Living and laughing with a disability - cerebral palsy; ordinary life, extraordinary circumstances.

Sunday, December 30, 2012

"Race is the stupidest idea in history"

Leonard Pitts is my favorite columnist.  He never shies away from difficult topics.  He smashes into them, head on, and brings forth commonsense and clarity.


"Race is the stupidest idea in history. It is also, arguably, the most powerful. It determines who goes to jail and who goes to college, who gets loans and who gets rejections, who gets the job and who gets the unemployment check. It determines the life you live and the assumptions that are made about you."
- Read more here: http://www.miamiherald.com/2012/12/29/v-fullstory/3159373/leonard-pitts-race-is-the-stupidest.html#storylink=cpy

There is no difference between the races, except for the the junk in our heads...and there is a lot of junk in our heads!

I have often thought of racism and disablism as being very similar.  We start categorizing people the moment we meet them.

The color of my skin or your skin...yes, there is junk in my head, and in your head, that goes with that.  The way I, or you, walk and talk, there is junk in my head and yours that goes with that as well.

Leonard does a great job analyzing some of this junk.


Sunday, December 09, 2012

A Very Special Christmas

Tonight I watched the special on GMC:

gmc TV – Gospel Music Channel News – 25 Years of Bringing Joy to the World: Ten Outstanding Musical Moments from A Very Special Christmas

I have been listening the "A Very Special Christmas" 25th anniversary station on IHeart Radio.  Rock stars and artists from other genes singing Christmas songs.  Very cool.

Okay, I have not grown up yet, in case you have not noticed.  ;)

I did not realize that this is a fundraiser for Special Olympics.  Stars, singing outside their zone, for a great cause.

My Favorites:

Blue Christmas by Heart



and Run DMC - Christmas in Hollis:



If you can spare a five, a ten or whatever, please consider joining my Polar Plunge team, "Team Witticisms" benefiting the Oregon Special Olympics.

Click here to join

Thanks!

;)


Saturday, December 08, 2012

Comcast, Xfinity...please have mercy on us!

We had a rude wake-up call as to what kind of company Comcast is back in October when they yanked $777 from our checking account.

Jodie called.  Because of their computer error, they had not taken the automatic deduction from our account.  The billing emails had come...I just figured the money was going out as usual with our flurry of early month bills.

The Comcast lady understood what had happened and said they would reimburse   the money to our account, but that we would need to call and set up a payment plan, because we did owe the money.  Fair enough we thought.

A week later, when the money was still not in our account, Jodie called Comcast back.  They said the accounting department decided that Comcast had rights to the money, that we should have been properly deducting the money from our account and balancing our checkbook.

Point taken.  After 22 years as keeper of our checking account, the responsibility has transferred from yours truly to Jodie.

In October Jodie requested that Comcast stop automatically withdrawing money from our checking account and we asked that they begin mailing us a bill.

It has been 2 months and they still have not sent us a bill.

When we looked up our account in November, it said we owed over $200.  Jodie called and they said we did not owe, but that we had a credit.  Jodie spoke to a guy named Joe who was really helpful.  He gave Jodie his phone number and his extension to call if we had any more trouble.

We downgraded our cable package to save some money.

December, still no bill.  Online still show the over $200 amount that we owe.  Jodie tried to call Joe.  Whoever answered thee extension that Joe gave Jodie kind of laughed at her and said "We can't let you talk to Joe!"

Jodie was told again to ignore the $200+ bill that is posted online.

Jodie was told there was a charge for downgrading our service.  Of course there is!  It's Comcast Xfinity...why would we expect otherwise!`

Jodie was told what we owe now. We are not sure where to send it now without a bill.  It has been a long time since we have scheduled a bill to go out.  From past experience I know that addresses and account numbers change...we really want to see a bill.

We are ready to try another company.  We have been with Comcast for so many years now.

I don't know how much we would need to pay to leave our contract with Comcast.

It feels like an abusive relationship...and we are the abused!


