Showing posts with label Success. Show all posts
Showing posts with label Success. Show all posts

Thursday, July 14, 2011

Change Is A Good Thing!

Hi Everyone!


Please join me as I continue to write my stories and blogs under the new name.  



Blessings,

Bobbie

© Robynn “Bobbie” Dinse / Bobbie’s World Blogs
Please note that this short story is copyrighted and should not be reprinted in any form without permission from the author
Feel free to link to "Bobbie's World Blogs"
Thank you!

Saturday, July 9, 2011

Awareness or Understanding? Finding The Courage To Be A Survivor

Vol 3, Issue 1

At any moment of any given day I can go online and find support groups for any illness or cause.  There are MILLIONS of them.  Chances are, each one I will find has all kinds of artwork, clever sayings and symbols that will direct me to take a look at any issue at hand.  If the cause you are trying to bring to the public’s attention is complex and difficult to understand, it’s even more difficult to raise awareness and bring attention to your cause that is positive and productive.

Fibromyalgia Awareness is one of those very complex causes.  Because no two patients have the same exact symptoms and FMS symptoms are so numerous and vary so much in intensity, I often describe FMS patients, treatments and the impact on their lives to be as unique as a fingerprint.

Not long ago, I happened to come across a comment under a piece of artwork supporting Fibromyalgia Awareness.  This is what was stated:

All of us with Fibromyalgia are aware of what we go through.  It's the rest of you who need to learn about how we suffer on a daily basis.

As I read this comment, something about it bugged me.  I mean it really unsettled me and I wasn’t sure why.  Was it that the statement was somewhat defensive or accusatory?    Was I feeling anger?  Sadness?  Confusion?  I was so unsure!  I couldn’t figure it out!

I don’t mean to be judgmental of the writer.  The writer had their reasons and feelings for phrasing this statement in this manner.  There is no right or wrong in the statement.  We are all entitled to our opinions and our feelings. Feelings are never “wrong”, they are just feelings.  Emotion.  It’s what we DO with those feelings that can be considered appropriate or inappropriate behavior.

One could ask themselves:  “Whom was the writer referring to when they stated the rest of you?”  Obviously it meant everyone without FMS, but could it be a family member who hurt them?  A friend lost because of the impact of the disease?  A spouse who left them behind?

Then I found myself asking another question: “What was the writer trying to accomplish?”   If it was awareness, it wasn’t going to be received well.  So perhaps they were not trying to accomplish anything.  Maybe the writer was just hurting and this was the only way they could express themselves at that time.

As I sat pondering all these questions, the original feeling I had kept pestering me.   Why does this statement bother me so much?  It was literally driving me nuts.  No, I’m not obsessive compulsive, but this was really getting to me.  Then it hit me.

I lived in silence for a period of time after being diagnosed.  I tried to hide my illness and live a normal life.  But the problem was I tried to live the life I had before my wreck.  I was trying to be just like everyone else.  But I wasn’t like everyone else anymore.  I was no longer a member of the “Healthy People Society” or as I have come to call it, the HPS.  I use that acronym because it fits so many different circumstances and still applies.  For example, I’ve encountered the “Haughty People Society”, the “Hurtful People Society” and the “Hopelessly Pathetically Selfish.”  That’s just for starters.  I’ve had many different encounters with HPS’s when it comes to my disease.

It is a fact that FMS patients live with chronic pain every day.  If it isn’t pain, it may be the relentless fatigue, or migraines, or nausea, or IBS, or sleep deprivation, or severe depression, even panic attacks and medication sensitivities.  All these different symptoms combine to make a very difficult disease even more difficult to manage.  My point being it’s always something, and its always every day. 

It was clear after my diagnosis that the days of “just push through the pain and do it” were forever gone.  I can push to a degree, but not without paying for it later.   Instead of pushing through the pain, I would have times where I was forced to change my plans at a moments notice.   Specifically, changing plans at the most inconvenient, embarrassing, once in a lifetime or turn on a dime moments.  Maybe it’s a migraine attack, or any one of the numerous other sister conditions that this disease brings with it.  Whatever the source may be, rest assured, if the conditions at that moment is bad enough that I have to change plans, it means I stop and rest or I risk being laid out on the pavement. 

