Adventures with Multiple Myeloma, a Brain Tumor and Tracheal Stenosis

Expiration Date

To preface most of this post, I was told at my diagnosis that, because of the involved kidney failure, I have a three to five year life expectancy. So most of these thoughts are based on that knowledge and things I have thought about the last few months. Sorry if this is morbid to you. It is a daily thought to me. Please take with a grain of salt, as I bring my sense of humor along.

Friends

A couple months ago, due to a random encounter involving a potato ricer, I ended up with a new best friend, Tyler. We say that jokingly, but the man brings me fresh barbecue and smoked ribs. I mean, seriously, the guy is a pit-master. Anyways, getting to know him better and hanging out a bit, things are great. However, he made a comment that I haven't been able to shake, and that was, "I wish I would have come up and said hi sooner, I feel like there was wasted time there." With so little time granted to me, is it fair to others to friend them? What about friends I haven't seen in a while? Do I keep in touch, reach out?

Stuff

Those who know me the most, know I like to collect things. I have an amazing collection of Star Wars Memorabilia. From a huge collection of Funko Pop Figures to large figurines of Darth Maul and some Storm Troopers. I also have various video game and Super Hero figurines. And I have an unhealthy relationship with the Kansas City Chiefs and probably should stop buying ball caps that tell everyone that I am a fan. With such a short time frame, do I stop buying stuff? Getting rid of it is going to be a pain, and I don't want Michelle stuck with it. Do I gift it away? Who is going to want all these Chiefs hats? I'm such a geeky dork.

Knowledge

One thing I have been really good at is teaching myself new things. My expertise with Adobe Photoshop, Adobe Illustrator, and Adobe InDesign has been all self taught. My computer expertise of hardware, software and all things Internet, self taught. I tell everyone that I bend the Internet to my will, and it is very true. It is scary some things I can do on there. My Facebook and Social media advertising, mainly self taught, though I had a great mentor at a previous job. Do I keep learning? Look at those skills, do you think they will be important in the next life? Everything there involves a computer. Are there computers in the Sky? Because "..I'm gonna go to the place that's the best..". Love that song..

New Vehicle

With the new treatment, I am getting stronger everyday. Hoping to be able to drive more frequently soon. I miss my truck, it is more a race car than truck, and she sounds so sweet. I even got to drive her the other day, and for those that do not know, it has been about 18 months of not being able to drive due to a health problem of some sort. And man, do I miss the freedom. But she is getting old and I think I am ready for a fun vehicle. (See the matte black Dodge Challenger) I know our first need is a replacement for my bride, and we are hoping to get something this summer. Needs to be able to make the run to the Mothership (Huntsman Cancer Institute), in the snow, in 12 parsecs.. oh and reliably. But then, do I think about my dream car? How would that work? My loan would have a longer time frame than me!

Final Thoughts

Please know I am not depressed. Some things about fighting cancer can be very depressing. Sitting with chemicals dripping into your chest for 7 hours each week with nothing but hospital to look at, yes, can be blah. I am strong. I am young. I have the bestest bride on the planet. I have great friends and family that keep me laughing and engaged. I have a lot to fight for. I know that I want to start travelling a bit, and hopefully will get some miles in soon. So, I hope that even though the topic is dark, that I was able to keep it a little light. But do know this. There are a lot of factors that are in play here, and I can beat it. I plan on beating it, at least, that is what I am fighting for. This lion has a lot more fight left in him.

Chasing Happiness

The past week two weeks have been a nice reprieve. Chris along with many family, friends and co-workers were so very thoughtful and their simple act of kindness was much appreciated. Last year for my birthday Chris was still in the hospital with his new trach. This birthday I was just glad to be spending making some happy memories. Thank-you to everyone who reached out in any way to wish me a Happy Birthday, it added so much joy to my week. I would try to least list each of you individually, but I don't want to leave anyone out. So let's just say I'm very lucky to have many sweet and thoughtful family, friends, employee's and co-workers who touch my life in many ways.

Last Sunday, my birthday, I had the opportunity to attend the re-dedication of the Jordan River Temple. Chris had put on a brave face trying not to damper my birthday, but I knew that he was feeling crummy. Luckily John came to keep him company while I went to the dedication. While sitting there waiting for it to start, I had some time to be alone with my thoughts. I was grateful to be there, but regretted that I hadn't thought to ask someone if I could attend with them. I was a bit lost in my thoughts when a sweet friend from the ward tapped me on the shoulder and asked if I wanted to come join her and her husband. It was an answer to an unspoken prayer. Not only was I not alone, but I even got to sit on a comfortable padded chair instead of a hard metal one. After the dedication I came home to find Chris sitting outside on the porch. We enjoyed an hour together sitting together watching the rain and hearing the thunder, we both love a good storm, it was a perfect unplanned moment I will treasure. Then my parents showed up with dinner and we had a nice evening.

Common advice to patients with a difficult illness is to not let your diagnosis run your life. But that in and of itself is a tough battle. With many complicated illnesses, it feels as if at each diagnosis they assigned us a pet monsters to be our constant companion. The gray brain tumor monster which has been our companion for many years has been joined by a a couple additional ones. With the burgundy myeloma monster being the loudest and most demanding of all.

Sometimes these monsters consume us. Other times there are rare moments when they sit somewhat quietly in the back seat. They are a constant reminder that our life will never be the same. Whenever we try to think about the future, or make plans, it always speaks up and says "What if?" "Are you sure you want to do that, what if...." "Do you really think you should get a new vehicle, what if..." "Do you really think you could plan a vacation, what if...." It's a battle to not let these unrelenting questions cripple us and keep us from making decisions or plans.