Friday, November 30, 2012

Team Witticisms for Polar Plunge Oregon

I have been volunteering with Special Olympics Oregon since last May.  They were looking for an intern to do some web design work.  I was looking for some web design experience.

My first task was to move one of their event website, PlungeOregon, from it's previous web platform.  I learned a lot about photo editing during that project. I am now a good cropper and resizer!

Currently I am handling the social media for the Plunge.  Most evenings I am putting together the Facebook posts for: http://www.facebook.com/PlungeOregon; and the tweets for:  https://twitter.com/plungeoregon.

Social media is a key way to promote stuff nowadays.  I really count it an honor to be getting hands on experience in such a greatly growing field.

Special Olympics is a great organization.  It serves individuals with intellectual disabilities.  Such a life giving mission!  As an individual acquainted with challenges, I like to have the opportunity to help make life better for others who face challenges.

Volunteering is great!  You get more than you give.  I have learned more about Twitter, Facebook and HootSuite than I would have ever learned elsewhere.  Lots of research, finding the Twitter handles and Facebook pages of sponsors.

Anyway, I thought it would be fun to start my own Polar Plunge team - Team Witticisms.  I am going to be there at the Portland Polar Plunge on February 9.  I  am officially "Too Chicken to Plunge".  I'm not taking the plunge...I can't swim!

I would like to invite you to join my team, Team Witticisms, by donating $5, $10, or whatever you feel you can part with at this time.


I set my goal at $50.  One donation and the goal was hit...thank you Aunt Jan and Uncle Bruce!

Lets push it up there!  The people at Special Olympics Oregon are very high quality, committed people.  The individuals with intelectual disabilities they serve, showing them respect and lifting their dignity...it is priceless.

Click the link below and join my team:

Click here to join my team

;)


Wednesday, November 21, 2012

Eric and Troy pardoned

My favorite episode of West Wing was when the President pardoned a couple turkeys, Eric and Troy:



I remember Eric and I just howled with laughter when we saw that.  How did they come up with those names...that just happened to be our names?

I have been neglecting my blogging responsibilities in a bad way lately.  Thoughts roll around in my head, but I can't find the words to spill them out in a coherent way.

Our budget has been squeezing us lately, for this, that and the other reason.  We are now living life in a much more disciplined and deliberate way.

This does not sound fun, I know, but in an odd way it has led us to a greater sense of family, friends and the multitude of blessings around us.

The blessings we already have are far greater than anything we want.  Maybe that is the true essence of Thanksgiving Day.

Peace and love to all.

;)


Monday, October 29, 2012

A tear or a smile...

It's my decision, I know, to shed a tear or to crack a smile.

I love these quotes from Albert Einstein:

"You never fail until you stop trying."
"I have not failed, I have just found 10000 ways that don't work."
"Success is not final, failure is not fatal: it is the courage to continue that counts ..."
"Try not to become a man of success. Rather become a man of value.” 

I got another "Dear John" email today...a job I wanted and did not get.  Another application, interview, and wait that did not end as I had hoped.  The online list says I have applied for 24 positions in the last two years.  I did not go all the way to interview with all of those applications...but still - it's a lot of apps.

Twenty three years ago I got my job with Child Welfare by starting as a volunteer, then a temp.  I showed what I could do and I was eventually hired.

Currently I am a volunteer with Special Olympics Oregon.  I go into their office once a week for a social media meeting.  I moved one of their event websites, PlungeOregon, from one platform to another.  I am working a Facebook page and Twitter page to promote the event.  The response has been awesome!  I am learning so much...and proving what I can do.

I am way better at showing what I can do rather than telling what I can do.  My cerebral palsy, coupled with nerves, makes the interview process very daunting for me.

I think of Einstein's words.  I'm not going to fail, because I'm not going to stop trying...after I shed a tear and crack a smile.



Sunday, October 14, 2012

That "B" word and Pastor Karl

I am distracted right now.  I have tweets to gather for Special Olympics Oregon,      but my brain is mushy right now.

