Too Much on Our Plait

Like Daughter - 52

Today's post comes after a lot of thinking. I haven't gotten my blood work results back, but I have a completely different issue to talk about.

All my life, I have struggled with my weight. I think it started when I was about 10. I was always overweight from that point on, and it was hard for me. It was the typical story - I saw other girls I wanted to look like, and tried so hard to look like them. I had a very different body type, and that was another setback. I have done countless programs - Weight Watchers, Jenny Craig, my own diet plans - and yet I always ended up gaining it back if I strayed. They worked, don't get me wrong. It was just very hard to maintain.

From about late 2010 to mid-2011, I was following my own plan. I was monitoring my calories, eating well, exercising almost daily, and making sure I was constantly moving. My job at the time was not as demanding as the one I have now, but I worked hard despite feeling tired after a long day. I felt so much better about myself. I lost about 20-25 pounds in that time, and I met my husband when I was at my smallest. Since then so much has happened - a new career, moving in with Jason, lifestyle changes - and now I am at my biggest. I'm over 200 pounds, which was unheard of for me before now. I lost weight before the wedding, but afterward, it came back on and then some. Due to certain medicine, lack of time and activity, and lack of energy, my body has become what it is now. I've been noticing more and more how much strain my body is under. I am short, so there is a lot of weight to carry for my stature.

I always blamed this on the cancer. I blamed my thyroid and constantly fluctuating levels. I blamed the medicine I took for almost a year that made me so lethargic I didn't care what I ate, therefore making me gain so much weight. I blamed myself.

As my mom says, I have the tools. This is true. I've always had the knowledge. It has been accumulating for over a decade of dieting, weight loss plans, and personal experience.

Three days ago, I had an awakening. I have had this before, but this is different. I had started to accept my body this way, but I think about my health and how much my body hurts just from climbing a hill. I can't live like this. So, I made a decision:

I won't.

This is the turning point. Over the last three days, I have watched my calories using MyFitnessPal, and I am starting to go back to Jazzercise with my mom. I already have lost about three pounds. I'm feeling better already. It's really hard working out with my body this way, but I won't let it stop me.

~~Hopefully,~~ by the time CancerCon 2016 comes around, a new, smaller, healthier me will have blossomed.

Next time I blog, it will be about the blood work results. I promise.

Until then, friends, I wish you love, happiness and - most importantly - good health.

Dori

Read More 0 comments | Posted by Adelina and Dori |

Like Daughter - 51

Good evening, my friends.

I figured it was about time I posted about my current situation with my cancer follow-ups. I have been seeing my endocrinologist every 6 months since my second surgery, which was November 2007. Up until about four years ago, my thyroid levels have shown little to no cancer evident. Four years ago, my numbers began to creep up. I went from below 0.5 to 1.9, to ~3, to 4.3, to 4.5. I just had blood work done yesterday, so I don't know my levels just yet. I'll update again with those along with the next steps that my endocrinologist wants to take.

My endocrinologist is amazing. Dr. H is straightforward and very proactive with my treatment. She has helped me become more independent and to take control of my treatment. She welcomes questions and answers them. I really appreciate her and all she has done for me throughout my cancer journey.

She told me she's ambivalent about biopsying and "cherry-picking," as she calls it. What she calls "cherry-picking" is going through my neck to biopsy and (eventually) surgically remove any lymph nodes that show any level of cancer, no matter how small. My numbers are not high enough just yet. The "magic number" is a thyroglobulin of 10. Dr. H told me she feels comfortable "sitting" on me and waiting. This has been her decision the last three years, so I'm not completely shocked. This time around, though, she is unsure if she wants to do a stimulated thyroglobulin test. A stimulated thyroglobulin means that the patient receives shots of thyrogen (right above the butt - Yay!) and at the end of the week, gets more blood work done to compare to the initial unstimulated thyroglobulin. If the numbers are higher, it means there is thyroid cancer still in the body. This test is much more sensitive in finding any leftover or recurrent cancer cells. When my numbers come back from this test and if they are higher than before, then she will do a stimulated thyroglobulin test.

