Julie and I are doing fine. It's been nearly three years since the stem cell transplant and I am feeling great. Both oncologist say we will cut back my visits to once each year...next one is in February, 2013, at the Medical Center. There are two hold over "side effects" from my treatments -- neuropathy in my left foot and daily naps. I find I really enjoy the afternoon naps -- very refreshing. The tingling in my left foot is annoying for me but dangerous for my massage therapist when I give an uncontrollable kick of my foot with the first touch.
If there are any pluses from this whole cancer experience, I guess giving myself permission to take a nap, gaining a truer sense of what it means to "be in the present", and allowing myself a regular massage rank right up there.
I am venturing out into social media. I have a Facebook page, twitter account and thought renewing the blog would be a good way to see how this goes in terms of our efforts to stay in touch. I say "our efforts" because Julie, although better at organizing "live" social engagements with friends and family, relies more on my efforts with electronic media to promote and support those relationships.
Julie and I have been blessed with our partnership for 39 years (plus 4 more years that we devoted to exclusive dating)...so far it seems to be working fairly well. We look forward to opportunities to break bread together and the sharing of our thoughts, prayers and joys with family and friends.
Tim.
Tim...Since you've been back to work, I've noticed renewed passion. I've thoroughly enjoyed the more "hands on" direction you've taken in some of the activities of Disability Rights Nebraska, ie the Community Advocate Network. I am better for my involvement with you and the agency! Thanks for the update!
ReplyDeleteMary - thank you for your kind comments.
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