It took a long time to wrap my head around that fact.  I grieved and hid from the world for awhile, just so I could avoid being put in that position.  I was so depressed and lost I shut myself away for 2 years and told myself it was safer than putting myself out there for the world to reject.

But then I realized, unless they find a cure, I’m going to have this disease for the rest of my life.  Is this how I decide to handle it?   Me.  The daughter of the most independent paraplegic anyone could have the honor to meet.  The guy who rather than miss a day of work, drove my sisters car using a crutch to work the gas and brake pedals when his handicapped equipped vehicle was in the shop for repair.  Possibly the most determined man I’ve ever known.  Would his daughter become known as a “VICTIM”!?!

NO!   TOTALLY AND UTTERLY UNACCEPTABLE! 

Things would simply have to change in my life.

Now, I’m sympathetic to the writer of the original statement.  I’ve felt the bitterness of lost friends and the rejection of people I wanted to share time with, but because of a form of HPS the relationships could not survive.  I’ve experienced feelings of not being “good enough.”  I’ve grieved HARD over the loss of my career and the hopes and dreams that I had planned to enjoy at this stage in my life. 


Used by Permission of Artist/Writer:  Manuela McPhee



FMS certainly wasn’t part of my midlife crisis!  I was suppose to enjoy the freedom of having grown kids!  Or deal with empty nest syndrome, or share time with my sons and their girlfriends so I would be prepared for the day my boys would marry and have children of their own.  I wanted to travel with my husband.  Just the two of us!

It was very clear that unless I made those near to me aware of my disease, I would continue to have problems maintaining relationships and I would continue to be lonely.  Which gets back to the subject at hand.  What bothered me about that statement?

THIS:
"The implication that those with FMS are DOOMED to SUFFER the rest of their lives as HELPLESS VICTIMS."
I completely and totally disagree with that conclusion with every fiber of my being!  This simple fact remains:

"If we do nothing.....nothing will be the result!"

My fellow FMS Survivors, how will the world ever understand us if we do not show them courage and strength in the face of chronic illnesses and devastating pain?  No one listens to whiners and victims, but they WILL stand up and take notice of those who survive the pain with dignity and grace.  Choose to be a survivor and never let the pain define who you are!  We have a gracious and loving GOD.  He will give you the courage you need to endure.  This is one of my favorite passages:

"I know the plans I have for you," declares the LORD, "plans to prosper you and not harm you, plans to give you hope and a future."  Jer. 29:11

In closing, this video is my story of how I eventually rebounded and fought my way back to a new life by God’s Grace.  This was my childhood dream.   I had never pursued it as I never had the time or gave myself the permission.  Had I not been afflicted with this disease, I might never have pursued this dream and had such wonderful experiences with Filly.  

The lesson here?  NEVER give up on your dreams!



Have a blessed life…..be a blessing to others!


Bobbie


© Robynn “Bobbie” Dinse / Bobbie’s World Blogs
Please note that this short story is copyrighted and should not be reprinted in any form without permission from the author
Feel free to link to "Bobbie's World Blogs"
Thank you!
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Wednesday, July 22, 2009

Horses, Friends, Teammates and Dedication. Our USEDC Success Story

Originally Written:  July 22, 2009
Vol. 1, Issue 7


Welcome back, Everyone! 

I hope you are all well and enjoying your summer!  I’ve been away from my writing lately as I’ve been out of town and recovering from our exciting trip to the United States Equestrian Drill Competition - the National Championships held near Lindale, Texas.

Since the beginning of February, our team members have braved freezing temps, walked through pastures to catch horses in sub-freezing wind chills, loaded them before we changed our minds, then headed to some nearby arena, (hopefully indoors) to get to drill practices so we would be “up to speed” for Nationals. Eventually, Old Man Winter would say his goodbyes and the cold wind would give way to high heat, humidity and sunburn.  Our ever-faithful horses performed like troopers.  They probably adjusted faster to the changes and the physical demands with far less complaints than we did.

