Category Archives: Uncategorized

And so it is

Two months ago, it was just a mere sentence thought. After trying the doubling of eye medication without success it was discussed as a possibility again. After my MRI, it was decided that the time was best to try–I have no other options.

I knew it was coming. Last week, the hopes was to have the surgery on the right eye this weekend, but that didn’t happen. My left leg still healing and switching from Warfarin (blood thinner pills) to the shots for surgery preparations, it still hadn’t really registered that surgery is coming. Until this morning; Or maybe two nights ago, when important questions started entering my mind; questions I didn’t think to ask at appointments.

I had just been to see my local family doctor earlier that afternoon for pre-surgery check-up procedures. At the end, he asked, “Do you have any worries?” I thought for a second and shook my head in a “No” fashion. Like a blank mind. I don’t worry about my body per say, but the outcome..the effects and details surrounding it. And so I am more thoughtful of how life will be after surgery-depending on the results. It is then, in those thoughts, my mind begins to see the worries of the actual physical portion of the situation.

I was talking to my aunt about this as I made my Starbucks refresher drink in the kitchen today. In telling her that I was seeing the negative, she encouraged me to hold to hope. And that is what I am prying until Monday–to see the hope, like the story of life, knowing whatever the outcome that God still has something special written just for me.

My surgery is set for this Monday, the 8th at 6:30pm. I sign in at 4pm. I will spend the night to be monitored; discharge is anticipated for early Tuesday morning and we might still have my Wound Team appointment (for my left leg) that day, since we are down there only a few blocks from Children’s. It’s no wonder the weeks seem to fly by so quickly. 🙂

I thought I would say a few specific prayer requests:

For peace–that I will continue to hold to hope (and being put to sleep is a fear of mine from a previous bad experience.)

For my family as they are in this with me and take care of me.

And for the surgeons/other medical staff..for wisdom and steady hands.

I won’t be on my blog until I return home; however, I may post updates on the Facebook page. 🙂 More to come…

9 Comments

Filed under Uncategorized

My Story

“Show off,” I sputter being very much out-of-breath. “Just because you can prance up the stairs…” I add with a laugh and having then completed all six stairs leading back to to main patio deck, I see Muffy flop down next to the picnic table. My whole physical being was shouting unanimously the same: SIT! But I still had two more stairs to climb to enter the house.

DSCN3727

DSCN3722

We had just been out by Mom’s garden taking pictures. I have been eyeing her growing flowers for quite sometime. The Zinnias from the kitchen window are like colored dots upon the green, but it is the sunflowers that I find most captivating. Although it is only a short distance from the back patio to the garden, it was my first time there all summer. It was my first time, because of the barrier between…the grass.

DSCN3750

Grass. I am not even sure why, but it is the biggest struggle for my body; talk about a serious case of painstiffy! But it was worth every moment, every bump in the grass, every nudge of love from Muffy, every laugh with my parents.

I’ve been having thoughts of life in a different perspective. Like a story. Dad and I were returning from Cleveland and I found myself gazing out the window to the biggest sunset that I have seen in a long time. Even wearing my sunglasses, I could see beautiful. As I started thinking, I told myself that if God knows my story, then it must be something good, because I can’t see it ending as a tragedy. Just simple faith talk to myself…then I return home to walk “the grass” of reality, find myself pleading for help and receiving grace and mercy in the time of need (Hebrews 4:16.)

DSCN3736

 

 

DSCN3735

My story is still being written, everyday that I live…

*My Mom shared this song with me. “Glorious Unfolding” by Steven Curtis Chapman. http://www.youtube.com/watch?v=Id2u3osFcp8

5 Comments

Filed under Muffy, Uncategorized

Painstiffy

I am not one of those morning people who get up around 6 or 7AM, fully set for the day, and singing jolly tunes (much to anyone else’s delight.) But, I also am not one to habitly sleep in until morning is over either. So I compromise: around 9:30 or so. I have, however, that my sleeping is getting deeper–and longer. And this morning when I woke, I was stiff and getting out of bed was just not something I wanted to do, but since it was almost noon, I was hungry. So I made myself get out of bed.

