Showing posts with label parenting. Show all posts
Showing posts with label parenting. Show all posts

Tuesday, December 28, 2010

Christmas

Today I remember Christmases past. I remember the year Colby was fifteen months old and kicked Santa Claus. The year he was a little more than two and was afraid to sled down my mom's slightly sloping driveway. We made snow angels instead. I remember the year he was three and got the choo choo train and the drum he had been asking for all year, every day, since the Christmas he was two.

By Colby's fourth Christmas he and my mom and I were sledding down the bigger hill in her yard like pros. That was also the year he begged to go to the dinosaur exhibit at the Minnesota Science Museum, then screamed when he saw the first dinosaur and refused to go in. By age eight Colby had graduated to sledding the hills at the local golf course and by age ten he was beginning to snowboard. We built snow forts and snow men (and snow women and dogs) and had a number of snowball fights.

In between the snow, there were trips to other museums, art exhibits, plays, concerts, restaurants, and lots and lots of movies. And board games. Colby always won at Michigan Rummy. And there were always projects Mom needed done. Colby fixed the gate to the downstairs when he was about twelve and it still works. He re-hung closet doors, helped clean out those same closets, and learned to drive on snow.

When Colby was maybe nine, he and Mom and I made cardboard swords and decorated them glitter, beads, and bits of sparkly fabric from my old skating costumes. He made cookies with the neighbor behind us and we went for winter walks in the neighboring woods. He and I checked out the neighbor's houses from the front by walking on the frozen lake, being sure to stay close to the shoreline. We snuggled during blizzards, went to church, and drove around in the evenings and looked at Christmas lights.

I am so grateful for these wonderful memories. Christmas will never be the same without Colby, without family. I struggle with this new reality, in finding my place in holiday doings and the family gatherings of others. For now I ignore them. Colby's loss is still too fresh, too painful. Someday, maybe, the holidays will mean something to me once again. In the meantime I am blessed to have had wonderful Christmases past.

Friday, June 18, 2010

Movement

I have a new "yard guy." My mailman is new and the neighbors behind me have a new dog. Colby has not met either of these people, or the dog, and that is another reminder to me that life for those of us who are still here goes on. There is movement in the progression of life and that movement does not include Colby. That thought makes me incredibly sad.

Every day I am reminded that Colby is not here, at least not in physical form. I pass his favorite drinks at the supermarket and put several in the basket . . . and then take them back out. My cable provider requires me to install new converter boxes, something that is not one of my strengths when it comes to skill sets. Colby could have done it when he was four--and that is not an exaggeration. I, meanwhile, will most likely spend and entire frustrating day and still not get it right. I find (yet another) pair of his socks (in a box), wash them and begin to put them in his sock drawer. Then stop.

Counselors say that the mind of a grieving parent is overloaded similarly to that of survivors of post-traumatic stress syndrome. That's why we "forget" our child is no longer here, why we have trouble focusing or remembering to do things we've done every day of our lives. It's one of the many reasons why we eventually turn into different people than we were "before."

That change, or the evolution in our stages of grief, is another movement away from our beloved child. We must go on without them, yet every time we turn around their absence is a gaping hole in our lives. I greet the new yard man. Wave at the new postman and introduce Abby, my dog, Colby's and mine, to the new dog behind us. I do all of this in a wave of grief, for they are more reminders that Colby has really and truly moved on.

Monday, April 26, 2010

Hats

Colby loved hats. From the time he was a baby, he always had to have a hat on his head. When Colby was just a year old, my mother and I were in a department store at 100 Oaks Shopping Center here in Nashville. She was trying on raincoats and I turned around and Colby was gone. One second he was there, the next he was not. Colby was a baby who walked at 9 months, so by 12 months he was zooming along quite speedily.

Mom and I were frantic. I began calling Colby's name and the sales clerks at the store rushed around looking for him under racks and inside shelves. I was heading up an aisle when out of the corner of my eye I saw something fly through the air. I stopped and changed course. There Colby was in the middle of the ladies hat section standing in front of a mirror, a dozen or more hats strewn around him. He'd grab a delicate flowery or lacy hat off a rack, put it on his head, then giggle at himself in the mirror and fling the hat into the air. Fortunately, even though he had stomped on top of many of the hats and they were squashed out of shape, none was permanently damaged.

