Category Archives: Family Times

Driving: Take Two

Yesterday started out like any other typical “It is an important day today!” —

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Let’s just throw out the fact that it was a Monday.

Yep, the day in which I was to complete part two of my driving evaluation tests could not have started out with any better of the typical important day fashion: sleeping past my alarm and Mom waking me up fifteen minutes before we had to leave. Her ever-calm assurance in these situations met my panic mode as I stumbled out of bed and started going through my morning list of important things I had to do (let alone getting somewhat presentable for the day): feed Muffy, take medicines, etc. “And I need coffee.” Mom said she would make sure Muffy is fed and start some coffee.

Only a few minutes past when we had to leave–with fresh coffee and an apple for breakfast–I get in the car and feel like I can finally catch my breath and looked forward to getting the test over and done! It amazes me that something like this can consume your mind. I do not have a problem with my driving–and yet when doctors first ordered the evaluation back in August, all of a sudden the restriction caused me to doubt my driving–so much that I was having dreams of being in accidents. After the first evaluation September 19th (even though I passed), I still had restrictions until I took this second part. I was able to practice in empty parking lots, which boosted confidence, but it is not a main road.

Feeling confident, I sign in and a few minutes later head out the door with the PT to the Student Driver car. I have only driven one of these official cars once for Driver’s Ed class…that was ten years ago. My instructor (who was also my history/government teacher) must have trusted his students as for our actual driving license test, we could choose between the Student Driver car or one that we had that we were more comfortable driving. I chose the latter of the two options…nothing compares to our family’s 1987 Honda Accord. It is like an heirloom. It witnessed at least thirteen years of high school drama from the parking lot between me and my sisters. Pretty classy!

Anyway, I would have felt more comfortable in my own car (logically), but since it was not a possibility in this situation, I tried my best to adjust to the Student Driver car even though there were many things very different from my car. I found my biggest frustrations being their steering wheel having these huge box-like attachments right above the “9” and “3” area..which is usually where I place my hands. (Note that this test was caused by the concern of my hand function in the first place, so the scenario didn’t suit well.) I also had a problem with the side view mirrors not having the small blind-view mirrors. (Those have saved me from numerous episodes of changing lane woes and proved so when I was doing some reverse exercises with cones in the parking lot.)

We finally get to driving around in a very pretty residential area–being fully determined not to mess with my chances of the evaluation, I kept my focus. Once we determined that the motion for “keep going straight” involved two hands (better clarification), I meandered, slowly, through the neighborhood. When we finished and headed back, the PT asked me how I felt about the driving and I told her my honest opinion (seeing no problems). Never assume a professional PT sees your driving the same way. As we met to discuss the results with my Mom, the PT explains her two things that she sees as a concern (which I do not see in context of the driving experience how they fit in properly to what I thought was the main concern : the grip and strength of my hands!) As soon as I figure out that I still do not have the official okay to drive and that I must return one more time, I bluntly express my point of view in one short sentence. I set up my next drive for the 21st and cry in the elevator–expressing my frustrations to my Mom. There are some things I just do not understand and what they want to see in these evaluations from me is what I do not understand.

There was good in the morning though…I can drive normally in my car as long as one of my parents is with me. Talk about feeling like being back in high school, but I am very thankful for this outcome (even if it is still an inconvenience to our schedules.) By driving  the roads, I can now get back to feeling like a normal driver and hope I spend less time dreaming doubts and trusting that God can use this time to help me gain more confidence as yesterday was my first time “on the road” since August.

But yesterday I also felt my conscience tug at my heart over my attitude at the PT right before we left. I did not mean to bluntly express my opinion, but it came out. And I feel bad for it; I hope I did not ruin her day. I am sure it was just as awkward and maybe frustrating for her to navigate a deaf person around a neighborhood and through cones in a parking lot. In my childish actions in response to the PT’s professional opinion, I see how wrong I was and asked God to forgive me.  Taking my driving evaluation as a lesson: These are events that I  cannot go back and change, but instead, learn from it and set out focusing on doing better next time.

Let no corrupting talk come out of your mouths, but only such as is good for building up, as fits the occasion, that it may give grace to those who hear.” ~Ephesians 4:29

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

Homecoming: thoughts of heaven

This weekend was Homecoming Weekend for the university in town. Although it meant nothing to me (besides a fun parade and getting pumpkin chai with my sister afterwards), there were many class reunions during the weekend where the alumni had returned to their Alma Mater to celebrate their years of attendance and also seeing the vision of the school continue through the current students. This year was also special as it was the coronation of the new university President.