Dreams are strange, mysterious. Most of the time, I don’t remember them; but lately, I awake with a few memories. This morning as I sleepily made my way to the bathroom to freshen up for the day, I thought of my dream. I don’t remember anything of my dream except that Mom and I were in a discussion about health and the word, “Painsty,” was mentioned a few times in reference to my pain.

As I am brushing my teeth, I decide to change the word just a bit to a better formula that makes sense: Painstiffy. It’s genius. It tells in one word how I feel: pain and stiff…well, the stiffness and numbness and muscle weakness or atrophy, especially in the neck, are the cause of the pain. It’s like a stiff pain…not excruciating pain. It’s hard to explain.

I decided this new form of a word would be how I answer my doctor’s opening question: “How have you been?”

“Well, I have been struggling with painstiffynes.” I assume they would want me to elaborate on the word with examples, so I already know my response: “It makes me grumpy.” Then I would probably laugh. 🙂 But it’s true–this morning I was grumpy and still God found me. Listing everything already going wrong or not working properly…like my hands, this hymn came to mind:

Count your blessings, name them one by one,
Count your blessings, see what God hath done!
Count your blessings, name them one by one,
And it will surprise you what the Lord hath done.

“Count Your Blessings.” Words by Johnson Oatman, Jr.

And I found myself literally asking, “How do I count my blessings?” Because I felt overwhelmed, to see past my painstiffyness for a moment and breathe in the reality of blessedness. You see, this past weekend was physically not the greatest, though from the outer sense, a person would never know. However, it was also a very fantastically fun weekend; I think God knew that I needed the balance. Yet as evening approached last night, fatigue and frustration set in my body. I found myself, yet again, using the bathroom and after I washed my hands, I just stood there in front of the mirror. Then started crying.

I’ve been so emotional as of late anyway, but last night, I finally had a chat with God. I said, “I need help.” At least that was my first sentence. It is hard for me to admit that I need help; admitting that to God was a first step in the full dependence and trust He desires me to have, to seek.

It’s a beginning…and I think that is why He wanted me to see past my woes, my paistiffyness and count my blessings. Because it keeps me focused on His Goodness.

3 Comments

Filed under Uncategorized

Letters on the Wall

It was my sophomore year of college that my hearing rapidly declined in the right ear at the beginning of the Spring semester. I was ordered a hearing test and having been a while since I had one last, I met my new audiologist. He was deaf, had cochlear implants in both ears and wore hearing aids. His assistant ran the tests.

As the “press-the-button-when-you-hear-the-beep” test started, I found myself in tears. A little embarrassed as the audiologist enters, I start to apologize and he kindly interrupts: “There is no pass or fail in this test…” It is the best medical advice I have ever received and I think in part that in coming from him, being deaf and knowing first-hand, made it not seem like a fake sentiment.

I’ve repeated that sentence to myself many times: at my last ever audiology appointment, where I beard nothing in the left ear; when doctors do the strength tests, “Don’t let me squeeze your fingers together” or watch me walk the hall. And the most recent: visual field tests and the letter chart on the wall. I suppose if I grew up playing Nintendo, I would find visual field tests more fun; I find holding the test button just as hard as trying to keep my eye focused on the orange light spotted in the middle of what my eye views.

I know my right eye has decreased since June, but it wasn’t until yesterday when I was reading the shown letter on the mirror on the wall that I realized how much I have been letting it slack. I know the greyness and bind spots are not cause of my slackness, but I am supposed to try to keep my eyes fixed straight ahead as possible and I have not–I am letting my right eye be lazy. Even if I were doing a better job at keeping it straight, my reading has still been effected greatly. My eye used to be near 20/20. Now I can read “E” and “HB”…then I start squinting. It’s not fair really–who puts “DO” together? 😉

My left eye has always been one for frustrations in this test, so no initial shock when I start squinting too after the annual, “HB.” The assistant shows a new slide, where I see an “A.” I think capital “A’s”are pretty distinct. But I am also seeing a large “O” that is heavier outlined on the bottom than by the pointy tip of the “A.” No pass or fail, I remark, “I know this is serious and I shouldn’t be joking around, but this looks like a baby penguin’s face.” Because it did! I had already talked aloud that it was either an “A” or an “O,” so at least they knew I was trying. I was half right,”DOAF.” Good grief. 🙂

