Friday, February 19, 2016

Day +81

Last night we took the family, Claire included, to a great event sponsored by an amazing charity. It was probably too soon to try something like that, but it seems like her doctors are encouraging her to do a few things to move back into normal life, so we went. Well, it turned out that Claire's feet, which still can't fully flatten to the ground when she walks, were causing her a lot of pain. And the event was much more crowded than I had anticipated, which made me very uncomfortable. So we ended up leaving shortly after we arrived. Then Claire almost fell going into our house, and she ended her day with a good cry in her room. In some ways it seems like the closer we get to this 100 day milestone the harder it gets. I lose sleep because I am so afraid of what might happen. My mind is often spinning because I don't know what things will look like next week, next month, in six months. I've said it before, but this is such a hard age to battle cancer. I know there is never a good age, but these young adults are in such a unique situation. My husband and I have six children, and when they were little we were pretty strict parents. I never had the primary goal of being a friend to my children. I always acted as their mother first, and the friendship came after that. And we have worked very hard as our children have grown to give them independence. I mean, six kids. We don't need any forty year olds living in our basement, right? But seriously, we make very conscious choices to try and support without meddling and guide without telling our adult children what to do. It's not always easy, but we went into this whole parenting thing wanting to help our kids become happy, contributing adults with their own lives. Then there is Claire. Independence is almost impossible. Encouraging it is sometimes painful. And the thought of her possibly living on her own later this year seems incomprehensible. I know four other kids Claire's same age who have or are battling cancer. Of course, there are more, but these are the ones that I know. I know their families. I watch their journey. I talk to their moms. Two of these young adults are, like Claire, still fighting. And two of them are, hopefully, done with their battle. One of those is a dancer and a college student, and I love quietly watching her life. The other  is serving as a missionary for the LDS church, which is so amazing. I want this for all of them. I want them all to start college, live in an apartment, find their passion, fall in love. Remember how exciting that was? But in this moment it is hard to see how that will happen. I have faith, it is just hard to have vision. The mom of one of these beautiful young adults who recently reached her 100 day post transplant milestone put it this way.
 " Unless you’ve lived in this world, you may not understand why we did not immediately jump up and down and shout with joy.  This has been our world for so long.  We’ve learned that with the Savior's enabling power, we can do hard, really hard.  We’ve taken up residence in a place we feared.  And we’ve found a home of sorts, here. We know how to do long hospital stays, multiple IV lines, beeping monitors, space age procedures, and a host of other things.  We’ve met people on this side of the door who have become lifelong friends.  We pray for those standing vigil each night beside a child’s bed and for “sisters” who are continuing the battle in their worlds of cancer.  Now, there is trepidation of a different kind.  Can we move outside this world somewhat and claim another? "
Beautifully said, don't you think? But for now we will just focus on this next goal. Try to live in the moment. Breathe deeply, love fiercely, and trust that we are in God's hands.

In parting, I leave you with a picture of some brand new hair starting to grow. Just in the back. Not on the top. I mean, come on! Seriously? Geez!











Saturday, February 13, 2016

Day +75

Wow. I am running out of insights and things to report. Which is kind of awesome, in a way, right? I love weeks with no drama. As we hoped, Claire's platelets have finally recovered from her unexplained fevers and hospital stay and are now up to a respectable, if still low, 121. She started Dasatinib last night and I had a hard time falling asleep for fear she would have another fever, but she didn't. I hate to say it out loud because I don't want to jinx it, but it seems like she has turned a corner. She is starting to eat again, and she is HUNGRY. She's also gained a few more pounds. (How would it be to have people be excited about that? I wouldn't know, but it certainly gives me perspective.) She hasn't been reading because, you know, chemo brain. But this week she decided she wants to reread all of the Harry Potter books, and she's almost done with the second one. She started and finished a puzzle. And for the first time since she relapsed in July she actually drove the car. It was just a few blocks, from the library to our house, and it was a little awkward because her feet don't flex very well. But I thought it was a very big and very important step toward 19 year old normalcy. Oh, and we snuck her up to Logan this afternoon to visit our son and daughter-in-law. Technically it was probably a little too far away from the hospital for her to go, but she was so excited to go somewhere! Especially since we are experiencing horrible air quality here in Salt Lake City due to our infamous inversion and going outside isn't the best thing for her. (There were blue skies today in Logan!) But she really had fun, so it was worth it. Now that I am writing this I am realizing that I actually do have things to report. Good things. And for that I am very, very grateful.



                          These two love a good puzzle.


                      Playing Extreme Candyland. It was hilarious!


       Two of our amazing nurses enjoying the cupcakes we brought into clinic for Valentine's Day. I guess we should have brought wet wipes ;)

Cuddling with the fattest cat in the world. (Don't talk to me about kitty diets. Believe me, we've tried.) Its like sleeping with a tiger. A very slow tiger who loves popcorn.



Friday, February 5, 2016

Day +67 (I promise. It's not day +68)

Clinic day. More of the same. There wasn't much change in blood counts, but with today's medication changes things should go up a little. I might have explained this before, but Claire has been on two different immunosuppressant medications to make sure that her blood counts don't recover too quickly. Things need to go nice and slow to prevent heavy graft versus host disease. Today we stopped one of the immunosuppressants, and in a few days we will stop her IV anti-fungal medication. The fewer the better, I say. Her platelets are not yet high enough to start her 10000.00 medication (Dasatinib) which we keep in a locked safe that we have buried in a snow cave in the back yard guarded by our fierce guard dog Jemma. (Just kidding. We keep it with the other meds. You wouldn't really want it if you didn't really need it. Trust me on this one.) We were done in an hour and twenty minutes, our shortest BMT clinic visit to date! Afterwards we went to the zoo to try and see the new baby giraffe (it is apparently too cold for her to be making public appearances just yet) then went to an Irish pub type joint for some fish and chips. (Claire had been craving them all week.) All in all, a pretty nice day. I'm sorry for the overuse of parenthesis in this paragraph. (Apparently I have run out of more effective writing tools.)

Once again this week I was asked, "So, what's the prognosis?" It was as casual a question as "So, what's the weather like outside?" I was silent for a few beats, then said, "Claire is hanging in there." Seriously, why would you ask that? And what makes you think my child's chances of living or dying are any of your business? Or that I would want to discuss it so casually? God has brought us this far, and He will carry us through whatever the future holds. I can't emphasize enough how much a cancer parent hates this question. Ok, rant over.

On a happier note, I was very excited to start the process this week of setting up a scholarship. Woohoo! It is The Claire Driggs Family Survivor Scholarship, and it will be offered to a survivor of childhood cancer or the sibling of someone who battled childhood cancer. Right now it is just for Olympus High School students, but I hope in the future to be able to have one Olympus only scholarship and one Utah scholarship annually. I know several incredibly bright and talented cancer survivors, Claire included, who didn't receive any of the national scholarships they applied for. Claire ended up getting a full four year tuition scholarship from her university, plus two Olympus scholarships, so she is in good shape. This scholarship is my way of giving back, expressing gratitude, including my kids (who will hopefully make up the selection committee. I could never choose!) and honoring some of the most amazing human beings I have ever met. I feel like I just had a baby :) So, if you ever need something to donate to...(last parenthesis of the post- I now have something to tell people when they ask what they can do for us!)