Homecoming is coming home. Ok, so maybe college is not home…nor your high school, but when you are saying “homecoming,” it is the welcoming back notion. I have to admit though, when I was in college, my term for “coming home” literally meant calling Mom and saying, “I am coming home.” Home. My mind has been thinking about this word…I think I started when we took a little weekend road trip to Toledo.

After my mom remarried, we moved to Toledo. I was about a year and a half old or so. We moved to Colorado a few months after I turned six years old; my first memories of a “home” were from there. As we visited a few weeks ago, I realized that all my memories of Toledo were of places, such as the tunnel you walked through under the main road to get to the zoo; the Bob Evans we passed to get to our house; the house itself (I can still see the inside); the church we attended (but when we actually attended church I noted how much smaller the sanctuary was compared to my five-year old mind); MacQueens Produce Farm and a really awesome ice cream place by car lot (which I finally got the name: Jan’s.) I remember things like my classroom at school, getting red tokens for lunch when you wanted pizza, learning the alphabet, and being Mother Goose in the end of the school year play. I remember singing a Honey Tree song for church and playing in the turtle sandbox or eating orange pushups. But what I don’t place is people’s faces. I only remember them through pictures.

All that changed in Colorado. We moved in the summer, meaning I started a brand new school that Fall. The kids in my class were the peers I attended the rest of my school years with, graduating together and continuing to keep in touch here and there (thank you Facebook.) Home was no longer just things or places…it involved people from town, school and church. Home, physically, was the house…a place where I could be myself, protected from the world. In the bigger picture, Colorado was home. I still consider it home. It is my Alma Mater.

Don’t get me wrong, I believe God moved me here for a purpose…especially in the area concerning my health. I now have friends, live closer to my extended family, a “home” church I have attended since the move and many open doors for my paintings. So why doesn’t it feel like home? Time may play a part in it: we lived in Colorado for almost twenty years (seventeen to be exact). Whatever the cause, I think it fits into the season of the soul..this current road I travel, with thankfulness.

Home brings thoughts of heaven. As my body continues to decline, [yet I am still becoming all that God has planned for me in this life] there are times when I do honestly question God in aspect, “I don’t know how much more of this I can handle.” Maybe I am using thoughts of heaven as an easy way out of this worldly suffering. Heaven is joy…and I look forward to that Homecoming. There will be nothing like it in comparison. But here, in the now, I should not be praying centered around myself, but God. It is only then that this temporary home (my body) will find strength in thanksgiving, even in the suffering:

Man-centered prayers tend to ask, “How can God help me with my problems?” while God-centered prayers consider, “What is God doing in this? How can I join in God’s purposes here?” This changes not only what we pray for, but also the way we pray.

Tim Challies. “Persevere in Prayer.”

Philippians 4:4-7

~Mel 🙂

*http://www.challies.com/articles/persevere-in-prayer?utm_source=feedblitz&utm_medium=FeedBlitzEmail&utm_content=5575&utm_campaign=Four-hourly_2013-10-02+12%3a15

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Like Plain English

I have never been a Shakespeare fanatic. Mostly because I never understood the language of his plays. In high school, I read and watched a few plays (movies) in English class and did the homework discussion questions but always seemed to grasp the scenes differently than others in the class.

“So what is going on in this scene here?” Or, “What does this character mean when he says this?” I would sit and hope that I would not be chosen. I didn’t want anyone to think that I was not understanding.

Don’t get me wrong, I didn’t have this problem all the time–only when discussing Shakespeare or poetry (like his Sonnets.) I love books, English class, creative writing and diagramming sentences. However, if I made a list of my favorite classic authors of all time, Shakespeare would not be in the top five. But I have discovered something that is helping me appreciate the works of Shakespeare. It is called, “plain English language.”

Barnes and Nobles could just very well be what I consider a great hangout place. It is almost like a huge library where you have freedom to chat and walk around with your coffee. I often go in to the local store just to look around at the bargain books, read a few children books and see what is newly released. In this meandering a few months ago, I headed towards the playwright section. Mom and I had watched James Stewart’s old film, Harvey, and I knew it was based on the play of the same name by Mary Chase. I wanted to see if there was a copy of the original play. There wasn’t, but I found the play Our Town, by Thorton Wilder, and skimmed through the text remembering seeing the play in the Creede Repertory Theatre and crying during the final scene. Excellent play.