The surgeon and his assistant come in and mostly talk to my Mom as I have been going without my glasses (they make me dizzy sick.) I get a few clues from hand motions: they were chatting about my leg, last year’s blood clot and my eye. Later the assistant fills me in: basically, the infection needs to heal, as they don’t want it entering the blood stream and getting to the eye. There is also the fact that I am on blood thinner pills. It was not an issue for the cataract surgery. However, for this right eye surgery, I have to follow the procedures of preparing for the surgery and change from pills back to the shots, until pills again in post-surgery. My doctor will regulate this, as they also don’t want me to get another blood clot.

The surgeon is hoping maybe the end of next week, but there are no certainties. And as I started to immediately try to plan and think of all the details of money and insurance and other family member’s upcoming appointments, Mom just tells me not to worry…I do’t have to worry.

It’s a reminder, like “No pass or fail in this test…” that I must believe.

5 Comments

Filed under Uncategorized

Infested

It all started Tuesday night a month ago, when I bumped my leg getting out of the shower, in which caused a deep gash on my left shin. A little background information might help explain the situation: It wasn’t my first time hitting my leg on the bathtub sides. In fact, both shins were already portraying an array of nicely blended shades of black and blue that had already been there for some time, due to the longer healing process in taking blood thinner pills. Add the delicacy of the skin, due to long-term use of steroids and complete numbness in the left leg, often I don’t know where most of my bruises come from–except the ones on the front shins.

I often think that I am un-observant. Or maybe things get so routine that it just doesn’t phase the mind that something is different. Such is the case on that day when I was exiting the bathtub. My bathtub already has higher-than-normal siding, not making it as an excuse, but my legs just can’t quite ever make it over the hurdles of a bathtub without contact, unless I am making a “leap in the air” look…which I am sure looks different in my mind than real life. I never ran track. Or hurdles.

My leg that day hit the rim, but I didn’t notice…actually, because it hit the heaviest portion of the bruises, I can’t even remember feeling it. It wasn’t until I noted scarlet red all over my new bathmat that I realized I had been wounded. Good thing I hadn’t ventured off the bathmat yet. I couldn’t reach the ever-present band-aid supply in my counter drawers by the sink, so I made myself presentable for assistance and then pushed my Lifeline button.

After several boxes of large band aids and keeping the wound as cleaned and protected as possible, it still was not healing properly. When I went to Children’s last week, doctors looked at the wound and my ankle as a redness and swelling of the skin under the actual gash had started. We set an appointment to see the Wound Team on September 9th, went to Cleveland for the weekend and started the new week. Then came Tuesday evening.

It hadn’t been until Tuesday that the redness and lower swelled ankle really started to hurt. That evening as Dad was helping me, he was carefully wiping the area with a warm washcloth before applying the new band-aid on the actual wound; it felt like pins and needles!! The next day was no better and by Thursday morning, Mom called my Nurse Practitioner at Children’s. I was just ending my early morning Skype chat with my friend when Mom comes in with a note saying that Children’s wanted me to their ER as soon as we could get there–more along the hopefulness that we could figure out the leg problem and still get me to my CEI appointment by 2:30. Like a two-in-one day. It’s not possible.

Already being set to go for the day, I just quickly put on my shoes, grab the rest of my half-eaten apple and a Fiber One streusel bar while Mom fills my Tervis with my morning coffee. Off we go. At the ER, we get into a room…do some waiting, watch an episode of Bonanza, talk with a few different doctors, more waiting and I fall asleep in my chair. Mom had already called CEI and explained the situation, and they kindly rescheduled my appointment to the following day (yesterday.)

It is in these situations that you learn patience; after much waiting, I got the ultrasound done one my left leg to ensure there was no blood clot problems. The good news is that there is no blood clot problems! 🙂 What the results show is that it is Cellulitis. It’s a skin infection. Germs, even the tiniest, enter through the wound and start to spread as an infection: infested…seems so gross. It’s not like I wasn’t keeping my hygiene or things like this, it just happened. But getting the proper antibiotics now will, in hopes, keep it from continuing to spread. It can get into the blood stream or the bones and that is something not wanted or needed at the moment!