Jodie was in tears at church today.  I was close to tears.  Eric didn't want to go to the lunch at church in honor of Pastor Karl.  Eric is having a really hard time with Pastor Karl's leaving...he has gotten real close to him.

Today was Pastor Karl's last day at our church, Resurrection Lutheran Church.  He is heading to a calling in Salem at Christ the Good Shepherd Church.

PK has been our family and youth pastor for the last five years.  Eric has been on mission trips that PK has led...to the Blackfeet Reservation in Montana, to Las Vegas,  and to the recent youth gathering in New Orleans.

PK was a high school history teacher before he got the call to become a pastor.  He came to us five years ago.  A geeky guy with a kid's curiosity.  Eric adores Karl.

Today was Pastor Karl's last day with us.  His sermon about the feast that was given for the returning prodigal son, and how we should always leave an empty chair (not the Clint Eastwood type...;)) for the guest that is yet to come.  I will remember this one.

We have been instructed that, as of today, we are supposed to stop looking to Karl as Pastor.  He will be removing us RLC members from his e-vos (a wonderful online weekly devotion that he writes) from his email list.

I told Pastor Karl today that he would still be my "E-Pastor".

We had a great catered lunch from Ristorante Di Pompeyo.  We played games, Karl style, and told stories.

I don't think I said the "B" word ("bye") though.  This song kept running in my head....the same song I remember from my college days when parting paths from my dear friends:





Friends are friends forever.

So PK, this is not the "B" word.  Today was a hard lesson of that for us, but especially for Eric who has not been though this a lot.

People do go in and out of our lives, but memories of the important ones never leave us.

Pastor Karl...my second Twitter follower btw (such a geek!) will always be in our hearts.

;)




Friday, October 12, 2012

Tip a cop - Yummm!

Swiss cheese, beer mustard onions, Black Forest ham, hamburger on a pretzel bun.  It's called the Octoberfest Burger.

Insanely good!  You bet!

I had one a week ago.  My taste buds have not been the same since.

Red  Robin.  We all love them.  Burger, salads, wraps, soup...they have so many great things on their menu.

Twenty two years ago, at the Red Robin in Beaverton, I got down on a knee and said "Woman, will you marry me?"  Jodie and I bought Red Robin t-shirts and we wore them with matching jeans the day after we got married.  Yes, they forever have a soft spot in our hearts.

I have another soft spot in my heart...Special Olympics Oregon.  For those who do not know, I have been a volunteer with them for nearly six months now.  My first task was to move their PlungeOregon event website from one website format to another.  Now, I am working on the social media team, learning the power of Facebook, Twitter and HootSuite.

Special Olympics Oregon serves children and adults in our community who have intellectual disabilities.    There are many great causes, I know, but this cause ranks very high on the list.  As a person with challenges myself, I know how important encouragement is.  Everything Special Olympics Oregon does is about lifting up people who might otherwise be  put down.

The Law Enforcement Torch Run is a worldwide partnership of law enforcement officers who join to raise money and awareness for Special Olympics.  Tomorrow, Saturday, October 13, 11-3 and 4-8, officers will be accepting extra tips at Red Robin restaurants in Oregon to benefit Special Olympics.  Yours truly help put thee blog post regarding this event - click here to view.

Below is a message from Red Robin about the event:





Saturday, October 06, 2012

I'm not wearing a lanyard!

We had our annual eye doctor appointments in August.  No change for Eric and I, but the doc wanted Jodie to return for a special vision mapping session.

When Jodie was young, part of her disability was that she saw everything upside down.  We all see things upside down...out brains just flips it right side up automatically.  Jodie's brain did not do that for her.  Through intense therapy, Jodie's brain was taught to see things the right way.

A couple weeks ago, we returned to have Jodie's visioned mapped.  Our insurance kindly agreed to cover the procedure...;).

Jodie knew something was wrong when the tech doing the vision mapping kept asking "Are you sure you don't see that?"...over and over again.

Jodie asked the tech if something was wrong.  A rhetorical question...proven by the tech's response..."I will let the doctor talk to you."

Indeed, good news it was not.