Last week was the start of his 2nd cycle of DRd and took us back up to the main Huntsman. We found out that he's already responding well to the new treatment. His specific myeloma currently represents itself with high Lambda light chains. An important part is also the ratio. At diagnosis his Lamda Light chains were 323. In February right before collection was the first time we had ever seen this test result with no flags. Going off treatment for just a short time and his numbers were already climbing again. Having everything back within normal range with just one month of DRd is excellent news! It's just one of the things that they are doing to monitor his disease, but it doesn't take a lot of knowledge to know that having things in normal range on any test is always a good sign. We are so grateful that DRd is working!

While the side effects of DRd aren't always pleasant and seem to be very unpredictable, they for now are easier than his previous CyBorD. The nephropathy in his feet and hands from Bortezomib is slowly getting better which is making it easier for him to walk and bit by bit he's getting stronger. The other day he was walking on the floor in our new bathroom and for the first time could feel the warmth of the heated floor. They say it can take up to a year for the feeling to return, and there's no guarantee that it will return at all or completely, so we are happy to be seeing signs of progress.

Saturday we packed up the monsters and threw them in the back seat with the oxygen tank and took a short trip. It's the first time we've traveled in over a year. We went for the afternoon up to my Grandpa's cabin (near the Soldier Creek Dam/Strawberry reservoir). It is a place full of many fond memories from my childhood. To hear the wind blowing through the aspen tree's, to feel the sun on our face and to see the clouds moving so quickly across the sky was a great distraction from life's troubles. We learned a bit of history about how the cabin came to be and enjoyed the conversation with my aunts and parents.

With signs that the DRd is working, we're hoping to continue to settle into and adapt to our "new normal". Life with the monsters is unpredictable, but when we can we try work in happy memories. When Dara was in clinical trials, the treatment usually worked for about nine months. However that was in patients who had already tried many more medications. There are many people who have had a longer response. This is what we are hoping for. Our hope is stay on the current course for many years. For this reason I likely won't be blogging as frequently because there won't be much to update. Don't worry, I still plan to write every few weeks when there is something to update. Chris will hopefully also write as well.

Pedicures and Rainbows

On Sunday last week we were taking the morning to sleep in and recoup when Chris got a text from Dr Sborov asking if he could call. A phone call from a doctor in the evenings or on weekend typically isn't a good thing, but in this case it was just a good reminder for us that we have an amazing man looking out for Chris. He was just reviewing things and wanted to make sure that he was doing the best for all of his patients. We talked for about a half an hour and he wanted to make sure that if there was anything he could do that he was doing it. We talked to him about some of our concerns and he asked to make sure that we let him know what happens with an upcoming meeting with our specialist. With all of the complicating and difficult things Chris has been fighting for the past 4 years we've really struggled to find the right doctors. When we weren't looking and needed an amazing specialist the most, he landed in our lap and for that we will forever be grateful.

Last year for my birthday, my family came and picked me up at the hospital. We had a nice breakfast and then several of us went and got a pedicure. It was a great break from the crazy month and I remember commenting that it would be fun to do it every year in May. It was such a nice surprise when I got a text from my aunt Gail asking if I would be interested in getting together again for another group pedicure. She took care of making all of the arrangements and this Monday I was able to celebrate the start of my birthday week in the company of my sisters and aunts. It was so nice to be pampered and escape for the evening, my Aunt Shari even was able to surprise all of us by being up visiting from California. Pictured: Gail, Roxann, Shari, me, Crystal and Jennifer.

Wednesday was the 4th infusion (and last) of his first cycle of DRd and for the first time it was out at the Huntsman in South Jordan. While the nurses and infusion center at the main Huntsman are familiar, being closer to home is a different kind of comforting. Next week we'll be back up at the main Huntsman and meeting with Dr Sborov as he begins the 2nd cycle of DRd. So today we went back for more testing so that we can know how he's responding. I've heard in a support group that often the numbers don't respond until after the second cycle, but we'll cross our fingers.

As we pulled into the hospital for the third time this week, the life flight helicopter was sitting on the pad, something we haven't seen before at our local UofU/Huntsman. It was a bit sobering and ended up being the theme for the day. After dropping of and getting labs done at the infusion center we headed to radiology. Dr Sborov wanted a skeletal survey. It's basically a whole bunch of xrays from his head to his knee's to see if they can see any lyric lesions. The waiting room was surprising empty, but before they could get Chris in they told us they just had an emergency patient that needed to be taken care of first. We gladly waited. The tech who helped us was amazing. She was patient and very understanding and did everything she could to make the process easier for Chris. The last time we did a skeletal survey was back in October in the early days of his diagnosis. It took all the energy he at the time and wore him out but he pushed hard to make it through. Today it did wonders for my heart to see how much stronger he is since then. It still was no walk in the park, but he's stronger today and it gives me hope he will continue to improve.

As we were going from radiology to the next appointment we stopped for a moment in the lobby and I happened to see a couple, about our age, sitting across from us. From what I could observe, the husband was breaking some tough news to his wife. She was struggling not to cry and I could feel the pain she was going through because I've been there so many times myself. I wanted so badly to go up and give her a hug and a word of encouragement but I had no idea what to say. They left and walked up the stairs and we went to his next test. I saw them again as we went to leave, tucked over in a corner talking, the emotion still etched on her face and the struggle not to cry a real battle. Going to the hospital so frequently, has become such a regular part of our life that it's easy to lose sight of how life changing hospitals can be.

