Sunday, September 9, 2018

Yin and Yang (Graphic. You've been warned.)





Yin and Yang describes how seemingly opposite or contrary forces may actually be complementary, interconnected, and interdependent in the natural world, and how they may give rise to each other as they interrelate to one another.


***

I used to work with a lady named Alice.  Alice appropriately chose a career in HR.  She just loved people and accepted them at their word.  I have never truly met anyone like her.  I shared a lot of my day-to-day life stories with her, and it amazed me how she would react sometimes.  

For example, one of our friends told me that she was going to get married.  I had serious concerns about the guy, whom I had only met a couple of times, and those couple of encounters left me a bit puzzled and concerned.  But, when I told Alice that our friend was getting married, before a single beat passed, she was screaming in excitement, saying, "How WONDERFUL!!! Oh how fantastic!!" Where my reaction was hesitancy and cautiousness, and yes, even some cynicism, Alice opened her arms widely to this celebration of someone else's happiness.  She didn't need to understand it, she just needed to celebrate it.  She is a truly wonderful friend.

True, Alice may have a snug-fitting, well-worn pair of rose-tinted glasses on, but I've seen her get serious when needed.  To be honest, it is people like Alice who surprise me and catch me off guard.  Of the several types of personalities people have, ranging from perpetual cynics to oblivious young souls, Alice was something else; she was electively, radiantly joyous.  I believe that Alice chose - demanded - to be contagiously joyous in spite of her surroundings.

When something a bit awful happened, from passing aggressive junkies in the street (we worked downtown Baltimore in a sometimes-sketchy area), to learning about her children being bullied at school... you cannot break this woman.  She whisks away the negative with the ease of a professional matador, and she hails and celebrates the positive like a trumpeting herald. 


I'll tell you why these types of people are precious.

I tend to end up in situations that others would not consider normal, but to me, they do seem to happen quite often.  I am going to share something with you that I have not told many people.  It has been a couple of years since this incident, and it has stuck with me.  In fact, I am often haunted by many stories like this which lurk around in my mind like tigers in the night.  



It was towards the end of a regular work day at my office downtown Baltimore when I decided to run downstairs to the Starbucks to grab a pick-me-up coffee.  This particular Starbucks is a Tier A location, meaning that there basically is not an hour of the business day that the place is not SLAMMED with customers.   

I ordered my drink, and then grabbed a seat at the long table, sitting next to some other customers, including a VERY GOOD LOOKING (there, I went on record with it) young man who was just there chilling with his coffee and reading a book.  I vaguely remember making small-talk with him, something about how he is in the military and in town for work...eh, that is all I remember, because what happened next paused the world.

This horrible screaming started coming from the bathroom area, towards the back of the store where we were sitting.  It was a man's high-pitched screaming.  My first reaction was that someone had slipped on the wet floor and fallen, since all I could see were legs on the ground behind the wall, and because the people around that area were not panicked.  I checked to make sure that the Starbucks associates were calling 911, which they were, and then started walking over there.  The Guy I Was Sitting Next To came with me.

It took me a beat to understand what I was looking at.  He had not fallen.  This mid-50s man was being attacked by a young-20s kid.  When we realized this, we started running, and Guy and I stepped between them.  

Can we pause the story here for a second so that I can highlight the above mention that no one was panicked, that no one else was helping?  There was a crowd of people, and in this fight-or-flight situation, everyone else flew.  Is it because they are so calloused because of our society, they figured it would sort itself out?  Were they really just scared and so they ran?  This is one of the things that haunts me. 

So, Guy had the Kid, and I had the older Gentleman.  It was hard to get him to stop sobbing, and his face was very jacked up, and his English was poor.  I am showing you these pictures because it has been a few years since this happened, and because I want to be clear about this imagery.




He started telling me that he has no idea why this is happening.  Why is he being attacked?  Why?  He was just waiting to use the mens room!!

I tell him to sit at the table, just sit and take a breath.

I go to the kid and listen in on what he is telling Guy.  I pick up on that Kid thinks that Gentleman has stolen his cell phone, and so he was beating the tar out of him to get it back.

I go back to Gentleman and ask if he stole Kid's cell phone, and Gentleman is completely confused.  What?  No.  My phone is in my pocket.  Here it is.   It is a black iPhone.  He puts the iPhone on the table.

I go to Kid and say, Gentleman is saying that is his iPhone.  Kid looks at the phone and says that is Kid's phone.  