I jokingly call it "cancer limbo." It kind of is, really. You're just sitting around waiting for something to happen. If it doesn't happen, you're happy (of course). The problem is the foreboding feeling. It's always there, in the back of your mind.

"Will today be it?"
"Where is it, and where is it going?"
"Why can't they just find it and get it out?"
"What's taking this so long?"
I just want it over.

These are just a few questions and thoughts that run through my head. I know other cancer patients and survivors can relate. The feeling that this appointment, this scan, this ultrasound, this blood test -- could be what shakes our current "normalcy" and turns it upside down once more. This has been my thought process since my last (second) surgery in 2007. I had 22 lymph nodes removed from the left side of my neck, two of which were malignant metastatic papillary thyroid cancer.

I've always told people that I'm just waiting for the ball to drop. The response I get more often than not is, "Don't jinx it! You're asking for it to happen."

Am I, though? Am I being dark and depressing, or am I being realistic? What's wrong with waiting for something to happen? Of course I'll be happy if my numbers never increase to the "magic number." The last time I felt like this was over was when my endocrinologist gave me the thumbs up after my nuclear scan post-radioactive iodine treatment. She said I was cancer-free and in the clear. All that needed to happen was get low numbers in my blood work. Guess what? They were not low enough.

Call me crazy, but I do not feel it is wrong to be ready for either event. If the ball drops, fine. I'll get through it just like the last two times. If it doesn't, fine. I will continue to live my life as best I can, just as I have in the 9 years since my diagnosis.

Feel free to leave comments with your opinions. Do you agree? Disagree? Do you experience the same roller coaster ride? Let me know!

As always, friends, I wish you love, happiness and -- most importantly -- good health.

Dori

Read More 4 comments | Posted by Adelina and Dori |

Like Daughter - 50

I can't believe this will be our 50th blog post! This is really exciting. What a great way to begin this entry.

Today's post is about quality of life for survivors and those who are affected by cancer in any way -- family, friends, caregivers. It is extremely important to be healthy, happy, and surrounded by those who love you and care for you. It is also important to be surrounded by those who understand what it is that you are going through.

When I was at the beginning of my cancer journey, I felt like I was the only one. I knew no one else who had thyroid cancer. It was 2006, and I had no one to turn to but friends and family who could sympathize, but not empathize. This is a big deal for anyone with an illness, especially a chronic or long-term illness. It can be very hard to cope when people listen to you, but can really only give words of encouragement or affection (which is also crucial).

My sister, however, had gone through cancer about a decade or so prior to my diagnosis, and she helped me through a lot of what I went through. Without her, I would have gone insane. I love her to pieces, and I wouldn't be who I am without her.

I'm a talker, in case you didn't realize. I talk about everything and anything, and have always been extremely open about my cancer journey. I need to be. I can't keep things bottled up. I wear my heart and emotions on my sleeve. Anyone who knows me (or doesn't know me well, really) can vouch for this. I also am very passionate about making sure my voice is heard for the sake of others who may need to hear what I have to say. When I was first diagnosed, I called everyone who wanted to know my results. I must have called about 10 people. The more I said it, the more real it became. I thought it a ~~dream~~ nightmare when it happened, but the more talking I did, the more...hardened I became. Not hardened as in cold and distant, but more strong and grounded. But out of all of those phone calls I made, not one of them were to a fellow survivor. No one who really grasped what I had just heard. No one who truly understood. It was a very lonely time, despite having so many people around to support me.

If you are reading this and are not a survivor, please do not misunderstand me. I needed my family, my friends, and those around me who were there for me. I needed that comfort and that support. If I didn't have them, I do not know where I would be. However, part of me still felt alone and completely isolated. I needed someone who was going through cancer, someone who at least had some understanding of what I felt and could take the journey with me.