The lower portion of Jodie's field of vision is gone.  I don't exactly know where the line is, but it explains why she has had a harder time seeing curb cuts when she is motoring along.

Jodie started to cry about it when we got in our van.  We talked about it.  The question as to why God would give us this to deal with came up.  Isn't having the disabilities and issues we have enough?  We don't dwell there too long.  God loves us and will see us through this like He has everything else.

We started thinking about the trouble Jodie has had riding in the van when Eric or I am driving.  She is constantly getting startled.  Well, she's not seeing what we see. With the lower part of her vision gone, other traffic is popping into her vision after Eric and I see it.  Eric and I see it coming.  For Jodie, it is just suddenly right there!

So, Jodie wears bifocals...as do I.  Since Jodie  cannot see anything in her lower vision, the lower lens of her bifocal is basically useless.

I told Jodie that she might need to have to sets of glasses "You know," I told Jodie, "with a lanyard like old ladies wear?"

"I'm not wearing a lanyard!" Jodie said.

Jodie is going to go back into the eye doctor in a couple months for another testing of her field of vision.  They want to see if there is any progression in Jodie's blind spot.  We are hoping there will not be.

But, whatever comes, we will get through it.


Monday, September 10, 2012

Major Inconvenience - part 2 - update

The email to Providence may have worked!

We just got a phone call from Providence.  They called ATG Rehab and were told that the parts for Jodie's power chair should arrive by Wednesday, and the chair will be ready on Thursday.

I wish ATG would have told us that...and I hope they are right.










Major Inconvenience - part 2

We are going on three weeks without having Jodie's power chair.

Providence In Home Services use to service Jodie's chair.  Now, ATG Rehab has the contract to repair power chairs for Providence In Home.

On August 23, I delivered Jodie's chair to ATG Rehab.  It took a week for them to get the authorization from our insurance so they could begin working on Jodie's chair.

Jodie has been calling ATG Rehab every couple days to see where they are in the  process of fixing Jodie's chair.

As of today, the answer is that parts were ordered on September 4 and it could take up to 14 business days for the parts to arrive.  My math puts that at September 21, almost a month after I dropped Jodie's chair off at the shop.

This has been a real hardship for Jodie.  She is back to using her crutches and a manual wheelchair, both really harmful to her shoulders.  This is really bad because the doctors told Jodie if she did not stop  stressing her shoulders, she could loose use of them altogether.

We hope the parts do arrive before the 21st, but how many days after that will it take for ATG Rehab to get Jodie's chair fixed?  If the shop cannot stock all the needed parts to repair a power chair, why can't they find a faster way to have them delivered when they are needed?

Jodie's chair is more than her legs around the home and around her office.  Her chair is fitted to her body.  It reclines in special ways to accommodate the stiffness of her body and to prevent swelling in her legs and back.

This morning, Jodie called ATG Rehab.  After they told her that parts were ordered and how long it could take for them to come in, Jodie called our insurance, Providence, to let them know how long it was taking to get her chair fixed and that it was not acceptable.  They told Jodie to call Providence In Home  Services and file a complaint.

The lady at Providence In Home Services that Jodie was transferred to did not really understand why Jodie was concerned...that these things take time...in the three-year-old kind of speak that disabled people sometimes get, with the attitude that Jodie did not understand what was going on.

Jodie called Providence insurance back and told them how the lady responded to Jodie's complaint.  They gave Jodie an email address to email a complaint to.

I am now working on the email  What to say...

Sunday, September 09, 2012

Twenty two years

Twenty two years ago today, Jodie and I tied the knot.

The Lutheran church on SE 39th (now Cesar Chavez Blvd.) and Brooklyn....St. Paul Lutheran Church.

I was telling my friends at Special Olympics Oregon how Jodie  and I met when I was three and she was four at Holladay Center in Portland.  At the time it was a school for the physically disabled where classroom instruction was augmented by heavy doses of therapy - physical, occupational, speech - whatever we needed for us to become as independent as possible.