Battling cancer is a something that is multi-factorial, with just one of the stressful things being financial. In general we've been pretty fortunate to have good insurance, and are surviving that aspect of the battle about as to be expected. However with insurance there's still often a lot of hoops to jump through. This week we ended up with about $5500 in bills for various procedures and medical equipment. They are things that should have been covered but were processed incorrectly. It's something that happens frequently and is very frustrating. We contacted IHC, Huntsman and our insurance to try and get them worked out correctly. It's something that happened frequently with his brain tumor and from that I learned all of the insurance lingo and to know how things worked. Many I'm sure get bills in the mail and pay them without question, but to me I'm not willing to just take it in the pocketbook without a fight. One of the bills that was sent incorrectly gave us a sneak peak of the cost for his Daratumamab. We knew it was expensive, but the $50,000+ price tag... per infusion... was more than I expected. That's also just one med. The Revlimid has a price of $14,000 per month, our portion is large but reasonable. Luckily the last drug, the little "d" in DRd is comes with smaller price tag, which we split about equally with insurance.

This week also luckily happens to be the week Chris has a break from Revlimid (his daily

chemo). Feeling crummy is pretty much just part of life with cancer, but we're hoping this week he'll feel just a little bit less crappy. With my birthday this weekend we've taken each evening to go out and get something yummy to eat. Getting out isn't easy, but Chris wants for me to be happy and we both want to have some happy memories mixed in with all the challenging ones. Tonight he wasn't feeling well and was worried about being away from home, but we were able to make the trip to Bountiful where we were able to have dessert with my parents at a place called Pace's. It's a favorite place from my childhood where you can get an ice cream treat called a rainbow, a fruity slush with soft serve ice cream. Just like the weather, life is unpredictable and you never know when you'll see a rainbow. So if you live in Utah, and are going through a stormy part of life and need a rainbow... now you know where to go to find one.

Longest Ever!

A year ago today on Facebook I posted this picture and said "Longest Day Ever". At the end of April we finally found the reason for his trouble breathing, which he had been struggling with since the fall... tracheal stenosis (narrowing in his airway). The entire next week we tried to get in for a CT. We struggled to get an appointment with a specialist, the earliest available being months out. After a long weekend with little sleep we knew that we simply couldn't wait any longer and on Monday we decided to head to the main UofU ER in hopes that they would see the importance of the situation and consult with the highly recommended specialist there, Dr Smith.

The nurse in the ER (named Michelle) was amazing, she was very concerned and a great advocate. They scheduled him for surgery the next day and then moved us up to a room where we felt tucked away and forgotten. Another long night with with only 30-60 seconds of sleep at a time, his oxygen would drop into the 70's (normal is 95-100) and set off the alarms and no one would ever come. We were both exhausted by the time morning came. They weren't sure when he would have surgery so he wasn't allowed to eat or drink anything all day. They finally took him back for surgery about 9:30 PM and I sat in an empty waiting room. The surgery was supposed to take less than 2 hours, but finally in the early hours of the morning, around 1:00 Dr Smith came and told me he was done. It was a difficult surgery unlike anything he'd seen, he put my mind at ease and said we'd done the right thing by bringing him to the ER. Shortly after a nurse came and took me to see Chris in recovery. It was great to see him, but shortly after I arrived it was apparent that he was struggling. He was on Bi-Pap and the look in his eye was pleading for me to help him. I felt so helpless not knowing how I could possibly help, so I held his hand and told him things would be OK. The nurses were doing what they could, but he was in respiratory distress. He needed more help. It wasn't long before they rushed him down to the surgical ICU and I was sent out to the waiting room. They said they would come get me in about 45 minutes.

The longest day ever became the longest night ever. Sitting in a new waiting room I waited anxiously wondering how he was doing, trying to sleep a little with only minimal success. Someone had come out and said he was stabilized and so I tried to wait patiently for them to tell me it was OK to come in. Finally at 5:00 I decided to try and figure out how to get back to the ICU. His airway was so small (even after the surgery to open it) that they had to intubate him with a pediatric tube. It was so short that they were very concerned it would come out so they had it carefully tied in and his hands restrained. The backup in case it did was taped to the shelf and every shift change the nurses would make sure they knew where it was at. He was also still sedated. As scary as it was to see him hooked up to so many things, he was so peaceful that it was a huge comfort compared to seeing him in recovery.

The longest day ever turned into the longest week ever as we stayed in the ICU. On Thursday they tried to remove the tube and allow him to breathe on his own, he did good for awhile but then it quickly became apparent it wasn't going to work. This time I was tucked away in the corner and watched the team as they had to re-intubate him. It was terrifying and comforting to be in the room as they did so. So many people making sure he was OK. Staying tied down, hooked to a ventilator wasn't a long term solution so on Sunday they put in his trach. It was about this time that I started this blog. Another week in the ICU and then to a regular room and eventually we were allowed to go home. Life at home with a trach was a tough adjustment. We weren't given the training that they promised and care for his new trach fell squarely on my shoulders. It was terrifying. At his follow up appointment at the end of the month his airway was still about 70-80% blocked.