Guy says, "Okay, well, why don't we call your cell phone number, to prove it?"  Everyone likes this plan.  I look at Guy and he kind of shoots me a look, which I know to mean that I have to do it because his phone is owned by the government and this could get ugly.  I dial the number, and guess what happens?

Kid's cell phone starts ringing... from within his very own pocket.  

Yep, they had the same exact cell phone.  Kid saw Gentleman's cell phone, and assumed that he had stolen it.

Kid kind of chuckles, knowing that he has just made a huge mistake, and he starts bolting for the door.

I start chasing him, taking his photo and telling him to pose for the camera.  We hear the sirens coming.



He ran away.  And that was it.

The medics and police arrive, and they start talking to Gentleman, getting his report, fixing his broken nose.  He has no health insurance, he is visiting from Haiti or somewhere.  He is supposed to go home next week.  He just bought these brand new eyeglasses with the last of his money.  What is he supposed to do now?

I take his eyeglasses while he is talking to police, and I bring them to my desk upstairs, and I clean the blood off of them, and use my little eyeglasses kit and some superglue to fix them the best I can.  They looked somewhat presentable.  I rush them back downstairs.  Gentleman is very grateful and laughs, swears they look like new.  I know that they don't... they are scarred.  We all are.

I was so sad for this man.  I still am.  All I could do is sit there with him, letting him be in the moment, letting him be sad and take all the time he needs, holding his hand as he cried, as he was so confused and lost and hurt.  

By the time we parted, we were joking with the paramedics, and everyone had a smile on.  The paramedics made sure to stick around for a little while, just to be in good spirits with us all, to communicate to this man that not ALL of Baltimore is a piece of trash; not everyone here is a terrible piece of scum.  I remember these moments very clearly.  The setting sun, the twinkle-light covered trees we sat under, the holiday shoppers going about their business, and people ice skating and having fun across the street. 

I had tons of photos and that kid's cell phone number that I was able to call into the police the next day.  I am not sure what ever came of it.  Probably nothing.

One thing that sticks out to me to this day is that, unlike that man, I never was truly surprised at the situation.  He was SO devastated, so shocked, so saddened that in an entire room of people, he was beaten to a near pulp, and 95% of the people in that room didn't say boo about it, didn't stop the beating, and went about their normal business. 

I could see it in his eyes, as they swept the room, that he could not actually believe that this was happening to him.  I wonder how a similar room would have reacted if this had occurred in his home town, wherever that is? And this was his learning experience with America? I am not surprised by it; I am exposed to this sort of atrociousness enough to consider it run-of-the-mill. What does that say about me?  What does that say about me???



So, I need people like Alice to help to bring some sort of balance to my life experience.  I need her because I am desperate to see that things are also being healed and celebrated, instead of only being destroyed. 

Thank you, sincerely, to the bright lights out there.  Thank you to those who are electively happy - not out of oblivion, ignorance, cowardice, or naivete, but out of sheer determination.  You help me keep my head above water, when all I see around me are bunch of perceived sinking ships, and all I hear are people screaming that the ship I am standing in is sinking.

Let's keep trying to bind ourselves together in a pact/life-ring of elected optimism.

Send me funny memes.

💓

Thursday, September 6, 2018

Good Ol' Favorite Things

Good ol' favorite things

I wish I saved more of my dance costumes.  
The good news is that I remember most of my dance moves.  😃


Do you have some "favorite things to do" that you have absolutely no explanation for (or so it seems?) Everyone loves things like walks on the beach, quiet time over coffee, hanging out with good friends, settling in for a few hours of Sonic The Hedgehog or Grand Theft Auto.  Some sickos even enjoy things like sweating over a garden, toasting themselves in a chair by a pool, or picking things up and putting them down at the gym.

A Strange Child


One thing I remembered a while back was one of my favorite things to do as a child.  When I was a wee lass, I used to love to stick my finger in the straw hole of cups.  I did this quite frequently. 


Do you see that razor-sharp star?

I always had to stick my pinky into it.


WHY???!!  Have you ever tried to pull a straw OUT of there? Do you see what the straw goes through on its way out?

I do not recall EVER being able to get myself out of it... in fact, all I can remember is time after time inevitably going to my dad, either bemused, or full on screaming in pain for him to cut it off of me.  I remember that several times, he'd have to pull the car over on the side of the road, bring out his pocket knife, and cut me out.  He's always say to me, each time, exasperated, "Why do you do this to yourself?????????"   I never knew.  I guess I thought I would be able to get out of it?  It was just one of my favorite things to do. 