From then on, Colby wore every kind of hat he could get his hands on. Fireman hats, cowboy hats, Air Force captain hats, construction hats. For years Colby received a different kind of a hat on special occasions and today, as I am going through boxes in the basement I find the "hat" box. There they all are. The sailor hat, the miner's hat, the civil war style hat, the hobo hat. All of them. I hadn't expected to find them. They were in a box that was not marked, so when I opened it seeing the hats took my breath away. I had to stop, regroup, begin again to breathe.

I had saved many of Colby's things for his children. He so loved playing with items that were mine when I was young that I wanted to pass that along to his children. Of course, those children, my grandchildren, do not exist, will never exist. I am ready I think, to give some of the hats away so I divide the hats into two piles. In one pile are the hats that I remember him wearing the most. Those I will keep. For now. I convince myself that young children are waiting for the hats in the other pile. They need to go to the Goodwill. But before I box them up I take a picture of them, and then I sit on the floor and cry.

Monday, April 12, 2010

Ragdolls

I see two piles of ragdolls. There must be a dozen or more in each pile. Each doll is seven or eight inches tall and is made of two pieces of material stuffed with rags and sewn together on the sides. The arms and legs of each doll are short and thick and each doll is made of a differently patterned red and white material.

Except for the dolls, which rest on a table that emits a soft red glow, I am surrounded by a misty, swirling blackness. I can see myself from about mid-thigh up. I can feel my feet and legs, but I cannot see them.

I gravitate toward the pile of dolls on the left. These dolls are well-loved. Their fabric is worn and the stitching has unraveled in places. I pick up one of the dolls and hold it, and I am overcome with emotion because I know that it provided generations of children joy and comfort.

Someone I know very well, yet am unfamiliar with, gently takes the doll from my hands and leads me to the pile of dolls on the right. These dolls are brand new. They are decorated with fine lace and bright, red jewels. Like the other dolls, each of these dolls is slightly different from the others.

I get the impression that I belong to this pile of dolls, that these are the dolls I am supposed to bond with. But I love the familiarity of the well-worn dolls and head back to those. Now several people I know very well, yet do not know, gently guide me back to the new pile. This is where you belong, they say without speaking any words. This is where you are supposed to be. The new dolls are lovely. They are breathtakingly beautiful, but I look longingly back at the old dolls. I am incredibly, heartbreakingly sad.

Then, as I turn back to the new pile I see Colby in the distance. He standing with his arms crossed on his chest and is leaning on something, a post maybe, to his left. I can't see what it is for it is shrouded in the black mist. Colby is dressed as I have seen him in other dreams: light blue jeans, white athletic shoes, light blue striped polo shirt. Colby gives me an encouraging nod and a smile before he fades into the swirling mist.

Reluctantly, I turn to the new pile of dolls, pick up a particularly beautiful bejeweled one, and begin to cry. The familiar people I do not know surround me. Everything, they say, will be okay. Is okay. Someday maybe I can believe them.

Thursday, April 8, 2010

Dandelions

When Colby was young he loved to garden. He could not wait every spring until we made the pilgrimage to The Home Depot or Lowe's to choose vegetables and other plants for our garden. He especially loved to plant herbs: mint, spearmint, lemon verbena, etc.

One spring when Colby was about eight, my mother was visiting and noticed we had a lot of dandelions in our yard. She made him a deal. For every dandelion he dug up with roots attached, she would give him a dime. Mom thought this would keep Colby busy on a quiet weekend and help the yard at the same time. Just think if he dug up fifty plants, what a difference that would make in your yard, she said. That's also fifty fewer plants that will go to seed.

Imagine her surprise, and mine, when Colby spent the entire weekend digging up dandelions. He dug not just fifty, or even one hundred fifty. Colby dug up eleven hundred dandelion plants. Shows you the state my yard was in. Mom made good on her deal and paid Colby $110.

Every year since then, paid or not, Colby made it his job to dig up dandelions in the spring. Today as I look out in my yard I see a number of them and I am torn. I can't bear the thought of digging them up because that is another hard, cold, reality that Colby is not here. But I should not leave the dandelions to seed the yard, either. I know this is something I have to do, hard as it will be. I will bring a lot of Kleenex along with Colby's trowel. And I will do this for Colby, to honor the many years he did this for me.

Wednesday, March 31, 2010

Family

Easter is just a few days away. It is another holiday I plan to ignore. But that is hard to do. Like Thanksgiving and Christmas, Easter is a time that is filled with references to family in newspapers, television, and radio. Even billboards and retail stores are filled with references to the holiday. Holidays, however, are for families. For those of us without, they are hard. The memories are bittersweet because there is no family left to enjoy holidays with. Ever. The years loom bleakly ahead.

