and still, she persists…

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And still, she persists…

The buzzing of the alarm is heard off in the distance. Her children’s eyes grow large with worry.

“Hurry Mom, dad needs you!”

She rushes into the bedroom, grabbing the silicone wedge off the nightstand. As gently as possible, she pries his teeth open and off of his tongue. All the while, his eyes are burning in anger at her. She didn’t come fast enough. His face doesn’t move, but it doesn’t need to. She can see his frustration in his eyes.

After she fluffs his pillows and readjusts his body, seeing to all of his needs, she can hear the children in the kitchen.
Moving from one fire to another, she rushes out the door to see what the next emergency is.

And still, she persists…

They are crying. Looking up at her with tear-stained cheeks. They want to understand why their beloved pet had to die. Her heart breaks. Not because the cat was killed on the road in front of their house, but because she knows that soon, these faces will be searching for an answer as to why their father had to die. Will she have the right words or be able to comfort them when that time comes?

And still, she persists…

Her eyes are bloodshot. Its after 2 am and finally, the dishes are put away. Her husband is sleeping, the children are tucked in and safe. She remembers that the only food she has had all day are the few bites from a package of crackers her baby had nibbled on, and the constant flow of Zipp Fizz, the only source of caffeine that keeps her moving.

She pours herself a bowl of cereal. Stifling a yawn. Her head heavy with exhaustion. She can’t remember when the last time was that she showered. She contemplates skipping her only meal of the day to take a hot shower, but her stomach is growling, her head is pounding, and she needs to lay down soon. The kids will need her in the morning as they get ready for school. Four blessed hours of sleep, if she is lucky.

And still, she persists…

Pulling and twisting his lifeless and limp body, she maneuvers him to an upright position. Trying hard to avoid pulling the hose that is attached to the mask, that is attached to his face; she uses all of her strength to pull him up and over to the wheelchair. The bedroom is small. So little room to guide the chair around. The bathroom, even smaller and more difficult.

The sweat beads along her brow.

She grunts, using her back, her arms and her legs to pick him up and place him on the toilet. Trying to maintain his dignity, she wrestles with his body, and the damnable hose. Wishing he could remove it for just a moment but knowing that his body no longer takes in air without its assistance. Trying to find a different solution, but knowing he will simply refuse her suggestions, she lifts once again, and repeats the entire process.

And still, she persists…

The voice is monotonous, but it doesn’t matter. She knows him well enough to know that he is angry. He is always angry. He hates this disease. He hates how he feels cheated. He wanted to do so much in this lifetime. It isn’t fair.
He takes out his anger on her. He uses words like a killer wields a knife. Piercing her heart with razor sharp words. He places the blame on her. He points his frustrations out on her. As if she were the reason he was diagnosed with ALS. As if it is her fault that the doctors never took his symptoms seriously. As if it were her responsibility to keep him happy and healthy, and she has failed him once again.

And still, she persists…

Was there a time when they were happy? She can’t seem to recall anymore. She can recall their wedding. She married a man, who was still so much a child in his inexperience, and his desires. Wanting to please him, she put her dreams on hold. Knowing that to make a marriage work, there had to be sacrifices that needed to be made. She never saw that she was always the one making the adjustments, in order to keep the peace, and because she loved him with every fiber of her being. Now, there is anger. She looks for the happy memories. The flashes of happiness, Traveling and exploring, his excitement with every new toy: a gun, a four-wheeler, or even the snowmobile. He was happy when he was out doing things…anything. Now, he lays in his bed, staring at a screen, pushing the world further and further away. She tries to show her love, with a caress, a smile. But still, he pushes her away. Every day, she tries again. Hoping this day will be different, and he will see how much she loves him, regardless of the disease that has ravaged his body…and stolen his happiness.

And still, she persists…

ALS has taken so much from them both, and yet she still searches for joy and gratitude in her day-to-day routine. She is exhausted but smiles when her children are excited in their adventures and discoveries. Her children are happy, and even though their father is bed-ridden, she continues to create a lifetime of happy memories. She manages to keep them occupied and distracted from the world that is just down the hallway from them. She hugs their hurts and washes away their fears. She carries a heavy load, but you will never hear her complain.
Her smile would break your heart if you understood what kind of sorrow and sadness she hides from the world.
Someday, she knows her life will look different. Someday, she will no longer be a caregiver to a man who cannot find beauty in his small world. She tries to encourage him and to remind him that there is still joy to be found, but he pushes her away.

And still, she persists…

Someday soon, she will have to look for a new routine, and find new dreams to dream. Hard work doesn’t scare her. In fact, she looks forward to the day when she can leave the walls of the house she is trapped in, and to have goals and aspirations once again. She catches herself feeling the familiar twang of guilt when she imagines the life she might have after…She stops herself just short of going too far in her daydreaming…knowing what that means for her husband.