I also loved to do normal things that little girls like to do, like play with Barbies, color, build tree forts, and tap dance/ballet.  And play Mario 3 with the cheat codes provided by my brother.  

As an Adult


I have lots of favorite things to do now which are far less painful. I love a good road trip, and a rainy day, and doing laundry.  I'm trying to force myself to get back into reading actual books and magazines, instead of just endless scrolling on The Screens. 

Last autumn, Prime offered me Oprah Magazine and some others for like $5 for the year, so I ordered it. 

Now, one of my favorite things to do is to scan where all of the contributors are from, and I always get excited when I come across far-off  (as well as near) lands which I have visited.  I catch a gasp of air when I see "Port Angeles, WA" come across... I have breathed the air and touched the sea waters of Port Angeles!


I also  have too many hobbies, and not enough at the same time.  Archery, Yanni, singing, the Hippodrome, church, writing, traveling, and crafting... it's a lot to keep track of.  And yet, I focus on none of them 100%.  What's the deal??  Human condition?  Wanderlust?  To tell you the truth, if I had a companion to join me, I would sign up for many more things... tap dancing, bingo, ballet, and more frequent hiking.  What are some of your hobbies and favorite things?


Monday, August 20, 2018

Orbeez

ORBEEZ


I am the type of adult who enjoys things like coloring, Disney, glittery things, Uno and other card games, and dancing in public, and so anytime I catch a whiff of a new fun thing, I need to have it!

One of my friends and happy hour champions, Lindsey, and I were chatting about this at a happy hour a while back with a bunch of our other friends.  She said some of the wisest words that I have ever not heeded:  Don't drink & Prime. 



In absolute full disclosure, she was preaching from experience, because she was telling me about some of the fun things she's come home to, without remembering ordering... however... this is not the case for me.  I don't actually drink that often, and so I always know what I order from Prime... and so there was a perfectly logical explanation for how Orbeez came into my life.


A bit over a year ago, I read an article about how some redneck in Florida (or someplace where this would not surprise you) was arrested, and his children were taken away from him, because he filled the back of his pickup with Orbeez, plopped his kids in there, and drove around town like this.

I needed Orbeez, whatever they were.  I ordered them off of Prime the same moment I finished reading that article.

So, I bought one bag of them.  They are water beads.  You can buy them, and even a little gun for them, which is like a marshmallow gun, and it is fun for hours.  People also use them in foot spa things, and you've seen them used in vases for plants and bamboo in various restaurants without taking note.  Oh, and you've seen them in those fragrance things.

Stop paying $10 for these.  Just grab a few of my Orbeez and some essential oils or something.   You're welcome. 


So, I bought them, and brought them into work, and distributed them.  Over a year later, and we are all still playing with them. (Also, I have moved to 3 different buildings over the past year, so sometimes I will be visiting a different building, and see Orbeez at someone's desk... They came from me.  My Orbeez are all over the company at this point.) They are so pretty, that people just put them in a vase and put them on their desks.  

There's regular size...
They start out the size of a seed. Leave them in water for a few hours and they grow... AND THEY BOUNCE. 

And there is GIANT SIZE:
After soaking a few hours... (they look like BRAINS)

After soaking for a day

"What is the point," you may ask.

Nothing.

They are fun to look at.  And they are fun/therapeutic to smash into one thousand bits of SQUISH.

And, once you are finished with them, you can toss them into the garden, to keep The Things a bit hydrated during the melty days.


Have you made any fun discoveries worth sharing about?
(Please send me the Prime link...)





Unpublished

I feel compelled to tell you that I often write blogs, but never get around to publishing them, because they don't feel quite finished to me.   In this case, I am going to just publish this one, even though 1) it is from October, and 2) it contains characters of the past.  It's okay.  Some events are timeless.  Enjoy this unfinished draft.
----------------------------------------------------------------------------------------


HELLO.
How is everyone??
October was insanely busy for me!  I am glad that I don't have to do anything for a few weeks.


Adulting

I email or text Gym Rat just about daily to inform of my spills and trips.


And this happened the other day...
3:22 pm Veronica: GUESS WHAT
3:22 pm Gym Rat: wut
3:22 pm Veronica: i just realized my shirt has been on backwards
3:22 pm Gym Rat : OMG
3:22 pm Gym Rat: that's so you
3:22 pm Veronica:  It IS so me.


Narrator:  It was so Veronica.