Cold temperatures are my worst enemy since my diagnoses with FMS.  There were some practices that all I could do was sit in the chair with a blanket and pray that when I got back up, my muscles would actually do what I told them to do.  Riding in those temperatures for me was out of the question.  Those times were strictly for Peyton and done out of love for him.  I would watch my son ride from the sidelines.  On these cold practice days, I would pay dearly the next day.  The knowledge of hot temperatures just around the corner kept my hope alive and I persevered.

Why do I put my body through this?  Well that’s easy.  I love my son dearly and I would do anything I could for him.  I have a deep passion for horses and have all of my life.  Truth be told, I love this team.  Some of the members are so dear to my heart I couldn’t even begin to tell them how I feel.  I just don’t have the words.   So I keep that inside, like a safe treasure only for me to hold.  Many of the veterans of this team I consider mentors, not just to me, but true examples for new riders of all ages.

This year there was a lot of excitement, new friendships were made and great times were had.  While there have been groundbreaking changes and thrilling successes, it hasn’t been an easy year by any means.  It has been hard for many of the people on the team.  Some members have been overworked, some are riding with injuries, and all of us were struggling with our children's church programs, school schedules and conflicts with performance schedules.  There were times when tempers were short, but the teams pulled together as always, to do what they do best, ride the drill.

I joined our drill team in 2005 when I was invited to ride in a parade late in the season. I loved it so much that the next year I purchased my horse and continued riding with the team in parades when I could.  It was that next season that Peyton also fell in love with my horse Filly and with a little encouragement he joined the youth drill team.  It only took one practice and he was hooked, just like his mom.

Since I rode in that first parade, there have been many changes in our club.  I have watched a team that was struggling to get enough people to win parades, loose a few teammates, and then come back strong the next season with 10, then 12 drill riders, and as of now we have 16 official riders, with several riders lined up eager to fill backup positions in a moments notice.  We have had to turn people away because there just has not been the room. 

We have also had fabulous blessings.  This team was the first ever to win two back-to-back National Championships.  In addition, the team won three consecutive Rodeo Division 1st Place Titles, and two consecutive Ride of Champions, quest for the SuperCup wins!   We have come a long way in those five years.  A team once severed almost in two, pulled together and came back stronger than ever.   Why?  I think it’s love and respect.  Love for the horses, love for the drill.  Respect for each other.  I believe that is the secret to the success of this team.  They rise and fall TOGETHER!

We added a youth team last year so our kids could ride instead of sit and watch their mothers and grandmothers compete.  They did well that first year with 8 members at Nationals and 10 at Regionals.  All along there would be sacrifices.  Equipment is expensive, uniforms and hats are costly, gas was almost $4.50 a gallon and pulling a trailer full of horses all over the country doesn’t get you the best gas mileage.  There were hotel rooms to pay for, stall fees, shavings and in some cases you had to pay just to get in to the event you were riding.  Meals on the road add up and take a chunk out of your pocket book.  But, every child deserves something to pursue.  I loved every moment I spent with my family as we drove to events and watched performances.  I did a little riding myself.  Last year I carried the team flag during grand entry at a local rodeo and had the time of my life.

This season [2009], we have been blessed with so many eager young children that we were able to put together a youth novice team of 8 and a youth advanced team of 12.  These children are the future of drill.  They will be the ones who keep the sport alive when we are too old and broken to perform at such a demanding level.

Our Novice team came in an impressive 3rd place at Nationals.  The Advanced Youth team captured the Advanced Youth Division Championship that eluded them last year by only a few points.  There were tears of joy, exhaustion and pride from both parents and children.  This is a family sport and by the time you get this far into competition, well, you become somewhat of a family.  I’ll never forget the smiles on the little faces of the 7 year old girls as they proudly carried their ribbons to mom and dad.  I still tear up when I see the three ribbons won by my son’s team, and I think of all the other teams that worked just as hard and are just as deserving of that respect.

While I would have loved to ride with these wonderful ladies on the adult team, I know that my disease will not be conducive to this sport.   That is okay with me.   It was in the beginning and it still is okay.  It’s okay for the same reasons.  Love.  Love for the horses and the sport.  I’m perfectly content to ride my horse on my own and enjoy the parades. I cheer the team on from the sidelines, just as the rest of the families do, and I love it just as much.  I also get tremendous joy out of assisting the team as part of their ground crew.  From water, to holding horses, to switching out tack, you name it I’m there to help out!  I want these teams to succeed!  If I can help in some small part, it is my honor for these wonderful families.

