Wednesday, March 23, 2016

4th Chemo Infusion - Pancakes, Naps, and Mrs. Doubtfire

Hey everybody. This is Lauren. Today I got to go to HCI with my dad for his 4th Chemo Infusion so it's my turn to update the blog. It was nice to spend some time with my dad today. I think we can all agree that life gets busy sometimes and we tend to forget what matters most. Needless to say I was excited to have some time off of work so I could slow down and have the opportunity to see where my dad has been spending a large amount of his time. So here is what we did today! Pictures included!

We arrived at HCI at 8:30AM and got dad checked in. From there he saw his nurse who "activated" his port. This process only takes about 5 minutes once taken back and from there we went up to get some breakfast. Dad got some giant pancakes (thanks Grammy and Grandad) and we got to hang out and chat til about 9:30AM. After breakfast we went down to start infusion. A nurse took us to Dad's "Pod" and took his vitals. His blood pressure was a little high which is normal considering you can be a little nervous. From there another nurse came and got Dad started on his "Hydration" phase. During this phase he got a little sleepy and took a 10 minute power nap. 


After the hydration phase Dad was given two bags of anti nausea medication. After each bag is done administering the machine beeps and the nurse comes back to start a new one. He scans both Dad's wristband and the bag of medication and the process starts over again. After all of those bags had been administered they started him on his chemo. The nurse informed us that this last one would take about 2 hours and that he should be done at about 2:30PM. At this point we decided that it would be a great time to turn on Mrs. Doubtfire which is a family favorite. After about an hour of technical difficulties we finally got it going. Multiple nurses stop by to check on Dad to see how he is doing and to see what movie we're watching. They also have snack carts that come by in case you get hungry. 

At 2:30PM Dad's machine beeped letting us know that his infusion was complete. He also receives chemo for the next 48 hours through his "chemo ball" so the nurse came and hooked him up to that before telling us goodbye. 

You never really realize what somebody with cancer has to go through until you actually see the process of everything. I'm glad I got the opportunity to get a tiny glimpse of what my dad is going through. I hope I will never have to know exactly how he feels. Cancer has been a constant trial for our family for a few years now, but Dieter F Uchtdorf gives a good example of how trials can actually be a blessing if we slow down and remember what matters the most. Times like these may not be very enjoyable, especially for those bearing the burden of cancer, but they sure make you realize the importance of family and how very fragile life can be. That's what I'm grateful for. So thanks for screwing my head back on, Cancer.

Have you ever been in an airplane and experienced turbulence? The most common cause of turbulence is a sudden change in air movement causing the aircraft to pitch, yaw, and roll. While planes are built to withstand far greater turbulence than anything you would encounter on a regular flight, it still may be disconcerting to passengers.

What do you suppose pilots do when they encounter turbulence? A student pilot may think that increasing speed is a good strategy because it will get them through the turbulence faster. But that may be the wrong thing to do. Professional pilots understand that there is an optimum turbulence penetration speed that will minimize the negative effects of turbulence. And most of the time that would mean to reduce your speed. The same principle applies also to speed bumps on a road.

Therefore, it is good advice to slow down a little, steady the course, and focus on the essentials when experiencing adverse conditions.

-Dieter F Uchtdorf

We love you dad! Keep kicking cancer's butt! 

Dad's Pod

 
 Dad's IV Tower

 
 Dad's Wristband

 

Thursday, March 10, 2016

3rd Chemo Infusion - A "Good Things to Come" Kind of Day

This is Arvonne and it is my turn to update the blog.  After Mikell’s post two weeks ago I’m not feeling very confident in my writing skills.  Thank you Kell for writing a beautiful and informative post.   Today was Cliff’s third chemo treatment.  I love being with Cliff on the days he is at Huntsman.  There is such love, compassion, and hope there and we always leave feeling optimistic. 

Cliff’s blood work came back really good today.  His white blood cell count is back up in normal range and we are hoping it stays that way.  One of the blood tests they ran today is called CEA, which stands for carcinoembryonic antigen.  It measures a protein level that indicates presence of cancer.  We all have a count, but normally it is around 3.  Yes, just 3.  2200 is where cancer is considered likely.  When Cliff first went to Huntsman his count was 2800. You are probably thinking, “Yikes that is really high”, but our oncologist says it can get to around 10,000.  Tonight we got a call from Huntsman telling us that Cliff’s number has dropped to 855.  They hope the number drops but were quite surprised at how “dramatic” the drop was.  Of course, we are thrilled!

In the next two weeks Cliff will have another PET scan and will meet with his oncologist where we will find out if the chemo is working in shrinking his tumors.  With the news we received today we are very hopeful.

A friend of ours sent an email out a week or so ago and she quoted Elder Jeffery R Holland, who is an apostle of our church.  It has touched our hearts and we would like to share it.  “Don’t you ever give up.  Don’t you quit.  You keep walking.  You keep trying. There is help and happiness ahead.  It will be all right in the end.  Trust God and believe in good things to come”. 

I too had an appointment at Huntsman today to meet my new oncologist.  Although I am two years cancer free I am currently taking meds that help my body fight off any possibility of recurrence.   My doctor spent a lot of time with me and educated me about my specific cancer.  It is good to know more and to feel confident that all is going to be okay.  For those of you that have dealt with cancer there is always that question in the back of your mind of, “What If”.  Today’s appointment put a lot of our concerns about my treatment to rest.

I want to thank my sister, Pauline, for coming and hanging out with us today.  She is always so willing to be with me when I need her and is the best cheerleader you could ask for. 

Before I end this, Cliff and I would like to send some love to our friends, Steve and Karin.  Steve starts his chemo tomorrow and we want them to know that we are praying that all goes well.  You guys are amazing and we are so glad that our paths have crossed. 

Today was a “good things to come” kind of day.  We believe in the power of prayer and are so grateful for the love and prayers that are being sent our way. Thank you, thank you, thank you. 

GO, FIGHT, WIN!!!!!!