3:22 pm Gym Rat: did you spill something on it too?
3:23 pm Veronica: earlier...  but fortunately, it was technically on the back of the shirt... so   now it's on the back and no one can see it.
3:23 pm GR: lolz.  smooth.  you should start doing that from now on.
3:23 pm GR: and switching halfway through the day
3:24 pm Veronica: yes... or just switching it before and after lunch
3:24 pm Veronica: i might need to go blog about this real quick
3:24 pm GR: YES!

I have been in very important meetings today and literally no one has said "HEY YOUR SHIRT AIN'T RIGHT." Sometimes people assume that I know that my shirt is on inside out, or that there is food or plants in my hair, or that there's food on my face.  PLEASE CORRECT ME.  I don't have a lot of mirrors in my life and also I never think about it.   I am a community effort, people!  

The other day when I was walking around Marshall's with a pair of jeans, and by the time I got to the Housewares department, I noticed that a cane wielding old man was walking directly behind me.  Probably 85 years old.  He followed me and followed me, and I tried to just be patient about the situation, as he examined every item that I examined, and touched every thing that I touched. 

Finally, he grabbed the pants I was carrying, and started speaking to me in Portuguese, saying what seemed to be something along the lines of, "These are nice, oh, they are black, I didn't know you needed pants."    I stared at him blankly.


Then he realized that I am a stranger, and laughed and laughed and apologized, and said he thought that I was his wife, whom he now had totally lost somewhere in the store.


These types of things happen to other people, right?  Is it really just me?


These funny little stories end up scribbled on post its and jotted down in my phone because they are silly and bring me out of myself a little.  The silliest things inspire me or make me over think.   




Friday, January 26, 2018

I have Multiple Sclerosis!




I have told pretty much all of you 1:1 by now, so I can post about it here. I have Multiple Sclerosis (M.S.)! It isn’t scary, so I don’t mind being a bit light hearted about it! Being diagnosed now versus being diagnosed 20... even 10 years ago is a totally different thing, so, we don’t have much to fear, my friends.

The Short Version!

If you are a totally lame person and only want the short point of this entry, scroll down to where you see the next M.S. Awareness ribbon:


For regular, nice people, continue reading here:

What actually is it?
Multiple sclerosis is... ready?... Multiple (more than one) sclerosis (scar tissue) on your brain or spinal cord.  The disease is an auto-immune disease, meaning that your body... your immune system (the central command for battling illnesses and viruses), is on auto-pilot ALL THE TIME, so it sometimes ends up attacking itself.  

So, the M.S. disease is basically a squirrel.
Think of your brain as the motherboard of a computer, and all of your nerves as the long wiring that goes everywhere and transmits the signals that makes your body move and breath and pump blood and drive and play video games.   And, wires, as you may know, have a nice, cushy covering, just like your phone cord does.  

Your phone cord is not just metal, otherwise we'd all get shocked and catch on fire all the time.  The coating protects the cord.  Your nerves work the same way, except the coating is called myelin sheath (covering).  

So, this squirrel, aka the disease, comes in, and starts chewing on the dang wiring.  This interrupts the signals sent to that part of the body.  Things do not go well.  That part of the body loses communication with the motherboard.




Sometimes, after the attack, the body can repair that myelin and signals are returned, and sometimes, not so much.  Unless you are on treatment, this squirrel is running around rampant and can attack any time.  
Maybe he goes for your nerves or your vision, or maybe he lays dormant for years.
Maybe your body can recover, maybe it can't.  
That's why the medicine is so important... it stops the squirrel, it just stops it!



We’ve only really started understanding how to deal with this disease over the past 20 years or so. The medications that have been released in the past 10-20 years have made it so that being diagnosed with M.S. these days is really not a big deal. The medications that are available have the ability to basically halt the disease/squirrel in its tracks. It’s amazing, really.  There's no cure, but at least we can hope to halt progress.






It is so frustrating to hear people give out fake news and alternative facts about this stuff. It is so important to take an interest in your own health, and when you have any sort of ailment, it is so important to make sure to never stop educating yourself. I know of quite a few people who have M.S., and for all sorts of reasons, they are not on any treatment. It’s a huge gamble… but also, I can’t judge, because everyone is different, and everyone deals differently with how they think is best to manage their soul vessels.


