Showing posts with label Chemo. Show all posts
Showing posts with label Chemo. Show all posts

Wednesday, September 3, 2014

MUGA

Last night, Patrick and I watched a super depressing cancer movie called "Now is Good." We went to bed late and then Bella got in bed with us at about 1:00. At 2:00am, Makenzie woke up and was whining, crying, and wanted to get in bed with her pillow (which is long and skinny), a necklace, a nightlight and its cord, and the iPad. Holy bananas. I just wanted to sleep. Eventually, I moved Bella to the foot of the bed and that sort of worked. I needed the humidifier since I've been catching a cold recently. 

Today, I had my MUGA test. Our insurance has been giving us some issues, so it's been a mess getting this thing ready to go. But it finally happened after a long day at work. 

A MUGA is a test for my heart.  http://www.cancer.net/navigating-cancer-care/diagnosing-cancer/tests-and-procedures/muga-scan

They had to draw some blood, mix in some tracers and radioactive material, and then put it back in and scan me to see what it did, specifically with my heart and how it worked. 

Well, apparently lymphoma patients have awful veins after chemo. I think I am the perfect example of that. Last week, I had a check-up with Nancy from Dr. Rich's office and when they went to draw blood, just to run some basic tests, it took two nurses and three tries. Then one had to spread my arm and apply pressure while holding the needle in place, while the other got the viles. I left with a rainbow on my arms from the pretty gauze. 



Today, there was a student working in the radiology dept and doing everything with me, with supervision, of course. I told them my veins aren't good, and he couldn't get it to work on his first try, so he asked the supervising fella. He just called in a snazzy nurse who is good at what she does. (Or maybe he did try it first... Goodness, I can't even remember.... I think he tried it.) anyway, she tried twice, left some sweet bruises, and called in another nurse. He tried twice, left two crazy bruises, and then stopped. They put my arm down, put the tourniquet on super tight, sang happy vein songs, and the veins just kept getting blown. So they called in a couple ladies with an ultrasound machine. They used that ultrasound to find a deeper vein. She tried twice and finally got it on the second try! Seven (or eight?) tries later and we were successful! She had one lady twisting my arm to the side (since I couldn't bc of my wrist surgery) and everyone else in the room helping with supplies or well wishes. It was such a feat! 



They got the blood and I sat as still as I could for half an hour while they mixed it with the tracers and radioactive stuff. I didn't want to blow that vein too! Finally, they put the blood/radioactive/tracers mixture back in, flushed with good ol' saline, and took the needle out! Woohoo! I felt so bad that it was taking so long. I wasn't mad at anyone and it wasn't actually that uncomfortable, for the most part. It hurts more now than it did earlier haha. I felt so bad that something that should've taken ten minutes took over an hour. I'm sure it was exhausting for everyone involved, not just me. 

There were only two series of scans, but I had to hold my arms above my head. I hate doing that. It's sooo uncomfortable, tightens up my neck muscles, and since my surgery, it was just hard to do. But twenty minutes, not too shabby! 

So the MUGA is done! I found out that last week, they missed one of the tests they needed to run with my blood so they need me to come back. Ah! After today's adventure, I am just not thrilled about that. I can't even straighten my right arm right now and I have a couple really hard, bruised spots. But I'll do that. Sigh. And probably go back next week for my MUGA results anyway. 

I'm totally pooped and I wish it were Friday, but I'll survive. I'm icing my arm and I sent my family to the pool so I could rest on the couch. I did learn today that all these vein issues could become another issue if I ever get pregnant again, including my ability to get an epidural. Eek. Don't know for use, but eek. Someone is gonna have to teach me how to breathe. Haha! 

In other cancer news....
I had two people send me emails today about a friend who was recently diagnosed with Hodgkin's. I think these two totally separate people were talking about the same person (based on their description of said friend). What are the odds of that? It's interesting to me how this really is now a part of my identity. I don't mind, though, because it has had such a huge impact on my life, and if I can help someone else, that's even better. 


I didn't intend for this to be a super negative post. I just wanted to document today's test and adventure. Happy Hump Wednesday. 

Sunday, March 23, 2014

Another Hair Field Trip

I created a "hair field trip" basically from radiation through present, but I forgot to add these. So here ya go. 

It's bizarre to see the changes - I knew it was happening, but I was in it, so I didn't fully recognize it. Not gonna lie, I miss my beautiful, long, curly brown hair. (It's just hair. It grows back. I know. I remind myself of this often, especially now that I'm entering the very ugly hair stage again.) 









Picture Update - the Hair August to March

I'm being lazy. One day I'll probably add "real" pictures. For now... Screen shots. 