Jodie and I knew each other back then, but we were in different classes and we didn't really hang out back then.  We both left Holladay Center, me in 1973 and Jodie in 1974, to be mainstreamed into public schools.  Before I was mainstreamed, my family moved to Southern California.  They took one look at the braces that I was wearing at the time and they said that I would never be mainstreamed down there.  In 1974 my family returned to Oregon where I was mainstreamed.

Jodie graduated from Portland Lutheran High School in 1982 when I was graduating from Beaverton High School.  Jodie's road took her to take classes at Concordia, Portland State University, and then to Western Business College.  She then traveled around the U.S. with a group called Break Through, educating churches about the need to become accessible for the disabled.

I went to Oregon State University.  I took hard classes and I did not do well.  Engineering, business...not my forte.  I took a class in journalism.  The professors in that department took hold of me and told me "Hey, you are a great writer."  I became a feature writer, a copy editor, and a columnist for the OSU Daily Barometer, a job I loved very much.  After college, I landed a job with World Christian Magazine as an assistant editor.  A great job it was, but the magazine was going under, and I had to raise my own financial support to be there.

In October 1988 I moved home and started looking for work.  I filled out applications and mailed out resumes.  Kind of funny, I remember being a little down at times, but I don't remember being too discouraged.  Something was going to work out...eventually.  I just had to keep moving and stay positive.

In the summer of 1989 I volunteered at a state office in Beaverton.  Don Bougher, the volunteer coordinator, had a Mac computer sitting on the floor in his office.  Kiddies, this is back when computers were still part novelty.  Don asked  me if I could  make that computer sing.  I said, "Yes I can!"  I created a spreadsheet with Lotus 1-2-3 for tracking volunteer hours.

A counselor I went to see mentioned that New Hope Community Church had lots of support groups.  I went.  They had a group for the disabled.  I saw the leader of the group.  "Jodie?" I said.  "Troy?" she replied.  I went to her apartment a few weeks later for dessert.  We really hit it off.  But, I remember thinking, Jodie had a job.  She was working at the Portland Center of  Hearing and Speech as an accounting assistant.  And I, well, I was still a volunteer.

In my quest for self sufficiency, I was packing and getting ready to move to the San Jose area.  A buddy had a room for me down there, I had family down there, and a community college down there had a good program for helping the disabled become employed.

A couple days before I was to leave for California, Don, the volunteer coordinator, spoke with Gary, the Children Services Division branch manager, whether he might have a job for me.  A day later, Gary put my "flying fingers" to work as a typist.

It took a few months for Jodie and I to reconnect.  She was so busy with church that she did not have time for anything else.  When we finally got together in February of 1990, it was pretty evident that we were meant to be together.

Jodie is a great people person and speaker,  I am a thinker and a writer.  We each have strengths and weaknesses.  Together we are greater than the sum of our strengths.   On September 8, 1990, in front a church filled with family and friends, with Pastor Dave presiding, Jodie and I exchanged "I do's".

Twenty two years.  I miss the people who were with us back then who are no longer with us, the grandma's and grandpa's.  Ken, Jodie's brother-in-law, who walked her down the aisle.  Two weeks after our wedding Ken was diagnosed with cancer and four years later he passed away.  My friend Erick, who was supposed to be one of my groomsmen, had tumors in his head, that prevented him from flying out from St. Louis to be in our wedding.

Twenty two years.  Jodie and I had no plans to have kids.  Our plan was to take care of each other and to be as independent as possible.  What's the old adage - if you want to make God laugh, tell him your plans.

Eric James was born nearly 17 years ago.  Yes, life has been a whirlwind since then.

Yes, I do have a book to write.  Do I have the discipline to do so?  Well.....


Monday, September 03, 2012

Judging disability

Judging others is generally seen as a bad thing to do.

It may be a surprise to the non-disabled community that we who are disabled, when we cross each other, tend to judge each other's disability.  It's not really in a bad way.

With my disability, my dexterity is quite affected.  Handwriting is hard for me...and it is not very legible.  Drinking from a cup or glass is difficult for me because of how my hands shake.  I can't button a shirt.  I probably could not drive your car.