Then again maybe my grief is just too new. Maybe holidays will get better. Maybe I can establish new traditions on my own. Maybe. I do understand that family is who and what you make it. Families these days do not have to biologically related to you. I think, though, when your life expectations of having children and grandchildren are suddenly taken from you, that the adjustment is harder than if you never had those expectations at all.

I try. I try to smile when other people talk of their families, their siblings, and kids and nieces and nephews. I try not to cry. This issue is, after all, mine. I do not harbor grudges for the joy others have. I am happy for them. Being sad for me is a separate issue and I am glad I can make the distinction.

I never expected life to be so hard. So grueling. I know this is what life must have been like for Colby, living with untreated mental illness. He felt so bleak about the future, about any possibilities of positive happenings, of success. Yet he managed to smile. He was able to be happy for others. I can do the same. I just have to dig deeper, try harder. And I will. Somehow. I will.

Wednesday, February 17, 2010

Dread

I don't sleep. From the moment Colby was born I was afraid he'd stop breathing so I'd stay up all night watching him breathe. Then when he developed asthma, he did turn blue several times. There were several ambulance rides, days and days in the hospital. Those years got me in the habit of not sleeping.

Now I stay busy during the day. Go, go, work, work. I stop several times throughout the day to think, reflect, but the pain, the anguish, is too great so I get busy again. By nightfall I am exhausted. I lie in bed and the anxiety returns and I find an excuse to get up, then another, and another. Before I know it, it is morning and I have dozed for less than an hour.

This happens most nights. I go through my days in a daze. Several times I leave the house and forget to turn the water in the sink off. Only one minor flood so far. Over the counter sleep aids make it worse. I shake, I am revved up, and sleep for the next several nights is impossible.

I try relaxation techniques, routines, zen tea, deep breathing, but the thoughts in my head rush in, overpower everything and I am up again, holding my arms around myself and pacing through the house.

In the mirror I do not look like me. A stranger's face stares back through the glass. Dark circles, baggy eyes. Old. Exhausted. Tonight will be different, I think. Tonight I will sleep. I think that every night and some nights, for a few minutes, I even believe myself. I have come to dread the night.

Monday, February 15, 2010

Donations

We receive our first donation for Colby's Army today. I am shocked, stunned, excited, for this validates the dream, the vision, the words I had of this nonprofit organization just days after Colby's passing. This means it is real, that others also believe we can take Colby's ideas and change the world, one step at a time. All Colby wanted to do was "affect change," positive change. This is the first thing I have been excited about in a very long time.

Just days ago Colby's Army received word that it was an official 501(c)3 nonprofit in every sense of the word. That I felt mildly pleased about, but I expected it to happen. I knew the paperwork was in order. But I was not ever sure others, strangers, people who do not know Colby or me, would also see the vision, also believe, even though there is a wonderful, professional group of directors in place, a board of directors, all of whom who are passionate about the cause.

Despite very limited finances Colby's Army is already helping others, has helped others, and will continue to do so. The donations mean we can kick off programs, get more people involved, and help many more. I am thrilled that we can do this for Colby, in memory of Colby, and for the people and animals whose lives will be improved.

It is also wonderful to feel something other than pain and anguish, despair, hurt, sadness, helplessness. I was not sure I could feel anything other than those feelings anymore. I like knowing other options are there to tap into. I have spent the last six and a half months crying and today I also cry, but these are good tears, tears of possibility, of hope. These tears give me a reason to live and that's something I have not had since Colby passed.

Dreamcatchers

Today I put the CDs aside to tackle Colby’s backpacks. He had eleven of them and after he became homeless he hid them in handy spots all around town. Some were at the homes of friends, others were tucked under bushes or hung in trees. Depending on where he was, he could find any one of them and have provisions. He stocked each of the backpacks with a variety of food, plastic, can openers, reading material, hygiene and first aid items . . . and a dreamcatcher.

Dreamcatchers originated in the Ojibwa (Chippewa) Nation, but during the 1960s and 1970s they were adopted by many other Nations. A typical dreamcatcher is made by tying strands in a web around a small round or tear-shaped frame. The resulting “dreamcatcher" is hung above the bed in hopes that it will protect those sleeping beneath it  from nightmares. Many also believe that a dreamcatcher can change a person's dreams and that only good dreams are allowed to filter through. Bad dreams are caught in the net, where they perish in the light of dawn.