And still, she persists…

She is the strongest person I have ever met. Her heart is pure, and she is beautiful, both inside and out. She doesn’t realize her strength, and she can’t see her potential. But someday, she will look back on these moments and realize that she accomplished more than most people will in a lifetime.

Long after the ALS memories and painful struggles associated with the disease have subsided…only then will she see what I have seen all along. No matter what life throws her way, I know that she will continue to do remarkable things. Her children will one day understand her sacrifices, and they too, will stand in awe of the strength of their incredible mother.

And hopefully one day, when they are grown and living lives of their own, they will know their own strength because of one woman who continued to push and fight for them, regardless of the incredible task set before her. Until then, she continues to get up, weary and almost to the breaking point.

And still, she persists…

 Matthew Wild

 

dinnertime…

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It’s my favorite part of the day.

The evening is winding down.  Books are scattered across the table as my studious child is bent over a book, brow furrowed in concentration. The other one is running in and out, doors slamming, as he tries to sneak past me once again. The dogs are watching, waiting for a small morsel to drop. I am laughing as I try swatting at my son to stay out of the pantry. He rushes just out of reach, a triumphant smile across his face.

It’s almost time for dinner.

The sound of onions and mushrooms sautéing in the pan. Fluid motions of chopping, the rhythmic sound of the knife slicing and dicing. With the flick of a wrist, the food is absorbing the heat and sizzle and beginning to meld into a meal. The smells are wafting into the house, and the sounds of laughter are mingling with the sounds of footsteps. My children are gathering around the table. Dinner is almost ready.

Matthew sits patiently, quietly. His chair turned towards me.  He loves to watch me cook. I know this about him.

Even on days when I barely have the energy to move, if my children are gathered around the table and I am cooking, I am in my happy place.

It was a subtle sound.  I didn’t even hear it at first.

As I am setting the table, my back is turned as I am dishing up pasta into a serving bowl.  My focus on gathering everything to take to the table.

There it is again.

I glance up, twisting my neck to see behind me.

Matthew’s face is red. His eyes are bulging.

He is sputtering.

Kaden and Peyton’s eyes widen.

My son jumps up.

Matt, are you ok?”  I can hear the panic in his little voice.

I set everything in my arms down, but Kaden is already rushing off towards the bedroom. Peyton is standing up out of her chair, unsure of what she can do to help.  I am walking quickly towards the bedroom, ready to grab the machine if Kaden is struggling.

Matthews face has gone from red to purple. He is trying to cough, but there is no sound.  A small wheezing gasp is all that can be heard.

Kaden comes running towards me, cough assist in hand. I can see the look of terror on his face as he glances from Matthew to me.

I smile, trying to reassure him that Matthew will be fine.

I press the “on” button, balancing the machine against my thigh, as I juggle the hose and mouthpiece.  It is taking forever to switch on.  I slowly count to three out loud. More for Matthew’s sake, to help him to remain calm and that he will be able to breathe again soon, than for myself.

One….Two…Three

Finally, the “swoosh” sound begins, indicating it is ready.

Matthew leans towards me, pushing his face into the plastic covering that encompasses his nose and mouth. The familiar sound as the machine forces the air in…then out fills the air.

After several deep breathes, Matthew leans back into his chair, relief across his features.  His face is still red. Tears streaming down his cheeks.  Snot dripping from his nose.

I set the machine down, grab a rag and begin to clean him.

This is automatic.  This is not the first time he has choked on his own spit….and it will not be the last.

I glance at my children, frozen in place. I give Peyton an encouraging glance and ask her to keep telling me about her day. Looks of terror on their little faces slowly dissipate and I can see their chest begin to rise.  They are only now realizing that they were holding their breathe.

And just like that, life returns to normal.

Our normal.

“So” I say, “What was the best part of your day?”

connections….

She must have noticed how my face fell in disappointment as my head turned, first to the right, and then to the left of me. I had run into the store to grab a prescription, leaving everyone waiting in the car. As I went to close my door, he asks me to quickly grab him something as well.

I nod my head, irritated as I hurry inside.

Matthew had a craving for Reese’s Peanut Butter Cups lately and asked me to grab a few. I tried to remind him that we had plenty of M&M’s and Kit Kats at the house, sitting in the freezer. The kids had been gone for several days, so the candy hadn’t been gobbled up just yet. But, no, his craving was specific, and judging from previous experience, if I don’t acquiesce, than the craving builds into some incredible hunger monster of epic proportions, often resulting in his “Go BIG or go home” philosophy that ends up with him miserable and having a stomach ache.

