There isn’t anything I wouldn’t do for you, we stick together and see it through

I am sitting in my recliner at chemo and wondering how life happened before the miracles of modern technology and medicine. I’m tired and really should close my eyes to sleep, but I’m down to less than an hour in the chair and it just doesn’t seem worth it.

I did speak to Dr. A about the depression on Saturday/Sunday and she offered 2 options. First, she doesn’t think it’s the anti-emetics, instead she thinks it’s likely the steroids. So, I can either go on an antidepressant all the time (which I really don’t want to do to manage the 2 days a cycle that I’m feeling blue), or we can try to lower the steroid dose. We are going to try that this cycle and see if that makes a difference. Unfortunately, Dr. A did indicate that this is a fairly common issue for people going through chemo. But, with today being cycle 4, that means I’ll have only 2 more rounds left. Two rounds left. So effing excited that today is 2/3 done.

Next, thank you so much for your name suggestions for my wig. I have shortened the list down to 7 names. I will see if I can shorten it even more tonight. Tomorrow I will give the boys the top contenders so that they can pick the winner

Goodness, I’m skipping all over the place today, and while I hate to, I’m going to end on a well-meant admonishment, because it’s my blog, and I can. I really hate how much people are keeping from me. I’m not talking about my doctors, I’m talking about my friends who don’t want to trouble me with things going on in their lives.

Like my friend J who has taken my youngest for more playdates than I care to admit. And who, about 2 weeks after the fact, I found out was in the hospital for 7 days with cellulitis. I don’t know whether it was a week I could have helped out too much or not, but I would have made an effort to take her son for a play date, or at least sent a meal over.

Then, there’s another family who I just found out that the Mom is having some health issues and will be out of town for upto 2 months. And, while there are things that I can’t or wont do, there are certainly things that I can help with: sending a meal or taking their kindergartner for a playdate, or something. People have been so generous with us, I want to give back.

I’m not offering to overextend myself, or do something that isn’t realistic or dangerous to my health. But really, especially on weeks 2 and 3, I feel mostly normal, or at least “new normal.” I would love to help and to do for others. I would love to give back to my friends and the communities that have given us so much.

Please let me decide what I can or shouldn’t do. Include me, and let me feel like I’m part of your community, able to give back. I promise I will be responsible for myself: I am with directing my healthcare, and I will with accepting the agreements that I make. Most of you have asked what you can do to help. There it is. Let me be a part of your lives as you’ve made yourselves part of mine.

4 Comments

  1. Betty Esworthy said,

    December 25, 2009 at 11:06 am

    You are in my thoughts and prayers! Hope they get a handle on the depression soon. I have it and know it is not a good feeling. Just know that I am here if you need me. Let’s have lunch soon!!

  2. sarahfeather said,

    December 29, 2009 at 3:57 pm

    Eileen:

    Sorry to hear about your depression. I was on Celexa for six months after surgery #2, and it really made a difference for me. Like someone put brighter light bulbs in all of my fixtures. I was reluctant to take something, too, but the crying was really a drag. It’s not a proud moment, but how many other things have you been through? You do what you must to keep going as “normally” as possible. (As my mom told me, “People take antidepressants when their lives don’t even really suck, and yours (mine) SUCKS. Do what will make you feel good!”)

    Keep your chin up and your kiddies close – have a VERY Happy New Year!

    Sarah (the Carcinista)

  3. Laura said,

    December 29, 2009 at 11:40 pm

    well-said, eileen. i love your blog! remember, we are all “new” at this too. having a friend with the “c” word. but you are right. we’ll try to do better. we love you, mate!

  4. Tanta Paula said,

    January 18, 2010 at 11:30 am

    You are truly a great person beenie; however, maybe your friends want you to get back on your healthy feet and then they will bombard you with paybacks…HAHAHA and boy oh boy they can be a witch. Love you kiddo and know just how you feel about helping out.

    Much Love,
    Tanta Paula


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