The longest month ever turned into a long summer as we adapted to his trach and new challenges and trials emerged. We learned and tried to overcome, but things got tougher and harder. Now, here exactly a year later from the "longest day ever." We are sitting at Huntsman with his 3rd infusion of his new DRd medications. Hospitals, blood tests, medications, side effects... it's something we deal on a very regular basis. Our lives have changed and it's hard not to long for the life before, the life we had hoped to have or to be frightened of what lies ahead. Many people in the support groups for myeloma talk about how hard they remember the first year being. We've still got about 5 months before we can put the first year of cancer behind us, but at least we have a different 1 year milestone to celebrate. We are so very grateful to those who have come to our aid and support during this difficult year.

Although life is tough and often overwhelming, it's something I'll gladly do as long as it means I keep my sweetheart by my side. Sitting beside him while he gets chemo, or helping him walk carefully to the car is the place I most want to be. Our love grows each day as does my admiration for him. He's so sweet, so tender, so loving, so thoughtful. He's going through such difficult obstacles and still always is concerned about me. He is my hero. I deeply hope that he'll beat the odds and that we'll have many, many more years together. This isn't a battle we chose, but we'll fight it together.
The lyrics to a Mariah Carey song come to mind....

And then a hero comes along

With the strength to carry on

And you cast your fears aside

And you know you can survive

DRD

Chris posted this picture on Facebook last week and I felt like it was just what we needed for the blog. Life with myeloma is hard and painful things but also many that are simply unpleasant. Compared to everything so far, last week was just a typical week with many unpleasant things and some uncertainties of how things would turn out.

Wednesday last week was a long day of his new treatment. He wore his cookie monster pants, I packed his favorite cookies and some of his favorite milk and together we got up and left our house about 6 AM. It was a long day and we didn't get back until about 7 PM. All things considered the infusion went about like we expected. There was a chance it could turn into an overnight stay, so we came prepared but it ended up not being needed.

After a whole bunch of "pre-meds" to help make things go smoother, they got the Daratumamab infusion started. They put the IV meds in a 1000 ML bag and started the infusion at rate of 50 ML per hour checking his vitals and increasing it each hour if he was doing OK. The first side effect he felt was a spike in his temp, nothing too crazy, and a cool rag worked to help him cool down. Shortly after they bumped it to 100 ML per hour he got a full body rash. It started in a few areas and quickly spread. They stopped the infusion and gave him some more IV Bendryl. Once the rash went away they started the treatment back up at 50 ML per hour. The Bendryl put him to sleep and he was able to get in a good nap. They increased it each hour by 50 ML. The monitored his vital signs on a regular basis and there were no more reactions for the rest. Once he was up to the max of 200 ML per hour things went much faster.

Our nurse Robin was awesome! She was his nurse the first day of collection and always makes us both feel welcome, she even remembers and calls me by my name. There are at least two infusion rooms that I'm aware of at the main Huntsman and we thought we were going to be in the main one however it was in the BMT infusion room. Doing the initial infusion's of Daratumamb is something apparently fairly new to the BMT infusion. Robin was a bit concerned and wondered why our infusion wasn't being done inpatient but everything went fairly smoothly and although we thought we might end up being transferred upstairs he was able to finish it in time to avoid being put in a room.

Chris's family from Washington, Montana and Texas let us know throughout the day that they were thinking of us by sending us pictures wearing their Team Chris shirts.

Once we got home Chris took his new chemo, Revlimid. It's a pill that he takes at home every day for 3 weeks, and then gets a week off to help his body recover. Having chemo around the house is a strange feeling. He's got to be very careful with it, it's not something I'm even supposed to touch. It also has a side effect of blood clots, so he also started a blood thinner. We thought they were going to have to be shots, but were relieved that they decided to do a pill instead that was much cheaper and easier to take. As well we now have another team watching over him, the thrombosis team. Until they figure out his dosing needs, they will be doing regular PT-INR tests every couple days to measure how thick/thin his blood is.

All of the new medications have come with a lot of fatigue. He's still pretty worn out and battling some of the effects from collection and it would have been nice to have the week off like planned, but it just wasn't in the cards. Unfortunately it also has really made him have insomnia. He has had hard time sleeping for while and is often up in the wee hours of the morning. Being exhausted and tired at the same time are two things that really don't go well together. Saturday I convinced him to go back to bed and he slept almost all day. He's felt a bit better since then, but has been again dealing with an itchy rash from the medication (a common side effect). We're both grateful that when he is awake he can often work to help keep his mind off things. There's no way he could work a typical 9-5 job, so we are glad he's able to work some here and there.

Today we are back up at Huntsman for another infusion. Our nurse this week is Amber, another one of our favorites. Instead of a 1000 ML bag, they've mixed the Daratumamab into a 500 ML bag. Starting again at 50 ML and working our way up, so far with no need to pause. He's been able to rest some this morning and the infusion room is oddly quiet. This morning as we walked in, Chris was resting in the lobby from walking in from the car. Dr Sborov happened to be walking by and stopped and came over to check and make sure he was OK. It was just something simple, but made me appreciate even more that we ended up with an amazing doctor at a time when we needed it the most. We're both so grateful and touched by his genuine concern.

Ferrari's

Today as I walked to church the sun was shining, a gentle breeze was blowing and the smell of blossoms in the air was sweet. It was a great balm for my soul. Spring is increasingly becoming my favorite season because of all of the reminders that life can be beautiful even after a difficult, cold harsh winter. I also couldn't help but notice that while some items are in full bloom, and others have already begun to sprout leaves, others were barren still hibernating from winter. It's was about six months ago that we found out about the multiple myeloma. Spring hasn't quite yet come to our journey, but the warmth of the sun and the gentle breeze I'm hopefully it's very close on the horizon.

