Since my own cancer was diagnosed in 2009, we have had a number of friends and neighbors who have also been diagnosed. Now the prairie dogs have surfaced even closer to us. Terry's daughter, Olivia-Shea has been diagnosed with stage 1B cervical cancer, which means the spot is visible but contained to that area. No evidence that it has spread beyond that area.
She will have an outpatient procedure on February 26th to remove the cancer tissue. At this time it would appear it has been caught early enough--but it has scared the hell out of her and her mother--as is understandable.
Please send your best Team Mike Good Vibes to Olivia-Shea before, during, and after her procedure. We'll keep you updated after we get the results of the surgery and any follow up reports.
Mike and Terry
I was diagnosed with a rare form of cancer at the base of my tongue in February of 2009, at the age of 57. My wife, Terry, and I use this blog to share that experience with our families, friends, and others who may be in this same situation, either as a cancer patient themselves or as the primary care-giver. We invite anyone interested in our story to read the blog and to reply with their own stories and experiences in fighting this terrible disease.
Wednesday, February 17, 2016
May I Have More Yogurt, Please?
Well, the theme from my last post turned into a bit of a bad story this past weekend. After several weeks of being tired of eating yogurt and my other limited selections of foods, things developed into a perfect storm that ended with me in the Emory ER on Monday. Make that "us," since Terry was with me the whole time.
Over the past few weeks I've not had much of an appetite--as I said before, probably just tired of eating much of the same foods over and over. Yogurt fatigue, I'll call it. The reality for me is that I have to drink a lot of water at every meal to help me swallow my food. So, if I eat less, I hydrate less. And, as I've now learned, when someone gets dehydrated, it can lead to an irregular heartbeat--atrial fibulation (a-fib), which I have had on occasion. The combination of fewer calories and dehydration also contributed to a general feeling of nausea and unsteadiness on my feet.
I woke up on Saturday feeling terrible, was very unsteady, and vomited several times during the day. All of that got a little better on Sunday, but come Monday it was time to go the the ER. The cardiologist found the a-fib, and the neurologist figured out the unsteadiness due to dehydration. After 6 hours there, and a bag of fluids, I was released--but with lots of advice (warnings, actually) about how this happened and how to prevent it. Pretty simple--more calories and more fluids every day. So, I've now started to track my caloric intake with a software app, and get back in the habit of drinking lots of fluids every day--and not just at mealtimes (such as those are).
I have a small procedure scheduled in late March to address the a-fib thing--a cardio inversion, and I'm on new meds for that as well. Hopefully that will do it.
But, all of this serves as yet another reminder that life as a cancer survivor does not necessarily mean a life without cancer playing some role. In my case, the permanent side effects from my treatments seven years ago.
Truth be told, I hate having to be vigilant with things that are basically nuisances, like taking meds, counting calories, watching my fluid intake, and making sure I eat enough yogurt and Boost every day. I'd much rather just go about my daily business and not worry about that shit. But, I don't have that luxury any more--cancer and its treatments have taken that away from me. I need to be much better at watching all of those things every day, to make sure I don't create another perfect storm that takes me to the ER, or worse, again.
mike
Over the past few weeks I've not had much of an appetite--as I said before, probably just tired of eating much of the same foods over and over. Yogurt fatigue, I'll call it. The reality for me is that I have to drink a lot of water at every meal to help me swallow my food. So, if I eat less, I hydrate less. And, as I've now learned, when someone gets dehydrated, it can lead to an irregular heartbeat--atrial fibulation (a-fib), which I have had on occasion. The combination of fewer calories and dehydration also contributed to a general feeling of nausea and unsteadiness on my feet.
I woke up on Saturday feeling terrible, was very unsteady, and vomited several times during the day. All of that got a little better on Sunday, but come Monday it was time to go the the ER. The cardiologist found the a-fib, and the neurologist figured out the unsteadiness due to dehydration. After 6 hours there, and a bag of fluids, I was released--but with lots of advice (warnings, actually) about how this happened and how to prevent it. Pretty simple--more calories and more fluids every day. So, I've now started to track my caloric intake with a software app, and get back in the habit of drinking lots of fluids every day--and not just at mealtimes (such as those are).
I have a small procedure scheduled in late March to address the a-fib thing--a cardio inversion, and I'm on new meds for that as well. Hopefully that will do it.
But, all of this serves as yet another reminder that life as a cancer survivor does not necessarily mean a life without cancer playing some role. In my case, the permanent side effects from my treatments seven years ago.
Truth be told, I hate having to be vigilant with things that are basically nuisances, like taking meds, counting calories, watching my fluid intake, and making sure I eat enough yogurt and Boost every day. I'd much rather just go about my daily business and not worry about that shit. But, I don't have that luxury any more--cancer and its treatments have taken that away from me. I need to be much better at watching all of those things every day, to make sure I don't create another perfect storm that takes me to the ER, or worse, again.
mike
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