What fascinated me the most in this section was the amount of Shakespeare plays available. I think all (even his Sonnets) were on the shelf. I didn’t bother to skim through them, but picked up this instead:

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It is genius! This morning I sat at Beans-n-Cream sipping my Pumpkin & Spice coffee and found that I was not only enjoying the play, but understanding the play. Shakespeare is on the left page–plain English translation is on the right page. Maybe this is considered a “cheat sheet,” but in my opinion…if it allows me to understand the text of someone who is considered to be one of the greatest writers in the English language, then it is worth the modern translation.

My everyday conversations can parallel much to that of a Shakespeare play. As much as I do my best to lip read, words and phrases constantly get mixed up; I miss context or transition clues to next conversation; and I sometimes just say, “I have idea what you’re talking about.” Lately, if it really important– after attempting fingerspelling, but obvious that I still am missing one or two words–my parents will write it down. Like plain English and I understand.

When it comes to translation in communication, I think I use a lot of different methods: sign language interpreters, text messages, closed captions on television or movies, and a Captel service when talking on the telephone. After my hearing dropped and I returned the Phonak Cros, I decided a better investment would be a Cap Tel landline phone. Up until this point, I have been using an internet caption service through Sprint. It was free and accessibly convenient in college. But it is getting more inconvenient: To make a phone call, I would have to start my computer, get on the site, log in, put my number in and then the person’s number who is receiving the call, press enter, wait for Sprint Cap Tel to call me, press send and finally be set up for the conversation.

It is not like a TTY or landline phone where captions are fast, accurate and promising not to cut out of a conversation. (Believe me, many times during chats with credit card companies gets frustrating as you never get the same representative.) I will say that I found humor though…because the captions are based on voice recognition, there were many laughable “read between the line” moments. I can relate–happens to me in real life daily.

But these woes are no longer my concern. I am now the owner of a Cap Tel captioned phone!!!

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It works fantastic and I finally understand the whole phone conversation! It provides accuracy and convenience (especially safety for emergency phone calls). On the bottom of the screen there are little boxes…the left is mine and the right is the person I am calling. When talking, the box flashes, so I know when to listen and when they are done speaking. My box flashes too, and st often in red, which means I am talking too loud. Ironic, since most of the time people say I talk too quiet. This phone allows me to receive calls, make my own appointments, and best of all-talk to my grandparents (as well as other family and friends.) Out of all the new accommodations made recently and still to come–this is placed in the top five favorites, perhaps even as number one.

Most people do not listen with the intent to understand; they listen with the intent to reply. ~Stephen R. Covey

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The Great Smoky Mountains

This past weekend my family and I ventured down to Tennessee for record-breaking short, fun-filled family reunion in the Great Smoky Mountain National Park. We stayed in Gatlinburg–a charming but busy tourist town full of souvenir shops and pancake diners (we enjoyed Flapjacks Monday morning!) It is no wonder that Gatlinburg is so popular as it sits right on the entrance to the park.

We filled our weekend with the beauty of the area…scenic drives in the mossy forests full of dense greens and streams of water; the mountain overlook areas; the ancient Cherokee history and the Trail of Tears; pre-Civil War life and the dedication of the National Park by President Franklin Roosevelt. (I found the history of the area, especially Cades Cove to be fascinating!)

Of course no family reunion is complete without lots of pictures, games, laughs, family meals (yes, pizza at 10 pm! and my aunt’s scrumptious lasagna), fresh coffee, good conversations, helping hands, and love.

“Family is one of nature’s masterpieces.” –George Santayana
I quite agree.

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Marcia and I standing by the “Thousand Tears” waterfall.

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Me and Grandpa ❤

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When my actions eat my words…

A few weeks ago I made a short trip to the grocery store after church. Because the previous time I had fallen coming in the entrance when my right foot caught the corner of the rug, I came prepared that next trip by using my cane. I went along with my shopping–cane in one arm, basket in the other. When I filled my basket of fresh produce, I got in line to pay.  I am already slow at getting out my payment from my wallet but try not to get flustered at the line behind me; this particular day I was also trying to keep hold of my cane while paying.