There are so many people out there right now who feel as I did back in 2006. However, there are now endless resources and support networks out there that can help those going through cancer not feel so alone. Stupid Cancer, Imerman Angels, Friend for Life Cancer Support, Hope for Young Adults with Cancer, to name a few. Go to this page on Stupid Cancer's website for countless more resources and websites.

In addition to these amazing resources, there is something new that will change the world of cancer for all. Survivors, caregivers, family, friends, let me introduce you to Instapeer. Instapeer - developed by the fabulous people at Stupid Cancer - is an app that will connect you to others who are like you. It is available on iPhone and Google Play. It is extremely specific, and will match you with others according to age, diagnosis, location, cancer stage, etc. The possibilities and options are endless. Even if you use it periodically, know that it is a place where you can go that will help you not feel so alone. You can message people privately, participate in the chat room, and create friendships and connections that will guide you and support you throughout your journey. Just know that this is there for you, and those using the app are there for you, as well. Including me.

As always, friends, I wish you love, happiness, and -- most importantly -- good health.

Dori

Read More 0 comments | Posted by Adelina and Dori |

Like Daughter - 49

Hi!

It's hard to believe it has been almost four years since my last post. A lot of things have changed. The blog may have halted, but life just kept on rolling!

Since the last post, I have gotten married and been very busy with my career. I took a hiatus from the cancer world (not completely, but I became inactive) for what seemed like a decade. Last month, my husband, Jason, and I attended CancerCon in Denver. The conference is hosted by Stupid Cancer, and is what the organization has been building up to since its inception in 2007. The OMG! Cancer Summit was the "main" conference in New York, and that is actually where I attended my first OMG! Summit in 2010. At the 2011 conference, I met my husband, a brain cancer survivor, and we began dating soon after. We got married last April, and are very happy (one would hope, right?).

The hiatus Jason and I took from Stupid Cancer was extremely hard, especially for me. I always felt like myself with the people from this organization, and they became family. There was always this hole in my heart, and every time I tried to get myself involved again, something happened to pull me away. Finally, this year, Jason and I said we would go to CancerCon, no matter what. So, we did.

It has taken me some time to put my thoughts together and write about the experience. Something like this is very difficult to put into words verbally, and even harder to "write" down. I am going to do my best, and hope I do the conference the justice it deserves, and then some.

The conference took place in Denver, Colorado, during the days of April 24-26. Jason and I flew in a day early to get ourselves settled and help out if needed. We saw many old friends and gained new ones. I met a fellow thyroid cancer survivor, and I was ecstatic to have a new friend who understood my diagnosis on a personal level. She and I really bonded. She brought her husband with her, and he and Jason really hit it off. It was nice to see Jason talking with another married man who understood his position. We had a blast reconnecting and making new memories while rekindling the past.

The conference officially began during the opening ceremonies on Friday, the 24th. The room was breathtaking -- the lights, the stage, everything was unbelievable. It was so hard to fathom that over 600 attendees -- survivors, caregivers, doctors -- would be in this same room! At the 2010 conference, there were over 150 attendees. In just five years, that number has more than tripled. Just the idea that Stupid Cancer has made this much of an impact and has reached so many people brought tears to my eyes. I hugged my friends on the Steering Committee and congratulated them, feeling so blessed and honored to be there and share that moment with them.

After Matthew Zachary (CEO of Stupid Cancer) and Alli Ward (VP of Stupid Cancer) welcomed us and kicked off the conference, I made sure to find Matthew to hug and congratulate him. I was still trying not to cry, and seeing him just made it harder to do so. I could hardly tell him my feelings, and I am pretty sure he understood. It brings me to tears even now to think of how that room looked that night.

There was a scavenger hunt scheduled for that evening, and Jason and I teamed up with Kristina and Allan (married couple; Allan is a survivor of lymphoma), Lauren (survivor of kidney cancer), and Nicole (Assistant Director of Friend for Life Cancer Support Network). We named ourselves "Team Badass" and tore through the city, racing to get all of the items done on our list. We posed with mimes, took selfies in a bathtub (don't ask), took pictures with a cop (no arrests, we swear), and came up with the most creative ways to check off the items on our list. 11PM was when the scavenger hunt was over and all pictures were to be sent to the judges to be evaluated. We were lying on the ground, tired and sore, but we somehow mustered the energy to go get some food and drinks. It was so much fun being with these new friends and working together to beat the other teams. Unfortunately, we didn't win, but we formed a special bond that one can only have as a member of Team Badass.

