Monday, July 30, 2012

Caregiver Podcast

Listen up! Caregiver Expert and author of The Medical Day Planner, Tory Zellick, discusses all things caregiver with me. If you have a caregiver or are a caregiver, click on the arrow to start the podcast and learn valuable things that will help you both.

And, don't forget to enter the contest for the book, which closes Wednesday at midnight CA time. Right now, the odds are excellent!

Go to All Things Caregiver for more information.

Listen to internet radio with But Doctor I hate pink on Blog Talk Radio

Saturday, July 28, 2012

The Medical Day Planner - Review and Contest!




I can't be more enthusiastic about the book The Medical Day Planner: The Guide to Help Navigate the Medical Maze by Tory Zellick. This book is just that - truly an amazing guide. It's a portable, easy-to-use planner, designed for patients or caregivers to keep track of information necessary during the course of a loved one's cancer diagnosis. It allows you to easily track doctor's information, medication history, treatments, procedures, tests and scans, appointments, hospitalizations and also includes a 52 week day planner. These sections all cross-reference, allowing you and your caregiver to be prepared during the course of your illness.

Not only are there spaces to write down and keep track of this information, there are pages with information on why you should keep track, what terms mean, and other helpful tips for both patient and caregiver alike.

I wish WISH WISH I'd had this book at the beginning of my diagnosis. I have advocated often that patients  get themselves a binder and put in all scan results, pathology reports, medical test outcomes, blood tests and other medical records as well as job/disability paperwork. Having a well-organized binder to flip through has come in handy more times than I have been able to count, but they can get unwieldy and there are things missing, such as appointments, scan dates, doctor information, medications that you will need down the road. This planner provides a place for all that and more - giving you the ability to keep all of that in one compact book. With the two things, a binder for your medical paperwork and this book to keep track of everything else, you will have every aspect of cancer treatment and history covered and will need no more.

I am the messiest organizational freak you will ever see.  I am a sucker for all organizational tools but I must say, this is one of the best.  I am in love with this book.

If you are newly diagnosed with cancer, start with this book. If you are metastatic, this is one place your loved one can go to find out all that information when the dreaded day comes you can't answer these questions yourself.  Take some time and fill it out for them.

Hmmm.....does my husband know when my last scan was? Who my doctors are? What my medications are? Probably not. All those are typical questions asked when admitted to a hospital, and there it is, right at your fingertips.  It will be so handy for a caregiver to have during that sad time - one less thing to worry about.

I haven't come across a product I like as much as this one in a long, long time.  Can you tell?

Because I like it so much, I've asked the author, Tory Zellick, to be my guest this Monday on my blog talk radio show, where we will be talking all things caregiver.  No, it won't be about this book only - we will discuss all aspects of caregiving, including how we as cancer patients can make it easier, how to best care for yourself as a caregiver, and how to emotionally prepare for the end.

And, here is the best news:  Tory  has agreed to give a book away to one of my readers! Honestly, this is a prize you want, whether you have just just been diagnosed with cancer, or are in the middle of your journey.  And, it is the perfect gift for that newly diagnosed person.

How do you win, you ask? It's easy!

Please either make a comment on my blog. (You may do so anonymously but please "sign" your comment with something that I can identify you with. Too many "anonymous" will get confusing.) Or, if you have trouble posting a comment, you may make a comment on my ButDoctorIHatePink facebook page about the book.  There will be a post dedicated to these comments.  If you haven't liked me by now, go right ahead.    And, as an added bonus,  if you "share" it from my page, I will give you two entries.

 You have until Wednesday, August 1st at midnight PDT. Thursday, I will take all qualified entries and draw them out of a hat and annouce the winner, probably via video.  Tory will then send out a copy to you.

Also, please  "like" Tory's page on facebook too. Extra karma points go for that one.

Enter. You will love this book!

Friday, July 27, 2012

Edumacatin' - C-Diff by Z-Dogg

I love me some Z-Dogg MD and especially this video, which is so close to my heart and rear. Listen up cancer patients - c-diff colitis is the worst thing I've gone through medically to date.

This edumacatin' is necessary - when sick with it, I had a hospital employee come in and see me, ungloved and ungowned. I made him leave but who knows, maybe a spore got on him and he spread it to the next patient. So if you work in a hospital, use soap and water and don't forget to glove and gown up when around a c-diff patient!

