Archives For lupus symptoms

Christmas 2014

December 17, 2014 — Leave a comment

It’s that time of year again when families send out their Christmas cards. Well, this is the fourth year that our family has opted out of the Christmas card and instead made a Christmas video. We absolutely love making these videos, it’s a lot of fun and we get to capture precious moments with our kiddos while making great memories.

Merry Christmas from my family to yours!

 

Layman Christmas 2014 from Chase Layman on Vimeo.

The Year of Pie

January 24, 2014 — Leave a comment

I absolutely love baking pies! And it goes without saying that I absolutely love eating pie!

Think about it…

Pie is just plain awesome! It brings a sense of comfort, and a comfy home feeling.

What is with all the cupcake love these days? Yes, I love a good red velvet cupcake, but it certainly doesn’t bring the nostalgia of a homemade pie! Am I right?

Look out world, I'm baking some pie!

Look out world, I’m baking some pie!

Ever since I can remember I was the kid that watched the cooking channels for all the baking shows. Besides making me crave what they were making, it would get my creative wheels turning. From then on I have had this insane desire to be an incredible baker.

I have tried my hand at baking the cool decorative cakes and cupcakes. While they turn out yummy (most of the time), they don’t always turn out pretty. Not to mention the immense frustration I get from my lack of skill with cake decorating. My kitchen ends up destroyed… flour everywhere, not a single pan clean in the kitchen and a lopsided cake that was definitely prettier in my head than on my plate.

But pie, ahhh that is another story. Last night I was creating a new recipe for my sister’s birthday and let me tell you I was loving every minute of it. Don’t get me wrong, I have had my failed attempts at recipes. But that is part of getting better, you learn from experience. I just feel like I am in my element when I work with pies. Oh, did I mention the pie that I made was a mix between an Oreo pie and a french silk? I’m thinking of calling it Oreo silk, or silky Oreo…

Get ready 2014, I’m baking lots of pies this year!

My forever accessory to life

My forever accessory to life

When my face is rash free, my joints are treating me nice and my fingers don’t go crazy white I can forget that I have an illness. Mostly when I have had weeks and even months of feeling better than usual. The thing about Lupus is that majority of the time it doesn’t show through on the outside. I look just like everyone else, I seem to be healthy but reality is far from that. There are times when I look into the mirror and think back to that moment I heard “You have Lupus” and find myself doubting those very words. Could it really be true? I have felt so good lately. I look okay. Maybe it was all in my head. But those thoughts come to a sudden jolt when I am reminded of my disease every day by my twice-a-day pill organizer. What twenty-something has a pill organizer? Just those that need one..

The truth is I am not in denial of my diagnosis. I’m actually okay with it. But sometimes I find myself looking and feeling like I used to and then everything becomes surreal. When I actually stop to think about those words “You have Lupus” it’s hard to believe. Not because I wish it weren’t so or because I fear what is ahead. It’s hard to believe because who thinks that they will have their world altered by words like that? No one. I seem to be healthy, and sometimes I even feel that way. But then I get reminded of just how invisible this illness really is when I wake up with achy joints and the beautiful butterfly rash to accent my face for the next several days and my stark white fingers that are my winter accessory. Truthfully it’s as simple as this… I don’t think about my disease all the time and if I am having several good days in a row I forget about this part of my life, that I have Lupus. But, I think that is a good thing because it’s pretty great that people don’t see me and see my illness. I will talk to people about it with all honesty, but I like knowing that it doesn’t have to be me. I think it’s okay to forget about your diagnosis because every day when I take my morning and evening medicine that is enough of a reminder. I don’t need to dwell on it.

I do not fear what is ahead. Rain or shine, God Has plans far greater than mine, and that includes my disease!

I am not patient. But lately I am finding that God is teaching me this very difficult lesson. There are so many dreams I have for myself and our family that I truly believe are dreams instilled in me from God. Sometimes those things just don’t happen overnight. In fact, that is usually the case! With the world of instant gratification the idea of waiting is unthinkable! Patience, who has time for that? I’ll just zap my food in the microwave and my “baked lasagna” will be ready in less than 3 minutes! Why on Earth would I actually bake my lasagna in the oven for half an hour? Patience! Ha! Do we even know what the world actually means?

Dictionary.com defines patience as the quality of being patient, as the bearing of provocation, annoyance, misfortune, or pain, without complaint, loss of temper, irritation, or the like. An ability or willingness to suppress restlessness or annoyance when confronted with delay.

Go ahead and make an entire meal from the microwave! Why wait an hour?

Go ahead and make an entire meal from the microwave! Why wait an hour?