The next day was chock full of breakout sessions and meeting the exhibitors. I attended two of the breakout sessions, but the one that stood out the most was What Cancer Stole From Me: Grieving the Losses Associated With Cancer. During this session, the speakers had us write on two sides of an index card. The front was about what cancer has taken from you. The back was for something that people don't understand that affects our cancer journey. On the front, I wrote about my grandfather (d. 2005 of non-Hodgkins lymphoma), and my family suffering from familial papillary thyroid cancer (there's more about this in previous blog entries, if you are new to this blog). This was not the difficult part. The difficult part was the back. I wrote about how I am about to "celebrate" my 9th cancerversary, and yet the stigma that "thyroid cancer is the good cancer" still exists. It hurts to feel like my journey is easier than others, when really everyone's journey with cancer is different and cannot be compared. Of course, I didn't write ALL of that, but it pretty much stated that. After we wrote on our cards, one of the speakers read our cards out loud. When my card was read, I started to cry. I didn't understand why, at first. I've thought about this so many times, repeated it out loud to so many people. Why did it get to me so deeply? Why was this even still something that COULD reach my heart in such a way?

That evening was Stupid Cancer Pub Trivia. Team Badass plus my new thysister and her husband joined us. We did pretty well, and it was so much fun! Italia Ricci (lovely lead actress in "Chasing Life" on ABC Family, and awesome Stupid Cancer advocate) joined the fun and was watching at a table behind us. She came in so quietly I didn't even realize she was there! She looked like she was enjoying herself, and was such a sweetheart when people talked to her. The night was full of laughs, love, and badassery. ;-)

The next day was the last day of CancerCon, with breakout sessions in the morning and the last few speeches before the end of the conference. I attended two sessions: When Did Cancer Turn Me Into A Control Freak? and Your Next Chapter - Making Your Survivorship COUNT! The first one was pretty powerful because I was in a room full of people who felt like they had no control over their lives, and that cancer and its side effects were taking the pieces of control that we thought we had left. We talked about our feelings and about how we can take back control and rely on those who understand and give us comfort. We all were given a little fabric bag and little cut out pieces of index cards. We were told to write down things/people/places that make us happy and bring us peace. We were also told to write down various things that stress us out or make us lose our sense of control. At the end, we put our "happy cards" into our bag, and the "stress cards" into a bin to later be burned. It sounds crazy, but I felt like a weight was lifted from me. I knew I had let go, and I had a better grasp on what was important to me. It felt nice to throw those little cards made of nightmares into that bin. Good riddance.

During the second session, I got to watch two lovely and beautiful ladies, Tamika Felder and Helaine Bader speak to us about telling our story. I spoke up at one point to respond to them about a question, and I talked about what I wrote on that card the day before. Again, my throat closed and cried. I had a harder time saying it than I did writing it. I kept contemplating afterward why this kept catching me. It dawned on me later on, and that epiphany was hard to swallow:

I had cancer.

You're probably thinking, "Well, DUH..." But, honestly, that never did sink in before. Not as much as it did during the conference. People in the cancer world used to get so frustrated with me when I told them that my cancer was "no big deal," and that I "didn't go through as much as they did." I used to shrug it off, and say how I felt bad that I didn't suffer as much. I was told over and over again, "Dori. Cancer is cancer. There is nothing 'good' or 'easy' about it, no matter which type you have." That finally got through. After 9 years of that stigma of "good cancer" being thrown in my face, it finally hit me. I have had two surgeries, two RAI treatments, countless biopsies, scans, and blood work tests. This cancer is still not gone. It is still in my body. In fact, my blood work numbers are going up every 6 months. It's only a matter of time, really, before they need to go cherry picking in my neck once more.

