Worry can best be defined as a chain of negative thoughts that have to do with fears about the future. Hmmm…pretty much sums it up for me, except that my chain can get really, really long, sometimes. So long, in fact, that I can no longer carry it. So what do we do when that happens? Well, Jesus put it quite bluntly during his “Sermon on the Mount.” He said: “On this account I say to YOU: Stop being anxious about YOUR souls as to what YOU will eat or what YOU will drink, or about YOUR bodies as to what YOU will wear. Does not the soul mean more than food and the body than clothing? Observe intently the birds of heaven, because they do not sow seed or reap or gather into storehouses; still YOUR heavenly Father feeds them. Are YOU not worth more than they are? Who of YOU by being anxious can add one cubit to his life span? Also, on the matter of clothing, why are YOU anxious? Take a lesson from the lilies of the field, how they are growing; they do not toil, nor do they spin; but I say to YOU that not even Solomon in all his glory was arrayed as one of these. If, now, God clothes the vegetation of the field, which is here today and tomorrow is thrown into the oven, will he not much rather clothe YOU, YOU with little faith? So never be anxious and say, ‘What are we to eat?’ or, ‘What are we to drink?’ or, ‘What are we to wear?’ For all these are the things the nations are eagerly pursuing. For YOUR heavenly Father knows YOU need all these things.” And yet, I still find myself worrying, day after day about what sufferings tomorrow may bring. I remember a time when I used to look forward to life…it held so much promise and excitement. I wasn’t prepared for June 3, 2008 , because on that day, in an instant, my dreams became blurry and disoriented. And the harder I tried to keep them in focus, the more I suffered. No, MS isn’t a “death sentence” they told me, but it is a life sentence…with no possibility of parole. I’m stuck in this body…A body that used to be athletic and strong and normal. And so began the worry…not the kind of worry you experience when there’s an exam coming up, or whether or not the mortgage will get paid. But, a kind of gut-wrenching worry I didn’t know existed. It rocked me to my core…I was devastated. The more I learned and the longer my symptoms lasted, the more afraid I became. No one could quite understand how I felt mentally or physically. They still don’t. Which is why I want to write. And since I love writing non-fiction, biographical stories…one about me is perfect. And in the midst of it all, everyday that I must struggle with my cross, I want to…I need to remind myself of Jesus’ take on worry. I doubt there’ll ever be a day that I don’t worry, but I’m going to try. And that is enough.
Tuesday, July 3, 2012
Shattered Dreams
Four years ago…my life was pretty close to perfect…or so I thought. Camryn had just turned 3 and I was loving being a mommy! I had everything I wanted in life…as well as a promising future! I was writing feature stories for my local paper and dreaming of what my next child might look like. All I ever wanted in life was to be a mom and have a big family. That’s it. Yet, little did I know…my worst nightmare was about to come true. In May of 2008 I started experiencing strange symptoms. My left hand felt numb on and off for a couple of weeks, but I wasn’t too alarmed. I’d always been healthy. I didn’t even have a doctor. Birth control and tylenol were the only medications I had ever put in my body. I had never drank or smoked…I tried to exercise when I could. But on June 3 of that year, my whole world came crashing down. I didn’t know what Multiple Sclerosis was. All I knew was that I was so dizzy I could barely walk, my hearing was very distorted and the left side of my body was numb. What did it all mean? When would I get better? Would it get better? No..no, they told me. There is no cure…this a life long chronic disease. You have scars on your brain and every time you relapse they multiply; your symptoms become worse and more intense. There are drugs you can take…in the form of shots. You will see a neurologist often, have regular MRI’s of your brain, (which, at the time, horrified me.) One moment I was lying in the sun on a beautiful June day, watching my little girl play in her blow up swimming pool. The next, I was begging my mom to take care of her if they found something bad…if they found something terminal. I shook from head to toe for months…I couldn’t stop. The symptoms persisted, I couldn’t drive, take care of camryn or anything normal. The pain was excruciating. At times I wanted to die. The why questions started. Why had this happened to me? What had I done to deserve it? I tried to think…I went to college, got married, had my first child…things were going like they were “supposed” to…the way I had “planned.” Whoa, wait a minute. ”planned.” I’m sure God got a chuckle out of that one. I honestly couldn’t fathom why? Yet the most agonizing question of all plagued my mind every second of every day…it still does. Can I have more children? When? How? Should I? Oh my God. This wasn’t supposed to happen. I’m healthy…wait..I’ve never even been sick! And you’re telling me my body wants to destroy itself and there’s little I can do about it? I will die with this horrible disease? I cried every day for months. I actually remember the last day I cried. It was sometime in August. Somehow I knew I had to make this about something other than me. I was focusing too much on myself…but I knew that it would come later. For the moment, I needed to worry about getting better so I could take care of my family. The answers would come soon enough. And they did. It has taken years…but they came…and now I know why I hurt every day. Why I am reminded constantly of my limitations. What I have lost…yet what I have gained…the precious lessons I have learned. I will write about them here. I want to share what I have learned and document it too. What I used to be so concerned about doesn’t seem to matter so much anymore. I have been beyond humbled by this disease and blessed because of it. Does my heart yearn every day for the life I had wanted to live? Of course! There isn’t a day that goes by that I don’t ache to hold another baby in my arms. There are times I feel so incredibly sorry for myself…I am still human, you know. Some days I cannot bare it. I feel so tortured. I remind myself constantly of my blessings…and there are so many, I know. I’m still learning…yet there is so much I have already learned. I will write about it…here.