At the last-minute or so, my cane falls to the floor. I had to firmly grasp the awkward paying counter ledge to maintain balance while bending over to try to grab the cane. As I regain balance and the cane, I come up to a standing position to see the lady in line behind me just watching. I say thank you to the cashier, grab my bag and head out to my car, replaying the scene over in my mind. I was so taken back that no one offered a helping hand. The polite gesture, in my mind, would have been to at least an offer to help–even if I was not using a cane, thus labeling me as “handicap”–it could be just offering help if I had dropped my purse and everything fell out. I dwelled on this event for a few days and told my doctors, “If I was the other person, I would have at least asked if they needed help.”

Today’s actions made me eat my words. Since my grandpa is visiting, we went to the state park for a picnic lunch then went to Young’s Jersey Dairy for ice cream. I was talking to Marcia on the way in the first door when I notice an elderly lady using a walker coming out the other double door. I even paused for a second to watch but she seemed to get to the exit door and from what I assumed could push it open. I should never assume these things; even with a cane it is awkward to get doors open–I can’t imagine using a walker in this case.

I get inside and turn around to see my Mom and Grandpa making their way to the other door. It is then that I get this sick-stomach-guilty feeling…I had just done the same to this lady as what had happened to me at the grocery store. I did not even offer a helping hand. I just paused, and turned away.

I should not dwell on my own misfortunes, but how I can help the misfortunes of others.

Jesus: “Which of these three, do you think, proved to be a neighbor to the man who fell among the robbers?”

He said, “The one who showed him mercy.”

And Jesus said to him, “You go, and do likewise.”

Luke 10: 36-37

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Living in a Fast Paced World

At Tuesday’s doctor appointments, we discussed transferring me to a neuro rehab clinic for my Physical Therapy and Occupational Therapy. This is still in the future plans, but because I currently have a driving restriction until I take a driver’s mobility test (based off the way I am currently walking, just to ensure safety on my reaction times)–it could be up to three weeks until I get the test completed even though I am on the current waiting list. Because of this, I am not able to get myself over to the rehab facilities and since I have already started with Home Health, the plan for now is to let them finish their sessions and then I go on from that point. I have been pleased with my PT sessions so far.

My first session of PT was last week and I start OT next week, which I am anticipating, because today in getting ready my hands lost grip of my makeup bag–momentary sadness to shatter a perfectly good bronzer. Anyway, while last week’s PT session was mostly talk and the “see where you’re at” balance, strength and mobility tests, this week was a full 45 minute workout. I have had PT twice already: one after my first blood clot to strengthen my left leg and the second session this past Spring to strengthen my neck and upper back muscles.

I have never experienced a singe PT session that would literally leave me so exhausted that I had to take a nap in the afternoon. To demonstrate how weak my muscles are–picture me on my knees, lifting the exercise ball over my head (repeat 4 times). By the last, my arms were beat. We also did a lot of balance exercises where I lift one knee while on the other and then rolling the exercise ball back and forth while maintaining balance. To the average person, these may seem so easy, but to a person such as myself, it was difficult. To be honest, today I felt like a toddler…learning to balance and lift things, freely falling over and struggling to get up. But the strength and retraining my mind to use the muscles does not happen over night..it is baby steps. 🙂

Of course, I overdid myself this morning after my session. I went downstairs and painted a canvas that will be on display next week at a pizza parlor in Yellow Springs. (more to come on that!) I finished but had some extra paint and don’t like to waste it, so I set out to finish a small abstract one as well. No joke, the last few seconds of “finishing touches” on the painting and the table topples over!! Thankfully, the painting was not ruined, but for the cleanup process, I was back on my knees like my PT session and struggling to get everything picked up without making a bigger mess. By the end of my painting session, I looked like a painting. 😉

I had been to Michaels a few weeks ago to pick up paints and a pack of 8×10 canvases. At the check out isle there were some extra-large reusable bags and on an impulse decision, I bought one in order to carry my paintings around when they go on display in Beans-n-Cream or anywhere else. Artistically decorated, the front says the classic line, “Stop and smell the roses.” I thought of The Story of Ferdinand by Munro Leaf. Growing up, Ferdinand was different. While his peers were shaping up to be the best for bull fighting, Ferdinand just wants to smell flowers. Only when he sits on a bee does anyone take notice of him. At the bull arena, he is adorned with roses…everyone expects him to put in a good show, and he just wants to smell the flowers. 🙂

Too often I try to rush forward in my physical body, even though it is no longer capable of the word “hurry.” I forget to stop, breath in, smell the roses (sweetness of God’s mercy and grace) and realize that I don’t have to feel pressure to keep up with the fast paced world. God can use me just as I am…like a child.