It is my hope that someday my disease will somehow be put in check so I can compete and enjoy that same thrill and excitement of success.  But, until that time comes, there is enough love in my heart to go around and be thrilled for all those out there giving their best and leaving their heart and soul out there in the arena dirt!

See you all next year!


Bobbie

[Writer’s note:  As of June 2011, the ladies team has won the Ride of Champions three out of the four years it has been in existence.   They hold three Division 1 National Titles and 3 Rodeo Division Championships.  The youth team returned to capture the Advanced Youth Division 6 Championship again in 2010.   The new youth team, a mixture of a few advanced and a few very young riders received ribbons and placed very well considering the age and experience they have had.]

© Robynn “Bobbie” Dinse / Bobbie’s World Blogs
Please note that this short story is copyrighted and should not be reprinted in any form without permission from the author.   
Feel free to link to “"Bobbie's World Blogs"
Thank you!

Sunday, June 21, 2009

A Father's Day Tribute, A Daughter Remembers

Originally Written:  June 21, 2009
Vol 1, Issue 6

Happy Father's Day, Everyone!

I hope you all had a restful and enjoyable week. I've been thinking a lot about my Dad, it’s only normal. Who wouldn't be thinking of their dad on Father's Day? I recently lost my father. We all knew he was in his last years, but it was sudden and very unexpected. I gain comfort knowing he is in heaven with Christ Jesus and I will see him again someday. I still miss him terribly, as does my step mom, Diane. To him, she was a gift that he had waited for all his life. It was mutual, they brought out the best in each other and his death has left an empty hole in her life and all those close to him. The 16 years they shared together were precious and their love touched all of us, their family, friends and co-workers alike.

He was an amazing man and lived well into his 60's, which given his circumstances was a miracle in itself.

If you have been reading my stories, you know that my Mom and Dad were both confined to wheelchairs in their teenage years. As a small girl, I recall my mom was the one to explained things to us about their physical circumstances. You know all the little questions we had like "How? What? Where?" and of course, "Why?" Dad's answers were never clear to us, at least not at that time. He would always say things like, "So what? Why not?" or "What does it matter?

One beautiful Saturday afternoon, while riding horses at my uncle’s place (I was about 8 or 9 years old), Dad asked if I wanted him to ride with me. I quickly responded with "But, you can't." Whoops! Dad asked me "Why not?" He was persistent...he repeated that question at least ten times until I started opening my mind to the possibility. Then I asked him the right question: "How could we do that?" He then gave me his ideas of how it could be done. I think he could have done it, too. No doubt in my mind. Let’s just say it involved a pulley system to get him up there, ropes to help keep his legs in place and some very imaginative ideas!

But, Dad didn't really want to ride that day. I was afraid to ride bareback and after galloping back across the pasture, I had asked for the saddle. He was trying to teach me something more important. In less than ideal situations, I need to look for other ways of overcoming challenges and doing things. Not assume that I can't do it because it might be hard or frightening. I needed to challenge myself.


Why not? So what? What does it matter?


You could sum up Dad's level of determination by those few short questions.

Dad never talked of his accident. What little detail of Dad's auto accident that I can recall (as it was told to me by mom) is that he fell asleep while driving his car (or truck...I never knew) on the rural highways that wind through far Northern Montana. He was apparently traveling into town when this happened and drove off the road and down into a steep ravine. I'm not sure if he remembered it, but he was trapped in his car for hours, upside down, with a broken back. He would never walk again and lost all feeling from the waist down. Dad never spoke of this experience with me. The one time he came close, he instead spoke of my grandmother, his stepmother, the woman he considered lovingly, Mom.

I recall Dad saying that if it wasn't for her, he would have given up and never done anything more with his life. She was the one that kept pushing him forward. She never allowed dad to say he wanted to die, although he felt like it at times. She said he had a future. She said, "There is nothing you can do about it now, it can't be changed, so don't waste your time worrying over it."

She was so right. No amount of worry or regret can change yesterday. We have precious little control over what happens next.

