Oh, Christmas Tree
I took down the Christmas Tree today. I packed up all the ornaments Jane made over the course of our marriage and all the ornaments we had bought or otherwise acquired over 21 years of marriage. For some reason, it felt like I was doing so for the last time. I cried through it all.
The tears keep welling up…
This was my sixth Christmas season without Jane. Somehow, it’s been the hardest of all six. None of them have been easy. I barely remember the first one. I spent it in Seattle and the shock of it is etched into the family picture someone took at my brother’s house that year. I am a ghost in that shot. There is no expression on my face–no pain, anger or disbelief.
Numb Christmas
People tell me you can tell the seriousness of a wound by how much it doesn’t hurt. Minor injuries hurt like hell. Major ones induce a numbness that masks the seriousness of the situation. I felt nothing for a very long time. I went through the motions of life and anyone who has seen me in public these past few years could almost believe I am OK.
I took down the Christmas Tree today.
I’m a good actor. And the numbness helps me create that illusion. Say something funny and I will laugh. Say something sad, though, and the curtain comes down. I may continue to interact with the people around me but my mind is far away. It is the only way I have to deal with the loss that does not leave me sobbing endlessly on the floor. I don’t do that in public.
Christmas then
Christmas was a special time for us. Jane would spend weeks selecting a new ornament to make for us. She would keep the design away from me–not showing it to me until it was finished and ready to hang on the tree. We would wake up on Christmas morning about 5 a.m.–we were like little kids. We would go out to the tree and bring our gifts back to bed, where we would unwrap them, starting with the stockings.
Minor injuries hurt like hell.
We would have cocoa and warmed chocolate croissants after presents–these eaten in bed as well. Then we would get up and Jane would bake bread and desserts we would take to her parents for Christmas dinner. I would wash the dishes as she worked and do whatever other prep work she needed done–chopping onions or veggies or beating eggs.
Christmas now
I spent the first four Christmases in Seattle after Jane died. I would stay with my father most of the time. We would sit up late into the night talking about our wives and remembering better days. Then he died and, because Jane’s dad was not doing well, I spent last Christmas here. I sat with our tree and looked at the lights. I had tea with my croissant.
…we were like little kids.
There were no gifts wrapped under the tree, no stockings, no Christmas morning card. Nor were there this year. I baked bread, a Quiche, and an apple pie and took them to Jane’s cousin’s house for dinner. I came home and watched It’s a Wonderful Life and wondered what George would have done without Mary.
The end of Christmas
Normally, I would have left the decorations up until January 6. Now that I’m retired I can wait until then. Jane and I always took the tree down the Saturday before we went back to work–and always hated doing it.
…I spent last Christmas here.
Last night, as I sat looking at the tree, I decided I would take it down today. I couldn’t stand looking at it. It reminded me of too many better days–days with Jane in my arms, days with her voice calling down the hallway, days when laughter was real.
Christmas tears
Part of me thinks I must be getting better. I wouldn’t hurt like this if the wound had not healed to the point that the nerves were coming back online. It’s what I tell myself. Maybe it will turn out to be true, this time. But the house is quiet tonight and I am alone. The tears keep welling up and running down my face. It’s been five years and 23 days and I’m still crying, still hurting, still wrestling with a loss I can’t describe or explain or escape.
…days when laughter was real.
Tomorrow, I’ll wake up and get out of bed. I’ll eat breakfast, exercise, and shower. I’ll take on the projects of the day, write the things I need to write, clean the things I need to clean, plan the things I have to plan. I’ll figure out new ways to go after the thing that murdered my wife in the hope I can somehow help to remove that arrow from Death’s quiver so that no one faces what she did–and no one faces what I have since.
Words fail me. Reading your thoughts helps me appreciate what I have and not to take it for granted. I’ve posted before and am a NETs patient. I’m on my 7th inj. of Somauline, and can only guess that it’s helping. I fall under the catagory of having had a diagnosis and surgeries. But unless I have surgery again (I’ve been told it’s too risky), my tumors cannot be seen or tested. I do however from my last surgery know that they are seeded, implanted, and too many to count in mesentery, pelvis, and a few other places. Jane sounds like a person who lived every moment of her life. I find that with the extreme fatigue I have, I wonder if it’s even worth fighting. Then I read some of your posts. I hope you’re able to raise the money for research, and reach your goal of bringing awareness of NETs to people soon. But in the meantime I just want you to know that because of your memories of Jane and all you do to honor her life you continue to make a difference to another NET patient. It is very easy for me to want to give up. But through your thoughful postings I feel I’d be letting Jane down if I did. I can’t imagine the pain you must be going through. I wish I knew what to say to help.
You’ve just done it.
Love to read ur stories.
So human and so full of love and angst. I am the one with net cancer but my husband is the one that passed away, suddenly in 2008. I can so relate to the feelings you express and know that i am not alone in how I feel.
I will spread the word and help fight the NET battle, for myself, for Jane and others that may be affected by this mysterious disease.
Thank you. I am sorry for your loss. I don’t know how anyone faces NETS alone.
Harry,
Each time I read an entry, my heart breaks for you. While reading this Christmas 2015 entry I was mindful of a quote by Rumi and I think it applies to you and your efforts on behalf of fundraising for research to cure NETS cancer.
“The wound is where the light enters you.” ~ Rumi
I pray that every day is just a little brighter for you and that one day, you will be lifted from the fog of pain.
On another matter, after writing back and forth with you a few months ago about a young man I know who was undiagnosed but clearly had a serious illness that I felt was cancer, I took your advice and urged him to go to a teaching hospital. The young man I am referring to has been in Emory University Medical Center since Thanksgiving. He is undergoing stem cell transplant and the process has been arduous. Every day I am praying that this young man will survive the cancers (he has more than one type) that are trying to take his life (34 years old). The young man’s wife sits a constant vigil next to his bedside. President Jimmy Carter wrote this man a letter of encouragement on the process he is undergoing in an effort to save his life.
The world keeps turning and you are making a difference. Thank you. Carry on.
Annie
Thank you. I needed this today.