Now, I am standing there, prescription paid for in one hand, and three king sized Reese’s packages in the other, hoping to get through the checkout in a minute or two…not the twenty minutes it looked as if it were going to take, judging by the long line of full grocery carts in front of me.

“Would you like to go in front of me?”

I looked up into a sweet face, waving for me to come closer.

“That would be great, thank you!”

I squeezed in between the cart and her, sucking in my stomach as I did this, shuffling my feet in a strange dance as I place the candy bars down on the conveyor belt. In full disclosure, sucking in my stomach does not, in fact, make my ass any smaller as I try this…but it is always worth a try.

I had noticed, as this older lady and I had done our strange shuffle dance, that she had a bandage just under her shirt. I assume it is a port, and I try to glance away quickly so as not to make her uncomfortable that I had been staring. My eyes venture over to the stacks of pizza boxes and frozen egg rolls, and various other over-processed foods. Maybe she has a Matthew at home as well.

She reaches over to rearrange the food, smiling.

“My grandsons are coming over tonight for a sleep over. They are bringing some friends and instead of cooking, I am hoping this might be enough to fill them up for a while!”

I know all too well how hard it is to feed the never-ending pit of teenage appetites. I learn that her grandsons are in their teenage years but still love coming over to Grandma’s house. I share with her I how I can’t wait to become a grandma!

Wait!

I quickly clarify that I can in fact wait, as my oldest is not quite 18 years old, but that I am looking forward to spoiling babies…only handing them back when I am done!

She mentions that she has enjoyed having her grandbabies over since she moved her almost thirteen years ago.

We talk more about parenting and the joys of kids.

She tells me how perfect her grandkids are. I nod, telling her that my children are also pretty perfect.

“It’s the parents, you know.” She leans in to tell me this as if it’s a secret between us. I laugh, telling her I don’t think I had much to do with it. I was really just blessed with great kids.

“When people tell me that kids today are awful, I just don’t agree! It’s the PARENTS that are awful!”

I can’t help but agree with her a bit on this.

She mentions the cancer.

She is doing really well with the chemo. In fact, today was her anniversary and she celebrated by having another chemo round. Her husband wasn’t doing anything to celebrate, but she seems content with feeding teenage boys with copious amounts of junk food.

She proudly pats the stylish grey bob on her head, “I did lose my hair, but I have plenty still to spare!”

I tell her I am sorry but that I am glad she is still feeling so well.

“It was more emotionally hard seeing all the other patients come in, looking sicker and sicker with each round.”

I nod in agreement again. I have no experience with that, but I can imagine it must be really scary and difficult not knowing.
She says how thankful she is, because she knows it can be worse.

I mention that my husband has ALS but that I have learned to find even the smallest things to be grateful for.

Her eyes widen, and then fall as they fill with sadness, her hand squeezing my forearm.

She gets it…

I give her a small smile, trying to comfort her as she tries to apologize for something she has no control over.

I don’t have any person experience with cancer. I know people who have had cancer. I knew people who have passed from cancer, but my experience with having a close loved one with cancer and caring for them is next to nothing.

However, there is something comforting about looking into another person’s eyes and finding compassion and understanding.

For just a moment, two complete strangers were able to connect about how life isn’t fair, but that joy can still be found in the love for family, a few boxes of pizza and maybe a Reese’s peanut butter cup or two.

And that craving of Matthew’s?

Yeah, those king-sized bars made their way into the freezer, along the other piles of junk food…

 Matthew Wild

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San Fran or Bust!

ALS Fact of the Day~

San Francisco or Bust!

Inverness, CA is solitude and beauty and quiet in a way that I have not experienced in years.  I want more, but I will be content with the few minutes I was able to enjoy before I was needed by the tiny travelers and the big guy. There is a part of me that could stay here forever, watching the tide ebb and flow with the seasons.  I must admit, the food and the local market leave much to be desired, but seriously…when was the last time you sat outside and listened to absolute quiet?  Just the gentle lapping of waves as they caress the shore.  No cars, no loud brakes or honking or engines revving.  It was peaceful.  I desperately want to come back someday.

Check out time is noon, which should give me enough time to shower Matthew, clean out the van and get re-packed.  The entire process should only take me a couple hours, but the kids are happy to watch a movie, and Matthew is laying back resting. And I don’t want to be the drill sergeant ruining the peaceful setting. So I wait…almost patiently.

