truck and say good bye to my father who has just lost his wife? How do I deal with tomorrow, the day after that...and the day after that?
I am a daughter without a mother... and my heart doesn't know what that means...
Posted by
TallGal
at
10:45 PM
2 comments:
My thoughts are with you, Kim. Though you've lost your mother, she will always be within you. You are her living legacy. It's still not fair. It's the deepest cut. I feel for you and your family. Hang in there. You have so much to offer your students and friends...
With prayers and sorrow,
Your PVNS Friend, Karen.
I wish there were a healing process that were easy. One day at a time is the best that you can do. Knowing that you're loved by the rest of your family and friends, as well as time will help. I wish you strength, much support, and the best of luck. Your heart will be comforted over time, and knowing what a wonderful daughter your mother has been blessed to have. Take good care. Always hoping for best.
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