When I need to take notes, I use a computer, a recorder, or I have someone take notes for me.  I chug my coffee and water through a straw.  I use a tool called a buttoner to button my shirts, though anymore I rarely wear a shirt that requires buttoning.  I drive a Sprinter van..an automatic with a steering knob.

I walk with some difficulty, but with my walker for shorter distances and my scooter for longer distances, I manage to get to where I need to go,

When I see another disabled person, I want to figure out what their disability is, what their challenges are, and how they have overcome them.

The Paralympic 2012 Games are on in London right now.  For those who may not know, it is Olympic games for people with disabilities.  Thank you Wheelie Catholic for the updates.

I came across this article in the New York Times that discusses how paralympians have their disability judged prior to going to the Paralympics to see what classification they will compete under.

What struck me in this article is how each sport has their own set of classifications.  Athletes can appeal their own classification if they think it's too high, or their opponents classification if they think it is too low.

Once classed, some of the athletes practice so hard and become so good at their event that other competitors believe that they should be in a higher classification.

Then there are 245 athletes who are classified as borderline, which means they could be classed high in one classification, or low in the next.

Judge not lest you be judged, unless you are a paralympian, where you are judged first so you can be properly judged later.



Saturday, September 01, 2012

Major inconvenience

A week ago last Wednesday, Jodie drove her power chair home.  It smelled really hot.  She called Eric and he met her in our garage.  One of the metal tube casings in back of her chair was very hot.

Jodie called our insurance.  They told us to take the chair to a shop in Milwaukie.  The shop in Portland is no longer servicing power chairs.  We were a tiny bit relieved to hear that, because they serviced it earlier this year, the chair has not been holding a charge.  Jodie use to be able to travel from home to her office (a mile) and back twice (4 miles) before her chair needed a charge. Now, a single one-way trip and the chair needs a charge.

I took Jodie's chair to the shop on Thursday...ten days ago.  They did not offer her a loaner, and we did not want one after the accident Jodie had in her last loaner.

It took a week for the shop to get authorization to work on Jodie's chair.  It could take another week or two for parts to be ordered and the chair to be fixed.  I can't begin to tell you the hardship this is on her.

She is using our manual wheelchair at work.  It does not fit her well.  We bought what we could afford, and we bought it for emergencies.

We are leaving the wheelchair at work during the week and Jodie is using her crutches to get from the van to her office.

I have trouble pushing Jodie in the manual chair.  Last night we went to a retirement party at the Fourth Street Pub.  I was having trouble getting Jodie up the curb cut.  A stranger saw me struggling from within the Pub.  He came running out to help us.  The guy had a prosthetic leg.  I was really amazed by his kindness!

Anyway, say a prayer that Jodie's chair is fixed as fast as possible.  It is more than just her ride now.  It is her comfort and her independence.



"People stare at you...it's fantastic!"

I am doing a bit of homework for my volunteership st the Special Olympics Oregon.

Yes, I know it's not a real word.  The position that I applied for was an internship.  When they saw how crazy old I am...and that I am way out of school...they classed me as a volunteer.

I like the internship feel of this.  Ryan, my supervisor, is giving me a variety of things to do.  Right now I am researching some material for SOOR to tweet.  I came upon this wonderful commercial:





Perspective.  It is all about perspective.

I know that mine needs changing.

I bet maybe your's...no,  I'm not going to go there.  I'm not going to start talking to empty chairs.

;)



Tuesday, August 14, 2012

Go Gresham Little League!

A couple weeks ago, on a Friday night, Jodie and I picked up some dinner and took it to the Gresham Main City park.  Eric was in New Orleans with Lutheran youth from across the country.

We were pleased to see a team of Little League All Stars practicing.  Jodie and I love to follow the Little League World Series on tv every August.  These kids were good.  According to the signs, they were getting ready for districts.

We were both thinking it...I don't know which one of us said it..."Wouldn't it be cool if these kids make it to Williamsport?