The night before, I had tried to lay Matthew on the bed, with pillows all around, under his head, his arms and legs.  However, sometime in the middle of the night, the pain was too much.  So, once again, I get up, trying desperately not to wake the kids as I grab the lift and put him back in his chair.  His knees and hips are hurting, regardless of what position he is in lately, so it means a lot of moving, and stretching and trying new ways to make an impossible situation bearable.

Finally!  At 12:00 pm, we load up and are ready to hit the road.  Everyone is in good spirits once again, and I suggest we get gas and a good meal before we attempt anymore of Hwy 1.  Our navigator thinks it would be better to get down the road a bit more. ( I silently disagree with his assessment, but I let him make the decisions, as he is the one who planned all of this!)

So begins the swerving, and curving..the topsy-turving.  In and out, and all around, we roll from side to side.  The kids begin complaining of headaches, and belly aches.  My arm hurts from holding Matthew steady.  Still, he wants to move onward.

Where the redwoods stood tall and proud behind us, the trees that come around the bend are different.  The only way to explain them is as if you were to take all the different kinds of trees from across the land, and then toss them haphazardly across the landscape.  There are trees that are leafy, that reach over across the highway to touch the fingers of the trees of their lovers across the road. It was almost as if they couldn’t bare to be apart, and even the simplest of touches would have to suffice.

The next trees were lined up, one-by-one, along the road, in an almost military style, as if they were saluting the cars as they passed by, standing proud and strong at attention.  Next were the trees that were a bit too lazy to make the effort to create strong branches. Instead, they had vines and moss that were hanging from limb to limb, as if with a small smile and a happy gesture to say welcome, but they were not going to offer any shade.

We were down to an eighth of a tank of gas again, and everyone was getting hangry. I have such happy memories of S.F. and I can’t wait to show them the sights!  But, my anxiety at letting the gas gauge get that low, and the kids are noisily munching on the last of the bags of baked chips and popcorn.

Matthew keeps repeating, “Its about the journey, not the destination.”

I know!

But I really want to get to our hotel room and then explore and it is already 2:00 pm.

We see the Golden Gate Bridge. I reroute us so we can get closer, but hauling a trailer behind us is proving to be difficult in a tourist hot spot.

We agree getting to the room and then coming back would be better.  I am getting antsy. I don’t want to be in the van anymore! I want to be out, walking around and seeing things!

We navigate our way through the back streets towards the Fisherman’s Wharf.  Only one problem…. The valet won’t take a vehicle with a trailer.

I have the kids unload everything, and I have them all go in and check in and get things to the room while I navigate the parking arrangement.

Each parking lot within a four-block radius refuses to let me in.

It is so bad, in fact, that they come running and won’t let me even enter.  They yell at me that I can’t park there, and they send me on my way.  One man glares at me, putting his body between the barrier and my can. All I can do is ask as politely as possible, and know that the prison system in California frowns against running over people for no reason. So I smile and back out into honking traffic.  Each place looks at me as if I have two heads for even attempting to bring a trailer downtown.

There was a moment, when one of the garage attendants was telling me to go away, that I almost started to cry.  It was close, but since I only cry when I am truly desperate, I backed that trailer up, in the middle of rush hour traffic like a true Mountain Woman, and short of telling him to piss off, I drove away with my head held high.

Until I parked and went into the hotel and saw their faces.

The kids were so sad.

I don’t know what is worse. The fact that they were ecstatic over the size of the large bathroom, so I would be able to help Matthew, and we had to leave, or the fact that they had to go back up to the room and load it all back up, while I brought the van and trailer around.

People are often unaware of what it takes to find accessible locations. I can’t say it was ever anything I ever would have considered during my life before ALS.  But, now, it is constant. I look at stairs, and steps, and dips and holes, I am constantly navigating and judging if it is something we can do.  Most times, we are unable to venture out to the highlighted attractions simply because Matthew lacks legs that can take him up or down a few steps.

I refuse to let this ruin our day.

I pull the kids off to the side of the trailer after we have loaded it back up again.  The damn valets and hotel guests can take a flying leap as far as I am concerned.

I kneel down, and I hug each of them and I tell them how much I love them and how proud of them I am.  Not once did they complain or become rude.  They did what was asked of them, even when they were disappointed. Not many kids could hold it together as well as they have today.  I told them that things weren’t always going to go as planned, but that we could only do the best we could do and go from there.

So off we were, once again.  A hotel booked about an hour south from here.  With the idea we would return in the morning.

I don’t know if I should thank San Francisco for permanently scarring my children to the effects of drugs and prostitution, but they got a pretty good idea of what it leads to.  As our safari bus tried to make its way out of the city, we went from light to light, witnessing drug deals, people literally leaning against the building to use the restroom…and I don’t mean #1!  There were people talking to themselves, and people dressed up in various outfits.  I tried to explain that some people were not given the same chances or advantages that others are given, and others become broken through a lifetime of bad choices.

