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Showing posts from June, 2016

Resources for sarcoma patients/families

Link to National Comprehensive Cancer Network guidebook --- written for patients and families. This booklet has a great flow chart and explanation for various stages of general sarcomas and treatment options. Great place for someone who wants answers, and can filter out what doesn't apply. The entire booklet can be overwhelming.. too many choices at once. But, it is a good place to learn your questions. Another sarcoma blog: Sarcoma blog - "Coping with the Big C"

Red Devil: Dose two

I've learned to be flexible and prepared for anything. Friday was a great example of why this works. There was a scheduling glitch. I wasn't scheduled for "chair time" at the infusion center. So labwork at 8:00 a.m., appointment with ARNP (Advanced Registered Nurse Practitioner) at 8:45 a.m. When I saw the practitioner, the office started getting a chair scheduled. It worked out that there was time for a quick breakfast at the cafeteria (glorious biscuit/gravy and a side order of cheesy grits.) Then off to the infusion center. I even got a private room for the infusion (that's a first, I've enjoyed chatting with the other patients when I shared rooms). We managed to get out of there before 12:30 p.m. So the day wasn't what I thought it would be. I was able to get the infusion. --- and avoid a second trip on Tuesday (which is my birthday). Red Devil is interesting. My hair was falling out, so I shaved it. Status report; toenails are

Shaving my head later this week.

My hair still looks good to others. I see the pile of hair by my sink. The final task is to get a passport photo while I still have hair. Then I can shave it. Oh, and I need to get some sunscreen. I'm still able to get things done. I have been doing laundry and outside activities. Although it takes three times as long to get anything done.

Driver License changed June, 2016

Today I went to the Tax Assessor's office, and changed the address on my driver's license. I know, I should have done that months ago. I also dropped the organ donation designation. I got my first driver's license in 1977. I've been an organ donor since then. But cancer changes things... and LMS changes a lot of things. Taking an organ from my body would quite possibly transfer LMS cells to the recipient. I was an organ donor almost 40 years. I donated blood for years. It just seems wasteful to put a perfectly good heart or lung or liver into the ground. Except my heart, lung and liver are not perfectly good.

Research update. Letrezole use for 10 years post breast cancer.

Below is a link to the original article. I realize that links don't live forever, so I've copied the article. I am currently on Letrezole.... and having bone pain. --Although that is something I'll be discussing with the doctor at Friday's appointment. Remember there are no easy answers... so a way to prolong life, also has side effects... pain, and reduced bone density. I'm grateful that I've drank as much milk as I have during the past decades. Hopefully, that will help strengthen my bones during this treatment. This also shows how treatments can cross from one cancer to another. I'm not sure there are any official treatments for my cancer, it is just too rare... so we keep trying new and interesting treatments. Washington Post Article about breast cancer and Letrezole Extending anti-estrogen therapy to 10 years reduces breast-cancer recurrence, new cancers CHICAGO — Researchers said extending hormone therapy to 10 years reduces the risk

Last cup of coffee... for a while.

The last time I did chemo, I gave up coffee. The taste was off, and I had been told that some chemo patients hate foods they used to love, IF they forced themselves to eat/drink them. Today the coffee is meh... doesn't taste good, doesn't taste bad. The last few weeks, I've indulged in the many tastes that I LOVE, but can't eat during chemo. Last weekend was a huge Sushi feast at a local Thai restaurant. I've been eating (and gaining a bit of weight) while enjoying while I can. From now on, I'm eating for nutrients, not for taste. If the last round is any indicator, nothing will taste good. I'm prepared. Last time I learned that I could focus on texture, temperature and tints. Since I couldn't trust my taste buds, I was trusting other clues. I was careful with expiration dates. Since everything tasted "off," I could easily eat something that had spoiled. more about adventures in chemo and eating later. I'm heading off to m