My mind went tripping back to when Eric was in T-ball.  Bright sunshine glimmering on the early morning dew at North Gresham Park.  The kids had to be pointed toward first base.  As the kids got older, the games moved to East Gresham Elementary.

I remember the jamborees at Gresham Main City Park.  Jodie won the raffle one year - a party suite at a Portland Beavers game.  I remember the lady that was in charge of the Gresham Little League was so happy that Jodie won.  We took the team and their families...so much fun!

So long ago.  Now Eric is 6'5" and a high school ace.

Even so, this week as the Gresham boys pursue their dreams in Williamsport, we will be watching.

Jodie will be rooting for them loudly until she is hoarse.  Eric will be saying, "Mom, they can't hear you!"

Go Gresham Little League!  We are proud of you!

The Wittrens




Thursday, August 02, 2012

Taking part of greatness

We are down in Coos Bay for a few days this week to watch our son's baseball team play in the state single A American Legion baseball tournament.

The aged vet who took our money at the gate - I saw him hop on his adult tricycle in the afternoon.  I was moved by that because that used to be my primary mode of transportation.  A lifetime of serving and he continues to serve in whatever way he can.

Clyde Allen Field, a classic baseball venue.  The flag that waves high above the stands was once waving on a flag pole in Afghanistan.

The look in the kids eyes as they were asked to repeat the words of the American Legion baseball code of conduct was read to them:


I Will: Keep the Rules;
Keep Faith with my teammates;
Keep my temper; Keep myself fit;
Keep a Stout heart in defeat;
Keep my pride under in victory;
Keep a sound soul; A clean mind; And a Healthy body

The kids were antsy and just wanted the game to start, I know, but I hope they heard the words and tucked the words somewhere in their hearts. Great words to live by.

A game with Central Point on Wednesday, and a game with North Medford this morning.  Neither game went as we would have preferred.

Even so, the great American pastime played with heart by Oregon high school boys from across the state, mixed with the patriotic tradition of the American Legion - how can you not feel awe of the greatness of it all?

I have heard some of the olympians say that winning is great, but just being there to witness the greatness of it all is almost as great.

My hope is that one day, after the sting of defeat has passed, the boys will remember with pride the American Legion state baseball tournament they were part of and the words of the code of conduct they recited will come to mind.

Winning is great, but taking part of greatness is never a loss.

Saturday, July 07, 2012

A Good Life

I was working at my volunteership yesterday down at the Special Olympics of Oregon,  I am there 10-2 on Fridays.

I am photo editing right now, going through hundreds of photos of last years Polar Plunge, re-sizing and cropping them for the new site.  I will be working on another site after this...the Bite of Oregon.

The intern cubical that I work at is pretty starkly decorated.  A couple notebooks, and a yellow sticky pinned to the wall.

Just a few simple words, but they say so much.

A good life is when you
Assume nothing
do more
need less
smile often
dream big
laugh a lot
And realize how blessed you are.


These words mean a lot to me right now, Even though I am nearing 50, I am still trying to grow up. I have ideas of where I want to be and what I want to do...but realities get in the way.

I searched Google to find where these words came from. What I found is that the author is unknown.


I wonder who posted these words on that sticky note?


My supervisor, "Avery" as everyone calls him, signs each of his emails with "Dream Big".


Hmm. Infectious optimism.


My heart knows the truth of these words.


Life is not about where we are going; it is about where we are right now.


Dream Big...Laugh a lot...And realize how blessed you are.



Wednesday, June 20, 2012

Me and U2

Some people have it all together.  Thanks to God and His great mercy, I have never been accused of such a thing!

I went to college in the 80's.  For a guy who has trouble writing notes, and even more trouble reading them, college was hard.  Some professors would give me that look "Why on earth are you here?"

The fun part of college for me was meeting Dave, Lisa, Frank and a myriad of other friends at the "Donut" shop to try to solve the problems of the world.  I also enjoyed my fellowship with brothers and sisters in Campus Ambassadors, the campus christian group I was involved in.