Colby loved history and studied the cultures of many people, including Native peoples across the world. He got his first dreamcatcher when he was eleven, when he came along on the Trail of Hope. This was where one of my clients arranged for five semi truckloads of books, personal care items, computers, blankets, etc. to be given to ten Native American communities. A number of us came along to help unload the trucks. Colby was one of them. It was a life-changing experience for him and I believe he got his empathy for those less fortunate from that trip.

Today, as I unpack each of the backpacks, it isn’t long before I realize every pack has a dreamcatcher. I find that incredibly uplifting, sad, and profound all at the same time. My emotions get the better of me and I sit on the floor of his room, surrounded by backpacks, and I cry. I hope so very much that the dreamcatchers did keep bad dreams away from Colby. I also hope they brought him good memories, fond memories, and I hope that in some way they brought him a little bit of piece. And, I am so very glad that Colby is now in a place where he will never need a dreamcatcher again. All of these feelings and emotion and anxiety leave me exhausted. Drained. I pick up the dreamcatchers and place them around the house. Now, whenever I see them I will think good thoughts of Colby. I even put one by my bed. I typically do not have nightmares, but . . . just in case.

Friday, February 12, 2010

Books

Colby had thousands of books and many of them he had listed for sale online. The books were spread out over five rooms and other than his personal collection (which numbered about five hundred) none of the books were organized. Lack of organizational skills was part of Colby's dysgraphia disability, along with writing, knot tying, and math calculation. It takes me more than six months but I have examined each book, categorized it, evaluated it for online sales listing, and then either kept it or given it away.

Several hundred books went to Grandpa's House a Nashville-based program for men with mental illness and addiction. About a hundred were so damaged they went in the trash. Several I kept, and I carted more than forty boxes of books to the Goodwill. I still have about two hundred books from Colby's personal collection that I will keep for a while . . . or longer.

The reason this is important is that I carried the last box of books to the Goodwill today. This sorting through thousands of books has taken a good portion of my time. Plus, it was important to move them out so I can begin evaluating, organizing, sorting, categorizing and moving other groups of items such as his hundred or so DVDs, VHS tapes, and video games. There are also several hundred CDs and CD cases in various bags and boxes, and stacked loosely on shelves. Of course none of the CDs are actually in the cases or any where near the case they belong to. I will begin matching those up next. That could take me another six months. At least CDs are smaller than books.

The work is tiring, boring, mind-numbing. But in doing it I feel close to Colby. These were his things, things that were important to him, that meant something to him. The best I can do is keep the ones we were both connected to and find homes for the rest. They do no one any good sitting in a box or on a shelf. Colby would want this music that he loved so much to be appreciated by others. And it will be . . . many months from now.

Sunday, February 7, 2010

Supplies

The dream is in black and white, like a pencil drawing with no shading. Just black areas and white areas. No gray. Colby is driving a Jeep and I am sitting in the passenger seat next to him. Colby's hair is longer and darker and messier than when I have seen it in other dreams, and his clothes are spattered with mud. The Jeep is also mud spattered. It has a stick shift and Colby's entire body is turned toward me, including his right calf, which rests on the seat next to the stick shift, his lower leg bent back toward him. If there is a top on the Jeep it is either folded down or has been removed. The temperature is perfect. I feel neither warm or cold.

There is no steering wheel or gas pedal in the Jeep, but somehow we navigate through a large area of rubble. Colby uses the stick shift a few times, but I can't tell how that affects where we are going or how we get there. We are talking in this dream, but we do not say anything; the conversation between us is in our heads. I am so happy to see that Colby is relaxed, at ease with himself, and confident.

Colby tells me he spends his time helping people in this Jeep and he is taking me to where he will be working this day. Soon after that we come to a stop. The area where we are is still littered with rubble and in the near distance people mill about. Colby tells me he is bringing the people supplies. Surprised, because I did not feel like we were hauling anything, I turn around to look in the back of the Jeep. The supplies we are bringing are not those kinds of supplies, he says.

I ponder that for a while and then ask why we do not get out and bring the supplies to the people. Colby replies that the people have to come to us. I watch the people and comment that the people act as if they do not know we are here. It's okay. Some will see us, he says. Some will come for the supplies. I have the feeling that the supplies are in the form of information or guidance, and I wake up then, not knowing if the people are here on Earth or over in Colby's world.