Like Grandma, Dad didn't give up either. He didn't stop living and waste away as a recluse inside the same log cabin in which he was born. He spent well over a year rehabilitating. A lot of that time was spent far away from home, away from the large family and the ranch life he was comfortable with. He eventually learned to accept the life that had been given to him. After rehabilitating and getting his High School Diploma, he went onto college and received his degree in accounting and business management. He wasn't going to sit by and take disability and never do more with his life. That wasn't good enough. He wanted to LIVE his life, not have it handed out to him or decided for him. So as his life began to unfold, when challenges arose, it was clear why he carried the mindset of "Why not?"

He eventually married my mom and together they purchased their first home. Now we had some unusual things in our home to assist in keeping mom and dad independent. We had what we named "reachers", nothing more than an oversized pair of salad tongs to reach the things on the top shelf of the cabinet. We had ramps in the front of the house, the garage and out the back porch. My dad's car (yes, he was a licensed driver) was lovingly named the "Green Lizard". A 1969 green two door Ford Fairlaine. I loved that car, hated the black leather interior in the summer, but we took many family vacations and road trips together in that car. Now dad had to make the normal and necessary changes. He built a sheet metal ramp to help get his chair in and out of the back seat. The ramp made it easier to pull the chair out so it wouldn't get stuck in the foot well. My sister and I fought over who sat on what side. If you got the driver’s side, you sit with your legs crossed during the entire trip. If you get the passenger side, you can get your feet on the floorboard. It worked well until we started getting to big and then it was time to make a change. We then graduated to a family van, which of course had to be modified to allow dad to keep as much independence as possible.

Now to modify the van in those days meant taking an empty cargo van, moving the seats into the back for the kids, attaching hand controls, an extended steering wheel and wheelchair locks. Our neighbors backed the van into the front yard, my parents wheeled into the back of the van from off the front porch, transferred into the van seats that were factory equipped, we loaded up the wheelchairs and headed for St. Louis, the closest place at that time where we could have a wheelchair lift and the rest of the modifications installed. At that time, we were talking about a six-hour trip in the hottest part of the summer. Dad was convinced everything was in order, all would be well and we would stay in a nice hotel off the Mississippi River while the modifications were made to the van. Modifications would be a cable supported lift off the side of the van, allowing my parents to ride up and down into the van with ease. From now on, there would be no need to transfer from their chairs to the car seat. Back then they did not have the motorized chairs they do today. They would be able to ride and drive from their chairs. Ah yes, Dad's ultimate machine would allow him even more independence! He named it the “Copper Coupe” because of it’s brown copper color. Dad named all of his cars, I never found out why.

There were a few "concerns" the neighbors had before we ever left the house. First of all, dad and mom would be stuck in that van until they reached their destination. Dad reassured our good neighbors that we had people waiting for us to arrive and they were supposed to help them get out of the van, check us into our hotel and then take the van to the shop for modification. No sweat, right? We had a brand new van, new tires, and a CB radio if heaven forbid something did go wrong. That way we could call for help. He reassured them that we would be fine and off we went. Fully armed with lunches, snacks, water jugs and Dixie cups. We were ready for the adventure!

Sounds like a piece of cake, right? WRONG.

Everything that could have gone wrong on that trip did.

Problem No. 1: Well, we hit St. Louis at high rush hour. I remember sitting in one place on the highway for what felt like hours. It had to be 100 degrees outside and at least 110 in the back of that van. We were late getting to our destination. Hours late. This meant that the shop closed before reached our destination. And it was closed for the weekend. So Dad decided the best course of action was to go to the hotel and see if we could check in and find someone kind enough to help with our problem.

Problem No. 2: Well, on arrival at the hotel, my sister and I were tasked with going to the front desk for a manager to come out and speak with our dad. The hotel had lost our reservation and they were booked. So we then had to find new accommodations and fast. Remember, this was back before cell phones, or even roadside phones that you could use while still in your vehicle. I started wondering myself how dad was going to get us out of this one! We drove around and found a nearby hotel. Dad caught the attention of a passerby who went into the hotel and asked if they had rooms available, he returned with the good news that yes; they could put our family in a room. So we had a place to stay, but this brought up the next problem.

