I don’t know how to begin this post. It’s been sitting with me for a while, but I just haven’t been able to write this.
On November 18, 2011, my mother-in-law called me and told me that she had cancer. She had been going through a series of tests, and we all had a feeling that the prognosis wasn’t going to be good, though we tried to to be optimistic. A few weeks later, at the beginning of December, we found out two things. It was pancreatic. It had spread.
Two days after Christmas, Mom started chemo. The doctor was great. The doctor gave us hope. He defied all of our expectations. Despite everything DH and I read online, we had years left with Mom. Years. 3-4 years. Not months. We all believed this.
On February 18, 2012, three months after she was diagnosed, Mom had been really sick. She had been having horrible stomach issues. We thought maybe she had gotten a virus on top of the chemo that was beating her up every week. The chemo that kept her from her grandchildren. The chemo that made her cry almost every day. We thought we were going in the hospital to get her back on track and bring her home so we could help take care of her.
A week went by, and she was still in the hospital. At one point, she seemed stronger and we thought we were going to bring her home and have hospice help get her through this. We met with hospice that Wednesday or Thursday. We were hoping to bring her home that weekend.
Friday. One week after she went in the hospital. I was at work, and this feeling came over me. It was the moment that I realized what was really happening. I called DH and said “I just want to prepare you. I don’t think we have much more time left.” I went home, and Googled end-stage pancreatic cancer and realized that we were not going to be bringing Mom home. Instead, I grabbed my iPad, went on Facebook and started pulling off pictures of my boys and my nephew. I pulled pictures of my husband, my brother-in-law and my sister-in-law. I took them up to the hospital to show her. She smiled and laughed at them. When the doctor came in, I had two questions. Can we bring the kids up? She has a brother on vacation in California. Should we call him? Yes. Yes.
People came. They brought food. They brought hugs. They made Mom smile. They prayed. They held her hands. They kissed her. They called us. They texted us. They messaged us on Facebook. We had a whole network of support. She knew everyone was there with her. She knew how much we all loved her. She knew it was time.
On February 26, 2012, at about 3:30 in the morning, the greenhouse alarm went off. It sounds like an old-time school bell, and rings loudly to let us house dwellers that the temperature has dropped too low. My father-in-law didn’t hear it. My husband woke him up. Dad went out to the greenhouses, stoked the fire and came in. The phone rang. Mom was gone. Just like that, we had lost her. 3 months after the diagnosis. 2 months after chemo. We never had years.
On February 26, 2012, my husband two boys and I moved in with my father-in-law. As we went through the next hellish 72 hrs of the wake and the funeral, I realized more and more how amazing she was. She did EVERYTHING for this family. She did it quietly. She did it with a smile. She did it all. Her inscription on her gravestone…Forever Adored. Nothing was ever truer.
And then there’s me.
I yell. I drink. I swear. Most of the time I mutter under my breath. I’m loud. I have what I refer to as a “busted filter”. I’m disorganized and I never put things back in the refrigerator or cabinets where they’re supposed to go. I have little to no patience. I get angry a little to easily. I’ve made major, major mistakes. And I’m living in Mom’s house. I’m living in Mom’s house and every day, I look up at the sky, cross myself and say “I’m sorry, Mom. Please forgive me.”
After some tough conversations, we decided that we would buy the house, jointly with my father-in-law. When we we signing the deed at the lawyer the other day, I came home and cried. This should have never happened. God should have never taken her to him when we all needed her so badly here. Mom kept a binder with all of the entire building process of this house. This was her dream home. This was the house she always wanted, and she should be living in it now. Not. Me.
Life doesn’t always work the way you want it to. Life throws you curveballs and knockout punches. Some days I just don’t want to get out of bed, and somedays I think of the alternative. Somedays I just don’t want to be here. Somedays I just want to get away from all of this. I want things back the way they used to be…before cancer and chemo and loss. Loss of so many good things. I would give anything to have Mom back with us.
The other day, I bragged to my father-in-law about fixing a toilet at work. I have no mechanical ability at all. I said “You’d be proud of me.” He said “I’m always proud of you.” I greatly appreciated his sentiments, but I have to wonder why he said that. I’ve done a lot of things I’m not proud of. Things that make me feel like I don’t belong here. In a house where there used to be so much laughter…and goodness…and baked goods. I feel like I’m black-sheeping up the joint.
I don’t know how I’m going to get through this. I don’t know how I’m going to deal with my own frustation and the pain that I feel every day, while trying to help my husband and father-in-law and my kids get through this. One day. One hour. One step, I guess. But some days, I just want to run and run and keep running.
I need to make new goals in life…starting now. Strive to be good. Strive to be a word that someone used to describe my mother-in-law…gracious. Strive to be someone that everyone could really be proud of. Always.