Please pray this infection heals enough by next week, as timing of the eye surgery is mostly dependent on this…

9 Comments

Filed under Adjusting to NF2, Hospital Trips, Uncategorized

Privacy, Patience, Public Restrooms

Don’t worry, this post is still G-rated, but the more I thought about how to go about this, the more I wanted to give you a better understanding of what a day in the life of Mel can present. Not that I am special; I just require a new format of special needs in certain areas of daily life.

I’ve talked about things before, especially during last Fall’s sessions of Occupational Therapy. A few: I have fancy big pens I use for “writing,” special handles on my silverware, plastic tableware to eat from rather than heavy plates and bowls, reusable straws to help when I drink, a shower chair and Dad attached a new, secure handle for me when I get in and out of the shower.

Out of all the additions, there is one–probably most significant–that I neglected in thankfulness and took for granted. Until I could not physically function on my own. Truly, if it were not this past weekend’s experience, I would still be living in the same denial of this helping hand: raised handles on my toilet seat.

It’s like anywhere else I sit–the couch, kitchen table or ca seat, I cannot physically stand without the use of my upper body and arms pushing against something. My legs and ankles are on the down-slide, but the fact I still get out of bed on my own each day is a miracle in itself.

So this past weekend, I find myself in a predicament: the toilet is too low to the floor and is next to the bathtub, unlike most others where it is near a wall or the sink/counter. The tub is about the same height at the toilet…too low to push from and my walker handles are too high. I am stuck. Humiliating and humbling, every time that I used the restroom, either my Mom or sister had to help me stand.

You know, I’ve been to Greece. At Phillipi, most of the ruins were still in good form: doors, stairs and walls of the First-century era. The main city entry and stone are original, making it slippery. We saw the amphitheater, the gladiator entries, and the hole in the ground that they termed as a prison. And we saw the public restrooms–

Greece0082

We’ve come a long way from this picture–much to be thankful for in privacy and patience. But this is what my life with NF2 is becoming: a special need that could one day require more assistance apart from my family’s helping hands. For now, there are no words I can express to my family for their sacrifices in those needs; and there are no words I can express to God for providing in those needs. It is learning humbleness, that I see the Love of God shine in others…and it’s contagious.

2 Comments

Filed under Adjusting to NF2, Family Times, Uncategorized

Being Heard

Over the past few months, I have noticed that when I speak, often it is not heard and ignored (unintentional.) There are other times when I am speaking and a family member will tell me, “I can’t hear you.” There are moments of patience and restating what I just said in hopefully louder voice and then there are the moments of frustration (pure annoyance from the, “I can’t hear you” phrase) in which I snap back, “Then why don’t you try reading my lips!” It’s not like I can hear loud or soft voices…step into my world, is what I am thinking.

My world once had voice; in fact, Mom often tells people that when I would sing as a little girl, I had a voice like an angel. We lived near Toledo until I was six, in during that time, I sang Honeytree songs at church and was Mother Goose in our Kindergarten play. When we moved to Colorado, I focused my stage career on the church plays, as it had both music and acting. I loved the memorization of lines and songs. My last performance was during my fourth grade year. I was the lead role of a tom-girl named, Morph. During my opening song, my voice cracked. I had hoped no one had noticed, but as I gazed out into the audience, I caught Megan’s eye and we both knew in facial expression. I had to look away to keep from laughing…concentration!

I entered junior high with a still changing voice. Not in any bully fashion, but I often got asked in the “You sound weird,” tone why my voice sounded funny. “I don’t know,” I had to say…because I didn’t and often I wanted to tell my family that too when they would state that I needed to relax my voice. Ironic, I could hear the pitches of my flute and piccolo, but not my own voice.

Although it would sometimes eat my self-esteem, it never stopped me from singing or talking. Half in love, I sang my boy-band songs so much at home, I was often told to switch the CD to something different. I only got into trouble in school twice: the first was in the 2nd grade. My “best friend,” Stephanie, and I were talking when we were suppose to be solving our math problem. Mrs. Brumfield wrote our names on the board and we missed recess that day. The next time it was Mrs. Baron’s computer class, in which we just typed (read and copied exercises.) Maybe Mrs.Baron didn’t know boring this could be day after day or the fact that Tasha and I were pretty much inseparable at the time…regardless, we were seated next to each other facing the library windows. Yes, between regular chit-chat and mouthing motions to passing friends out the windows, it didn’t take long for Mrs. Baron to move me across the room to face the wall.

