Yesterday, wishes were granted. I had my head examined. I was overdue.

Testing was intense. 5 hours of sitting in a small office, doing all types of things to show how my brain works, if at all. This is necessary because of several brain injuries and Alzheimer’s being rampant in my family. As I prepare to move, I need to plan based on my hope to live independently.

My good fortune is finding humor everywhere in life.

The man (psychologist) was just as you would expect. He ‘tried’ to be fun, but is, after all, something of a scientist, anal, orderly, and controlled. My polar opposite.

While I took tests, he observed and surreptitiously scribbled secret notes. I asked if I might please have some water. He grabbed a coffee cup and obviously saw the horror on my face as he started to fill the dark brown-stained cup for me. He stopped. I had not meant to show my concern. I must have been fatigued. He said, “This bothers women,” pointing to the stains inside the cup. I agreed (wholeheartedly). He said, “It doesn’t bother men, why does it bother women?” I told him that most of us would fear the cup was not clean. I went on to say my brother had a heavily stained coffee cup. He carries it with him everywhere. Once, without realizing my transgression, I cleaned it. Thoroughly. I did the old ‘Polident’ tablet in the cup, twice. Then, I took a scouring pad to the offensive stains. The next morning, after putting it through the dishwasher, I proudly handed him his pristine cup. He asked what I had done. I told him I had just cleaned it, as if it were no big deal.

My brother left. When he returned, he had a new cup. He did not openly complain. After a year or so, his new cup looked just as bad as the one I had spent hours cleaning. He was happy again. I had clearly ruined his cup. I learned the lesson.

This man across from me asked if I needed a different cup. I said no (I lied). After another section of testing, he asked me how to remove the stains. Amazingly, men know that women fight stains. We get no extra salary for this. We get no recognition but men know we fight stains. We are wonder women without the snazzy costume and lasso. I told him to put a Polident tablet in it.

The look on his face was so odd. He almost looked embarrassed. Then he explained that he does not wear dentures. I smiled slightly and leaned over the table. I said, “You know, it’s interesting. You are allowed to buy them anyway. ‘They’ don’t even check.” He just stared at me. I could see I was not getting through to him. So, l leaned in a bit further and said, “In Texas, men are even allowed to buy sanitary napkins.” That did it. He broke. He laughed. He saw the humor.

We went back to the testing.

Two hours passed, immersed in the paperwork and the various tasks I was given. He finally saw that I needed a break. He told me I could take 10 minutes. I almost felt as if a lock was taken from the chain that held me in place at that small table. I bolted.

When I returned, I carried a large cup of coffee, extra shots. He was noticeably concerned. I apologized for bringing something into the exam room, assuming that was some sort of ‘rule’. It confused me, though, because we had been sitting there, drinking water from cups. He explained that the testing materials were very expensive and spilling coffee on them, it would be a problem. I was mortified that I could not be trusted with my cup of coffee, even though I am not known for being sloppy with beverages. Each time I took a sip, he watched carefully. It was an agonizing drink. During the time I consumed it, he explained twice more the expense of the materials. I knew I was on thin ice.

He turned a page in my booklet in front of me. There was crayon all over the page ahead of it. I asked how crayon got on this expensive booklet and how he could possibly expect me to use it, thus ruined. He was serious: “children are not easily controlled.” He went on to explain he had tried to get the crayon out of the page, to no avail. He asked if I might know of a way to remove the crayon. He asked if I needed a new booklet. He simply cannot help himself. He is a serious type.

During one part of switching materials, I asked him how long he had been married although I felt certain he was divorced. He did not want to share that information, which was fine. He DID mention that the crushing blow to the union was the desire of his wife to have a pet. He explained that a pet means there would eventually be a pet hair somewhere that it “doesn’t belong.” I had enough of a mental picture and needed no other explanation.

As we were reaching the end of the testing, he was rushing me. We were behind schedule. I realized what a huge transgression that was so I was doing my best to accelerate. He announced that we would not be able to finish but he thought he had enough to complete his analysis.

As he rushed me to the door, he explained that I would need to return for his results. We made another appointment.

I am edgy about the results. I am hopeful but recognize it is just going to be my life and I cannot control the outcome too much. I want to take a piece of cat hair. I just can’t help myself.