We met with Dr Sborov again Friday to figure out what the next step is. Chris was originally supposed to have a break from chemo until May but just prior to collection we found that his Lamda Light Chain numbers were high. In October his Lambda light chains were 323 (Normal is .57-2.63). Starting chemo they dropped fairly quickly and were down to 4.67 by December and dropped regularly each subsequent test. They were normal for the first time in February at 2.03. Just prior to collection they were 12.6, and when tested again this week they are at 18.4. So all the plans to start treatment were moved up. Dr Sborov would like to start again as soon as possible, he would have started this week if he could have.

Trying to describe the status of myeloma is tricky. There's approximately 724 trillion blood cells in the average human body, so there's a lot of places for myeloma cells to hide. There's a lot of debate about using the term "remission"" for myeloma. Most myeloma patients, even those who do transplant, are on maintenance chemo to keep the myeloma at bay. Compared to most other cancer patients when in "remission" are not currently being treated. One term is "Complete Response" which I interpret to mean that the drugs are doing their job. I've learned that when they decided to do collection Chris was in SCR (stringent complete response) meaning that according to his blood tests and bone marrow biopsies things were in normal range. The meyloma was behaving so they used the opportunity to collect. Because his numbers are climbing he has "relapsed". Since he hasn't been doing chemo it's to be expected but they had hoped it wouldn't come back quick so quick.

When Chris was originally diagnosed, because of his kidney failure their options for treatment were limited. Now that his kidney's have improved he's eligible for the "Ferrari" of treatments. While Dr Sborov meant it in terms of the quality, it's hard not to be staggered at the cost two of his medications are each both likely 6 digit figures in terms of cost per year.

Years ago I remember standing in line picking up a prescription in St. George. The person in front of me was picking up one that was about $250 and trying to figure out how to pay for it. I was shocked and wondered what the costly medication could possibly be. I remember then picking up mine and being grateful that it was only about $10.

Over the years we've been shocked at the prices of medication. $600, $900, $1000, $1100, $3000...Several times it was common to hear the timid pharmacists carefully ask "You know this is expensive right?". We are very fortunate to have insurance that covers a large portion of the cost. Especially since his chemo usually has a 5 digit price each treatment. However one bit of knowledge that I can highly recommend to anyone is that if you get a prescription that's very expensive is to see if the company has an assistance program that can help bring your co-pay costs down to a reasonable amount. Not sure what would be covered by insurance and what we would have to pay, I looked into this as soon as I got home to get signed up for anything available.

Next week he'll have his first treatment of DRd

daratumumab (Darzalex®)

revlimid (lenalidomide)

dexamethasone (Decadron®)

His previous treatment was all done once a week on the same day (an infusion, a shot and pills). DRd will be different. It is a weekly infusion (Daratummab), Revlimid (daily pills) and dex (weekly pills).

Daratumamab is a monoclonal antibody. It targets the CD38 protein that is highly expressed on myeloma cells and attacks and kills them or allows the body to kill them. The way I picture it is like a military operation and we are sending in reinforcements. The body doesn't know that's what they are, so for the first couple infusions most people experience a reaction and in varying severity. When a reaction happens, they will stop the infusion, treat the reaction, and then when safe to do so start the infusion again at a slower rate. Because of this the infusion can take a long time, usually about 10 hours. After the first couple infusions, the body seems to realize that we're sending reinforcements and instead of causing a reaction they become allies and fight the myeloma. He will do these infusions weekly for a while, eventually going to bi-weekly and then eventually monthly.

Revlimid is an oral medication that will likely be taken for 21 days followed by a week off. Revlimid is an IMiD (Immunomodulatory drugs). This Immunotherapy treats the disease by inducing, enhancing, or suppressing an immune response. It can cause low blood counts, fatigue and blood clots. They will monitor his blood counts carefully and because of a family history of blood clots he will also be on a blood thinner. It's a powerful drug which required several pages of consent, and regular phone calls with the company to make sure he's taking it correctly.

Dexamethasone is a corticosteroid that is very common and included in most myeloma treatments. It is used at almost all stages and sometimes even alone when nothing else works. It can help with inflammation, help decrease nausea, and at high enough doses can even kill myeloma. It can also help make other myeloma drugs work better.

Anyways, enough of the technical and informative. The next couple weeks are likely to be tough, but we've been through many tough weeks and survived. This new treatment will hopefully provide relief from some of the difficult side effects and improve the quality of life for both of us. The first treatment CyBorD served it's purpose and was able to get the myeloma under control and save his kidney's. That is no small achievement!

After the first couple weeks things will gradually get better and getting down to only one infusion a month instead of one a week will be amazing. The past six months we've had little time or energy to do anything else. It will take time, and these new medications will surely have it's own side effects to deal with but I'm hopeful there's a chance to to reclaim a part of ourselves and have time to make some happy memories. Treatment, in one form or another, are likely a permanent part of our life but with a few windows of opportunity opening it hopefully won't be all encompassing.

Milestones

The past week and a half of collection were exhausting and we are both so glad to have that milestone marked off the list. We haven't had time to celebrate yet and instead have just been trying to recover. However this is a huge and potentially life preserving milestone! With so many new treatments on the near horizon we hope that one of them can bring the cure for myeloma and that it will come during his lifetime. However transplant is the best treatment to give him the longest life expectancy to wait for this cure, so collection was a very critical step. It was very long days for me, however I'm so glad I could be there with him to support him because as exhausting it was, it was so much more difficult for Chris.