I spent a lot of time in college by myself, studying really hard.  When you have a disability, such as the cerebral palsy that I have, your whole life is about overcoming.

I had a secret stress relief.  When nobody was around, I would slip a cassette tape into my boom box.  One tape in particular I listened to over and over again.

And I would dance.

The lines played through my soul like a prayer:

"Where the streets have no name"

"I have climbed the highest mountain...but I still haven't found what I am looking for"

"And you give...and you give...and you give yourself away"

U2...the Joshua Tree.

When I heard about the event that our intern at church, Vicar Ray, was putting together, I was beside myself.  U2christ, a social justice and worship event to the music of U2.

Click on this graphic below for event info:




Here is a song I hope they do...with BB King, of course...;):



Sunday, June 10, 2012

Breaking out of the groove...going to the Hub

I am liking my new 4/10 schedule with Fridays off.  My supervisor at the Special Olympics was out of town Friday, so I had a day to myself to fill up.

Jodie had a meeting at the district office, so I dropped her off.  I came back home. I had a few hours to kill before my lunch downtown with Sam.

Last February I had gone to a meetup in Portland to learn about search engine optimization from Mr. SearchCommander himself, Scott Hendison.  Scott use to coach Eric's baseball team a ftew years back.  

At that meetup I met Haley from Lewis Creative.  Their job is to brand your image, which I think is really fascinating - "Mad Men" type of work.  She gave me her card.

Haley invited me to come to a meeting that she and cohort Sarah (of Garrison Marketing Solutions) host on Friday's from 10 to 2 in Gresham.  It is called the HUB - a place for local business owners to meet and collaborate.

I have been leery of going to the meeting.  I am not a business owner and I am not a professional.  I have way more to learn than I have to share.  I know a little about everything but not a lot about anything.  Even so, I am learning what I can about creating websites with WordPress, and about promoting websites.

I nearly talked myself out of not going to the meeting.  Lately I have been experiencing anxiety when I am confronted with new situations.  I don't know why.  With my disability I seem prone to stay in my defined world.  I have a life in my own little world that is totally accessible to me.  Why venture in unknown territory where I might run into people who might not understand me or my disability?

Insanity: doing the same thing over and over again and expecting different results.
Albert Einstein

I am finding a lot of inspiration from Einstein these days.  A genius, yes, but he knew more about failing than he did about succeeding.

I made my way to Park Place Coffee.  There were lot's of people inside.  I went to the front of the shop and bought a cup of coffee.  I asked the barista to bring the coffee to my table when she finished helping the customers who were in line behind me.

There was a bunch of tables pushed together with people who all had laptops set up.  I set up at a table behind them.  When they realized I was there for Hub, they invited me over to their table.

Haley was with a client.  Sarah came over to find out what kind of projects I was working on.  I told her that I was working with WordPress and that I could use some advice.  Sarah told me to talk with Al at the end of the table.

Al was talking  to the barista, helping her with internet marketing strategies for the cafe.  It was nice to hear how business at the cafe has gone way up on Fridays since the Hub has been meeting there, way beyond the Hub members themselves, leading us to wonder if a busier cafe draws more business.

When I was able to talk with Al, he wanted to see some of my work.  I had him look at wittren.com.  Al said it was a nice, simple and clean site.  He read some of what I wrote and he said to me, "Wow, you are really a good writer!"

The compliment was very nice - it really surprised me.  Al had some helpful hints about the projects I am working on.

It was a very encouraging being around other creative people.  It reminded me of my six month stint on the magazine back in 1988.  The idea of talented, creative professionals coming together to help each other rather than compete against or one-up each other is such a positive environment.  No bad ideas, just better ideas...letting the creative juices flow.

I am still a novice in the world of WordPress, SEO and other technical matters, but I have dreams of learning what I need to know to become successful in such a world.  I have further dreams of one day helping other people with disabilities find economic self sufficiency using these kind of skills.

I may not ever get there, but it is really more about the journey rather than the destination.  It is nice to know there are people like the people at the Hub to help along the way.