Posted by ConsideringLily at 7:39 AM 0 comments
How Can a Good God Allow Suffering?
Posted by ConsideringLily at 7:39 AM 0 comments
Doubting God's Enough
Posted by ConsideringLily at 7:37 AM 0 comments
An (Unlikely) Unanswered Prayer
Posted by ConsideringLily at 7:37 AM 0 comments
To suffer is gain
Posted by ConsideringLily at 7:36 AM 0 comments
Grace
Posted by ConsideringLily at 7:35 AM 0 comments
Monday, July 2, 2012
Tears in my milkshake
So today I had my 4 month appointment with my neurologist. He's so happy with how I'm doing, compared to last year. This drug I'm on is working incredibly well. He chuckles as I walk down the hallway, watching as I try my hardest not to fall to one side or the other. "You definitely shouldn't become a tightrope walker any time soon" he says. Soon? I think. Try, never. But I quickly dismiss those negative thoughts. I know he is just trying to make light of my clumsiness. There is a pertinent question looming in my mind. One I had been waiting to ask for weeks...but at the same time, scared to know the answer. "What about the baby thing?" I say. Stupid way to ask, I know. I figure he'll understand what I am getting at. And he does. My nurse has already prepped him...she and I had talked about it during my monthly infusions. "In your case...well you need another 2 years of stability," he says hesitantly. I literally feel like someone has just punched me in the gut. Every breath of air leaves my body. Tears begin...the kind you can't possibly control...the kind that comes from the depths of the soul. Four years of anguish and anger...questions and pain and terror...it all floods out. I cant stop it. I apologize. Through my little pity party, I tell him "I wish it would just go away." "Me too," he says. And I know he is sincere. His children are about my age. I'm sure it must be heartwrenching to be a doctor...to see pain...whether physical or emotional...every day. "Don't give up yet...you're still young. Believe it or not, 31 is still young." "I know," I say. But I really don't know. As always, he tells me to "hang in there." After a quick handshake, he is gone. I slowly slide off the table and into my sandals...I make my way down the hall to schedule my next appointment. I stand there for at least 10 minutes, waiting for a lady and her kids to schedule her son's MRI. I wonder what is wrong with him. I feel so sorry for him...for myself. My eyes well up with tears again. I brush them away quickly...it is my turn. I am met with a cheerful "How are you today?" I just look at her...surely she can see my tear streaked face...my chest, beet red as it always gets when I'm upset. "Fine." I reply. I make my appointment. "Have a nice day," she says as she hands me my appointment card. "I will," I lie. I wonder how often people lie when asked how they are doing. I don't like asking that question anymore when I see people, especially if I know they have endured any kind of suffering. Because I know they will lie. I numbly walk to my car and climb inside. I call my mom, even though I know she won't share in my grief. Somehow, it still feels right to call mom when you're upset. She has chosen to take the high road with me and ms. She, like everyone else, feels like I should be happy that I have Camryn...that I should just enjoy her...and stop worrying about another child.