I’m pretty sure that our microwave zapping, instant streaming, world in our hands by the touch of an iPhone generation doesn’t have much of a chance! And I am right there with the rest of the population. If my iPhone is taking a hair too long to upload a page I’m annoyed, don’t even get me started when there are three commercials on Hulu instead of just one! Speaking of commercials, my child doesn’t even know what they are! We don’t have cable. Instead we bought Netflix and Hulu, made our lives cheaper and no commercials! The first time he experienced the world of commercials he was at his Aunt’s house and the Mickey Mouse Club House was rudely interrupted by a commercial. He energetically let out “I want more! More Mickey!” This continued until the show came back on. Little did we know getting rid of traditional cable would make my child impatient! It wasn’t our intention, I promise!

I’m not sure about your family, but we like to dream big! Chase and I will be driving down the road and one or both of us will start dreaming of having more children, when we can take a big Europe vacation, update our kitchen, get a second car, Chase’s businesses grow even larger and I write full-time. Our list of dreams go on and on. Here is what I am learning, rather slowly, these things might actually be our future but they won’t come easy and they won’t come with the push of a button. Sometimes we have to patiently wait where we are, work hard and enjoy the blessings of our current circumstances because as long as we are following God’s path, the blessings are sure to follow! This is something that I am having to remind myself of more often than not. I see what we are working towards, the steps we are taking and the amazing benefits of our sacrifices to get where we are wanting to go. But I still struggle with the microwave mentality. Can’t it just happen now? I’m trying daily to overcome this awful mindset because I know that when you are so focused on what you want someday, you miss out on the amazing of today! And I don’t want to miss out on the blessings of my here and now!

The following is a guest post by Mandy Karo. I first met Mandy in college when we both joined Pi Zeta Phi during college. After hearing about my diagnosis Mandy reached out to me as she is also living with Lupus. I am so thrilled to have her share her story. She has wonderful insight, show her some love! 

Middle school is a tough time for most kids. When I was in eighth grade, I was in the midst of a very difficult transition with my two best friends. We had been inseparable in fifth, sixth, and seventh grade. I remember the gym teacher saying weMandy's guest post were “joined at the hip.” But in eighth grade, they were drifting away from me and becoming a part of the popular girls group. For a young teen this felt like the ultimate abandonment and rejection. I remember feeling a lot of loneliness, stress, and anger. It was in the middle of this drama that something much worse was piled on to make my teen years even harder. I was diagnosed with Lupus.

I had been having odd symptoms for a while. In sixth grade I started having strange stomach aches. The doctors thought I might have ulcers so I had to have a stomach x-ray. It was awful—the stuff you have to drink so they can x-ray you is disgusting! There were no ulcers found so life went on. In seventh grade I began feeling tired in the afternoons. But what happened in eighth grade was what led to my diagnosis. I started getting purple spots on my feet and ankles, especially when I was upset or stressed out. My feet and ankles would also swell up. At first we thought maybe I was allergic to the laundry detergent my mom used but switching it didn’t help. The worst time was when one of my teachers accidentally ran over my ankle with a TV cart. The purple spots showed up and I got so swollen I couldn’t walk on that foot. It hurt to put shoes on.

When we showed my family doctor the spots, she was perplexed so she looked up what it could be. She named off a number of possibilities and one of them was Lupus. I really had no idea what Lupus was, but I had heard the name before, and I knew it was some sort of serious disease. I started to cry. We were sent to Children’s Hospital in Denver to see a rheumatologist. They did blood work and the doctor asked me a few questions about my symptoms. Then just like that, he told me I had Lupus, gave me some packets about it, and prescribed medications for me to take. It felt odd that it was so quick. Even my parents continued on acting normal. Didn’t they know that I was just diagnosed with an awful, potentially life-threatening disease? Shouldn’t we all be crying or yelling or something? I know that they were just trying not to freak me out. Inside they were scared too.

I’ve been diagnosed with Lupus for thirteen years now. I deal with fatigue, unexplained fever, swollen joints or muscles, sensitivity to the sun, susceptibility to sickness, and the spots (which are called purpura and are caused by bleeding underneath the skin). The medication I take has helped me in controlling the flares. I know I am actually very lucky because many people with Lupus have much worse symptoms, and thankfully my symptoms are not life threatening.

There are a lot of questions that come with having Lupus. Will my symptoms get worse? Will I be able to have a healthy pregnancy? Will I have the energy for a full time job? Will I have the energy to raise children? Will the men I date be able to handle the fact that I have Lupus or will it make them want to head for the hills? The real question becomes, what do I do with all of these fears and anxieties?

When any sort of fear comes into our lives, no matter what it is, we must remember the power of God. God is bigger and stronger than any scary thing that looms in our path. Just imagine the universe in its incredible vastness and remember that God created it! That is power. Then remember that he loves you. When something bad happens in life, we might be tempted to ask if God loves us. If God loves me, why did he allow me to get a disease? But that question is focused on the physical, and God focuses on the spiritual. Yes, bad things happen on this earth. But God allowed his son to die for us in order that we might have a new life. That is love. This world is temporary, and we must use the struggles that come with it to strengthen our relationship with God.