The process was very interesting and even though we tried to learn what to expect ahead of time, there were side effects we didn't know to expect. We were prepared for 1-2 shots per day, however in total he received 32 shots, not a fun surprise. As well, Tylenol and Claritin only took the edge off the pain. We also did not know that it would cause fluid shifts and retention. We've been trying so hard to get the extra fluid off, but are back again at square one.

Dr Sborov's goal for collection was 10 million, and Chris exceeded the goal and was able to collect 11.5 million. Yay for reaching this goal! The minimum that they need for a transplant is 2, but closer to 5 is ideal. So depending on what they choose, he has at least for 2 transplants. Multiple transplants are pretty common, and sometimes they even do them one right after the other (called Tandem).

During collection, we had three different tech's overseeing the process and running the machine. These techs are the ones who also work in the lab processing, counting and prepping the cells for their time in the freezer. They are also the ones who are responsible for thawing them and helping with transplant so perhaps we will see them again. They were great at answering questions and we learned a lot, or at least had a lot explained to us that we tried to absorb. Much of the details go above our head, but they explained that they use the marker CD38 to count the stem cells. I had researched about the new medication they want to start him on that had mentioned CD38. Daratumamab (Darzalex), is a immunotheraphy drug. It helps the body's immune system to find and destroy the cancer cells by binding to CD38.

If you haven't gathered it already, myeloma is complicated!

Because of collection, the meeting that we've been anxiously awaiting with the cardiologist, Dr Ryan, that was scheduled for the week of collection was moved to the week before. His father has heart disease and has been in and out of the hospital for the past six months so hearing that there may be problems with Chris's heart has had a very worried for the past couple months. The appointment was a bit anti-climatic but we came away with some assurances and clarification.

Pulmonary Hypertension is high blood pressure in the arteries to his lungs. All of the respiratory issues we have been dealing with (the tracheal stenosis and trach) have been difficult for his heart. However, the condition will likely not have any impact on his life expectancy. It is both good and safe for him to exercise.
Dr Ryan does not feel that it is a barrier to receiving a stem cell transplant.
The swelling in his legs that we have been battling is a symptom/side effect.

One aspect of our marriage that I've always loved is how much we enjoy talking to each other. He's someone who I can talk to about anything and we never run out of things to talk about.
Before his most recent challenges, he would often take me to and pick me up from work. I work only a few miles away, but it was nice to have this time in the morning and at night to look forward to. He hasn't been yet been able to do resume doing this, but with all of his appointments we have a lot of time to talk while driving and waiting. I'm so glad he proved the doctors wrong when they said he likely wouldn't speak again! Among other things, we've talked quite a bit about a bucket list. Even before the cancer diagnosis we would toss out ideas, but with a bucket that developed holes and is leaking out precious moments we are trying to figure out how to find the balance to accomplish some of the things that we've always wanted to.

We'd love to hear some inspiration,

what's on your bucket list?

Collection

Today started very early, driving to Huntsman while the moon was still up and the sky was still dark. Often while making the drive my thoughts wander and I try to focus on being grateful instead on on some of the other things. Today in the dark with Chris silently sleeping beside me I turned to where we were headed. I'm amazed at how lucky we are to have a top notch cancer center, that just so happens to specialize in his rare cancer nearby. Being treated by a myeloma specialist is important in his key to his survival. While the drive is often filled with traffic and usually takes an hour, it's a blessing that most don't have. Today we learned that the older man in the bay next to us had to come all the way from Oregon. With all of our appointments so far this year, we've driven about 1,000 miles, I can't fathom the logistics of trying to coordinate everything even if we still lived in St. George. Being able to sleep at home, and just visit the doctors in the hospital is a blessing. Collection was delayed from the original plan of February but we grateful that he's being able to do the process as it's an important one in his treatment.

Today marks the first potential day of actually collecting. We've driven here several days already to receive Nupogen shots to tell his body to over produce stem cells so that we can collect them. We weren't sure how quickly the shots would kick in, but shortly after getting them the bone pain kicked in. Strangely Claritin can help, so he's been taking that and Tylenol to try and keep the edge away. They only take the edge off, I'm so grateful that I'm able to be with him as sometimes the simple act of human touch is the greatest for pain relief. The pain tends to come in waves sometimes in his hips, sometimes his shoulders or his legs or arms. Often in multiple places at once. He's described the pain a few ways.... like his bones trying to get out of his body, like someone is taking a chisel and hammer to his bones and also like a vice grip on his bones. The pain ebbs and flows in each area and he's been a champion and handled it pretty well. I'm touched with his thoughtfulness as each day he's thanked me for being with him and for being patient with him. He's going through a lot, yet he still things daily of how it is for me.

Yesterday in addition to the Nupogen shots, he also had a line placed for the collection. This one is very similar to the line he had for dialysis but with an additional catheter. It usually sticks up out of the patients neck but we were able to request that they tunneled it down through his skin instead.

Yesterday was an unusual day at Huntsman. While in the waiting room waiting to be taken back to IR we were both surprised to see two young little toddlers. Being treated at a cancer treatment is strange because unlike a regular hospital, you know that everyone there is either being treated for or is there to support someone with cancer. We usually feel so out of place with so many around us the age of our parent's or grandparents. Having a toddler walk by and say "bye-bye" and wave sweetly brought a smile to both our faces.