They say that I can move the mountains
And send them crashing into the sea
They say that I can walk on water
If I would follow and believe
with faith like a child

Jars of Clay. “Like a Child.” Self-titled debut album. 1995.

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Two months ago…

Yesterday marked two months of taking the chemo therapy, Sirolimus. Seeming like we had just made the trip to Children’s Hospital in Cincinnati, Mom and I embarked on yet another early morning drive. (And that was sarcasm…we literally had done the same routine on Friday morning for my MRI.) The only differences were (1) traffic–yesterday reminded me of why I don’t miss city driving; and (2) Friday I could drink coffee on the drive down–I could yesterday but not until after my lab work was drawn. I am very thankful for my Mom’s driving as I would have never made it on my own yesterday morning.

Yesterday’s appointment covered a LOT of things. We discussed my walking and balance, PT and OT therapy, the need for ankle braces, driving and safety, better communication methods for me between the team of doctors, and a few fun things like my paintings. 🙂 My initial intent was, as always, to blog the details and keep you informed on the latest like a news anchor, but I don’t think that it is best to do that this time. Everything is changing and more appointments are appearing; I will just blog as it comes.

Tonight I begin with my MRI results: I went to the appointment with a neutral emotion. A few weeks ago, under frustration, my thoughts were that if the tumors had grown more in the brain, then I would just want to stop the chemo. I don’t know where the attitude changed, but I realized last week that I found myself thinking differently. I reasoned that maybe two months was not long enough time for the medicine to have a chance, so regardless of the MRI results, I was fine with continuing the treatments. However, I didn’t want to be a pessimist, but because I have experienced continuing downside side effects, especially in my right hand, balance and right ear, I assumed the scans would show growth.

I assumed wrong. The MRI showed stable in the brain. 🙂 I still could be experiencing hearing loss and physical side effects from the tumors but that is where it gets tricky, because MRI scans only show growth, not density (if the tumors harden they squeeze more on the nerve)…but since there is no way to calculate this, I will just take the good news: there was no change. What a praise and answer to prayer! Two months ago I saw nothing but growth.

Overall, the MRI of the spine looked stable too. I learned something though; instances such as this amaze me at how much I seem to miss…then when I learn about it, my curiosity comes out as a weird question, “I have that??” It seems to happen more often than not…I seriously should do more study on my disease. Anyway, what I learned yesterday is that the tumor that grows in the spinal cord from C-4 to C-7 area has cysts resting on top and on bottom of the tumor. I never knew this. While the tumor has not grown any nor the bottom cyst, there was more fluid in the cyst on top of the tumor. They don’t know where the extra fluid comes from, but the cyst now rests in the brainstem.

They showed me the scan and the top cyst appears to be “ballooning” from the extra fluid (it literally looks like one too). It took me time to understand this effect of the cysts being like balloons, but basically it is like holding a water balloon and squeezing one end so that the other gets bigger. I asked if the extra fluid could be from the tumors in the brain that were growing…just maybe added pressure, but doctors were not sure.

Besides the physical challenges I typically blog about, the thought occurred to me that because this cyst is now in my brainstem, I should probably have more headaches (but I don’t have any) and more neck pain but that is minimal too. I could have a big list of side effects from the chemo, but so far I have only experienced a minimal few. I will remain on the chemo for another two months, then another MRI. Then go from there.

As my parents helped me today with the phone calls for the next step appointments, I thought of how I am surrounded: I have a circle of doctors who want the best for me, a family that sacrifices their agendas for me, friends who encourage me, prayer warriors who faithfully pray for me, and a mighty God who holds me in His hands. Changes are going to come and I am not the best at shifting gears…but as my Mom told me tonight, “You have to be flexible with this.” So as the calendar starts to overflow with different appointments over the next few weeks, I think I should just drop my expectations of how and when things should be done and just let God write in the details. It will make this complicated chaos more livable.

May all your expectations be frustrated.

May all your plans be thwarted.