I want to end these false ideas about thyroid cancer. I want to bring my knowledge, my story, and my family to as many people as possible. I want to inform and move people into being more aware of this disease and what it can do. I want to get to know and help those who already fight this every single day and feel so alone because they feel like no one understands. I want to be a person who really makes waves in the thyroid cancer world and in the outside world.

So, to close this long, long entry, I will say this: I will be more involved in the young adult cancer community, and I am going to do everything in my power to accomplish the goals I have set upon myself. You will see me again, and this blog will continue.

Until then, friends, I wish you love, happiness, and -- most importantly -- good health.

Read More 2 comments | Posted by Adelina and Dori |

Special Entry: Good Housekeeping Article Response

If you are an avid member of the thyroid disease/cancer community, then you most likely already know the controversy and outrage that surrounds this article, written by Susan Carlton and published by Good Housekeeping. If not, this article and all comments and concerns about it still apply to you. Why? It’s as simple as this: knowledge is power. Knowledge of the diseases and cancers that are out there, and knowledge about what information is accurate, and what information is dangerous. Below is my take on certain portions of the article. Admittedly, I am no expert. Some of the information that Ms. Carlton presents is without documented sources. Therefore, I can neither credit nor discredit her claims. However, since I currently (some formerly) endure four different types of thyroid diseases, I am able to use my 5 years of acquired experience and knowledge to refute several points made by Ms. Carlton and Good Housekeeping. Questions, comments, complaints, and commendations are not only requested but encouraged.

Introduction – Section 1

"My eyes lit up. Could the problems I'd assumed were inevitable be blamed on the tiny thyroid gland — and be reversed with a tinier pill? Maybe I didn't have to renew my gym membership after all."

What I feel Ms. Carlton is inferring here is that Synthroid and its brothers and sisters (Levothyroxine and such) will simply cure all of her symptoms – fatigue, weight gain, lack of energy, brainfog – and then she will happily carry on her life. That is a piece of information that should never be relayed to anyone. It isn’t as simple as that. While she does state that it isn’t simple in the next paragraph, I don’t think she should have used such a comment as a clever quip. It sends the wrong message to individuals who are not privy to the ins and outs of thyroid problems. I’ll explain further on this as the article progresses.

"At least 13 million Americans have some form of hypothyroidism, says Jeffrey Garber, M.D., who (literally) wrote the book on it — The Harvard Medical School Guide to Overcoming Thyroid Problems."

When I Google’d the general quote from Dr. Garber, I noticed that this statistic was in an online review of this book, but it was written very differently. You can view it here under “Editorial Reviews.” It clearly states the following in the review, “More than 13 million people in the United States suffer from some form of thyroid disease, and that number is expected to rise precipitously as the baby boomer generation approaches its sixties.” This changes the meaning of Ms. Carlton’s statement entirely. It isn’t solely hypothyroidism that over 13 million people in the US deal with on a daily basis – it’s every thyroid disease. That includes, but is not limited to: thyroid cancer, Hashimoto’s Thyroiditis, and Hyperthyroidism. Not only did she misquote, but she also did not even use this book to her advantage. She only uses one statement from the entire book in her three-page article, and even in that statement there is no evidence of how to “understand thyroid problems”, as her article claims to assist the reader to do. She does quote Dr. Garber later in the article, but I (nor anyone else) am not sure if that quote is from his book or if she spoke to him personally (The evidence that Ms. Carlton did not speak to any of the doctors she cited in her article and responses to her “advice” can be found here). Even with the secondary quote, it is obvious that Ms. Carlton did not put forth as much effort as she could have to include more information from this source.

Ms. Carlton then proceeds to give a statistic about how many people are affected by hypothyroidism, following it with this:

"(Hyperthyroidism, meaning thyroid hormone production is in overdrive, is a less-common condition.)"