Problem No. 3: How to get mom and dad out of this van. With our help we brought dad’s wheelchair out of the side door of the van and around to the driver’s door. Remember, this was a 70’s model full size cargo van. It was a LONG way to the ground. To my mother's horror, he jumped from up on high, down into his wheelchair. Hit his target, no harm, no foul, no problem. He was quite pleased with himself! Then it struck mom, she would have to do the same. In tears she cried out that no way was she going to do that. NOT. GOING. TO. HAPPEN. The next twenty minutes were filled with a lot of words I'm not supposed to use and was told to cover my ears. I could still hear what was going on and let's just say she let my dad know that she was displeased with him and sick of all his adventures and ideas. In between the "I hate you for doing this to me" and the "I'm not doing it, I'm not!" My sister and I sat on our suitcases thinking about how much fun the pool would be and how hungry we were! Then my dad had enough and finally said calmly, "You don't have any other options, you will be fine, the kids are here, now get your ass out of the van." She gave him one last cussing and then landed square on her backside in her chair. After catching her breath and getting settled, she didn't talk to him for the rest of that night. But for the rest of us, it has made for an entertaining story and a fond memory that I will share with others for years to come. Ah yes…my dad and his determination to be independent, his idea of comfortably “normal”.

We spent the rest of the week at the hotel, watching the boats on the river from our 12th floor balcony, swimming every day and spending time as a family. It was a really great vacation. Filled with the type of relaxing moments that you hope you can have with your children, once you have grown up enough to look back and realize just how good you had it as a kid.

This is just one of many examples of how my dad took the every day normal tools of our life and modified them to work for his life. So he could have that same freedom of choice that all able bodied people are entitled to have. I have mentioned that dad had many gadgets to accomplish this. One of my favorites was his lawn mower.

Now, there were so many things that Dad did that you just would not expect a paraplegic to attempt. It would be too hard, take so much more work...just pay someone and save your energy, right? Nope, no hired hands for my dad. Yard work and mowing the lawn was one of those things. My dad had a green riding lawn mower that yes, he modified. He ripped off the seat and replaced it with a regular bucket seat from a car. Never mind the bucket car seat was bright burgundy leather/vinyl material, it worked for him. He took off the steering wheel and replaced it with bicycle handlebars, carefully welded to the shape he needed to reach. He added foot rests for his legs, designed a "stop and go" bar that attached to the throttle so he could control this function by hand. It was the most ugly lawn mower known to man, but it worked. Every Saturday he was out in the yard, without fail.

We had a system when Dad mowed. Take water out to dad often and listen for the mower to stop. If it stopped anywhere but in the garage, time to go rescue dad. It did break down and often, but he would doctor it back up and get it through another season. Mowing the lawn wasn't the end of the job. Dad would then rake and bag his entire front and back yard. Why? When for a small amount of money someone could do it for him? Well, he wanted to be independent. Just like everyone else. It was his perception of "normal" that he could be happy with and accept. A well tended yard, complete with the trimming, done by his hand. What a sense of satisfaction he must have had at the end of the day!

Eventually my parents divorced, Dad moved away, eventually landing in Denver many years later. Dad and Diane purchased a nice home together and gave the yard work over to a young boy down the street. But, Dad’s green thumb prevailed so he also hired someone to build an elevated garden complete with irrigation systems, so he could grow his tomatoes, carrots, green beans, squash, you name it. His garden was his pride and joy and each time we visited him we loved going out to see what veggies were ready for picking. He had a gift for gardening and grew some of the sweetest baby carrots I've ever eaten. It had become part of our trips to Denver that we all looked forward to.

Finally, I want to share one of my fondest memories that I have of my Father. It was dancing with him at his wedding reception after marrying Diane. Yes, DANCING! He would get out there with his chair and "get down" for lack of a better adjective. Now, I'm a horrible dancer, but that night at the club he said to me; "Please honey, I want to dance with my daughter on my wedding day." How could I refuse? I had the time of my life. Once our dance was over and the slow dances began, Diane took her place on his lap. They shared a very special moments on the dance floor that night, and all the people in the club took notice that there was something different and very special about him, about both of them. Not having legs that worked did not mean anything to him or her. He showed the world that his disability wouldn't stop him from having the life he dreamed of. I cried tears of joy for my father. I was both incredibly proud and happy for him that he had found his place in this world and found someone equally as special to share it with.

