Well, it's June 2015.
The last post I made on here was February 2014.
I think it's safe to say I have a little bit of catching up to do.
Months in Review
In the fall of 2013, following our failed Frozen Embryo Transfer, I started to feel quite strange. I expressed to my physician that I have was experiencing some "out of body" experiences. It is hard for me to explain what it really felt like but it was just NOT RIGHT. My doctor understood right away. She said that some women who are going through Menopause will express that they feel that way. She didn't believe I was at that stage but she began to wonder if it was just all of the hormones working through out my body. She decided to send me on to an endocrinologist just to get his input on things.
November 2013
After an in depth visit to a highly recommended endocrinologist, they discovered that I had nodules growing on my left side and middle part of my thyroid. He expressed to me that they were quite large and he wanted to keep an eye on them. After doing some very painful biopsies they declared that they were benign. The doctor made plans for me to see him in 6 months. I started some thyroid medicine to help shrink the nodules, as well.
June 2014
I had my 6 month follow-up with my endocrinologist. This included an ultrasound and some blood work. After the ultrasounds were looked through it was discovered that the nodules had grown by almost 30%. The doctor did not like that at all, and wanted to remove this as soon as possible. So he sent me to an ENT doctor to start that process.
July 2014
Wednesday July 23, 2014, was the day of my surgery to remove the left side and the center of my thyroid. They planned to leave the right side of my thyroid due to no nodules being found on that side. Leaving this side would help balance my levels out in the long run.
I was in a lot of pain following the surgery but by the next day I was ready to go home. I was discharged and sent home with a large bandage on my neck. I was pretty sore but overall felt pretty good. I pushed through and by Saturday, I was feeling pretty good.
On Monday, July 28th, 2014,
I decided to take our little guy to a park. I was having a pity party and just needed to get out of the house. My extended family was in Chicago visiting my younger sister and my hubby was eye ball deep in the cornfields. I needed some fresh air. After lunch and some time at the park, we headed back to the van. I got my son situated. My phone started ringing and it was my surgeon. She was calling with the Pathology reports from my surgery. She goes on to inform me that there were two spots of cancer (1.5 cm papillary; 3.8 cm follicular) that were found.
I went NUMB.
My ears were ringing.
My ears shut off.
I felt like I couldn't breath for a moment.
I began to sob uncontrollably.
The doctor consoled me on the phone and tried to help me collect myself.
It is a routine for them to go back in and remove the rest of the thyroid when cancer is found. The doctor told me that I needed to come back in on Wednesday to have the rest of it removed.
Wednesday, July 30th, 2014
It was like a really bad nightmare, actually.
Driving to the hospital.
Being admitted.
Starting an IV. (which is the WORST part)
Lying in a bed waiting for the doctor.
Being rolled back into the same operating room you just saw 7 days ago.
Going through anesthesia again.
Waking up IN the operating room.
Having a scar that is partially healed, cut into again.
Waking up in a recovery room.
Being confined to a hospital room for two full days.
AGAIN!
I remember just wanting to cry and throw the biggest temper tantrum on this day. I didn't want to go. I didn't want to go through all of that CRAP again. I wanted to clinch my hands on the doorway as my bed rolled through and tell them NO, I DON'T WANT TO GO. I remember crying uncontrollably as they wheeled me in to the OR, again. I just didn't want to do this.
But I NEEDED TO.
This surgery was by far the most PAINFUL experience. I didn't expect this much pain due to not only removing the rest of my thyroid but also all of the lymph nodes that were located around it. I had to stay an extra day so they could monitor my incision.
6 weeks later~
I had a follow up with my ENT doctor and the endocrinologist. They felt I was healing very well. Both of them expressed their state of shock in the findings from pathology. My biopsy from six months prior was benign so when they found malignant cells they were very surprised. It isn't all that rare for it to happen, they just weren't expecting it.
September 2014
I had to prep myself for the RadioActive Iodine Treatment that is done with patients that had thyroid cancer. This treatment goes in and "zaps" all of the thyroid cells that may be left and makes sure that they are gone so no more cancer can develop there.
I had to be on a Low Iodine Diet for 30 days. This was a terrible diet to be on. It was so difficult to find anything to eat.
Pretty much NO IODIZED SALT.
If it had salt in it, I couldn't eat it.
The thyroid absorbs iodine.
So this diet was starving any thyroid cell that was left, of iodine.
This 'starving' process, would help the radiation to be absorbed better.
Tuesday, September 23rd, 2014 (My birthday)
I had to get a shot to prepare my body for the treatment.
Wednesday, September 24th, 2014
I had to travel, by myself, to the hospital to take a Radioactive Pill.
This was a frightening experience for me because I had no idea what to expect.
Wednesday-Saturday
I had to remain in our basement in isolation.
My body was absorbing the radiation, so I was essentially "radioactive" and needed to be away from small children.
I had to use rubber gloves so I didn't contaminate things.
I was still on my restricted diet.
I missed my family.
And I felt very alone.
October 1st, 2014
I had my follow-up with the doctor with the RAI treatment.
I had a body scan done so they could see if the radiation was located in the right places (around my neck and jaw line). This confirmed that the treatment did what it was supposed to do.
This body scan also showed that there was NO OTHER areas of concern.
*SIGH OF RELIEF*
Need to have a follow-up in 6 months.
October through April
These months have been spent trying to figure out my new medicine and the right dosage for me.
Severe sluggishness.
Weight gain.
Tired all day long.
Muscle fatigue.
Mood swings.
I have never dealt with a mental illness but dealing with all of this has really made me question my mental state. I have expressed all of this to several different healthcare professionals, they all assure me that "its all a part of the process". I had NO IDEA that I could feel SO BAD, for so long.
May 5th 2015
I had an Ultrasound, blood work and an appointment with my endocrinologist.
I expressed to him that I still didn't feel "normal". He evaluated my blood work and felt that we could increase my medicine that will help move me back to a "normal" range....I HOPE!
He looked through everything and gave me an
ALL CLEAR and SEE YOU IN A YEAR.
*SiiiiiiiGGGGGGGGHH*
So there you have it.
A RECAP.
Over the past year and half, I have just wanted to forget most of it.
I haven't really wanted to talk about it much because it STINKS. It sucks to have to talk about health trials that you go through. I have no idea why all of this has happened to me right now. I do know that in talking with my doctor, he shared a perspective that we had never thought about....
He said
"You know your frozen embryo transfer that was a failed attempt may have been a blessing in disguise."
I am a firm believer in GOD'S TIMING IS PERFECT.
He knew all along that all of this needed to take place.
He was paving the way all along.
As painful as it all has been,
I know that:
We also glory in our sufferings,
because we know that
suffering produces perseverance;
perseverance, character;
and character, hope.
Romans 5:3-4