My personal story:


About 5 years ago around Thanksgiving, my right foot started getting really tingly, like the pins and needles you feel when you’ve been sitting too long and your foot or arm or whatever goes numb. Except it didn’t go away. Eventually, it crawled up my entire right leg, and it got to the point that I literally couldn’t feel that right side of my body, from about belly button down my right leg. I knew I wasn’t having a stroke, and I felt otherwise fine, so I really didn’t freak out about it, because I didn’t have time for such an inconvenience. I had just started a new job and didn’t want to be that guy who takes off work right away, and I was traveling to visit my aunt in Florida for the holiday.

Miraculously, I was still able to drive and walk just fine, I just couldn’t feel anything on my right side. You literally could have shot me in my leg and I would not have known. I had to wear shoes that strapped to my feet, because I wore flats one day, and looked down to realize that I had been walking on my now-sideways facing shoe. That’s a quick way to break an ankle, and I wouldn’t have known it… but thankfully it was winter boot season, so I just wore boots for about 6 months.

Eventually, the tingling and numbness started moving to my other foot, and that’s when I knew I was in trouble. Thankfully, I had a very good friend at the time who asked me when we were going to celebrate her birthday with a happy hour (December 1), and I told her that I didn’t know how far I could walk, and explained the situation. She, being a paralegal and all-around badass, screamed at me on the phone that “YOU SHOULD BE IN A MACHINE RIGHT NOW… NO… HANG UP THIS PHONE AND LEAVE WORK AND GET IN A MACHINE…” and she basically kept screaming and terrifying me until she met me at the hospital very soon afterwards. I’ll always be grateful for her snapping me out of myself.

Another symptom I had going on was a TERRIBLE misfiring nerve in my chest, almost by my armpit. It’s kind of hard to explain, but basically, it felt as though someone had shot a smoldering arrow clear through that joint area of my arm, in the front and clear out the back. It was extremely itchy, to say the very least, and in fact sitting there in bed rolling around in discomfort that morning that I went into the hospital, after already haven gotten ready for work, it was the actual last straw. It was torture, and I was terribly bruising myself by trying to find relief.

Lots of testing later, we didn’t know much, just that it was possible that I could have M.S., and that I had transverse myelitis, which is inflammation of the spinal cord. My spine for some reason started viewing my legs as a virus or something foreign, and so it had been cutting them off. The body is amazing, that it can do that. 

So, it took many months and lots of rounds of steroids, but I eventually could feel my legs again. The misfiring nerve got a lot better, too, but I do still struggle with the discomfort of it on an almost daily basis.



M.S. is really hard to diagnose, because no two cases are alike. You need to have a combination of at least two things to diagnose someone…. Either two “events” (which is what I went through,) or progress on an MRI (meaning that new lesions, or scars, are visible on your brain or spinal cord.)

I never had the combination, so they could not diagnose me. Meanwhile, I went to multiple different doctors at Johns Hopkins and University of MD to get more opinions. No one could diagnose me for years, and that was fine by me. I didn’t want to start treatment anyway… first of all, it’s a major commitment not to be taken lightly, and secondly, it’s about $45,000/year. Who was going to pay for that if I lost my job? Obama? Oprah? Trump? (LOL nah, it’s pre-existing condition…)


Annual or semi-annual 3-4 hours long MRIs! I don't mind them.

Finally, my main neurologist, who is amazing, said to me, “Look, you’re putting yourself at risk every day you are not on treatment.” He told me that they can get conclusive data by testing my spinal fluid, so that’s what we did. This led to a spinal fluid leak, which was misery for about 2 weeks… but I digress…

So, I started treatment after that. That was almost exactly 2 years ago.

Picking a treatment is almost literally like choosing your poison. Each has its terrible side effects, none of them are without risk. I’ve been on the same one since I was diagnosed, and it’s been rough.   The good news is that Smidgen has been extremely aiding, and always seems to know when I feel like death.  


((( engage extreme cat healing )))

I get flu-like symptoms every other week, and spend the better part of every other weekend ill. Over time, I’ve grown accustomed to it, and my doctor says that I’m part of the 15-20% of patients who don’t seem to totally acclimate to the side effects. There’s not really a solution. I’m basically allergic to my medicine, which, btw, is a shot that I give to myself, and my injection site swells up and bruises for about 10 weeks. It gives me a really cool cheetah pattern. Check it out.



Dangit, I thought I had more pictures of the cheetah print, but it turns out that I do not.

The worst part

Probably the worst part about going on treatment was that I couldn’t figure out how to do archery anymore. The treatment (especially in the first year) gives me hot flashes like crazy. I already had a pretty severe aversion to heat and sun (WHICH, btw, is common for M.S. patients and kind of a symptom,) and the treatment made it so much worse. In the hot Maryland summer, I couldn’t figure out what to do. I remember one day I was at a shoot at my club, and I simply couldn’t go on anymore – I had to walk off and go home.