As well, after they wheeled Chris back and I was sitting waiting for him to come back they wheeled another patient into the curtain next door. His voice sounded very young and I could tell he was alone, it made my heart ache and I nearly peaked around the curtain to introduce myself. About that time a visitor stopped by and I learned that his indeed was very young, likely about 19. He had just until recently been serving an LDS mission in California. He, like us, was grateful to be in good hands with his diagnosis.

Most people don't collect on their first available collection day, but the preliminary numbers testing for the number of cells in his blood stream looked good so instead of having to wait 3 1/2 hours for the blood tests to come back, they were able to get him started a little bit early. Chris has been very optimistic that this will go smoothly so being able to collect some today was a win in our book

They usually process 15 liters of blood in a session of apheresis and the speed that they do so can vary the time that it takes. Today's session was about 3 hours. They collected about 175mL of stem cells and 200 mL of plasma.

As well, there is approx 250 mL of blood in the tubing, but at the end of the process they put most of it back in, usually returning about 230mL.

To prevent his blood from clotting in the machine and tubing, they add an anti-coagulant as part of the process. This anti-coagulant binds to calcium which can cause his calcium levels to drop which can cause tingling in your lips and extremities. Because his calcium was low before even starting this morning they started a calcium drip shortly after they got him all hooked up. Because it can mess with your other electrolytes (potassium, sodium, etc) they run additional labs to make sure he's OK to go home. More waiting for those to come back, but they all turned out good and he was given the OK to leave. About 9 hours after we left this morning we arrived back home and both took a nap.

The tech today said it's really hard to estimate but that his best guess would be about 1.2 million. We're now getting ready to head back up to the hospital for a new nightly shot. This shot, called mozobil, tells the stem cells to "get out" of the bone marrow and into the blood where they can collect it. This also is pretty common and something we expected. He will continue to get the Nupogen shots in the morning as well.

While hanging out in a hospital hooked to a machine isn't fun, and brings back memories of doing dialysis, we know this is a good thing and a step in the right direction. We also are touched by the support and thoughtfulness of others. Our friend Rachel stopped by for a visit, wearing her Team Chris shirt. We're getting to know all of the nurses, techs and support staff but it's always nice to see a friendly face and reminisce about her recent trip to Hawaii. Also, we returned home to a delivery of groceries on our porch from Smith's. Our good friends from St. George had promised Chris a Dr Pepper and had Smith's deliver a case along with a whole bunch of other goodies and essentials. I had started a small list of what I knew we needed and planned to try and go to the grocery store sometime this week but they saved us. While I'm sure there are several who would have picked up groceries for us if we had just asked, we weren't quite sure what this week would be like so having it just show up when it was needed to me was a tender mercy and someone following a prompting. So lucky to have such good friends!

Off we head to Huntsman again, but at least we get to return home again tonight to sleep in our own bed!

Sunshine!

The weather outside is transitioning from winter to spring and for that I'm so very grateful. I love the blue skies, the spring rain, the feeling of sun on my face and the spring flowers coming up through the dirt after a long winter as life begins again. Today as I was out in our backyard I looked over to see "popcorn" on our little apricot tree and interrupted the pair of ducks courting in our front yard. I love the smell of flowers and the uniqueness that each flower brings. Spring is a wonderful season of transitioning.

Our lives are also changing and hopefully providing new life. Because most people proceed directly from collection to transplant, we were a bit nervous that insurance would decline collection only, but we heard this week that they have approved collection and things are moving forward. Collection will start late next week.

We're still learning about collection and will understand more after our consent appointment next week. I thought however I'd try to share a bit about what it is. There are two types of transplant, autologous (from Chris) and allogeneic (from a donor, usually a sibling). In order to do to transplant they must first harvest stem cells. Stem cells are the basic building block of many cells in the human body. The collect these "baby" cells, then during transplant us a high dose of chemo that kills everything. Shortly after they reintroduce these stem cells into his system in hopes that these new cells will develop correctly.

There are two overlapping parts to collection. It starts with daily shots that will cause his body to overproduce stem cells, which can often cause bone pain as they kick into overdrive producing stem cells. As described above stem cells then develop into other types of cells. In the case of blood cells they will become red blood cells, white blood cells, and platelets. Luckily stem cells are found in the blood as well as the bone marrow, and they will be collecting them from his blood.

In a process very similar to dialysis (and likely plasma donation) called aspheresis they will temporarily remove blood from his body and filter out the stem cells and then return the blood. The cells will then be taken to a lab, processed and then stored until transplant. Most people tolerate it pretty well and there are usually very few complications.

So as we celebrate Easter this Sunday we are very grateful for the opportunity to be soon undergoing collection. A break from chemo has been a wonderful blessing. It has allowed Chris to continue to regain some of his strength. He's had a bit more energy, and is in great spirits. We both are still reveling in sleeping in bed, and also enjoying the luxury of a safe and relaxing shower. We've enjoyed going out a couple times together for errands other than doctors appointments and driving around with the sun roof open. May all of you enjoy this weekend and the coming spring weather.

He is Listening

The past couple weeks have given a reprieve from the endless appointments and procedures with the main item on the agenda each week being chemo. Being able to meet Jonah and catch up with Carmen and Jim is something that we've looked forward to. Life is so very unpredictable from week to week that planning anything besides medical appointments is tricky but we enjoyed the time that we were able to spend together.

Today we met with Dr Sborov for the beginning of cycle #6. He explained the results of the bone marrow biopsy from the March 1st and it was.... good news! The chemo has worked very well and he's doing well enough that instead of another cycle of chemo that they canceled his chemo for today (and the next few weeks). Instead (pending insurance approval) we are doing collection in about 2 1/2 weeks. Until then he won't be doing chemo. Actual transplant is still on hold and possibly won't happen until next year, but we are OK with that. Aside from the one week off we got the week of Valentines, he hasn't had a week without chemo since he started in October.