So, I get this one precious childhood to enjoy...but I hadn't planned on that. "Mommy's so sorry, sweetheart," I whisper. So sorry that I can't give you a baby brother or sister. So sorry that I got sick. My plans were to have a big family and now, somehow, I've got to figure out what to do with my life. I'm at a loss. I finally get up with Mark to tell him what the dr. has said. He reminds me of the tattoo I got on my hip a couple of months ago. "Never lose hope," right? He says. "God has other plans for us...for me." I tell him again for the millionth time how frustrating it is to have a perfectly biologically normal body, capable of having babies, but at the same time, a disease that threatens to destroy it. I want to scream. I want to rid myself of this fate. But I can't. I know I can't. I think of all the trillions of people who have had babies without having had to deal with ms at 27. I become angry. I think back to a time when I was so full of hope and looked so forward to my life...wondering what my children would look like....what their names would be. I smile. Those were good times. But what do I do with my life, now so riddled with disease and disfunction? I pray. I ask God to take it all and make it into something beautiful...something only He can do. And that means I must stop trying to figure it all out myself. I should throw the pieces in the air and let them fall where they may and allow God to put them together. I swing through the local Chick-fil-A drive through for a cookies and cream milkshake (a treat I seldom allow myself to enjoy.) In minutes I'm headed toward home again. And with milkshake in hand and tears streaming down my face, I give it to God. I'm so tired of wondering...of wishing and waiting. The truth is, I will never be better. This is my fate, whether I like it or not. It's how I deal with it that matters. But let it be known that I hate it, yes. That this wasn't supposed to be my life. But for whatever reason, it is and I must accept it and move on.
Posted by ConsideringLily at 4:52 PM 0 comments
Friday, June 1, 2012
Adversity
As children, most of us are protected and nurtured by our parents; we are often sheltered from the sufferings of others. I was. I'm doing things a little differently as I raise Camryn. Of course I still want to protect her from the evil in this world. But I believe it's imperative that she begin learning now that not everyone has it as good as she does. A psychologist once told me that children with parents or siblings with disabilities or illnesses often develop into more empathetic, compassionate adults. I had been horrified of what my 3 year old had seen and would see in her coming years. At the time, I thought my disease would ruin her. It never dawned on me that it would be the exact opposite. As we grow and thrive as children, we are bound to face some sort of discomfort, no matter how much our parents would love to protect us from it. For most of us, this is the beginning process of learning how to cope with adversity.
As we age, the adversities can sometimes hit us like a ton of bricks, crushing even the strongest and the fittest. Adversity can be small and make us feel uncomfortable for moments, days, weeks, months or even years, and for some people they seem to have a lifetime of hardships and battles which they must endure.
How we deal with adversity will determine how it will affect our lives and the lives of others. Even as children we can learn from experience in order not only to help ourselves, but to use our own pain and sufferings to help people when they are going through what we may have already endured. Learning to care for others through empathy will greatly reduce their suffering because you will know how to help them and comfort them through your own life's experience. I've learned this first hand. I now pay such close attention to anyone who may be struggling, young or old. Three out of the last 4 summers, I have been nearly unable to care for myself. The dizziness and inability to control even my own eyeballs was, for me, the height of adversity. Although I recovered from my relapses, I am left with residual permanent damage. And knowing it can and will happen again is so discouraging. I just wish I could get better, fully, without having to worry about this disease every single day of my life. But it could be worse. I came across a blog of a woman who lost her 4 year old daughter in a car accident. What she writes about will rip your heart out, especially if you have children. It's painful to go without see Camryn for a few days, much less never seeing her again. I thank God that he let me get MS instead of losing my child. I don't think I could survive that.
I long for a carefree life. But is that what God intended for us? Or does He want us to know the depths of adversity, empathy and compassion. We can't fully help carry someone's burdens unless we've been through it ourselves. Without MS, I'd probably still be focused only on my own family...with no regard of the trials that so many people go through every day. Right now, hospitals are full of people suffering. I know first hand because I was one of them several times. Now when I drive by a hospital, I am painfully aware of what's going on inside. I'm trying to teach all of this to Camryn. That life isn't always fair...that adversity WILL be a part of her life, so she better get ready now. I don't want it to catch her by surprise like it did me.
On a happier note, we are all off to Disney World tomorrow for 8 days!! I just pray I can endure the heat and walking. But it's a challenge I'm willing to take on. I can't wait to see the looks on Mark and Camryn's faces!!
Posted by ConsideringLily at 9:52 AM 0 comments