When I reached high school, the aspect of my voice and hearing made sense. I no longer took stage to sing, act or play the flute–but there was just one more acting performance that I took part in, and I didn’t even have to audition. And there was no audience…well, maybe the FedEx deliverer counts? Yes, the height of my career…the big grand finale, our own Hollywood in the making–

The Three Musketeers

I’ll give you three seconds to control your outbursts of laughter…3, 2, 1.

And this is just a picture; the movies are none to compare with, except maybe the real Lord of the Rings trilogy. If you hadn’t noticed, that is me with the home-made (and most itchy) hat and neon looking beard. I was cast as the “talk at the wrong moment,” lover of roasted pork and ale, but tough as a nail in battle–the stubborn Dwarf, Gimli. We filmed all our favorite scenes across our property the entire day. By the end, my voice hurt, because not only did I have to try to talk loud over the wind, but also, I had to change it to a deeper tone. Some sacrifices are worth the finished product. 🙂

The adult world didn’t ask about my funny voice, but expressed concern: “Do you have laryngitis?” they would ask as they pointed to their throat. If I ever got bored at work, I could have just started a mental tally of how many times I got asked during my shift. Why does voice matter so anyway?

I know for my doctor, this was a concern. He noticed my softness right away…things have changed since I saw him in February. I too have noticed the changes in my face, but maybe have not realized how significant they may truly be. As we continued our discussing of numbness in the face and hands, it dawns on me, like everything else effected by the pressed nerves: “Can your vocal cords go numb?” My doctor said it could be a possibility.

And so I have a quiet voice. Sometimes that is a blessings, sometimes I desire to be heard; but if I am living a life full of praise, my actions will speak louder than words.

I think that all of us have a responsibility to sing the songs as though this is our last day on earth. And we have a responsibility to live them out. Because when we sing and live together like this, uniting as one voice, it can literally shake nations.

Martin Smith, lead singer of Delirious?

7 Comments

Filed under Uncategorized

In a few words…

Normally, I like to give my MRI results in a full detailed account. However,in thinking of last week, the past few weeks, the past few months of complexity–I just want to tell you simple. In a few words…

My parents told me the results before my eye appointment, because I would be seeing my neuro-ophthalmologist and would need to discuss my questions and tell of my changes in the right eye vision. I suppose too, my parents wanted to tell me themselves and not have it come to me as a shock or surprise. It didn’t. “I saw this coming,” I told them. And even though it didn’t make it any easier, the fact that I knew in gut-feeling that my scans would reveal something, somehow made it easier to comprehend.

“There’s good news and bad news,” Dad begins. The good news: MRI of the spine showed stable. That is good news; although I have had more weakness in my legs, I probably would have been shocked if there was growth, because the lower half of my body (besides intense bruising on the legs from bumping into things) has not been a problem.

The bad news is that most of the tumors (besides the ones on the acoustic nerves, which wouldn’t matter to me since I am deaf already anyway) have grown…some significantly, some in areas by the skull that are likely causing pressure and the effects seen in my curling right hand, weaker left hand and numbness in the face/neck area adding to the choking, chewing and voice changes too.

These changes are slower, more “normal” to me to adapt to in everyday as compared to the right eye vision. The scans showed that there is a tumor growing next to the right optic nerve. “I am trying to see God’s goodness in all this,” I type to my best friend. At the time, I didn’t see it, but now I catch a glimpse…the fact that the tumor is next to the nerve and not on the nerve, is goodness.

This is what has been causing the grey veil and blind spots in the right eye. I don’t know much about eyes–I truly regret not taking Anatomy in high school or college, but there’s nothing I can do about that now; so I learn from my physical woes. I was told that your optic nerve is protected by a sheath, in which my right sheath is very swollen (thus pressure on the nerve.) I meet a surgeon on Thursday to discuss the surgery to release that pressure in hopes it helps the vision.