If you have a lowered immune system and must take an antibiotic, for reals, then also consider taking Florastor along with it.  While studies are not conclusive that it will prevent c-diff, there is some evidence that it might help.  Yo, if you have a port, take the capsules and not the powder. As always, ask your doctor before you take anything. Word.

Thanks to c-diff, I am a cancer patient who can never take antibiotics again. Scary.

Enjoy.

Monday, July 23, 2012

Uproar in the Blogosphere - Angelo Merendino Photos - Updated News

So, it looks like there has been a resolution to the uproar about where to exhibit the moving photos of a woman dying of breast cancer. The Cleveland gallery has agreed to exhibit them.

I, for one, am very glad they found a more appropriate home, and I would encourage and hope that everybody go see these powerful and emotional photos. As you look at them, think of women, like me, who are undergoing the same things that Jen went through and know that she represents thousands of us across the country.

Also, I'll be on blogtalkradio in one hour. The topic will be a more fun one - the crazy things people say to us with breast cancer - and what should they say?

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Friday, July 20, 2012

Uproar in the Blogosphere - Angelo Merendino Photos

It's funny, but as I continue plodding along in my journey with breast cancer, I feel less and less like fighting about anything. Hell, I even used the phrase, "journey with cancer" which would would formerly have me up in arms.

My, how I have changed.

So when the blogosphere exploded with the latest cancer controversy, I immediately decided to ignore it and maybe upload more photos of my dog.

I'm having second thoughts.

The controversy involves a man, Angelo Merendino, who took some absolutely beautiful photos of his wife as she went through her treatment and died from metastatic cancer.  Apparently, these photos were exhibited in a building called the Gathering Place, and because they upset the people who, uh, gather there, they were taken down. That news went viral, and everybody online who is involved with cancer in some way exploded with anger, feeling that cancer patients were being dissed or shoved aside. They were encouraged to like this gentlemen on facebook for a show of support.

Go ahead, his photos are beautiful; he honored his wife. I like him.

Gayle Sulik, his friend, did a post about it called "The Battle They Don't Want to See" saying about the pictures: "They are a vision of breast cancer that is too often sugar-coated with platitudes, sassy t-shirts, fun-filled fundraising galas. For some, this reality is too much to bear. But until we as a society are willing to see cancer for what it is, our capacity to support the diagnosed will always be limited."

Her post was tweeted and shared throughout the blogosphere as another example of society wanting to ignore the reality of breast cancer.

And yet, an important point is being overlooked.

And that that in this case, the ones who feel that the reality of these photos are "too much to bear" are the ones who actually have to bear the disease. It isn't society who doesn't want to look, it is people who are dying from cancer themselves who don't.

Speaking as one of the diagnosed, and one of the ones diagnosed with metastatic cancer, I agree with Gayle's overall premise.  In fact, almost exactly three years ago, as a cancer newbie not knowing what was to come, I named this blog "I hate pink" for that very reason - I didn't want to be part of the pink culture that prettifies cancer. Even back then, I knew it was ugly.  I wanted to detail it with words.

Yet, since I have become metastatic, since I am dying of cancer, my original thoughts have expanded.  If you look deeper into the story, you will see that the photos that were taken down were exhibited at a place called The Gathering Place that describes itself "as a nonprofit, community-based cancer support center to fill an unmet need in the greater Cleveland community. The programs and services offered address the social, emotional, physical, and spiritual needs of individuals with cancer and their support network." Reading deeper into the site, they are focused solely on nurturing those with cancer. They have classes, such as movement to help with low energy, nutrition information, caregiver classes, and emotional support groups.

In reading what it is they do, and after hearing the photos upset some patients who go there, I think it is wholly appropriate that they took the photos down. The better choice would have never to have put them up to begin with, but given the nature of their mission statement and their goal to support the emotional needs of cancer patients; given that they got complaints from those with cancer, I agree that they should not have photos of a dying woman displayed in their lobby.

But why?

As a woman with metastatic cancer, I have nowhere to go where I am not confronted with the magnitude of my disease. In my personal life, I comfort my family, telling them I'm okay, it'll be okay. Weekly, I have chemo. Monthly, I see an oncologist. It's always on my mind.   I am in pain and exhausted. I will forever be in treatment. I am going to die, and I have paperwork to do, things to finish. I look at photos of my own deterioration, without even wanting too, just by flipping an album.  I don't know any other terminal people.  I rely on me.