I want to eat what I like
I want a drink when my long day is through
I don’t want to gain any weight
I want to look just the same as I do

I want to play in my garden
I want to watch “too much” tv
I want to fool with my computer
I never want to run out of money

I don’t want my parents to die

But I want to be brave if I must

I try not to obsess about so many things

But try as I might, it’s a bust.

So these are my hopes and my dreams

And I don’t think my list is that awful

My dreams run me crazy but I don’t really mind

’cause at least what I love is still LAWFUL!

Alexa

I am selling everything. Ok. Almost everything.

I consider myself to be ‘divesting’. It is all very odd and different since I spent much of my life ‘collecting and holding’.

I wrote once about letting things go that you hold due to love and memories. I still adhere to that lesson. I recognize that ‘things’ are not people and ‘memories’ are not ‘things’. Therefore, I get the fact that by letting things go, I have not let go of people and memories that are important to me.

I am in new territory. Things I have owned and used for years and still see huge asset in owning. Point here is someone else should own them. I have had my time.

I have a shelf unit. My husband hated it from the get-go. During a time of particular stress in our family, I moved in with a relative to help him save his house. This shelf unit was almost our “un-doing.” The fight about this dumb thing was huge and scarring. My dad came to me one night, explaining that he could ‘cut the bottom of the unit’ to make it go to the basement and fit. That was heartbreaking to me. Nevertheless, I was the intruder. Saving the house did not mean I was welcome. We cut the poor shelf unit. Nobody would ever know it had been changed. I lamented. It was my custom-built shelf unit.

When my husband realized I was bringing it along to our marriage, he balked. I was surprised to recognize his dismay over my shelf unit. It has a drop down desk in the center, beautiful oak, cubbyholes, and all of the shelves fit onto dowels so you can mix, match, and create any design you desire, with your changing needs. What’s not to love? I just did not understand his upset. It ended up in our daughter’s bedroom. She could use the desk. She had lots of books and stuffed animals. It worked. We moved again and it was too tall for the ‘basement’, which we refer to as the ‘lower level’. So again, I allowed it to be cut. Again, I am the only person aware of the cut. This thing has been impervious to pain.

In one place I lived, no wall was long enough for this unit. So, I disassembled it. I put the desk into my bedroom and used the two rectangular shelf units in the living room, on each side of my picture window. Worked just fine. Perfect. I do not see the problem with this unit. Every time I move, and I have moved 6 times since I got the unit, I just work the puzzle of the thing to manage my new space. However, in the meantime, since it goes together immediately, sitting on dowels, I can get about 16 boxes off the floor, to create space. When you move, that is a huge deal. I love this unit.

Now, I am divesting. The shelf unit no longer suits my life. I know I will miss having the ability to get so many boxes off the floor in my next apartment or house. That was always a lifesaver, making a pathway through so many boxes. But. I have grown. I don’t use 70’s shelf units anymore. The fact that this is relegated to the ‘basement’ of several houses says everything. I am letting the shelf unit go.

Someone looked at it and suggested $80. I almost threw up. A contractor came over, looked at it, and said there was probably $200. of good wood. Well, now we were talking! The problem, he explained, was how the wood was all tied up with this shelf unit. Oh.

It took me another 6 weeks to digest this. I am now asking $80 for the shelf unit. Someone will get a great unit, or a bunch of good usable wood.

Am I crushed? No. I finally saw the light: I have had use of this shelf unit for 34 years. If I get ANY money for the wood or the unit, I am way ahead of the game. It is like selling a house. When you are leaving, you need to disengage yourself from what the next people might think or do. It is not longer important because you are ‘selling’, “divesting,” moving on.

I am moving. It is time. I am ready. And whatever anyone wants to buy, I will be willing to part with so that I can move forward. Looking into my past has not served me. Looking forward, to what I might create next is the only logical step I can take.

I love a bargain.

It is that time again and I am already deep in denial and dread. I go through this every year. I have always been great about occasions even though we hear complaints that occasions are really drummed up by ‘card companies’, like American Greetings or Hallmark. Now the advertising wheel is enormous and you become drenched with every possible occasion.

When I look at my calendar, I am surprised at all of the pre-marked dates. Secretary’s day, bosses day, grandparent’s day, teacher appreciation day. The greeting card areas are enormous now. Its nuts really but we bought right into it and now it is just a way of life.

I have tried very hard to tune all of this out. I always try. It never helps.

