Thursday, August 13, 2015
Dear Dad (#4)
Sunday, June 21, 2015
Dear Dad (#3)
I’m going to Washington D.C. this week, and I find myself missing you all the more. The one and only time I was in D.C. was with you, when you chaperoned our 8th grade trip. It was one crazy busy day, and I’ve found myself wanting to back there for a long time, but it has a different meaning now that you’re gone.
Wednesday, December 17, 2014
Dear Dad (#2)
Today is your birthday. You would have been 63. I'm not really sure how I feel about this day or how I am supposed to feel. I miss you...a lot...that's for sure.
Thanksgiving was better than I thought it would be. Except that you weren't there, which was huge. But it was the first time that I've been home since you died. And I had no idea what to expect.
It's weird because I often caught myself thinking that you were at work or sleeping in the next room. But I had to keep reminding myself that, that wasn't the case. That you're gone. Permanently.
And that still hurts terribly.
It's been a little bit more than a year since Zaydie died. So when I was home for Thanksgivng, we had the unveiling for his stone. I didn't want to go because I didn't want to face the reality that you died, too.
We went, and it was fine. Until I walked to where you're buried. Around the mound of dirt, they've put a concrete barrier. And it's still so new that it isn't flush to the ground. It was creepy. It's still too fresh and new. Maybe it was too soon for me to go back there.
I don't know how I was supposed to feel being there. Connected to you in some way? The place I can go to "see" and visit you? Because I didn't feel connected or comforted. I felt empty.
I feel like it's a bad consolation prize for not having you physically around.
Things are moving forward on my project for you. And I hope that after the New Year, I'll be able to share with you amd everyone else what has been going on. But for now, mums the word.
Andrew and I started looking for apartments. Yay! And I'm sad that you won't be able to see our relationship grow and evolve. But I'd like to think that somewhere, someway, you know.
It's hard to imagine life moving forward without you, but it has to. We don't have a choice, or we die too.
As things start to get a little easier, we are hit with Thanksgiving or Chanukah or your birthday or some other even that you're not here for. And it brings everything back again.
I'm not sure what else to say except that not a day goes by when I don't think about you. And wish you were here. And miss you. And love you.
I love you,
Leslie
Friday, November 21, 2014
Dear Dad (#1)
Tuesday, February 24, 2009
Building A Better Me, Part 1: Being A “Smart Patient” Matters*
“Wham! From the very first moment of a health crisis, you’re unprepared and not in control […]” (170).
Welcome to my first blog series. I’ve been on a self-improvement kick lately, so I’ll be exploring a variety of issues, some which deal specifically with chronic illness, others that do not. I hope that you find some of these posts useful for your own life, and that you’ll humor me as I do some rather public self-exploration.
When I embarked on this journey of self-discovery, which basically meant scouring the shelves for books related to various aspects of self-improvement, and devouring them as quickly as possible, the one thing I promised myself is that I would try and stick to looking towards the experts for advice on the things in my life I was looking to improve.
That said, I wasn’t too impressed with myself that I scored a 19 out of 40 on the “Smart Patient” Quiz. On the other hand, though, I wasn’t all that surprised. When you’re not expecting more than annual visits to the doctor and a few minor ailments here and there, when you’re hit with a chronic illness, you’re thrown feet first into the medical “ocean”. And honestly, it’s not always that easy to keep up. It’s literally sink or swim…
While I don’t pride myself on being enamored of Oprah’s cronies, I’ll admit that “You: The Smart Patient” by Drs. Michael Roizen and Mehmet Oz was very useful and user friendly.
They say, “[…] our patient really plays a triple role, he or she is our partner and our chief, and also the very citizen we’re protecting and serving” (13). I really like this analogy because a lot of times, the doctor-patient relationship can be very unbalanced. It’s nice to hear doctors acknowledge that we are their business, front and center. However, much of the onus is still on us, the patients… “Most patients don’t do a great job of communicating with their doctors […]” (41).
In my opinion, these are the top 10 tips that I gleaned from the book:
1. Ask questions of your doctor. “Sweat the small stuff.” In other words, don’t lay low. “Speak up!”
2. Know your family history.
3. Find a doctor who is experienced, but young enough to see you through the majority of care over your lifetime (Not sure this is one is doable for some us in the young and chronically ill category).
4. Explore cutting edge techniques, the best doctors, and hospitals (“size matters”).
5. The pharmacist is a great resource for medical information.
6. Always get a second opinion (you shouldn’t feel guilty about doing so).
7. Appoint a health advocate.
8. Don’t believe everything you read on the Internet.
9. Even though you are a patient, you have rights. So use them or lose them.
10. Be skeptical about and cautious of alternative medicine therapies and remedies. That doesn’t mean you shouldn’t utilize them, just always make sure to consult your doctor in order to avoid any interactions with medications you are already taking.
And remember, all of this is the advice for the (currently) healthy folks… Means some of us “sickos” have a lot to learn…
Overall, “You: The Smart Patient” is a good resource to look things up in as needed, but I don’t recommend you read it cover-to-cover like I did, and I don’t feel it is particularly useful for chronically ill people (especially those of us new to this camp). For instance, one suggestion is that you take all of your actual medication bottles to doctor’s appointments. Really? You’re lucky that I take my medication, so don’t push your luck…
The main thing that this book emphasizes, which I think is critically important, is that we have to be our own health advocates. While it’s also good to have someone appointed as your health advocate in case you can’t make decisions for yourself, we are the keepers of ourselves. We have to be the first line of defense in finding the right doctors and providing those on our medical team with the information they need to help us get the best care possible.
There are so really useful handouts in the book, though, that you can use to keep track of all of your health and medical information. You can find versions of these for free at www.realage.com.
*My friends have had it with me, but they’re going to have to hang in a little longer. They can no longer ask for book suggestions because all I read are patient narratives and books for my self-improvement “project.”
*****
(Roizen, Michael, and Mehmet Oz. You: The Smart Patient. New York: Free Press, 2006.)