NL #35: I have noticed a blog change that you may be only partially aware of, so I thought I'd fill you in. As some of you have noted, comments on the blog have decreased since I moved to a new platform. In that same time, more of you have contacted me directly, in person or via email, to tell me of your own struggles and the struggles of those close to you. Each of you has shared that the blog has been helpful to you in this time and many have mentioned that you have shared the blog--or particular entries--with others.
The community of commenters here is and has been a real source of support for me. Hearing from those of you who are facing changes in your own lives and who are finding this blog a source of support for you means the world to me, too. Having you share your stories with me--in either venue--helps me to feel a part of community and not so alone in this struggle.
Without your comments, on the site or in more personal communication, I can feel a bit like Who-ville praying for a Horton: Is anybody out there?
Thanks for being here. Mary
"For me a brain tumor and its treatments are not a pause in the adventure of life, but instead a part of the adventure of life." Mary has survived big hair, a brain tumor, coming out, distressed bowel syndrome, hallucinations, radiation, and a car wreck. Here Mary takes us from public transportation horrors to the joys of sharing life with you. Though you probably won't want to have a brain tumor; you will wish that you could see the world through Mary's eyes. Sister Jen
A Photograph of me without me in it
Monday, June 7, 2010
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I am here! Every day. No thoughts yet, as I haven't had my morning coffee. Keep on writing, Mary.
ReplyDeleteEm,
ReplyDeleteI am here too! I have some music to share with you at some point soon. Let's get together soon!
Pea