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Leiomyosarcoma, the rare and unknown disease. We are blessed in that one of our beloved Board Members, who was a caretaker for her husband with LMS, wrote a book about him through her observations.
It is not just about LMS, it is about living with LMS as Joe battled through his diagnosis and fight with the disease.
Through the efforts of Gloria Schwartz, we are now published and our disease is no longer an unknown. I recommend this as a gift for all your family and friends as a way to open communications and help understanding.
Gloria lost her own battle with metastatic breast cancer in June 2008.
She was gracious in having all royalties from the book donated to this Foundation.
Last Edited -
20 September 2010 22:58 pm
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