The last years of his life I think were some of his happiest. He and Diane shared such a wonderful relationship. Together they shared many experiences that he may not have had if they never met. They went hot air ballooning, snowmobiling in the moonlight and took many more trips across this great country. The last time I saw him was when he came to visit for my oldest son's high school graduation. Their van had broken down and needed to stay at the shop for repairs. Problem? How were we going to transport my dad two miles from the dealership to the hotel, without a wheelchair accessible van. Not to fear, Dad had a plan. He told me on the phone, "No problem, I have a ride, I'll meet you at the hotel." Okay. My family hoped in the car and headed toward the hotel. All of a sudden, in the dark I see this image on the back of a flatbed truck. Just behind the cab, holding onto the light railing, was proudly perched my Dad, in his wheelchair, happy as a clam. He was waving to people, there were people honking and waving back, he was having the time of his life! He said the breeze was great and the view was even better! We got him to the hotel and unloaded Dad the one man parade and then I laughed all the way home. It was typical Dad. No fear, ever. Just go with the flow. There is nothing you can't overcome by God’s Grace and a set mind!

What an inspirational human being he was. I was the luckiest daughter in the world, because I was able to share his life!

Even if you don't have a disabling disease, Dad's life lessons were far reaching into all areas of life. We just didn't know it as young kids. Every person who met him, liked him, respected him or loved him. He was always outgoing and full of humor.

On a personal note: Dad, I miss you terribly, but you have left me with so many positive memories and examples of courage and strength. Sometimes when I'm down with my own disease, I wonder how you managed. It’s then I remember that I have to keep going and I CAN keep going. I have choices. I need to make them and go forward, even if it's just a little bit everyday. Although I miss our long talks, I'll never be without all those wonderful memories that you have given to me and your grandchildren. I know we will be together again someday and I want you to be proud of what I have accomplished, too. I won't give up; I'll fight this disease every day and get my life back in balance.

To my readers, I hope that you will gain strength from what I've shared of my father. There is so much more to tell. I could write for hours. Even in his death, he never lost his sense of humor or his practicality. He wanted his ashes spread on the ranch in Montana, under the same tree that Grandpa and Grandma asked for their ashes to be spread. At his memorial brunch, held in his home last spring [April 2009], Diane took my hand and walked me to the pretty oak box containing his ashes. It was engraved with the following: "Now wasn't that cost effective?"

Save me a dance in heaven, Dad. I'll be there in God's time.

Your Loving Daughter



© Robynn “Bobbie” Dinse / Bobbie’s World Blogs
Please note that this short story is copyrighted and should not be reprinted in any form without permission from the author
Feel free to link to "Bobbie's World Blogs"
Thank you!

Sunday, May 31, 2009

Life Doesn't End When You Have A Disability

Originally Written:  May 31, 2009
Vol. 1, Issue 2

Hi Everybody,

Today I wanted to share with you how my evening went.  Tonight we had youth team drill practice.  We have a rodeo coming up this weekend and Nationals are coming up the end of June.  I managed to stay on the horse and actually remembered all of the different moves in the drill.  Needless to say I had a wonderful time and for a few hours forgot all about this horrible disease.

As you know, I suffer from severe Fibromyalgia.  I have good days and I have bad days.  Today was one of those good days.  You couldn't tell the difference between a healthy person walking down the street or me!  My passion since I was a little girl has always been horses.  When I was young I collected the Breyer model horses because mom refused to let me put a pony in the back yard.  Go figure!

Anyway, my son and I ride with a local drill team.  Since my disease is so severe, I cannot ride on the drill team with the rest of the ladies.  On good days I can ride in the parades and I can help out with ground support during competitions and rodeos.  Where am I going with this?  Well, since 2005 I've been trying to control my horse at a lope and still be able to walk the next day.  I've managed to accomplish one of the two...guess which one!  Unfortunately, it’s only during the warm season and only on days that my Fibromyalgia is in agreement.   You all know that FMS has a mind of it’s own and what it decides to do ALWAYS takes lead role.