They seemed oblivious to the seriousness of what was happening around them, and as we went up the steep embankments and then down again, I couldn’t help but laugh so hard I was snorting.  The kids were freaking out at the almost 70-degree incline (so not joking here!) and I was literally trying not to crash as I help with one arm to keep Matthew from slamming his head into the dashboard on the way back down.  Brakes are good!  I know, because I was on them for quite a while!

But alls well, that ends well.  I managed to drive us through the city and to our hotel in San Mateo, where they are above and beyond accommodating!

We have hotels figured out for the next six days, and now we will attempt to see San Francisco once again..this time without a trailer in tow, as we will be leaving it behind to navigate a bit easier!

Some important life lessens here:

  1. Don’t do Drugs! They do scramble your brains!
  2. Don’t use the bathroom on the main thoroughfare..at least go the alleyway!
  3. Even when people are assholes, try not to lose your patience. They are only doing their job
  4. NEVER! I repeat…NEVER! Attempt to take a trailer into the city…EVER!!!!

 

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San Fran! – Take 2!

ALS Fact of the Day~

If you must know, I never write if I’ve been drinking. Matthew says its because I refuse to be truly vulnerable.

Pff!.
That couldn’t be further than the truth.

The truth is that I simply don’t have the ability to form complete sentences if I have had a drink or two. It’s similar to drunk texting your ex at 2:00 am after a night of too much indulgence, or getting on stage with a microphone after knocking a few back and thinking you can speak coherently.

It’s just a bad idea!

You’ll end up thinking you sound intelligent. But in reality, you’ll come across as desperate and probably a bit inept.

I left off on our California adventure having had a less than ideal experience in San Francisco. We had hoped to have two days to explore, but after the hotel and trailer fiasco, we would have to make due with only one day left..

I stopped writing for the remainder of the trip because, as you can probably guessed by now, I began drinking every night.

Don’t raise your eyebrows at me!

It’s hard work, daunting even, to be solely responsible for a paralyzed man, two children and all that that entails, thousands of miles from home, or help of any kind. Falling into bed exhausted, the last to close my eyes, and the first to open them. I took my respite once everyone had fallen into their slumber. I would pour myself a glass of my favorite red wine…or more often than not, some cheap crap from the gas station with a twist top, poured into those little Styrofoam cups from the bathroom counter and relax for just a while, thankful no one is needing me for just a while. Some nights I stopped with one glass; some nights required a bit more of the tranquilizing liquid.

However, Matthew is holding me hostage. He says I need to finish the story and post the pictures so that we can move on with the next adventure!

So here it goes….

San Francisco – Take 2

The city is a hodge-podge of messiness. It is almost as if it can’t quite make up its mind what it set out to be, so it took everything and everyone and wrapped its arms around in a welcoming embrace. Before the gold rush, the city consisted of about five hundred people. One year later, it was five times that size. There was no planning or time for adjustment. They began building in the least desirable location possible. On steep mountains and dense forest on the edge of the ocean.
Just ten years later, the population was over one million.

Yet, now, it feels as if the hippies, the yuppies, the homeless, the hopeless, artists and businessmen alike, have molded into a beautiful condensed mess. There are redwoods mixes with cypress trees, military with peace and love. Vines, flowers of every texture and color mixed with weeds growing in impossible locations. Fog, so thick you can’t see ten feet in front of you, only to traverse a few miles, and see brilliant blue skies, and birds gliding seamlessly across the horizon.

Every ethnicity, culture and race can be found within a few miles of one another, stacked upon each other, not unlike the buildings they co-habitat in. In a matter of just a few hours, we ate at the Fisherman’s Wharf, with Alcatraz looming off in the distance. We walked, following the masses along city sidewalks, when the kids jumped up and down excitedly.

Could they please???

Now, I am not much into the whole Ripley’s Believe it or Not kind of entertainment, but after looking aghast at the prices, I kept walking. Matthew rolled up alongside me and gave me the look.

“What??”

I tried to ignore his scowl.

It’s one I get quite often actually. It’s the “You are being cheap!” look…

Fine!

The next building had wax figures, some so life-like, you could almost sense their eyes following you as you tiptoe around them, inches from their face. The kids were creeped out yet enthralled by Madam Trousseau’s Wax Museum. The Virtual Reality exhibit was open, and this time, when I was given the
“Can we please, mom?!”

I shrugged and left it up to Matthew.

Okay, to be fair, the virtual reality was really cool. A quick walk back to the van and this time, buckling Matthew in to avoid him making a face plant on the dashboard, we went on to the next location.