After collection he will likely start a new chemo. Bortezomib which is likely the biggest offender for his neuropathy will be discontinued, so hopefully his numbness, pain and tingling will get better. Instead of CyBorD (Cyclophosphamide, bortezomib and dexamethasone) he will likely do DRd. His drugs go by different names so it also has several aliases it can also be called DLd, Dara-Rev-dex, Dara-Len-dex.

daratumumab (Darzalex®)

revlimid (lenalidomide)

dexamethasone (Decadron®)

The best news about the new chemo is that depending on how he responds his infusions could gradually be dropped to bi-weekly and eventually monthly. I can't even put into words how glorious that sounds.

Compared to the news we got today this seems to pale in comparison but we've reached also an amazing significant event. For the first time in about a year and a half we've been able to return to sleeping in bed. When Chris started to have problems breathing in the fall of 2016 we moved to sleeping on the couch. I could have stayed in bed, but being together helped us sleep the best we could in the circumstances. When my Grandpa got him an amazing recliner Chris started sleeping there, and I was able to claim the couch for myself. We're fortunate that our couch is fairly comfortable but still nothing quite compares to a real bed. Luckily he's been able to build strength and his new trach has made sleeping back in bed a reality. Sleeping in a real bed and being able to cuddle up next to your sweetheart is incredible. It does however come with one drawback, getting out of bed and facing the day! I treasure the days I get to sleep in.

The slower pace has been great to allow us to recharge and recoup. It's also provided time to reflect, which is in many ways overwhelming. All that we've been through and all the medical challenges we've dealt with in the past few years have been unrelenting. Last year I think we were so busy surviving that we haven't had time to really process much. I cried very little during those many days in the hospital, but looking back tears instantly come to my eyes. Several people have told me recently that I'm strong. I know they mean it as a compliment, and I should take it that way, but it reminds me that just below the surface most days I feel like a fragile porcelain figurine. As I've been searching for bamboo items to carry over the theme from our bedroom into our new bathroom I came across this quote. "The bamboo that bends is stronger than the oak that resists". We both have really tried to just take things one day at at time and go with the flow. I'll have to remember being bendable is different and that I am strong, like bamboo! Today's appointment was a perfect example. We went in expecting it to just be a typical appointment only to take a 180 degree turn and go in a different, but good direction.

As someone who likes to be prepared, not being able to plan anything much in the future is a challenge. In pondering the difficulties of the past I want to do what I can to make the future easier. I think one of the most difficult challenges of his myeloma diagnosis is that the future is terrifying. I try to focus on living in the present, but it's not an easy task and it's the prime reason why tears are always just below the surface. Very few people know how long they will live, or when they will lose a loved one. I don't know this either but I do know that there's many difficult days in our future, transplant being one of them. In a caregiver support group I'm in people so frequently post about a loved one who is now on hospice or who has lost their battle that it's hard not to be constantly reminded that myeloma is not curable. We hope and pray that he will beat the odds, or that the new treatments on the horizon will drastically increase his life expectancy but we know the odds aren't in our favor. However now while he's feeling better we are talking about plans for his funeral. It's not easy to do but it will be a lot easier now than whenever in the future when it might be needed.

At church recently the closing hymn made me cry. At the time I couldn't understand why the tears, but in rereading the lyrics again later they again touched my heart. The pioneer's weren't able to stop when things got hard, and neither can we...

Then work and watch and fight and pray

With all your might and zeal.

Push ev’ry worthy work along;

Put your shoulder to the wheel.

Put your shoulder to the wheel; push along,

Do your duty with a heart full of song,

We all have work; let no one shirk.

Put your shoulder to the wheel.

With the good news today a "heart full of song" seems a bit easier tonight than it was this morning. Even though collection isn't a walk in the park, it's a relief to be storing his stem cells for the future. Having things be easier for a little while will make it easier to fight will all our might and zeal. So we'll put our shoulder to the wheel and keep pushing. We're developing the strength with need for the challenges ahead. We're being given the opportunity to gain strength that likely will be needed.

When looking to pioneer's who have overcome difficult trials I need look no further than my mother. In 2010 she suffered a stroke that drastically changed her life. It took away from her all of the things that she enjoyed doing and made life incredibly difficult. Even though basic things like reading, writing and even driving are now difficult she has taken then time to send me several encouraging notes. It is always such a nice surprise to check the mail and instead of bills, ads or junk mail to find an envelope with my name on it written with love. She, like many of you, prays daily for us to have "strength to handle the challenges". This week she mailed a small package with the reminder to celebrate my worth. I know it wasn't easy for her to mail the package, and I know she knows hard hard it is to face and overcome very difficult challenges.

The first blog I wrote about the diagnosis of multiple myeloma was called "Close Around Me" and as part of it I quoted the song "A Child's Prayer". Here is part of the the second verse, applicable to today as I feel like we are soon to be entering the second chapter.

Pray, he is there;

Speak, he is list’ning.

You are his child;

His love now surrounds you.

He hears your prayer;

He loves the children.

Thank-you for all of the prayers, thoughts and concern on our behalf, it is because of them that we've been able to make it this far. As you say a prayer, please express gratitude for our wonderful news today and for continued strength. May hopefully this coming chapter be easier and have time to be filled with happy memories.