Just so the readers know, this is the only statement she makes throughout her entire article on Hyperthyroidism. Word to the Not-So-Wise: If you are going to write an article about “understanding thyroid problems,” then you should probably write a little bit more than just one line about another thyroid problem that exists. If your focus was simply on Hypothyroidism and Hashimoto’s Thyroiditis, then state that in your title and description so it does not mislead the readers. This title is, in a word, insulting. You, my dear Ms. Carlton, claim to have all of the secrets we want to know about our thyroid problems, and yet, you only focus your attention on Hypothyroidism, with Hashimoto’s Thyroiditis being a close second. Where are the others? And how dare you make such light of Hyperthyroidism and only describe it in six words, then say in a single breath that it is a "less-common condition"! All that would tell a reader who is still learning about these conditions is that Hyperthyroidism is not a disease that should be worrisome since it obviously couldn’t possibly happen to that reader. It’s "less-common!" Let your mind be at ease, dear one! You are saved from Hyperthyroidism! Here’s a little factoid for you, Ms. Carlton: I have hyperthyroidism due to being diagnosed with papillary thyroid cancer when I was 17 years old. These are two thyroid diseases that you failed to mention and explain in your article. Hm. Fancy that.

It gets so much better (oops, I mean worse):

"Hypothyroidism has been recognized since at least the 17th century, yet it's become a disease du jour…"

Excuse me? Okay, Ms. Carlton. Here is another factoid about my thyroid cancer battle for you: In order to receive radioactive iodine treatment (RAI) to treat my thyroid cancer, I was forced into hypothyroidism. When hypothyroid, iodine-suppressed, and then given iodine, the thyroid immediately takes it in and uses it. There is also a low-iodine diet that contributes to the thyroid being so deprived that it will suck up all of the iodine given to it during treatment. Believe me, my dear, being so hypothyroid was not a walk in the park. It is certainly not a “disease du jour,” as you so flippantly called it. Who says we wanted this for ourselves? Who says I wanted to become so tired and exhausted that I couldn’t even enjoy my summer with my friends and family like I wanted to at 17 years of age? Who says I liked being so cold in the middle of July that I was wearing sweatshirts, sweatpants, gloves, thick socks, and a blanket in 70-degree weather? Who says I enjoyed my weight gain when I was already overweight (and struggling with it) to begin with? Ma’am, you have some serious rethinking to do. None of us asked for this, and none of us want to be a part of this club. When your hypothyroidism starts to affect you more than it has (because it will), I hope you begin to feel the same way.

"'…people have lots of questions.' There's no shortage of answers for them. Hundreds of websites, a virtual cottage industry, profess to educate women about hypothyroidism."

It is certainly one thing to have hundreds of websites dedicated to providing information on hypothyroidism to the public, but how do we know that these websites are giving accurate facts? It is easy to find information, sure, but how are we sure as to which websites are legit and which are a farce? Ms. Carlton does respond to this later in the article, and really gives some valuable website information, but the list definitely does not start and end with the sites that she listed. I also firmly believe that she could have listed websites for the rest of the thyroid diseases and conditions that she did not discuss in the article. (I list my own list to add to hers later.)

Testing Roulette – Section 3

"To confirm a hypothyroid diagnosis, many doctors suggest two additional blood tests: one to check the levels of T4 hormones (low levels confirm hypothyroid) and another to check for antithyroid antibodies (to see whether you have Hashimoto's)."

Whatever happened to T3 hormones? Sure, T3 tests are important for diagnosing hyperthyroidism and Graves’ disease (again, another disease not mentioned in Ms. Carlton’s article), but the T3 triiodothyronine brand medication called Cytomel, can be (and sometimes is) used alongside Synthroid (Levothyroxine) to relieve symptoms of hypothyroidism and speed the buildup of Synthroid in the body. Personal anecdote: While I was undergoing treatment, my endocrinologist (God bless her) prescribed me Cytomel for the first two out of the six weeks I spent in prep time for treatment. During those six weeks, I had to become hypothyroid, and the Cytomel helped relieve my symptoms of hypothyroidism for the first two weeks. If I had not taken that medicine, I would probably have been in an even worse state than I was after the six weeks had passed. Once treatment was completed, I was able to resume my Synthroid, along with two weeks of Cytomel. The Cytomel was a lifesaver for me while I was in college. If that medicine had not been given to me, I would have struggled greatly through my first two semesters of college. I would probably not have passed most of my classes. To learn more about a study that proved T3 triiodothyronine medications to be helpful alongside Levothyroxine, see Mary Shomon’s article here.