August 2013

January to August 2013

September 2013, at Grandma Velda's house. We all just happened to come out of our rooms for church dressed alike. Haha. 


September 2013, shopping with my mom. :) and goofing off. 




October 4, 2013


October 5, 2013


October 2013

October 2013

October 2013 - my aunt had my cousin and his wife drop off real Coke. Yummy and the best! 


November 2013
When he had family pictures. 


December 2013


December 2013

December 2013 - finger waves 

December 2013

December/January 2013/14


January 2014


January 2014

February 2014

February 2014


February 2014

February 2014 - I let the BareMinerals lady put makeup on me

February 2014

February 2014 (and July 2013, comparison) 

February 2014

March 2014

March 2014 - I love us. 

March 2014 - I got my hair trimmed before going to Idaho for my grandpa's funeral. 

March 2014


March 2014


And there you have it. A crap ton of pictures of my lovely face and hair. You're welcome. 

Wednesday, January 22, 2014

Well, Hello There

It's been three months since I blogged, and it was about two months before that the last time I was blogging "regularly."

I do apologize to anyone who cares, including an apology to myself for not tracking the last few months.... So here goes some post-chemo story-telling.

Like I said before, I finished radiation in August and my mom came to visit in September.

I learned that my side burns and neck hair were from the steroids I was given during chemo - NOT from a "broken" thyroid. :) In fact, I went to the OB for the good ol' annual check-up and they wanted to run some blood tests to check cholesterol and whatnot, since I've never had it tested before. Well, apparently those blood tests also included a thyroid levels check and my thyroid is all hunky dorey. So that's good. :) I do have slightly elevated cholesterol, but I'm guessing most of the reason for that is my diet and lack of exercise in the last year...

My hair is a lot thicker and I still have cute little baby hairs growing in, so progress is coming! :) My hair is A LOT different from a year ago, but it's better than it was six months ago.
A few weeks ago, before I got my hair trimmed. Long and thick enough to use hair ties!
Top: When we chopped my hair last year, Bottom: tonight. About 11 months difference.

My curly post-chemo hair, getting thicker and longer every day. Growing out a curly pixie cut is awful!

I have been struggling with a lot recently - depression, anxiety, confusion and frustration about me. The heart problem I thought I had turned out to actually be a giant anxiety attack - caused by the physical stress on my body from chemo plus the emotional and mental (and physical) stress from the car accident. Since then, I have discovered that when I am super anxious, the muscles in my chest get tight (not uncommon), so I have had those muscles massaged and I have actually learned where to find the trigger points so that if I feel the anxiety coming on, I can start to work it out and keep it from escalating.

I'm still going to various appointments relating to the car accident - manual therapy (massage) and chiropractor once a week, physical therapy once a week, and now I will go see a wrist specialist because my dominant wrist where I had a mild ligament tear has not improved, so I will probably do specialized wrist physical therapy. I also have at least one school/work meeting a week and am going to counseling. Counseling is helping me a lot - working through holding onto the burden of lost/betrayed friendships, handling the emotions of the loss of control from everything that has happened to me in the last year, etc. Lots of great things are happening because of it and I'm grateful for it. I know a lot of people are very judgmental about counseling/therapy, and this is definitely my own business that I am putting out on the Internet, but I believe that it is just that - MY business and MY choice and it is helping. I have one hell of a year and it has helped SO much to work through it all with an objective person, who happens to be a professional. ;-) Our old bishop is a marriage family therapist and he recommended the place I'm going to and man, I'm grateful.

I got strep throat in December. And Patrick got it. And then we ended up around extended family who had it and didn't realize their sick symptoms were strep, so our kids got it too. That was fun.
Christmas in Idaho, a wonderful holiday and break from life. 

I'm in a cancer support group for moms on Facebook and a mom in the group recently finished her treatments. She was asking about how quickly the weight comes off and stuff like that. I'm six months post-chemo and five months finished with all treatments (chemo/radiation) and I still don't have all of my energy back. I started going to the gym a couple of months ago and working out at home. Then I fell into a funk and stopped going. I'm starting to feel better and more into it, so I've started working out again. Since I finished my treatments, I've actually gained an additional five pounds - well, really, I gained that in the last couple of months. It is sooooo incredibly frustrating to have the extra weight on my body brought on by a life-saving treatment. An outsider probably sees it differently than I do. It's so frustrating and difficult. I am surrounded by people who are getting fit and healthy and losing weight and blahdy blah blah blah, and I don't even have the energy to work out regularly. I don't even have the energy to take care of my house. I thought that, for sure, by now I would have the energy to make my house beautiful again and not a total disaster zone. But it isn't true.