Friday, January 29, 2010

Nine

I am maybe 3/4 of the way through sorting Colby's things. It has taken six months of steady work to get this far. Now it is time to sort and organize what I have gone through. So far I have nine cell phones, nine flashlights, nine cassette players, nine speakers, nine backpacks. There is more to sort through. He was a pack rat. I may find more.

This sorting is bittersweet. Some days I can't even think about it because it is too real. Sorting through Colby's things means he is really gone. He is not coming back. Other days I rummage with a vengence, clearing space, clearing clutter, needing the process to be finished so I can move on. If one ever can. I am not convinced that is possible. I am forever changed.

Every time I sort I hope to find something of meaning. And often I do. I have found a box of Christmas and birthday cards his grandmother and I gave him over the years. He saved every one. I find photos of us, of a dog we had for many years, of his grandma, all in the backpack he had with him when he passed. There are many scraps of song lyrics and poems, and abstract acryllic paintings he did. There is a collection of old coins he used to study and pour over, and lots of music, his music, that I haven't gotten to yet.

Schizophrenia sucks. It really does. It and its effects, the paranoia, anxiety, depression, panic attacks, and resulting use of drugs and alcohol to try to feel normal, has devastated so many branches of my family. My mother's side of the family. And now mine. I am the last. On one hand I am glad that there is no possibility that our genetic makeup will contribute further to this disease. On the other, I am still so very lost and alone without my son. Researchers are making strides in understanding schizophrenia and its ravaging effects. I support them and pray that someday this disease will be completely treatable, or even curable. No one needs to hurt this much.

Saturday, January 23, 2010

Remembrances

I am behind on my tasks for counseling. Today I drive to a small town near where Colby and I used to live and have lunch at a restaurant where we used to eat. My task is to remember good memories we had there. I sit first at a table, but that is too hard. Colby should be in the seat facing me; his absence is too strong so I move to the counter. There, I first see Colby making sailboats out of his fish sticks and launching them in a sea of tartar sauce. Then I watch as he makes letters and words out of his french fries. I see him through the anorexic years and remember my anguish every time he left to use the rest room. Later, I visualize him loving a steak salad he ordered.

For some reason I can't swallow my food so I get it boxed up and drive a short distance to a park Colby and I liked. His second grade field trip was to this park when they had a festival honoring the area's history, and I remember the smile on his face as he wandered through the area with his classmates. Then I drive up to the road to a spot where I used to take Colby and his friends fishing. I can't recall them ever catching anything, but they sure had fun trying.

I am not sure what this exercise is supposed to accomplish. Maybe that's part of it, I am supposed to figure that out for myself. Today I learn I can face places where Colby and I spent happy times, and that's a good thing. I know I could not have done this a few months ago. I also learned that if I have a choice, I'd rather not. I got through the day, but it made me sad, wistful. I have been putting off errands in other places Colby and I had fun. I think I will put them off a little longer, even though I know that if I have to do them, I can. Maybe I'll try again in a few months.

Friday, January 22, 2010

Research

One of the things I struggle with most is Colby's schizophrenia. There were many in my family who had this complex disease, so I know he inherited it from me. I feel tremendous guilt over this, even though I know one cannot help what genes he or she passes on. Nor can a person control how those genes mix with the other parent and manifests in the child. Schizophrenia is hard to predict. It skips around like a tornado, landing here and there, missing this one and that one, but causing horrible destruction to everyone who is even on the periphery of its path.

What family I had when I was younger was not close, so I did not know until recently how many were affected. But even if I had known, in the years leading up to Colby's birth, there would not have been anything I could have done. There was no genetic screening back then, no way of predicting whether or not a person was carrier of a specific gene. But now all that is changing.

According to a study conducted by researchers at Mount Sinai School of Medicine, variations of a gene related to brain development and function (OLIG2) may cause the development of schizophrenia. Researchers have already classified schizophrenia as an hereditary psychiatric disorder. Earlier research suggested that schizophrenia is associated with changes in myelin, the fatty substance (or white matter) in the brain that coats nerve fibers and is critical for the brain to function properly. Myelin is formed by a group of central nervous cells that are regulated by the gene OLIG2.

The new study showed that genetic variation in OLIG2 was strongly associated with schizophrenia. In addition, OLIG2 also showed a genetic association with schizophrenia when examined together with two other genes previously associated with schizophrenia, CNP and ERBB4, which are also active in the development of myelin.

