May 28 is an important day in my family.
It is a day of remembering and a day of celebrating.
Remembering how fragile life is.
Celebrating that there is still life left to live.
May 28 is a day that changed me.
It changed my life.
It changed my family.
2 years
730 days
17,532 hours
1,051,898 minutes
63,113,852 seconds
May 28, 2010.
(This is taken from my post May Twenty-Eighth from 2011)
One year ago today my life flipped upside down. One year ago today everything I knew changed. One year ago today my dad was diagnosed with Multiple Myeloma, a blood cancer.
The Background:
In December of 2009, my dad graduated from nursing school. Throughout school, he kept saying he wanted to work in the OR, ER, or critical care unit. He enjoyed the blood and guts of the operating room. But once he graduated he didn't go out looking for a job. Mom and I became concerned. We later learned that he wanted to work on his nursing skills before he specialized in anything. In March of 2010 he finally went to the hospital and he got a job on the spot, which they never do.
Problems:
Everything started off great. Dad had awesome mentors and he enjoyed the work. But after a few weeks he started to get pain in his legs and back. We figured it was from working 14 hours days nights, standing on his feet, lifting people, etc. It got so bad that dad wouldn't leave his bed unless it was a day he worked. After his 8th week of orientation mom told him he couldn't go back to work until he went to the doctor. We knew something was wrong and we knew he needed to be looked at.
On May 27, 2010 dad finally went to see our regular family doctor. Dad couldn't hold up his own leg. The doctor knew something was up so he did some blood work and scheduled an MRI for June. 3 hours later mom got a phone call from the doctor's office saying my dad was in acute kidney failure and had to get to the hospital right away. So they packed up and headed to the hospital not knowing the worst was still to come.
During this, I was in Kansas City, where I go to school. I was planning on staying there for the summer with hope of getting a job. When I heard my dad was in the hospital I decided to drive home the next morning.
That Morning:
May 28, 2010
I remember I woke up kinda early. I wasn't feeling to well with my allergies and just wanted to go home and be with my family during this rough time. The entire hour ride home I played different scenarios in my head. If this happens, then I move back home. If he is ok, I will go back to KC, etc. The next thing I knew I was arriving at the hospital. As I pulled into the parking lot I got this horrible sickening feeling in my stomach. Something was wrong and my mom wasn't telling me everything. I even told her that as I picked her up from the parking lot to go run a few errands. She didn't say anything to my comment and it was soon forgotten.
It's bad. I have cancer.:
When we got back to the hospital dad was in a prep room for surgery to have a central line put in. Once we did all the normal greetings, things changed and got a little more serious. I remember dad put his hand on my arm and told me the news was bad. He had cancer. They found out early this morning. I immediately started crying. My dad cried with me. I was 21 years old, and it was the first time I saw my dad cry.
The next few hours were a blur...literally. Everything happened through rounds of tears. We didn't know what he had. We didn't know what the life span was. We didn't know if he would fight. We didn't know anything.
As time went on we learned dad had stage 3 Multiple Myeloma. There is no stage 4 in this type of cancer. But the important thing was to fix dad's kidneys first, then we would work on fixing the cancer. For those who don't know, kidneys functioning level is determined by a protein called creatine. Normal is around 1.0, 12.0 is critical. Dad was at 11.98. According to his doctors there wasn't much hope that dad's kidneys would come back and if they did it most likely wouldn't be to normal level. In fact, he had less than a 5% chance. We were told he would need to have dialysis 3 times a week for the rest of his life. As far as the cancer, he needed to have a transplant once the cancer came down to a certain point and when his kidneys got a little bit better. Our oncologist said he hoped dad's creatine would be around 3 or 3.5 when the transplant would take place, but we wouldn't worry too much about that right now. So they started dad on dialysis right away for about 6-7 hours every day. By the third day they stopped because his kidneys responded so well and they wanted to see if his kidneys could hold their own. They did. After a few weeks, his kidneys came to a normal range. Daddy never had dialysis again.
Dad had bone scans done and we found out he had some fractures in his legs, back, and skull. This happened because all the protein and calcium was leaking out of his bones and going into his blood. This is part of the reason he was in kidney failure, because your kidneys filter your blood. These fractures were also part of the reason he was in so much pain back when he was working.
Fighting Cancer:
Once dad's kidneys came back we were able to fight the cancer full force. He started chemotherapy a few days after he was admitted into the hospital and by October he was able to have a bone morrow stem cell transplant. I won't go into much details of the transplant process, but it was the roughest thing I have ever seen. Basically the transplant process kills your entire immune system. Dad had to go into isolation (from other people-mom and I were able to be around him). Daddy lost all of his hair and became incredibly weak. For about a month the only way he could get from one place to the other was in a wheelchair. Dad finally got a little bit stronger and was able to make it out of his room by Christmas time.
Follow Up:
In February, he hit his 100 day mark (after the transplant) and his cancer progression was reassigned. They found a little bit of the cancer left in his body so his prognosis was 'pretty good' remission, not complete remission. He went back on a low dose of chemo, which they do even if the patient is in complete remission--studies have shown that it prolongs life. In May of 2011 he began is inoculation again (he has to get all the basic shots a baby gets). And just a few days ago they found that there is only a teeny tiny line of cancer still in his body.
After:
It has been exactly one year. My little family has been through so much. We experienced numerous trials and triumphs. And most importantly we experienced many, many miracles. I moved home immediately after dad was diagnosed and spent many evenings watching movies with him through his recovery time. We have become great friends with our doctors. They have experienced all the hardships and joys right along with us. But most importantly we are all still here, fighting together as a team. A friend of mine once told me that God doesn't play by numbers. She couldn't have been more right. We have overcome what science has told us. Because according to science, my dad wouldn't be here today.
And now.
We are given a little hiccup.
If you have been following this story you would know that dad was recently in the hospital.
He was sick with a gangrene gall bladder, which is not cancer related (we don't think).
But what I didn't share,
what I didn't know how to share,
is that the cancer is coming back.
At the moment, dad's white count is low so they had to take him off of his maintenance chemo in order for his white count to go up and for him to heal completely from the surgery.
So right now, we just wait.
I don't know what will happen when he gets the all clear, but we have various possibilities and options to fight this cancer again.
Maybe putting him back on the maintenance drug will help, maybe trying different drugs will do the trick.
I don't know.
But what I do know is that all we can do is wait and hope that this is just a bump in the roller coaster and not for the long haul.