I am faced with this illness every day, every night, without respite. I am not really welcome at support groups as I frighten the lower stage women - I am, after all, their worst nightmare. Their concerns are not my concerns.  I can find some relief and companionship online but even on the forums for Stage IV cancer, we have the family members of cancer patients turning to us for comfort and information and all too often describing their family member's death in vivid and disturbing detail - never realizing or thinking they are asking for support from women who will soon be in those same deathbeds, unseeing and unblinking and moaning in pain, same as their loved one.

If I had been able to find a place like The Gathering Place that gave me comfort and support, maybe I wouldn't want to see those photos either. That doesn't mean I don't think they shouldn't be seen, or that I bury my head in the sand - not at all. I've looked at them, and they are beautiful. My regular readers know I have always faced the truth. But, the Gathering Place is designed for cancer patients, to find healing and comfort and a sense of peace. Maybe even a little hope. Seeing graphic photos of a woman in the process of deterioration and dying from cancer every time you walk through the lobby, photos described by Gayle as filling "many of us with deep sadness and a sense of dread" has turned out to be emotionally upsetting for many who are suffering with cancer.

I am not saying the photos aren't beautiful or touching. I'm not saying they shouldn't be shown. In fact, a few are on on CNN's website. They will be in Gayle's new book.

It isn't the photos, it's the place.  And, it's all to easy to dismiss a cancer patient who doesn't want to see them as "putting their head in the sand" but you know what?  Why shouldn't we have a place where the sand is warm and comforting if that's what we want?  We have too many people telling us how to handle our disease as it is.

What I'm saying is that maybe our "capacity to support the diagnosed" as Gayle says, includes giving us, the diagnosed, a tiny space - just one - where we aren't always compelled to confront our future.

Seems to me if liking something on facebook provides support, than "The Gathering Place" deserves that same honor.

As do I.

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Tuesday, July 17, 2012

Sponsored Video: More Birthdays


As you all (should) know, I support two charities in the fight against Breast Cancer.   One, that I just wrote about, is Stand Up 2 Cancer for their pure research. The other is the American Cancer Society.  They do research as well, but they are also big on supporting cancer patients individually.

How do they do that? They put on the Look Good, Feel Better classes, which are so important to those of us who are doing chemo for the first time. They provide money that will go towards a wig reimbursement. They provide gas money for rides to doctor's offices, and they have classes for cancer patients on the subject of nutrition, emotional health, and so much more. I have called them with questions myself, and every time have gotten a live person to answer my question, with no hold time.

And a kind live person, one who, if they didn't know the answer, found out rather than giving you the runaround.

They also provide information and statistics that I have used hundreds of times on this blog and for supporting research.  Each spring, during chemo, I have received daffodils in my infusion center to brighten my day.   They put on the famous Relay for Life which goes directly to support people with cancer.  At some point on my bucket list is a goal to sponsor a "But Doctor I Hate Pink" Relay for Life team.   Back in the early, frightening days of a new diagnosis, the American Cancer Society was the group that provided me with the most help and information, and I will never forget it.

The ACS catch phrase is "more birthdays" and they work on that with ongoing research, but what they also do is make the birthdays you have left enjoyable, managable ones, by supporting you and educating you and actually helping you.   A big plus - they are not focused on breast cancer alone, or "awareness."  They will help my uncle with Prostate Cancer, my Aunt with Lung Cancer, and they surely have helped somebody in your family and if they haven't, well, you are pretty lucky.

Of all the charities out there, this is the only one I have personally benefited from. You can see how I feel about ACS in former posts about them here and here and here.  So, while I have just asked you to donate to Stand Up 2 Cancer, I also would like you to consider donating to the ACS.

The world does need more birthdays.






This post is sponsored by the ACS, but don't think that I don't mean what I say.

Monday, July 16, 2012

Little things

My blogtalkradio show starts today at 2:00 pm PDT, 5:00 Eastern.  The topic is metastatic cancer. Share your story or ask a question.  The number to call to talk to me is 347-215-7838.

As alluded to, I am starting a newsletter.  The subscribe button is to your right. --->   My plan is to do it monthly, and put in things I don't want to clutter up the blog but find interesting: recipes for a healthful life, helpful products for the cancer patient, stories about the latest in cancer research and just general fun stuff.  If I get a ton of interested people, maybe I'll do it bi-weekly.  If none, maybe quarterly.  :)

I used MailChimp because they comply with the Can-Spam Act of 2003. That means they won't spam you and I won't spam you.  You will be able to unsubscribe at any time, and I will never use your email address for anything but the newsletter.