As researchers further unravel the role of OLIG2 and myelin in schizophrenia, it is possible that medications like those being developed for the treatment of multiple sclerosis, a disorder associated with a breakdown of myelin, may have a future impact in the treatment of schizophrenia. This news is so exciting to me. None of us know how difficult life was for Colby. He was the only one walking in his shoes, but I do know that he struggled, daily, hourly. I would not wish his circumstances on anyone. But it is quite possible that future generations may not only have more effective treatment, there may someday be a cure.

Friday, January 1, 2010

Resolutions

I always make New Year's resolutions. From the time I was small I used the opportunity the new year brought to try to better myself. More recently I made two resolutions around the first of the year: one for me and one for the betterment of the world. For example, the resolutions might be to walk more and to pick up more litter. Or they might be to eat less ice cream and do one nice thing a day for others. This year, however, I have no resolution.

This year I can't wrap my brain around a resolution because I can't think far enough ahead to sustain such a commitment. In my grief, I am still operating day-to-day, hour-to-hour, sometimes minute-to-minute. Right now, to me, next week seems an impossibility.

Colby also had resolutions. Together, we thought about them over the holidays, and made careful choices. For many years we wrote our resolutions down and put them in the family bible. It's too painful, today, for me to look at them, but I remember several of his resolutions were to call his grandma daily, to read more, to take better care of his clothes, and for years he was able to keep his resolutions. For what are resolutions other than ways to build good habits? Once you do something every day for long enough you don't think so much about it, you just do it. And he did. More recently, though, it was a struggle for him to simply survive and that's where I am now.

Some days are better than others, but each day of grief still brings inordinate challenges in personal strength, optimism. Daily tasks that were once very easy have become very difficult. Going to the store, the post office, interacting with people, just getting up in the morning is sometimes nearly impossible. But I do all of it, each day hoping it will be easier than the last. So instead of a resolution I have a wish, that I just get through the year, day-by-day, hour-by-hour, minute-by-minute and that by next year I will be strong enough to have the resolve to make a positive addition or change to my life. I am not sure if this is a reasonable wish, if it is even possible, but it is a goal, something to strive toward and that in itself, is almost a resolution.

Thursday, December 31, 2009

Snow

The New Year's Eve that Colby was ten it snowed. Big, fat, silent flakes drifted from the sky and by early evening most Nashvillians were either tucked away safely in their homes, or already at their chosen celebratory location. On our street, in our neighborhood, not a single car had gone by since the snow began that afternoon. By eight, there was a good five inches of snow on the ground and we decided to go for a walk.

Outside the silence was stunning. Cocooning, if there is such a word. On the west side of town not a hint of freeway traffic could be heard. Not a door slamming, no voices, no planes. Not that it was a particularly noisy neighborhood where we lived then, but there were always city sounds in the background. Not so tonight. We walked down the sidewalk and when we reached the street we turned right. We started on the side of the street, but as it became apparent that we had the entire neighborhood to ourselves, we moved into the center with the crunch of our feet in the snow making the only sound we heard.

Colby and I marveled that the only tracks we saw were our own. Not even a dog or a rabbit had ventured out before us. And while most of our walk was in complete silence, on the way back, when we doubled over our own tracks, Colby said he hoped all the people and animals without homes had found a place to stay that night. Then he offered his room to anyone we might pass who was shivering in the snow, and I began to cry. While the chances were very slim that we'd come across anyone, Colby's offer was made in earnest. I was reminded once again what a gift Colby was, not just to me, but to everyone he met.

That New Year's Eve was by far my favorite of all my many new years. When we got home, we made hot chocolate and watched movies until it was time for Colby to open the door, run around the yard, bang on a few pots and yell "Happy New Year!" And, for the most part, it was. Although he had some problems, Colby's mental illness had not yet fully reared its ugly head. Today, I remember that magical night fondly. Like Colby, it was a gift, a treasure, and it reminds me that the best things in life truly are free.

Tuesday, December 22, 2009

Premonition?

Last year at this time, as Colby and I drove to Minnesota to visit my mom, he turned to me in the truck and said, “I want this to be a really good Christmas; I think it is the last one we will all spend together.”

I, of course, thought Colby meant my mom might not be around this year. She was 85 last year. At that age, every day, every hour, is a gift. And that is, probably, what Colby meant. Colby had plans, things he wanted to see, do, experience. I know it was not his intent to leave us.