The Fine Arts Museum, with columns and arches, complete with a beautiful Indian wedding taking place in the center of the columns. Women in colorful gowns, jewelry jangling at their wrists, eyes darkened to accentuate their almond shaped beauty. Men, dressed in their wedding attire, trying not to look nervous, their feet shuffling, as they readjust their vests for the hundredth time that minute. I felt as if we were trespassing, so I ushered the kids along the path, shushing them along the way. Matthew unable to follow us along the pathway by the pond, turned his wheelchair around and began to navigate his way around. We watched the swans swimming gracefully along. The idea of staying still and simply watching life move by for a while was tempting, but my children are unable to sit still for long and I should probably make sure they stay out of trouble.

Instead of simply walking along the path, enjoying the sights, and sounds, they have to run, whoop and holler. The next thing I know, my children are attempting their skills as modern day Tarzans, climbing onto massive limbs, so far high above the ground I began doubting their ability to get down safely.The limo pulls along side the street, and the wedding is about to begin. It is time for us to go.

Chinatown:

The streets were jagged, the buildings looked ragged and old. Paint peeling from the walls, and steep steps into nooks and crannies that promised intrigue and ancient secrets. As soon as we find a somewhat level parking lot, Matthew wheels himself out of the van, we are ready to explore!

Damn…

Each street is cobbled stone and cracked beyond repair. Most sidewalks are crumbling concrete with no gentle slopes to be found. Matthew would not be able to go far. We settled for a restaurant as close as possible to where we parked. We weren’t going to be able to explore this part, but we could at least try the food. Yelp reviews be damned!

Imagine the look on my children’s faces…no one spoke English. No English on the menu, no English to be found anywhere! The menu had strange marks etched beneath photos of food. There was no way to distinguish pork from chicken or beef…All we could do was point to whatever looked appetizing and hope for the best.

The circular platter in the middle of the table was soon filled, and they delighted in spinning it to and from, reaching for new delights. Besides sitting in an area where no one spoke English, it felt like any other restaurant. Families walking in, toddlers misbehaving or whining, and parents scolding them for wiggling. The tone, inflection of the stern voices, and the parental “evil” eye cross all boundaries!

I want to say that we had all the time to explore, but really it was more about racing from one site to another, since we only had this one day to see it all. A drive-by to visit the Painted Ladies (no one seemed to impressed..) to Coit Tower, and the last part of the day, driving down the infamous winding Lombard Street, all before the sun set on our adventure for that day.

I can’t say that it was easy to get around, and I am sure that it is even harder in a wheelchair, as Matthew was bounced around in his endeavors! However, the kids didn’t seem to mind only getting quick sneak peaks here and there, and Matthew was happy to finally see the city that I had told him so much about.

Stay tuned for our next few days of adventures along the California Coast!

 

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T.M.I.

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Disclaimer*** TMI!
 
If bodily functions make you queasy…I suggest you just keep on scrolling…Nothing to see here…
 
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Almost five years ago, when I tepidly decided we could date, but that I really wasn’t looking for a serious relationship at the moment, I had no idea the adventure I was headed towards with Matthew.
 
Take for example shortly after we began dating. Matthew thought it would be great to take a quick weekend and explore Glacier National Park.
 
Having no children of his own, we packed up my (then) 6, 8, and 13-year-old children for a fun excursion. Things were off to an awesome start. Fun things to see, hiking and all the smells and sights, in majestic mountains. After day 1, we headed into Whitefish for dinner. I believe Yelp was the go-to app that directed us to a lovely café, on a beautiful street filled with quaint stores, and all the Montana paraphernalia a person could buy.
 
I remember the kids chose the customary mac and cheese dinners, while Matthew went with a burger and fries.
I chose a warmed spinach salad.
 
A healthy and delicious meal that I smugly ate, assured in my choices to help my waistline as well a great example to my growing children.
 
A decision I quickly began to regret.
In less than an hour, my stomach was rolling and gurgling…a sure sign I had food poisoning.
 
Now, if you know anything about me, then you would know that bodily functions are something I don’t want to announce. So with all the strength of an elephant, I shakily kept my face neutral, while the goosebumps spread across my skin and the sweat broke out across my upper lip and forehead. I quietly prayed I was wrong, and this was just a little stomach bug and nothing more. This would pass, I know it would. I would not throw up. The very idea was ludicrous!
 
I forged ahead, willing my stomach to hold its contents and not embarrass me in front of my boyfriend on our very first vacation together. And, in less than an hour I knew what was coming, and I was hoping against hope that my body would not embarrass me with what was sure to be an eruption of epic proportions.
 