My oncologist told me not to expect much for the first year and that I may not even be 100% a year after finishing treatments. I might be even at like 70-90%. It's bizarre. Such a strange thing. One minute, I feel like I have loads of energy and the next, I'm totally pooped. I don't have the energy to wash the dishes or even start a load of laundry, let alone work out. And when I do have the energy, sometimes I don't have the desire. I feel in a funk a lot - and I'm taking a medication for the anxiety, but sometimes I just don't WANT to workout. Sometimes I just want to lie on the couch and eat ice cream.

So many things I have experienced in the last year are beyond foreign to me. It seems so surreal. I'm grateful to have a few friends who are there for me through the good and the bad and who I owe my life to for their support in this last year. I pray that I won't ever have to give them support for the same reasons they have given me support, but I do know I will give them anything and everything that I can. I love them and they are very treasured friends. My patriarchal blessing tells me about the friendships I will make in my life and that I will have life-long friendships I will treasure. I'm grateful for those friends who have been stronger than me this last year and who let me rant when I feel fat or sad or upset and who boost me up when I need it. I'm grateful for the friends who have treated me like I'm totally normal and, yet, supported me like the sick I have been. I'm grateful for their kind and honest hearts and how absolutely giving they are.
My friend, Leah, and I at B.O.'s Christmas shindig. 

Aaaand that was a side rant I did not expect. So anyway, it makes me sad that this woman will probably go through many of the same things I have gone through, particularly mentally and emotionally, in the last year. I wish she didn't have to. I wish I could take that from her and I wish she could go back to being totally herself. And I hope that she does have more energy and drive than I do. Like I said before, finishing treatments does not make you the same you you once were, and I really thought that I would go "back" to being "me". I'll never be that version of "me" again. That scares me. Well, sometimes it scares me and sometimes it brings me strength. I am a better person. I know more than I did before. I have experienced more than most people my age and it has given me a unique and special perspective on life. Sometimes that is really challenging because others my age don't understand and don't have this view. I think that is part of the reason I have lost some of the friends I have lost. Or, at least, I think it has added to it. At times, it is frustrating to have this perspective. Sometimes I wish I could be carefree, but ultimately, I'm incredibly grateful to have a perspective that allows me to KNOW that spending time with my kids is more important than doing dishes and that life is short, but of great value. I know now that my body isn't everything - it's a vessel and it carries my spirit through this life. I know that it is important, but that it will be made whole in the life to come. I KNOW these things now. I'm still learning and growing from this "experience". Sometimes I hate learning from it and I wish we could move on. But I'm still learning. I'm still growing.

I've avoided this blog, really. It's been a hard six months. Really, really hard. The last six months have made chemo and radiation seem like a cake walk (to me, at least). I haven't known what to say, what to share, what to keep in, and sometimes, I haven't even really known what I have been experiencing. It's been really rough. If I can help anyone with cancer, I want to help them with this part of cancer. It's been the hardest part so far. I know there is a lot more to go and maybe that opinion will change, but this part is so hard, so mysterious, so confusing, so traumatizing, so bizarre, so... challenging.

And there I go on another side rant. My scalp doesn't itch anymore - I use Head and Shoulders shampoo now. The advanced formula kind. I love my baby hairs. Most people find them to be super annoying, but I adore them!

We had family pictures taken in November. I wanted to have pictures taken throughout the year, so we did another shoot in the Fall. There was also an art exhibit/gala thing in October (I think October) featuring Heal Courageously (the organization who took our photos in July) and we attended that. It was really emotional to see the photographer, Anna, and Michelle, who runs Heal Courageously. I didn't realize it would be so emotional, but it was. It brought back so many feelings, and yet, I also felt like super woman for having gone through that.
I absolutely LOVE this photo - I think it perfectly expresses the end of our 2013 and so much more. I LOVE it.

Me in November (crazy to think that just a few weeks later my hair went crazy curly!)

Oh, and speaking of Heal Courageously, they were featured in the Utah Cancer Connections magazine and they wanted a photo of a family, soooo... we were on the cover! :) And then had a couple of photos inside. So we're on the cover of a magazine, albeit a cancer magazine. Haha. :) Patrick has a regular customer at work who saw it a the doctor's office and wanted us to sign their copy. That was weird, but cool I guess. Random, right?


So anyhow, now we are getting ready for Patrick to go to training for Army National Guard. He'll be gone for a while... more than I want him to be gone. And I'm teaching. And life is life. And I think I'm ready to blog more often.
We got tickets to the Christmas devotional that The Church of Jesus Christ of Latter-day Saints does every December. We ended up sitting REALLY close to the front (possibly thanks to my handsome hubby coming straight from drill and still being in his uniform from their inspection... It was a beautiful devotional and I love the date night with our friends.)