When Colby said those words it never crossed my mind that it was going to be Colby who was not with us this year. If it had, I wonder what I would have done differently? Anything? Everything? I know I would have hugged him more, told him I loved him more. I would have asked him that, when his time came, to find relatives and loved ones who had already passed and tell them how much I love and miss them.

While Colby always felt he would not live to be old, I do not think, a year ago, that he felt he only had a few days left. If he had, I also wonder what he would have done differently. How would he have spent his remaining days? Would he have traveled? Played more music? Eaten more junk food? Spent more time with friends? What would any of us do if we knew this holiday would be our last?

Were Colby’s words a premonition, or just the reality of having an 85-year-old grandmother who is not in great physical shape? We will never know and even if we did, knowing this particular fact would not make any difference. What will make a difference is to let those around us know we care. When we greet friends, we need to let them know how truly glad we really are to see them. We need to listen closer, help and support more, smile when we can, give as circumstances allow. I hope everyone reading this has many, many wonderful holidays ahead, but even more, I hope everyone makes the most of each and every day, whether the days number 100 or 10,000.

Monday, December 21, 2009

Wishes

Several people have sent me the following, and it is so true that I felt I should share.

"A Bereaved Parent's Holiday Wish List"
Author - Unknown

1. I wish with everything I have that my child hadn’t died. I wish I had him/her back.

2. I wish you wouldn’t be afraid to speak my child’s name. My child lived and was very important to me. I need to hear that he/she was important to you also and I treasure your stories.

3. If I cry and get emotional when you talk about my child I wish you knew that it isn’t because you have hurt me. My child’s death is the cause of my tears. You have talked about my child, and you have allowed me to share my grief. I thank you for both.

4. I wish you wouldn’t “kill” my child again by removing his pictures, artwork, or other remembrances from your home.

5. Being a bereaved parent is not contagious, so I wish you wouldn’t shy away from me. I need you now more than ever.

6. I need diversions, so I want to hear about you. I might be sad and I might cry, but I wish you would ask about my child; I love to remember him.

7. I know that you think of and pray for me often. I wish you would let me know those things through a phone call, a card or note, or a real big hug.

8. I wish you wouldn’t expect my grief to be over in six months. These first months are traumatic for me, but I wish you could understand that my grief will never be over. I will suffer the death of my child until the day I die.

9. I am working very hard in my recovery, but I wish you could understand that I will never fully recover. I will always miss my child, and I will always grieve that he is dead.

10. I wish you wouldn’t expect me “not to think about it” or to “be happy.” Neither will happen for a very long time.

11. I don’t want to have a pity party, but I do wish you would let me grieve. I must hurt before I can heal.

12. I wish you understood how my life has shattered. I know it is miserable for you to be around me when I’m feeling miserable. Please be as patient with me as I am with you.

13. When I say “I’m doing okay,” I wish you could understand that I am not okay and that I struggle daily.

14. I wish you knew that all of the grief reactions I’m having are very normal. Depression, anger, hopelessness and overwhelming sadness are all to be expected. So please excuse me when I’m quiet and withdrawn or irritable and cranky.

15. Your advice to “take one day at a time” is excellent advice. However, a day is too much and too fast for me right now. I wish you could understand that I’m doing well to handle an hour at a time, or a minute.

16. Please excuse me if I seem rude; that is certainly not my intent. Sometimes the world around me goes too fast and I need to get off. When I walk away, I wish you would let me find a quiet place to spend time alone.

17. I wish you understood that grief changes people. When my child died, a big part of me died with him. I am not the same person I was before he died, and I will never be that person again.

18. I wish very much that you could understand understand my loss and my grief, my silence and my tears, my void and my pain. But, I pray daily that you will never understand, that you will never experience this loss.

Monday, December 14, 2009

Planting

My house has burned down. In my dream I am fine with that. It had been a nice two-story log house, an older home with square, dark brown logs and white chinking. The ceiling of the living room, which was to the right of the front door, had been low and white with heavy beams made of the same logs. The house was located somewhere in New England. I sift through the ashes and lovingly place charred mementos in a small metal tray about the size of a sheet of paper. The tray is tarnished gold and the lip on all four sides is about an inch high. There is no top. I carry the tray in both hands in front of me, reverently.

With me inside the ruined interior of my former home is a horse I trained about 30 years ago. She is a bay Appaloosa mare and she is to my right, but stays very close to me throughout my dream. Often, I can feel her breath on the right side of my neck. I know that she is my trusted companion and is there to help me.