Thankfully, I was able to hold it together until they were asleep. Then I hastily crept into the bathroom, running the shower water and sink water, and expelling, quite violently, all the remnants of the rotten, warmed spinach salad.
 
This event lasted well into the wee hours of the morning. I remember gingerly placing the small waste basket, unassuming to the poor passer-bys, outside the hotel door for the poor housekeepers that morning. I don’t even want to go into details of what happened, but let’s just say, it was violent and from both ends… And poor Matthew…he had to load up three children and myself, weak and unable to move, to drive the five hours back home.
 
Now fast forward three months after that…
 
My first trip to Cabo San Lucas! My first vacation in I don’t know how many years.
 
Matthew has, as usual, planned the most amazing time to be experienced. We went on bottomless boat rides, and sunset cruises. We had drinks on the balcony and walked the beach, watching the sun melt into the ocean.
 
It was perfect…
 
He excitedly grabbed my hand one evening, wanting to show me the very location where he personally partied the night away with the very famous Sammy Hagar as well as various other celebrities. His eyes lit up like a school boy at Christmas as he excitedly showing me where he sat, drinking and dancing with wealthy socialites and bodyguards, and how he was invited to the after party, long after most people would have called it a night.
 
The place was called Cabo Wabo. Maybe you have heard of it?
 
He ordered his usual Coors Light and three tacos.
 
He raved about these tacos.The flavors and the fact that we just had to try them…
They were good, I guess. Nothing too mind blowing that I can remember. The atmosphere was fun, but I guess without Sammy Hagar, it was just another one of those overly hyped up locations in a tourist trap. And the tacos?
 
The damn tacos gave us E. Coli that lasted at least fourteen days.
 
Yep..the same thing that happened to me just three months earlier, only 100x worse!
 
Only this time…we both were sick…
 
The rest of the vacation was spent staying within ten feet of any bathroom…and we both were walking a bit funny after the rest of the week, when our bathroom breaks were still happening at least every ten to twenty minutes..
It was less embarrassing, since we were both suffering together, I guess.
 
You might be asking yourself why I am telling you all this…
 
Well, I think the Poopy Curse has struck again.
 
Let me just give you the little by-play last night.
 
11:00 Pm – I finally close my eyes.
 
12:00Am – Matthew needs adjusted.
 
2:30 am – he groans. I sit him up. He tells me his stomach is gurgling. We wait a few minutes. He seems content to go back to sleep.
 
I lay there for a while. I can’t fall back asleep. I grab my phone. I know better, but I catch up on the news, and waste away an hour. Finally, I set my phone down and close my eyes…
 
3:30 am – He moans again. He needs to use the bathroom.. ASAP!
 
Well, shit!
 
I left the hoyer lift in the trailer. Bad planning on my part.
I quickly dress and run outside into the parking lot, unlock the door and wheel it out. Quickly, I throw the deadbolt back on the hatch and hurry as quickly as possible back into the room.
 
If you haven’t figured out by now, bodily functions while having ALS is a process…and never a quick one.
 
Without going into too much detail lets just say, there were sad eyes, apologies and a lot of gagging on my part…and his. And a lot of groaning from him, and comforting words on my behalf
(btw..how I had three children and changed diapers daily is beyond me! I can do anything…literally, I can handle anything…but poop!)
 
The damn waste basket was put outside the hotel door again. A pile of towels, and about two hours later, Matthew was all cleaned up again.
 
When we had checked into the hotel that evening, there had been a mistake and we were placed into a regular room. At the last minute, I switched our rooms. (Just in case, I told myself.) There was just no room to move around. After the last two hours, I was so thankful I made that switch..or the mess would have been much worse.
 
And the kids…yeah, they slept through the entire ordeal!
 
5:30 am – I close my eyes and finally sleep
 
7:00 am – my children are giggling, ready for the day to begin
I am determined not to let a little lack of sleep ruin Day two of our vacation!
 
We load up and are right on schedule!
 
Well, shit!
 
Matthew has to poop again. ( I groan a bit inwardly here, not gonna lie..)
Deep breath…Okay, no biggie…
I send the kids out to begin loading up the trailer.
 
As this is early in the morning, we have plenty of time to make Crater Lake and then a short drive to our hotel in Klamath CA.
 
I wheel the hoyer lift out to the parking lot…determined not to make that mistake again!
I pull the deadbolt key out of my pocket. Ready to hit the road, the kids are bouncing around, feeding the local chipmunk and being generally goofy.
 
The damn key won’t fit.
 
Well, Shit!
 
In my rush last night to get the hoyer, I had slammed the deadbolt on upside down. Now the key won’t fit in the hole.
 
Freaking wonderful.
 