I was thrilled that Nationals were going to be in Washington State that year, because Washington State is my favorite place! It is cloudy and cool! Finally! It would only get to be like 70 degrees at the worst! I would shoot and it would be amazing!!

Except, it was the hottest summer they’ve had on record with temperatures hovering around 100 each day. Of course. 

It was a heatwave the entire week we were there, and I got sick and couldn’t shoot well. I had a really really great trip over all, and got to meet up with lots of friends, but the archery was a loss.
I didn’t touch my bow again for months.

So, I am going to amp myself up and try to see what I can do, again. I don’t know how I will manage. But I would hate to give up so soon.



Why are you only now telling me?

Well, I wanted to see what I could do on my own. I told my small circle of trust, and put everyone, including my mom & Mario, on strict lock down from discussing it. I have my reasons. Mostly, because I didn’t want people to know half the story. There is such a stigma with M.S.. People hear “M.S.” and they immediately think… wheelchair… or some other awful fate. 

 The truth is, it simply isn’t like that anymore with the treatments that are available, and I never feel comfortable telling people that I have M.S. without being able to make eye contact and tell them the full story.

It’s important to me to be able to open up the conversation. They say it’s a “rare” disease… but I’d say about 4% of the people I know have it. (That’s a lot, actually.) And that’s only the people I know about.




There could be other people who, like me, aren’t public with it, or haven't been officially diagnosed yet. I know that before I was diagnosed, the one person I knew had it at the time wouldn’t talk to me about it. I felt resource-less. I don’t want anyone to feel like that.





Why this is important

Just as importantly, I have seen the benefit in sharing. I have a friend from my last job who is a C-level employee, and will be for the rest of his life… he’ll always be running some company somewhere. He happened to get scooped up in the news, because we caught up not long after I started my new job, and he has a medical background, so I shared with him. We catch up every 4-6 months.

About a year ago, we caught up again, and he shared with me the most heartwarming story. He told me that even though he had no previous experience with M.S., by knowing me, and hearing my story, and seeing how the whole thing developed and my journey to treatment, he has been able to support his own employees. He had an employee who recently opted to go through the most rigorous M.S. treatment (which is basically a chemo and was just approved by the FDA last November), and he said that by my sharing my journey with him, he was able to support her in a way he would have never even considered before. He had previously never given much thought to M.S., but by learning through me, it became real.


And, in other employees, he has a compassion now for their medical journeys that he was blind to beforehand. He never had to think of people like that before, and he thinks that he is a better boss, and a better person, directly because of seeing me through my experience. This, THIS, is everything to me.


Remember, if you know someone with M.S., it's okay to talk about it with them, but unless you are a professional counselor or a physician, please remember that you are not a professional counselor or physician.




If you actually just skipped from one ribbon to the other, I am so upset with you right now.  I know who you are.


So, the timing of this is for a reason. March is M.S. awareness month. There are many M.S. walks, all that can be found here (click here) at the National MS Society, along with TONS of really, really, really, really, really, really, really, really, really, really, really, really, really, really, really helpful resources and tools.

The walk I go to is in Annapolis on April 8th, and I want you to come with me.

I did the walk last April, and allow me to share with you my experience. 
I signed up, expecting to go by myself, but I invited my mom, and she said she’d do the short walk. 
So, I got up that morning and got ready, and drove to the Navy Stadium, where it starts, and felt so incredibly silly. 
I was thinking, 
I can’t believe I am doing this, this is pathetic. There are going to be 10 people, and we are going to walk around Annapolis, and people are going to think, “wow, 10 people walking for something-or-other, big deal.” 
I felt incredibly silly.

Even as I pulled into the stadium, I couldn’t wrap my mind around what I was seeing. The parking lot was FULL. There were vendors galore, and bubble machines, and loud music, and TONS of people! And free food! I was moved to tears. They make such a big deal. It’s fantastic.




People were there supporting family members, friends, colleagues… I even saw some of my own colleagues, there supporting I don’t know who. I couldn’t believe it, I really couldn’t.




And crossing the finish line, no matter how long it takes you or how far you walked, they have people cheering you on, pom poms and all, just so happy that you are there.



Update:
Here is the link to my Team Page for the walk, if you can donate/join the walk!  For the full scoop on fun stuff,  Click here to be directed.