I finish looking through things and the horse and I emerge from the house to see Colby crawling around the front yard. He is about six months old and wears a white diaper and t-shirt. I shift the tray of mementos to my right hand and pick Colby up with my left arm. I hold him close and notice he has a toy in each hand. Both are red. One might be a plastic duck. He is gurgling and very, very happy.

We walk toward a garden on the other side of the street, but on the way several people intercept me. They already know my intent and urgently try to dissuade me. One of the people is a salesman in a light gray suit and large, brown-framed glasses. He has come out of a hotel that is up the street to the left, and up a small hill from my house. The hotel is two stories and is the kind of bed and breakfast you might find in a small town. It is painted light gray and has white shutters. There are flowers in the window boxes. The salesman is tall and thin with thick gray hair; he wears a white shirt and gray tie, and his suit jacket is unbuttoned. He is known to be untrustworthy. Some say he sells “snake oil.” The man hails me by raising his right hand and calling my name. He hurries to catch up with me. I know this salesman well, and he is especially firm that I change my mind. To his extreme disappointment I stay my course and go into the garden.

The people who have tried to get me to change my mind do not enter the garden with me. Instead, they stand on the sidewalk by the garden gate. There are maybe half a dozen people, including the salesman. Once inside the gate I walk to a specific spot. I know this is the right spot and I sit there, on the ground, placing Colby and the tray to my left. I dig up a small patch of grass to the left of some iris. I dig while sitting with a trowel and my hands. The ground turns over easily. Enclosing the iris in their special patch of the garden is a low, black garden border, the kind that sinks 4-6 inches into the ground and keeps the grass out of the flowers.

When the ground is prepared I place Colby on top of the metal tray of mementos and plant them both in the newly dug ground. Colby is still very happy. He is sitting on the tray with his legs in front of him as he is planted, and is waving his arms and holding the red toys. I plant him waist deep. Within seconds of the planting, Colby morphs into a small tree. The tree is about a foot high and has many tiny branches. Within minutes, however, the tree is fully grown and leafed out. It shades the entire garden and sunlight now filters through the leaves as they wave in a light breeze. While I don’t feel happy, I am pleased and satisfied.

I am not a dreamer. Not usually anyway. When I do dream, all I normally remember are vague colors and feelings. Since Colby passed that has changed. Granted, his loss is a lot to process, but the clarity and detail in which I remember these dreams is startling. There have been a number of such dreams and their frequency is increasing. I hope that, over time, if I put them together they will make more sense to me as a group than they do individually.

Sunday, December 13, 2009

Snoqualmie

Eighteen years ago today Colby rode with his cub scout pack in the White Bluff Christmas parade. The boys rode on a float, dressed in their pajamas and Santa-style caps. We both had a wonderful time, but when we came home early that afternoon it was to find our beloved horse, Snoqualmie, in distress.

Snoqualmie was 30 that year, about to turn 31, and a few days before she'd had a minor stroke. The veterinarian said she'd either pull out of it or she wouldn't. It was obvious when we got home from the parade that she would not. Snoqualmie had been my best friend since I was 12. For 23 years she had been my sister. More recently she had been Colby's trusted friend, serving alternately as pirate ship, diving board, ladder, Indian chaser, Cowboy mount, alien, and rocket ship. Whatever his active imagination came up with, she was ready to play the part.

This afternoon she was down, breathing hard, stretched out in a grove of trees and I knew she'd never rise again. Colby stayed with her while I ran to the house to call the vet, then he ran back to the house to retrieve the blanket I had forgotten. Colby went to the barn and brought some grain to Snoqualmie. She loved to eat and was an "easy keeper" so she never was allowed a lot of grain. It wouldn't make any difference now, I thought, as Colby fed her little handfuls until the vet arrived.

I quickly explained to Colby that Snoqualmie was old and that it was time for the angels to take her to heaven and I sent him to the house to gather the dogs and cat and pray. In a few minutes it was over. I covered her with the blanket and went to the house to call a local guy who had a backhoe.

Every year on this date, the anniversary of her passing, Colby and I took a drive out to the farm where we used to live so we could visit her gravesite. This year I couldn't do it. Mourning both Colby and Snoqualmie was too much. I feel bad that I was not able to honor her with a visit this year, but I hope she understands. I hope she is now with Colby, that they are once again friends who are having one adventure after the other. Colby would like that, and so would she.