As a result, I really am in a fog about the date. I don’t pay much attention. Today I had an appointment that I truthfully knew nothing about. I’m under the weather but missing an appointment instead of cancelling is unheard of in my world. I will start paying attention next week. I will get back into a cycle and life will be so much better. I just need to get past the weekend.

I always miss her the most on Mother’s Day.

I’ve been thinking about my friends. Learning who your friends are is important. Your friends are people you can reach for when you need to lean. I recognize how fortunate I am to count so many.

I have many friends from my airline days. These men and women have been physically absent from my life for decades. If I need any one of them, they will  immediately respond. That is friendship. I just got a phone message from one. She lives in Atlanta. We haven’t seen each other in 25 years but stay in constant contact. Her husband had an affair. Then her next husband did the same. She is living on social security, close to the bone, after marrying with houses and investments. She is now bereft emotionally and financially. She is a wonderful friend to me. We have the same pain. However, we had such fun and wonderful memories. We laugh. Everyone needs to laugh. It reminds us to live and enjoy life. We are fortunate. Sometimes we just need to remember.

I have friends from so many neighborhoods where I had homes. Manhattan, Orlando, Miami, Boulder, Colorado Springs, St. Croix, Gainesville, Salem, Spokane, Nuremburg, Munich, Frankfort, Oberammergau, Ft Knox, Redstone Arsenal, and others that I can only remember vaguely. Incredibly, I still am in touch with friends from almost all of those locations.

Now I have many friends I have never met. They are all on Facebook. According to my profile, I have 176 of them. Amazing. These men and women know of my impending divorce, know I have a cat and recently lost one, know I live in Washington and know I love to write. They know I flew, they know I care. They are my friends.

If these friends were around me on a daily basis, I wonder how much they would still want to be my friend. Am I whiny, controlling, difficult, dumb, or boring? Who knows? The beauty of this group of friends is the instant connection we all know. If I need help, look to Facebook. My friends there will immediately rally. I have seen them come together as a force whenever needed.

I have a wonderful friend nearby. We never see each other. We plan, we swear, we promise, we mean well. It simply does not happen. Like me, she is recovering from an ‘indiscretion’ from her husband, the love of her life. As he has moved on with his mistress, she has had to pick up the pieces of their lives, sell their home, and find a new place to re-start, saying goodbye to so many memories and so much pain. We ‘get’ each other completely. She is about 1 year farther down my road. It helps me to see that. I remember when I learned of her pain. Now I recognize I was not supportive enough. We all just go through the motions of help and support. We do not necessarily tie that to our hearts when we should, as friends. My lesson came later. Gratefully, she has continued to be my friend in spite of my lapse.

This is friendship. We ebb and flow. We understand and forgive. On a daily basis, it might not work so well.

As we each move through our lives, some friends come and some simply stay forever. I am blessed with both. You need some of them for a bit of time. That time finally passes and the friend needs to pass with it. They did their job. You did yours. Time to move. Time to change.

A friend just called. Incredible. We have not spoken in so long. She just asked me to come for the weekend. I am going. What could be better than a weekend with one of your dearest friends?

We have so many and they are so willing to help.

A friend of mine is not in great health; his time is short.

I have lost so many people in my life and my family. You begin something of a routine. It becomes necessary to continue in your daily life while you monitor the person who is leaving theirs. Routines help us cope. Knowing the ending is difficult but you still must keep moving forward, toward that difficulty.

It’s almost like a movie you love, but cry when you watch. You enjoy the good parts yet you know the worst is to come and regardless of many repeats, you will still cry. You love that movie.

Family and friends gather in a hospital. It is a kindness for them to come to a grim place like this. They want to pay their respects to the family and the friend. It is true respect. That respect carries through a funeral service. You do not attend a funeral for the person who is gone. You attend for the family to see how valued their beloved member was in life. It is respect.

When my mom passed away, I was determined to have a gathering of the fun and joy she created. Several people were kind enough to relate their stories of time spent with her, laughing or being amazed. Everyone in the chapel laughed, even though many of us had to give into our tears. My mom was always laughing. We said good-by in style and I know she enjoyed watching.

Because of my mom’s service, I do my best to attend those for my friends. I go because the family deserves to feel their loved one touched many lives. Respect.

I was talking to a friend today about respect. Specifically we were sharing the importance of being certain our next generation of women learns respect. So many lives change due to a lack of respect. Naturally, you cannot respect others until you respect yourself. Young women are especially in need. Our society still operates on ages-old routines. Many continue to make young girls obsolete in favor of young boys. Women will always be necessary because we give birth. However, young girls have consistently been pushed to the back. If these young girls do not learn their importance while they are children, they will have a more difficult time standing firmly for themselves as adults.