May all of your desires be withered into nothingness,

that you may experience the powerlessness and poverty of a child

and sing and dance

in the Love of God the Father, the Son and the Spirit.

~Blessing given to Henri Nouwen by his spiritual mentor

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Looking Upward

Over the weekend, I finally accomplished putting into chronological order and placing my college to present pictures in photo albums. It brought back many great memories. As I sorted, I found these pictures that made me laugh at the memory of the evening:

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During my years living in the Denver area, I lived in a neighborhood called Bel Mar. On the corner of Wadsworth and Alameda, this was the rising place for living and shopping. The Target I was employed at was about fifteen minutes from Bel Mar…connected to a flat mall that had an indoor mile track that ran its course around the stores. I enjoyed a mile walk on my lunch breaks. I think every mall should be modeled after that one.

Even though there were a few Target stores in the area, Bel Mar also built one a few months before I moved. It was one of the “new city” model styles where the parking garage was underneath on the “first floor,” making the actual retail store on the second floor, all of course equipped with escalators, a stairway, and an elevator. I opted for the escalators.

Mom came to Denver every other week to help me on my chemo weekends. After the grand opening of Target (we had watched it being built over time), I wanted to show her the inside of the new Target. Up until this point, I had only been in a few times, because it was more convenient for me just to get my needs and groceries from my Super Target rather than stop at another one on the way home. But with Mom, we had grabbed a few groceries and as we left, I made a discovery: they even had an escalator for your carts!!! I was laughing so hard, Mom was afraid I would fall down our own escalator. 🙂

Currently, I have recently developed a phobia of walking down the stairs. Going up the stairs is not a problem; just coming down. Too many falls in the past few months has triggered this phobia, but I can’t say that I had really classified it as a fear up until a few weeks ago when I mentioned it to a friend. Now I am not even sure if it is just the stairs I fear falling–I think it is falling in general.

With my balance continuing to worsen, I have now restarted Physical Therapy, but it takes place here at my house. Due to the decline of function in my hands (especially the right hand), I will also be starting soon some sessions of Occupational Therapy. The reason for having the sessions here at home is to help me with my everyday living. For example, because I started my first PT session last week, we did a huge overview of my current conditions and discussed the areas in which I need assistance. Most of my current frustrations deal in the realm of OT, but balance was a major issue for me in PT. She gave me a suggestion for going down the stairs sideways, but to be honest, it doesn’t make me feel any better about the decline. As for right now we are mainly focusing on extra balancing exercises to accompany the PT strengthening exercises I have been doing already.

To access my current conditions, my therapist had me perform some “strength and mobility” tests. I can only stand on one foot for a mere one or two seconds…and standing with one foot in front of the other depends on which foot is placed first. Considering I have had two blood clots in my left leg, don’t be surprised to hear that it is my stronger leg. I think it always has been to be honest. When we lived in Colorado, I did get the chance to learn how to snowboard before my balance would no longer permit the activity. My Dad insisted that my sister and I take a half day of lessons before we just went out on our own. At the rental shop, when deciphering which foot you will put forward on the board, the rental personal did a little test. He had me turn around and gave me a slight nudge. I put my left foot forward first. He said, “You’re a regular foot.” (A right foot is called a goofy foot.) I think if anyone gave me a little nudge today, I would just fall over.

I am seeing the reality that my balance and falling will worsen. I have no control over it. There are days when I am to the point of tears at my balance. Other days, I find humor in it. I think it parallels the balance of life: days when strength is strong and days when strength is weak…in both I need to keep looking upwards, knowing when I fall, He still stands.

I lift up my eyes to the hills. From where does my help come? My help comes from the Lord, who made heaven and earth.

Psalm 121: 1-2 ESV

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A cup of tea

Mr. Tumnus: “Daughter of Eve from the far land of Spare Oom where eternal summer reigns around the bright city of War Drobe, how would it be if you came and had tea with me?”

“Thank you very much, Mr. Tumnus,” said Lucy. “But I was wondering whether I ought to be getting back.”

“It’s only just around the corner,” said the Faun, “and there’ll be a roaring fire–and toast–and sardines–and cake.”

C. S. Lewis. The Lion, the Witch and the Wardrobe. Great Britain: (Geoffrey Bles, 1950.) pg. 116.

I think Mr. Tumnus was on to something: tea is best when shared with a friend (or a way to make new friends); tea is always better served like a tea party (although I question his choice of sardine refreshments); and tea no matter what time of the year it is…is tea, and can be fully enjoyed whether on a sunny day or in the winter chill by a roaring fire. (In my opinion, rainy days make great tea days.)