The maintenance man is summoned. After about thirty minutes, he moseys along, hacksaw in hand.
 
With a shake of his hand, and a $20 bill, I tell him I appreciate his help. He seems to take it in stride and gives me a toothless grin in return for the tip.
 
Okay, NOW we are on our way. An hour and a half behind schedule now, but all’s well that ends well!
 
A quick stop for another deadbolt, and we are off!
 
Kids still have no idea where we are headed or what adventure awaits.
 
Crater Lake was breathtaking!
 
Souvenirs are purchased, and without WiFi or a map, and the wrong turn, we finally figure out we were going in the wrong direction for 45-minutes!! Ok, NOW we are finally going towards our next destination!
 
The Redwood National Forest!
 
We stop for gas, a quick stretch and a pee break.
The kids and I run in, as I am ushering them through the aisles, sending them towards the snack aisle. FInally, I make my way towards the restroom.
 
I fumble with the top button of my pants, my mind scattered, trying to hurry so as not to leave Matthew alone in the car for too long, and make sure this time we are headed in the right direction. My jeans are shimmied down and..
 
Plop!
 
My cell phone, which was in my back pocket of my jeans, lands in the toilet bowl…
 
Well, shit!
 
 
 
 
****Disclaimer #2
Day 2 of Vacation is still awesome! Even with all the little unplanned for quirks!

slowly, they all just disappeared…

Image result for sayings of losing friendship

You didn’t think it would happen. Not to you. You had it all. You had a loving and supportive family. Siblings and cousins you saw or talked to almost every day. You had friends. Friends who grew up right down the street from you, buddies who had gone through thick and thin with you.

Slowly, so slowly at first, it seemed almost as if you might be imagining it all.

First, the words of condolences.

“I am so sorry you are going through this.”

“I heard about the diagnosis. I am so sorry.”

Next, they see you out and about, but instead of the happy greeting you would normally get, they avert their eyes. You sort of stop. Unsure of how to proceed. You see them look away. You clearly make them uncomfortable now. They are hoping you don’t call out or draw attention to them. They duck, they turn away, they do anything to avoid having to face you.

It seems awkward at first. You take it personally. You feel as if you have inconvenienced them in some way, but you aren’t sure how.. After a while, it becomes such a common occurrence, you do them the courtesy of simply not even looking in their direction.

The pain is less sharp with every ripped page of a calendar month. It seems that time has a way of helping you adapt. You adapt to the loss of mobility. You adapt to losing your independence. You adapt to losing camaraderie with co-workers you used to see daily. You simply adapt to losing something, each and every day.

You think you have managed to come to terms with all the changes, but then you realize that the changes never stop.
After your body has morphed into something you no longer recognize, and you only slightly look like the person you used to be, you must now adapt to a new challenge. The friends and family you hold so dear. have all just slowly dropped out of sight. You had no idea that this is the part that would test you.

You thought dealing with the disease would be the hardest thing you would ever have to deal with, but you discovered you were wrong.

The hardest part, in fact, would be watching everyone around that you love move on with their lives, and all you can do is stare at a screen and watch it all happen.

You do everything in your power not to click on that icon, you try so hard to stay away from social media.

You don’t need to be reminded of all the Christmas parties, the weddings or the birthday celebrations that you are no longer invited to.

You don’t get to be included in the phone calls, or the invites for a drink to commiserate a friend’s breakup or loss of their favorite sport teams championship game.

The connection is gone.

Funny that you didn’t notice at first. You were so focused on the loss of your legs, you hadn’t noticed that those friends who used to talk to you every day, haven’t reached out in almost a year now. No one has stopped by to visit in so long, and you don’t even bother asking for visitors. They all promised, but its been so long, you finally quit anticipating anyone knocking on the door.

The invitations you had gotten were either to someplace that cannot accommodate your new situation, or it was a pity invitation. At least, you assume it is a pity invitation, so you politely decline. You feel you have done everyone a favor by not going.

You thought the disease would be what caused your body to stop functioning. Now, you no longer believe that. Your heart is breaking, and you begin to imagine that it is possible to die from a broken heart.

If you had only known the disease would not be the hardest part to deal with. You found out the most difficult part of each day would be to live and then die from isolation, depression and sadness. The ability to see all those people you once had a connection with, posting pictures of their lives, their loves, and their ups and downs, but you somehow, realize that you were forgotten.

You want to turn away, but you so desperately need to feel as if you are still worthy of their time or effort.
Now, you scour the internet, Facebook, Instagram, Twitter…anything that connects you in some way to the people you used to know. The anger is gone. Now, you simply want a connection with them. Even if the only link to them again is by pressing the “like” button.