Our school systems believed that young women could not really grasp math and science. Astonishing. My father did not think a girl needed college. He pushed my 3 brothers to attend, even though none of them did well in high school. For me, it was not an option. He decided I would just find a husband. This idea is still alive and well in many families even though women are now more than half of the workforce.

Once a young woman values herself, she begins to expect equality in her life. Men do it so easily but women have to be taught by parents, teachers, and relatives. We need to change this. Once done, I believe many teen pregnancies will be avoided. When a young girl realizes she has more in life than to ‘catch a boy’, her options open fully. Once open, they rarely close. This has nothing to do with being pushy. It has everything to do with pushing yourself. Respect.

Being strong and respecting yourself means there is no sign of weakness to tears. Crying when your soul aches is a sign of love felt. You can only be as happy as you have allowed yourself to be sad. The valleys and peaks must balance. That is respect you owe yourself in life.

I wish for women. I hope for humanity. I pray for leaders who will make rules. I do not know how this will end. Movies and books cannot tell me. I have to play it out to the end. Nothing can foretell this.

How much do I wish I really knew? I wish I knew. Sometimes knowing the end isn’t all it’s cracked up to be.

The winter Olympics made me sick. I remember vividly that they made me sick last time. I can watch the summer Olympics but the winter Olympics just make me sick. Maybe I make myself sick.

I lean, move, and try to jump. I am helping. I am doing my very best to help them bobsled, short-track, race, do moguls. I cannot help myself. I have tried not to lean and move to no avail. Then, I get sick.

I recognize it is a mind/brain issue. I know my eyes have something to do with it too but I get so sick trying to lean into the necessities. Boy it makes me sick. I talked to my brother about it. Turns out he is doing the same thing. Made me wonder how many people in the world are leaning, trying to help, leaning without meaning to help. We just cannot stop leaning, helping. However, for me: it makes me sick. I get nauseous. This time was bad. I’m wondering if it’s my brain injury. It really doesn’t matter. I just know that I get sick to my stomach now. Consequently, I had to stop the program repeatedly, giving myself time to recover. I really did get sick.

My dad’s brain is not working too well all of a sudden. He has no injury. Yet, many people are older and they function fine. He does not. He has good days and he has horrible days. His brain is not working well.

My brother is somewhat ill. Cancer keeps stabbing at his body. He continues to fight it off. He is not as he was, but who of us is? I want to help. I need to help.

One of my dearest friends will not eat. She has been too thin for years and refuses to recognize it. Many of us are not doing as well as we had imagined we would at our respective ages. Illnesses and such were for the old.

We watch these incredible athletes every four years. We remember when we used to ski, to skate, to dare. It’s wonderful. Nevertheless, it really makes me sick. I just cannot continue helping them. I try not to lean. It does not work.

Where I live, my birds have begun to return. I have a wildlife habitat in my back yard and the birdhouses are already filling. It seems early but I am not in charge of the schedule. I had a large hawk here yesterday, hunting. Anytime I walk up on that huge bird, we are both startled. It flies, I watch in awe. Such grace and such deadly ability to take out little animals I am helping hatch.

One of the birds makes a sloppy mess of the birdhouse. I believe this is a Hammond’s Fly Catcher. The nest sticks and straw protrude from the opening in the birdhouse. The first year they were with me, I noticed the ‘mess’ and pulled those strands out, making the opening more tidy. It was only for me. I did not give a thought to the bird. I did not want it to look unkempt. The next morning, the sticks and straw were again sticking out of the opening. I got the point. A friend of mine mentioned the very same thing in one of her houses. We both realized that this is a trait and we need to stay out of the nesting ritual. I know the birds are back because suddenly I have sticks and straw making obvious notice in the birdhouse. I walk past, refusing to touch anything. I barely glance.

They don’t need my help. Neither do those golden athletes. Sometimes I have to sit on myself to leave things alone. This is not my job, is not my business, and is not my niche.