That is my last and only option. For the remaining tumors, I have no treatment options. “Your tumors will continue to grow,” my doctor tells me. We have had the discussion several times and I know that he and the rest of the team of my physicians feel helpless in the situation. He expresses his concerns on my current physical state and then asks, “What can we do to help, for you and your family?” Minutes before, I had just been in a state of tears and floods of emotions. Without a moment’s hesitation, I reply, “Well, you can start by getting me a limo and a personal chauffeur. That would help my Mom.” It made for good laughs; it released pressure.

I have not been abandoned though–I do have one more option: “Do you trust Me?” As I sat at the kitchen table that night with my parents, I started asking my questions as if I had already gone blind. My biggest was communication: I’m already deaf and couldn’t learn braille with my hands being so numb–was what I reasoned. How will we do this? Dad gets up and comes to my chair, gives me a bug hug and says, “Like this.”

It’s the picture of trust…”Do you trust Me?” Because in good news or bad news, God holds me.

Hold me Jesus ’cause I’m shaking like a leaf

You have been King of my glory

Won’t You  be my Prince of Peace

~Rich Mullins

9 Comments

Filed under Adjusting to NF2, Hospital Trips, Uncategorized

The Blob

Yesterday had me feeling like a blob. There’s nothing worse than feeling like a blob–I had entered the room with great defense, but left like a weak and helpless one. Being a blob in your mind will have you wallow in this way. I put my brain on mental stand-by as we made our way to the car and dozed while Mom and Dad made their way in construction and traffic to the nearest Cracker Barrel.

Comfort food, I started to regain composure. I can’t say it was back to Mel, but I was trying, although I just wanted to be home. That was comfort. At home I make tea and start a new book on the library app that I have downloaded on my Nook. A black background and white words. It’s like a photo negative effect and I read the text so clearly.

It reflected my day completely. My inner blob was my defense. Turn the room of people around like viewing from a negative in the light: and see the defense signs from the bleachers, from loved ones in the crowd; those around cheering me on, those around working ideas to keep me going, those around hindering my path that leads to the blob.

The Blob. It’s pain, suffering, confusion, justification, frustration and fear, selfishness and comfort, unfocused purpose. It’s the complete negative (literal meaning) of the Fruit of the Spirit.

The blob in me comes and goes as I embrace the newness of realty: “Man is like a breath; his days are like a passing shadow,” Psalm 144:4. It is not easy lowering your defenses..but it is not a weakness either. In living, I am learning this…

3 Comments

Filed under Adjusting to NF2, Uncategorized

Secret Codes

When we were little, my sisters and I played “Spy.” If you have never been associated with this game, allow me to explain. It all begins with a sheet of wide-ruled paper and a wooden No. 2 pencil that was usually used for math class, hence, it lacks the eraser. After spending half of your spy time by creating a detailed floor plan of the downstairs areas, especially the kitchen, the game has now begun.

It’s a parallel to hide-and-seek with follow-the-leader. The objective is to pinpoint the non-playing family members and spy on them without being seen or heard. Melissa, being the eldest and cunning, always seemed to end the spying eye on her at first notice; Mom just played along, even when we giggled or accidentally moved the table chairs while trying to knee past them on the tile floor. It was the era of Carmen Sandiego and our games of Spy just happened to help us solve our curiosity mysteries.

Fast forward to junior high days–it was in these days that I learned two fundamental traits that would guide me as I started losing my hearing in the end of eighth grade: sign language and lip-reading. I first learned sign language from Melissa my sixth grade year, as she had learned a song at summer camp. That next summer meant that I was old enough to attend church camp as well, but I did not take the signing class–my friends did, however, and that year I learned, “I Can Only Imagine.” My junior year of high school, I took a community ASL class with my Dad; I had been self-teaching myself from a few signing books I purchased at the local college, but the course helped increase my vocabulary.

Until my lip-reading rehabilitation course during my first rounds of radiation in 2002, I never realized how much I was already reading. I sometimes get asked when I first started, and I honestly don’t know. I do remember once getting a talk from Mom after getting into trouble, in which I read her lips…but I always thought that may have resulted from a guilty conscience rather than hearing loss. 🙂

We may have no longer played our games of Spy, but we sisters developed in the junior high years a code. A secret code, and we would relay this message to each other in our times of need: SPR!! Yes, these three letters were part of the foundation to my lip-reading career. Best part was that we could say them to each other from across the dining room table or Sunday School room. The message was simple, so loud and clear: Secret Private Room. It usually was the closet, but some of our best secrets and cases solved were a result of the SPR!

