Portrait of a Cancer Fighter!!
Finally, I figured out how to post a picture to this blog!!! Some of us are slow learners. And I can't blame the disease for my brain malfeasance. . . .
Anyway, this was taken the morning before the first treatment. We'll see how it goes as the weeks progress. . .
So today began with radiation treatment #4 (31 more to go) and the second day of fluid infusion after chemo. So far, so good on the chemo - I did feel a slight wave of nausea late last night but the prescriptions that I got set me right. It will be interesting to see how it goes once the anti-nausea drugs that were in the IV cocktail wear off. I have to say that cancer is not for wimps - there's a new adventure every day. And I'm finding all the routines I have to follow to try to retain dental health, to treat the mouth ulcers that will soon begin to form, and to keep up with the five time a day swallowing exercises is near a full-time job. If you don't think you're up to the regimen, don't sign up for the disease, I tell you!! (Yes, that is a feeble attempt at a joke. . . ;-)
But what is not a joke are the revelations I've been having about where I see my life going after this. I know I had mentioned working for/volunteering at Hospice after David passed 9 years ago as I was very, very impressed by the organization and the people that work there. I will admit that my interest waned for a while, but it is definitely coming back and I know that I will ultimately volunteer there, with the perspectives of both someone who has seen a loved one's passage eased by the angels of Hospice and of a cancer survivor my own self. But what I have learned these past few weeks grappling with the disease and meeting and talking with others with the disease, I realize how to be the most effective volunteer I can be. What I'm finding is that people want to talk about their experiences and that's what comforts them. So, when I become a volunteer, I'll certainly have the 'street cred', but that's not what my 'clients' are going to care about. So, instead of telling them about what David and I went through, my entire personal introduction will go something like, "My name is Joe, my son David had a very satisfying Hospice experience x years ago and I'm in my nth year of becoming a survivor. Now, tell me what's your story". I will be able to listen and I will mean it. I will only mention my past history again if they ask. People are listening to me right now and I want give the future patients of the disease the empathetic ear they deserve.
OK, off of soapbox.
Peace and love to all!!!!
Joe
You are a trouper Joe. Great post - thanks for keeping us sane way over here in Seattle - wondering about your treatment and health. Love! Diane
ReplyDeleteLooking strong!
ReplyDeleteTalking is theraputic, but listening is meditation for the soul. Love your outlook. Stay strong! - Kristen Little
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