A friend of mine cannot let her garden be natural. Anyone who knows me, realizes I am a fan of cottage gardening. My flowers and grasses are sprouting hither and yon. I love the carefree idea. She cannot live with that. She could not let foliage die. She had to cut it so it would look better. Cutting tulip leaves and daffodil leaves will cause less growth for the next season. Soon she had no flowers. Remember that ad: “don’t fool with mother nature”? It’s true. We need to learn to leave things alone. Sometimes that is too much for many of us.

So, as my dad’s brain continues to misfire and my brother has his battles, the birds and the deer and everything wild will do pretty well. They don’t concern themselves with much of anything except survival. They will eat as needed to fuel themselves. In their world, you are not too fat. You just ARE.

In the world of flowers and grasses, they will overgrow and the weaker will not. In my world of the Olympics, the summer is good; the winter is difficult. I still try to help.

It makes me sick.

Don’t you hate it when your child is sick? They whine and complain, they ‘hurt’ but cannot explain exactly where or how, they cry, wanting more ‘mom’ time but refuse to do as you plead with them to do. They cannot understand the meds they dislike. They don’t want to be ordered about. They are not quite honest about what is at stake and how they really are dealing with the day-to-day.

You want to scream. You want to run away. You want them to grow up or let you parent. Either side would work better than what you have in the here and now.

I just visited such a household. It was difficult. Who raised this jerk? I’m sorry. I know he cannot help it. I know his mom is almost ashamed, as is the sister who had to take on the task of raising this child. However, if he will not admit something is wrong when the TV show comes on, he should not be allowed to suddenly be at death’s door when it’s time to help with the dishes or the laundry. You cannot have it both ways. Neither can a sick kid, but that’s just my opinion.

What I know is I spent a horribly frustrating time with family, some overindulgent and some just plain angry and frustrated with the attention needed by one member being under the weather. What is the solution?

The obvious one is that you wait until the illness is past. That always helps. Everyone can relax. But, what if your child is brain-injured? That child will never really ‘recover’ from this illness. Those parents don’t get the opportunity to ‘wait it out’. They live this 24×7, and have no outlet unless they are fortunate enough to have a huge support group. A huge support group. Huge.

I am seeing commercials about health care. Morgan Freeman is a spokesperson for ‘something’. I get the message. We need to help each other more often than we do. I understand that volunteers are needed. I know we should be doing more for our own. What I do not have the answer to is: how?

How does the normal family get the much-needed help when someone in their household is not going to improve but takes a majority of your time and energy? We are all so busy now. We have so many needs to fulfill.

I came home a crying fool. Afraid I had not done enough for my family unit. Sleep-deprived, angry, upset, scared. What I left behind is the mom who still has to deal with this while I fly away. I did laundry, cooked meals, cleaned the house, made beds, pushed meds on a kid who refused to take them, ran errands, and did medical appointments so that she could finally get a break. It completely wore me out. I am spent. Finally, home, I have no energy left. I have a full week ahead of me and don’t know how I’ll manage it. Tomorrow she starts with more doctor appointments, meal prep, housework, and laundry. Taking the medicine we need is not easy. He needs medicine. She needs rest, medicine, and they both refuse it because they are not capable. He needs to be fed and clothed, not simple. He wants things his way; she wants him to wear his underwear UNDER his clothes, not on top. She wants him to eat and is exhausted with the work that entails. He will not drink his juice, wants specific foods and because he is not well, she wants to provide but is close to illness herself as a result.

When I left, we all cried. I promised to come back soon. I always make that fruitless promise. I cannot afford to keep flying there but these people are so important to me. My family is so scattered. Travel is expensive and of course. I have to pay someone to care for my pet, my home, my routine, in my absence. Money. Medical. Misery. What in the world is happening in our lives? Who should be taking care of this, of us, of lives in illness when something has prevented us from having family members to do it? Moreover, with those family members, where do you draw the line? They cannot do everything. We cannot expect anyone to do anything. What is the solution?

Forgive my soapbox here, but why is our country continually working on a new health care program instead of making the program that our elected officials have, the national norm? Shouldn’t everyone have the same option at the same price? It certainly makes sense to me.

So, my stepmother will continue. I know she is exhausted. And the recalcitrant sick boy is my father. How does something like this happen? Until we find solutions for our family members whose mind has eroded, we are all sick.

I live in Spokane, WA. The US Figure Skating Championships are here, and I am normally in a front row seat. I have followed skating avidly since the mid 80’s. Fortunately, for me, attending championship contests have been constant. If I were not able to be in a great seat, I would watch it on TV, never missing a second.