Fast forward to the present day: I no longer play Spy or hold SPR meetings in my closet, but I do enjoy the game of CLUE. My college roommate and friend from Denver days surprised me with a visit on the weekend of the art show! Considering my past history in solving mysteries, one would think I would have not been so confused at the situation, when Callista taps my shoulder and I look up to see her smiley face. I was at the kitchen table reading, so I had my glasses off; Mom had just been discussing the new neighbors, resulting in my next sentence understanding of who I portray Callista to be in my mind: “You look like my roommate from college.” The lip-reading, because in my mind I know it is Calista, but I think it’s the new neighbor–it just threw me off completely.

“Hold on a sec and let me get my glasses on,” thinking of how I don’t like new introductions as I am terrible at names. I turn back around, see Kate and glance back at Callista. “What are you doing here?” It finally settles in–yes, these are my friends and they came to see me. 🙂 Later that night, we played CLUE. My hand of cards was not the greatest. I had all characters and two rooms, no weapon options. We play a few rounds and I had two characters left–still no weapons marked and only one room (besides my own) marked off the choices. Deciding to subject my own character to checks and balances, I place him in the nearest room and random grab a choice weapon.

“I think it is Mr. Plumb, in the kitchen with a candlestick.” Kate had no cards, Callista had no cards; they look at me like I am pure genius. “It was just a guess,” I had to assure them. Back came the conversations of Carmen Sandiego and I mentioned the show Sue Thomas, F.B.I.–inspired by the true story of Sue Thomas, who solved crimes by lip-reading: a deaf F.B.I. agent.

I must have been inspired by all these memories when it came to Monday’s MRI. Being an older, complicated body patient, my scans usually get scheduled for the last of the day. Monday was no exception. I was to report by 5pm for the preparations (which is translated as paperwork and questions); the scans starting at 5:30. I am comfortable with the long scans–usually they are my nap time when scheduled for earlier in the day. With this scan scheduled late, I knew if I napped, I would not sleep when I got home. Selecting my movie, I toyed with the Lord of the Rings, but once I start one–I must watch them ALL. To escape this, I selected Star Wars V: The Empire Strikes Back.

They get me settled in with the head-gear, strap my arms in, blanket and knee lifter; I am all ready for the scan and movie, although the goggles pressed hard into my nose. The opening overture and text starts–I find that looking at the screen with my left eye is actually blurred. So I allow that eye a break, close it, and view the movie from my right…aside from color differences, I saw things pretty normal considering its condition.

We’re still the beginning parts of the movie: Rebel forces are fighting the Empire on the ice planet Hoth and aside from that action, there are a few scenes with Darth Vader and his top commanders on his spaceship. It was right at the moment when the light, snowy planet Hoth gets cut off to the scene of the darkness of the spaceship that I am thinking I am seeing a secret code! You’ve heard of it before–movies will flash messages to the audience: “Buy popcorn.” Or something to that extent.

As the camera zooms in on the outer of the spaceship, I am seeing words, in what I think is the little lights from the inner of the spaceship. All excited, I start squinting to decipher the code, thinking, “Wow. My right eye problems give me a chance to see things different!” I start to see it is in sentences:

“This movie is 2 and a half hours long….” It goes on to tell me that it is not good for my eyes and that I should shut it off and sleep. But just in case I still wanted to view the movie,”Press [*].” So much for codes-Luke hadn’t even gone to Dagobah to find Yoda yet and it wants me to sleep! Thinking that my eye had recently gained some sort of cool lens power made me laugh.

In life, there are secrets and mysteries. Some will be revealed, some will not. Instead of solving them, I am learning to live in them.

Call to me and I will answer you, and will tell you great and hidden things that you have not known.

Jeremiah 33:3

3 Comments

Filed under Adjusting to NF2, Books and Movies, Family Times, Funny Stories, Hospital Trips, Uncategorized