To Treat or Not to Treat – Section 4

“The goal isn't just to ease symptoms — it's also to preempt new ones.”

I think she meant “prevent.” Hey, typos happen.

“A recent Danish analysis of a small group of newly diagnosed hypothyroid patients found little or no change in patients' fat mass after one year of thyroid treatment.”

Where is all of the information for this study? Where can we find it? Dori to the rescue! The brief overview and results of this study is located here. Does it really take that much effort to keep track of your resources and then cite them?

Treatment: Old-School Versus New-Age School – Section 5

Explain, explain, explain. When writing an article that people will read for information, you need to explain as much as you possibly can. The “why’s” will always jump off the page for readers, especially when information that is deemed crucial is stated in one sentence or quote. Here’s why:

"'The goal is to take the lowest dose possible to get the TSH in the 1 to 2 range,' says Daniel Duick, M.D., an endocrinologist in Phoenix and president of the American College of Endocrinology."

Why do we want our TSH in the 1 to 2 range when hypothyroid? I’m sure most if not all of the readers of this article were asking, “Why 1 to 2?” Well, our beloved Mary Shomon, About.com Guide for all things Thyroid, explains that in this article.

Online...And On Guard – Section 6

While I do believe that she posted some informational websites, I believe that she could have listed so many more, if only she had discussed the several other thyroid diseases that exist. Below are several websites that I adore and want to add to Ms. Carlton’s collection:

http://www.thyca.org/

http://www.endocrineweb.com/

http://www.stupidcancer.com/

http://www.thyroid.org/

http://www.cancer.gov/cancertopics/types/thyroid

http://www.medicinenet.com/thyroid_disease/article.htm

This is just too good of a conclusion to skip without commenting:

"So here it is: Six months later and after a retest, I find my TSH is...exactly the same. Given my family history, my doctor recommends I check again next year. With all I'd learned about hypothyroidism, I had already decided that even if my levels had nudged up a bit, I would opt out of treatment. In the meantime, I'm drinking more java (for energy) and honing my crossword skills (for focus). As for the unwanted pounds, there's a spinning class on Saturday with my name on it."

While I am no expert, I do know that coffee, crossword practice, and [insert workout class title here] will not eradicate symptoms of hypothyroidism, nor will it even lessen them. While hypothyroid, I had so much trouble concentrating on my Sudoku puzzles, even coffee would not suffice. I still would fall asleep! And I sure as hell did not want to work out while feeling so horrible. I sincerely hope and pray that Ms. Carlton’s health does not decline, but unfortunately, there is a very good chance that it will. As Dr. Datis Kharrazian states in Mary Shomon’s article in response to this controversy: “The research shows that by ignoring an autoimmune thyroid condition one raises the risk of developing future autoimmune issues. Also, the brain is highly dependent on sufficient thyroid hormones to function normally and she is accelerating her own brain degeneration, memory loss, and autonomic dysfunction by ignoring her declining thyroid health.” If you read her article and have the choice of treatment or ignorance (like Ms. Carlton), I truly hope you will choose wisely.

My Final Thoughts

Just so that I make myself clear, I am not holding Ms. Carlton solely responsible for this article being available. I do also blame the editors at Good Housekeeping for deeming it appropriate and factual enough to publish. You can view the editor’s response to the thyroid community’s comments, concerns, and rants about the article here. In short, the response to our outrage is stating that we are not careful readers and Good Housekeeping is avoiding taking responsibility for this dangerous article and its contents. I am horrified by this and still am amazed that they are standing by this publishing, and personally am offended by their simple yet bogus reply.