This year I have been asked to ride with the novice youth team in their competition this June.  I was elated but cautiously optimistic.  After explaining that there was a significant need to have a back up, just in case I was too weak on the day I needed to ride, I was told "No problem"!   So, my life long dream may finally be coming true.  Not only do I own a horse, I may actually be able to ride with the team in the drill.  I will be filling in this weekend at a rodeo, since there are 3 riders that cannot attend.  My first real live performance!  I'm both excited and terrified at the same time.  I'm sure I will be sore afterwards, but the more I ride, the less severe the pain is afterward.

It is very exciting for me and I hope that I can give others with this terrible disease hope that if they can find the right mix of medication and therapy, there lives don't have to be over.

I'm 41 years old.  I refuse to let this disease end my hopes and dreams.  Just because I may have to slow down and rest, I still have the God given right to dream and strive to reach the goals I have set for myself.

Have a blessed week everyone.  Remember to be thankful for your health.  We all don't have healthy strong bodies to lean on and even the strongest of people can have their health removed from them with one doctor’s visit.  Don’t waste your good days!   Rejoice in every day that you have and get out in the world and see God’s beauty!  It’s all around you.  All you have to do is open your eyes and your hearts and you will see the blessings that are there for you!


Bobbie

© Robynn “Bobbie” Dinse / Bobbie’s World Blogs
Please note that this short story is copyrighted and should not be reprinted in any form without permission from the author
Feel free to link to Bobbie’s World Blog’s” 
                 
Thank you!

Saturday, May 30, 2009

A Word About Unseen Illness and Disability

Originally Written:  May 30, 2009
Vol. 1, Issue 1


Hello Cruel World!  Just kidding, welcome to my first personal blog!

Today I want to talk a little bit about unseen illnesses.  The people closest to me know that I suffer from severe chronic migraines and severe Fibromyalgia.  When I was 34, I was in a really bad car accident that resulted in neck surgery. I now live with a titanium plate in my neck to help support the vertebrae that were fused together as a result of damage from the impact.  I recovered from the accident just fine, but then about a year later I noticed a sharp increase in my migraines and a lot of all over body pain and severe fatigue.  I went to my doctor and after extensive testing was diagnosed with Fibromyalgia.

Many people don't know what Fibromyalgia is and because it isn't something you can see like an amputated leg or a disfiguring injury, people won't know that you have it unless you tell them.  What I have found is that the fatigue and pain slows me down so much that it does get mistaken for laziness or a lack of drive, which is both unfortunate and unfair.  I have good days and bad days.  On my good days I can function for a short period of time almost as normal as everyone else.  On bad days I may not even be able to get out of bed. 

On the up side, I try to make the most of each day and on my good days I thank God and treat them as precious moments.  They are making advances all the time in the treatment of this unfortunate disease and it is my hope that someday they will find a cure.  At the moment, there is no cure.  You treat the symptoms and hope for the best.  I think my biggest peeve is when someone says, "If I can do it, I don't see why you can't."  Well world it's like this.  If I only get three hours of sleep or push my body past my personal limits, I can end up hospitalized. Or at the very least in bed for a day or two, perhaps weeks, and maybe even have to take a steroid dose pack to control the pain and regain my ground.  Everyone has limits and we need to respect those differences.  God did not pull out the cookie cutter from his kitchen drawer when He created man and woman.  Not everyone was made the same and we all struggle with different problems, be them physical, mental or family issues, we all have hardships!  A healthy friendship is based on respect.  Without that respect, the friendship cannot flourish and grow deeper.  So before you judge someone because they cannot do what you do, perhaps you should ask yourself if there is more to the situation than meets the eye.

So my quote for the day is from the Bible. "Love one another as I have loved you."  The next time you open your mouth to say something about another person, first ask yourself:  "Do I know what is really going on in this person's life?  Am I being overly critical?  What is the benefit of my comment?  Am I lifting this person up or tearing them down?   Is it possible that I feel that I am better than this person and by stepping on their feelings, I affirm myself?" Hmmm…..food for thought.   I hope the right choice is made for the benefit of everyone involved.

Have a great weekend!

Bobbie


© Robynn “Bobbie” Dinse / Bobbie’s World Blogs
Please note that this short story is copyrighted and should not be reprinted in any form without permission from the author  Feel free to link toBobbie’s World Blog’s  
 Thank you!