Skip to main content

Tired and hungry

One of the things about preparing for the radioactive iodine treatment is I have to be off of my thyroid medication until the treatment AND I have to eat a low-iodine diet. I had no idea what this meant until I delved into the internet and the materials my doctor gave me, but here it is in a nutshell:
  • No dairy of any kind (milk, cheese, yogurt, butter). With really no suitable substitutes either.
  • No commerical bread products. No bread from the grocery store.
  • No sea food of any kind.
  • No iodized salt, which at first seems simple (replace the salt in the shakers with non-iodized salt). However, that also means that you can't have salt in the products you buy too, which means practically everything. For example, I found out this weekend that red licorice has salt in it....grrr. I'm a constant food package reader now.
  • No chocolate
These two things (no thyroid meds and the new "diet") are sure to make me crazy. At the soccer games yesterday, the team went to Subway between games. Subway was next to Harris Teeter so I went in there in search of something to eat (I did bring some food but thought I would check it out anyway). I found that they had a salad bar so I had lettuce, mushrooms, chick peas with no dressing and some apple slices.

The funniest thing is people look at me eating this salad at Subway and say things like, "Wow, you are eating healthy." I smile and then want to scream "I really just want a subway sandwich and chips like you!" I'm not that salad eating girl we all know. I'm from Oklahoma and eat because I like to (plus, it's a family event)...and love milk. Instead of coffee for breakfast each morning, I still have chocolate milk for breakfast like a four year old (well, not NOW). Yes, I'm 40 not 4, but it's what I do.

Chris has managed every night to make us all dinner that I can eat. At first, I had visions of the family dinner with me with my sad plate of non-iodized food. However, we found this PDF cookbook at http://www.thyca.org/ with great recipes and alternatives. He has made delicious garlic chicken, pasta, etc. My favorite is Chris's salsa made with fresh veggies using non-iodized salt and he made homemade tortilla chips with the non-iodized salt.

What does the no meds and special diet combo do for me? Prepare whatever thyroid tissue and thyroid cancer cells I have left (could be in lymph nodes, lungs, or bones) to be killed by the treatment. The more you make it "hungry" for the iodine treatment, the better your treatment is. This combo also makes me very tired (could sleep all day), and my metabolism is screwed up, which means all of this healthy eating will probably result in a weight gain! Geez...

So I'm tired after all of this exhausting typing...and want to take a nap now.

Comments

Popular posts from this blog

Quite a pay raise!

Today I received a press alert via email from my alma mater, Oklahoma State. Check out the first two paragraphs below: Following only the sixth nine-win regular season in school history, Oklahoma State University today announced a contract extension for head football coach Mike Gundy, giving him a new seven-year contract worth $15.7 million. The contract was announced following action by the OSU/A&M Board of Regents at its regular meeting in Miami. With the new contract, which is effective Jan. 1, 2009 and runs through December of 2015, Gundy’s average annual compensation will be more than $2.2 million. His current six-year contract paid him $1,053,000 this year. What the heck? That's quite a raise, and he didn't even beat OU, Texas, or Tech! Now, I went to OSU when Mike Gundy was the quarterback there. He was the quarterback during Barry Sanders' Heisman year. He seems like a nice guy and a great coach, but wow... In all fairness, I have to point out that I also read

Changing the Focus

I will turn 50 this month. In honor of this milestone -- and just because I want to -- I am changing the focus of my blog. 10 years ago at the age of 40, I was diagnosed with thyroid cancer -- papillary carcinoma. I started this blog after my first surgery as a means to communicate. I had lost my voice for about three weeks, and speaking was a challenge. Many well-meaning folks called in the days after my surgery to check on me. While it was fine that Chris and my mom provided updates, I missed being in contact with people. So I started writing. Along the way, I learned that I liked to write and also found other cancer patients and survivors along the way. I needed an outlet, and, unexpectedly, my blog provided some perspective for those newly diagnosed as well as those of us who must endure the various follow-up visits and the anxiety that accompanies them. My last cancer blog post was three years ago. Believe me, the anxiety is still there, but after two recurrences, I&

On my soapbox about "the best cancer to have"

Those of you who follow me on Twitter know I was on my soapbox this morning after reading yet another article about the dreaded subject of how thyroid cancer is "the best cancer to have." Think about that...the best cancer? Why would someone say that? In an attempt to make you feel better about having thyroid cancer, some health care profesionals try to convince those of us who have or have had thyroid cancer that it is "the best cancer to have" because it has a high survival rate. An aside here, that high survival rate applies to papillary carcinoma, one of the three types of thyroid cancer out there. Survival rates are lower for medullary carcinoma and anaplastic carcinoma, the other two types of thyroid cancer. Back on topic...OK, so tell us that papillary carcinoma has a high survival rate. Truly, that is good news. But because of this "best cancer to have" statement, and the fact that I was told my thyroidectomy would most likely be just an easy, ove