Please, my friends, be aware of what is out there, and make sure you are receiving accurate information about your diagnoses, and any other disease out there that you are trying to understand. It is articles like this and people like the editors of Good Housekeeping that/who mislead us and potentially harm our bodies further due to their lack of proper guidance. Know your body and know that you have valuable, reliable resources at your disposal. Use them wisely.

Wishing you love, blessings, and most importantly -- good health.

Dorienne Plait

5-year Papillary Thyroid Cancer Survivor

Read More 7 comments | Posted by Adelina and Dori |

Like Daughter - 48

Wow, it's been a while, hasn't it? Sorry, it's been pretty stagnant in the Cancer Clan. We're all doing fine for the most part. Mom and Janina are doing well. They both are still on 6-month follow-ups, but their scans showed up normal as did their blood work. Aunt Rea, Aunt Gracie, and Melissa are all well, also. They didn't need any radioactive iodine, so they are on yearly follow-ups. Aunt Gracie is the most recent addition to the Clan, so she's probably having more follow-ups, just to check her scar. I did see her at my cousin's 10th birthday, and, let me tell you, her scar is barely there! It looks wonderful, as does she.

I do want to let you all know that Mom and I will be on The Stupid Cancer Show on Monday, May 2. The 'Stupid Cancer' Show is a radio show hosted by Matthew Zachary, CEO and Founder of the I'm Too Young For This! Cancer Foundation, and Lisa Bernhard, Executive VP and Media Development for the Foundation. The show is entitled, "Parents of Young Patients." I will be on air as the Survivor Spotlight, and Mom will be one of the two guests on the show. It's going to be a wonderful show, so please mark your calendars and tune in! The link is here.

I'll more than likely post again later on in the week. I have more to tell! All good things; I promise. :-)

As always, I wish you all love, happiness, and -- most importantly -- good health.

Read More 2 comments | Posted by Adelina and Dori |

Like Daughter - 47

We got my Aunt Gracie's results from her thyroid surgery. Turns out she does indeed have papillary thyroid cancer. This makes her our 6th member of the PTC Clan. Fabulous.

Mom texted me with the news while I was at work. Of course, my phone was off, so I didn't get the message. I did, however, get a call from her with the news before I could even check my messages. To be honest, I couldn't help but laugh. Does this make me inhuman? I don't really like how I've been reacting since my aunt and cousin were diagnosed, but to be honest, isn't it just second nature now? It's sad to think that way, since this is one of the worst things to consider an everyday occurrence. At the rate this is going, though, it almost looks like it.

Let's put it in timeline perspective:

Me: June 2006 (outlier)
Mom: December 2009
Janina: January 2010
Aunt Rea: February 2010
Melissa: February 2010
Aunt Gracie: November 2010

This is absurd. Do you not agree? I hate feeling like this is just going to keep happening, but I can't help it. How else am I supposed to think otherwise?

I'm always the optimist in any situation that occurs. I do my best to think about the positives of each situation. The only one I can think of in this one is: No one is dying or is going to die.

Please tell me I'm not abnormal in my thinking.

Many blessings of love, happiness, and -- most importantly -- good health.

Read More 0 comments | Posted by Adelina and Dori |

Like Daughter, Like Mother: Our Thyroid Cancer Journey

Behind the Blog

Adelina is a full-time wife, mother, practice manager, and medical transcriptionist. After receiving an ultrasound and countless biopsies, she was diagnosed with papillary thyroid cancer on December 11, 2009. She successfully underwent surgery on December 29, 2009, and had her first radioactive iodine treatment in February 2010. Following treatment, Adelina now sees her doctor once a year for follow-up. She has been doing well, and refuses to let cancer slow her down.

Dori is 26 years old. She was diagnosed with papillary thyroid cancer at the age of 17 on June 1, 2006, just three days prior to her high school graduation. Dori endured two radioactive iodine treatments and two surgeries to remove her complete thyroid and 39 total lymph nodes from her neck. She is now under close watch by her doctors, and only time will tell if the cancer stays at bay.