The concept of tea started for me at an early age. We sisters would sometimes have tea parties. My older sister had a tea set and Mom would serve tea (apple juice) with refreshments (usually graham crackers.) Tea time was serious excitement.

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Melissa and I

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After the apple juice excitement faded, tea was non-existent in my youth–although I applaud my Mom’s efforts in having us try herbal tea. “Add some honey.” Even honey was not sufficient. I never touched tea again until college. Then everything changed. Tea is now a hobby.

Socially, I don’t throw tea parties but I have thought about it a few times. Back at my birthday, being in the south where the best tea resides, my parents gave me a book on tea party history and etiquette. It is fascinating. Books and tea, what could be better?

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You don’t necessarily need a tea party to share with friends. Over the past few weeks, I have been given in gracious amounts–tea–resulting in the enjoyment of a few cups during the day. I have been given teas that I have never tried or even heard of in flavor. Once again, excitement resides!–because as far as tea goes, I usually stick with flavors I know or ones that help my stomach (such as peppermint or Bigelow’s Lemon Ginger Plus). But now that new flavors are being given to me as gifts to try, my knowledge of tea choices is expanding and in turn I share the new favorites with my family or other friends.

In order to give, we must also receive.

In life, we have been given a divine invitation…more than just a tea party, the invitation is for eternity, “For God so loved the world, that he gave his only Son, that whoever believes in him should not perish but have eternal life.” ~John 3:16.

The gift has been freely given–freely receive.

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Recap: Art on the Lawn Festival

Hi everyone. 🙂

Can I just say for a Monday, today was good! I read Psalm 23 this morning in my study of finding the phrase “steadfast love” within the Psalms. Psalm 23:6 says, “Surely goodness and mercy shall follow me all the days of my life.” I never took note of this before, but today I read the numerical at the bottom reference to the word “mercy.” It says, “Or steadfast love.” So I noted the verse in my notebook.

I found Psalm 23 exactly what I needed to read after getting through the rest of last week and the weekend. God’s mercy and goodness was evident, but I cannot say that I held on to the steadfast love in all areas like I should have–instead I chose to cling on fear to a few health related issues…forgetting the peace and calmness of the still waters; forgetting how He restores the soul.

I am entirely grateful to my family who put up with my frazzled grumpiness and helped me immensely in the preparation (writing the price tags, putting in the thumbtacks and twine on the back of the paintings for hanging), set up/take down of my booth on Saturday and stayed all day with me at the festival. I could not have done this without them!!

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I will say though that overall I was better prepared this year than past year, including getting a better nights sleep. It is interesting to see the difference one year can make, even within my painting style. As Mom and I were pricing on Thursday, I took note of my work: focused on smaller paintings, more abstract and ones with media. I stretched myself last year in my paintings to paint detail and broad themes; some of my best work is from last summer.

But over the year much has changed and I can see the paintings this year represent my style of what I am comfortable with and best at painting–a more relaxed approach yet detailed in its creativity. I would be lying to say that I don’t miss details, because I do. But sometimes even painting my “Mel” at the bottom corner is enough detail for me. I am just thankful that I can still paint!

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So how was the art show? Fantastic! It was a LONG day…I could have gone for a second round of coffee, but the day could not have been better. We were blessed with beautiful weather and my booth sat right in front of a huge tree, which offered pleasant shade in the afternoon. In conversation, I did fairly well. It is hard for me, because I talk more than I listen just because I can’t hear…but as time went on, I felt more relaxed–enjoying watching people point to paintings they liked and meeting people or talking with the friends who came to my booth too. At the end of the day, I survived staying awake through dinner but then fell asleep on the drive home (last year I fell asleep AT dinner).

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I want to say a thank you to the staff at the Village Artians, who coordinated this event. They went above and beyond making sure that the vendors’ needs were met. I can’t say that I will be in next year’s festival (who knows what another year will bring), but if the door is opened, then I would love the opportunity to participate again. Either way, painting this year will not stop for five months as it did last year–doors continue to  open and I am ready to restart on the journey through art.

Creativity takes courage. ~Henri Matisse

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Filed under Adjusting to NF2, Family Times, Paintings