Last night a very nice friend of mine took me as her guest to the championships. It was wonderful to see again.

However, what I actually experienced was not what I was accustomed to seeing.

I’ve mentioned before that I suffered a TBI (traumatic brain injury) a couple of years ago. It really has changed my life, my outlook, and my future. Last night I recognized it has also changed my past.

My mom had Alzheimer’s. Horrible disease. She lived in Fla and I lived in Colorado, then Oregon, now Washington. Farther and farther away from her, needing to be with her, hating to see what she was.

I made a decision about my visits with mom: I would meet her wherever she was. Toward the end, she had no clue who I was. I would watch her before I approached, to get a feel for how she ‘was’ at that moment in time. she would look at me, blankly, smile, and ask how I was. that’s mom. the more ill she became the more she morphed back into her ‘hostess’ mode of making others comfortable. because she did this so well, most people had absolutely no clue she was so ill. she managed to fool people for almost 5 years, with this disease eating away at her memories, her being. Now, visiting her in the lock-down ward was always unsettling. I wanted to scream, I’m ALEXA!! I’m your DAUGHTER!!. that would have done no good. she simply did not know me anymore. so, I decided to try to get her to like me, every time I visited with her. she had always helped everyone, everywhere. huge volunteer, all of her life. I decided that whenever I ‘met’ her, I would try to get her to enjoy my company. for an Alzheimer’s patient, that is no small feat. they are angry, frustrated, isolated, and tired of being bossed around. they have no clue who anyone is and they want ‘out’. I would go to her, smile, call her by her name, and beam at her, “HI”. she always responded favorably.

sometimes, rarely, she would chat, laugh, and almost manage conversation. Alzheimer’s robs people of their ability to use their words. I learned to listen to her cadence and her tone. amazingly, I usually could converse with her, on her terms. all I wanted was for her to like me. just for that ‘time’.

a brain, robbed of its use is not pretty. people do not act the way we expect them to or the way we are accustomed to them acting. when I injured my brain, my husband had his hands full. I had outbursts, my language went to the gutter, I was angry, crying, unable to do things and unable to figure out why. the doctors had warned us several times but until you live it, you really don’t ‘get it’. when I was going through this with my mom, I was still intact (almost brilliant, or at least really smart, IMHO). I just wanted her to like me. I loved her enough for both of us. I wanted her to like my company. so, we would chat. sometimes we would hold hands. she had no idea who I was. I was careful not to intrude. I just wanted to be with my mom, or whoever she was at that time.

sometimes I would visit her and it would go really well. so, I would stay longer than normal. those rare times were golden and I didn’t want to miss a second of them. we would talk and laugh, her conversations would make little sense, but she liked me. she was happy in my company and I was thrilled to almost see a piece of her, coming through. if anything or anyone interrupted her, she was lost again. sitting with a stranger. I would start from the beginning. again.

brains are pretty interesting. she was ‘there’ in pieces. the pieces weren’t necessarily the good ones. my brain was here but not functioning very well. as a result, I was difficult and unable to care for myself.

now I have the after-effects. my marriage is in shambles, over essentially. my brain has returned as much as it will manage we believe. if I am tired, I cannot form sentences. my spelling ability has completely vanished. I was an english whiz, math whiz, science whiz. now, I cannot multiply. sometimes I cannot add, no matter how hard I try. I spoke 4 languages, I seriously struggle with my english today. it’s just the way the cookie crumbles. I’m mobile, I can drive and run errands and cook and garden. I am just a bit more diminished. that’s life.

last night I realized I don’t know a damned thing about skating. that was astonishing. my friend had gone with me as my guest years before. she evidently relied on my knowledge to help her understand the competition. it made me remember the first month I was here in Spokane, the championships were here (Skate America, I think) and I took my very best friend to every event all week. she was an athlete but knew absolutely nothing about this sport. so, I explained to keep her appraised. last night, I could not answer the most basic questions. that was stunning to me. I simply don’t know anything much about this sport I have spent thousands of dollars on for 25 years or so. I’m a newbie.

so, just like my visits with my mom, I decided to just be ‘there’. I decided I don’t need to be in charge, don’t need to know the answers, don’t even need to know the questions. I could just be there, with my dear friend, watching a program of great challenge and superior athletes. I had been here the month I moved to Spokane, and now, 8 years later, as I am making my plans to depart, I was here again, but a different person, in every way.

and it was ok.