Sunday, June 26, 2022

Karate kicking..........

I’ve been thinking about re-starting my blog for several months. Then things keep happening and I get so far behind and it’s the least of my worries. However, as challenges have presented in 2022 and continue to block my lane, I decided to finish up this post I started many weeks ago and set it free.

As gentle as an angry 42-year-old with health issues of that of an 95 -year-old could, I flung the door open to my Jeep, jumped out and proceeded to karate kick my garage door that was erroneously bouncing up and down in my brand-new gold and hot pink monogrammed sandals. I didn’t know whether to cry or laugh. I honestly wanted to slide down that garage door and crumble into a ball and sob. And here’s a good place to add, in my driveway, which earlier in the day had been swept clean of the neighbors TREE which had landed across it in a storm the night before. Also, should be noted this is the SECOND time said tree has taken up space in my driveway in the last few years.
Why is it when things go wrong, they just plain go wrong? Or they keep going wrong? One wrong turn leads to another, and you are in deeper and deeper. Since February, I have battled what I consider my most challenging fight with myasthenia gravis. Two surgical procedures with complications, one a pretty big one, fluid on my lungs which has resulted in very low oxygen that are likely reflective of the work my lungs are able to do at this point and time because I do have a rare neuromuscular disorder. Some days I just live with the condition I am in, but early last week as a breathing machine arrived at my house to use at night and I lost my sh*t.
Like many things with MG, I am not sure why this is happening. My first question was how soon can I get off this machine to which the tech responded people don’t usually ever get off this machine.
I’ve spent more time on the phone, emailing and googling trying to piece this all together and get it fixed”. It’s literally like having a second job managing my health right now. There is NOTHING like nothing, I wouldn’t do to feel like a normal person again. And I use the word “normal” loosely because after all I’ve been battling MG since I was 5. I’m not exactly normal. I get plasmapheresis treatments on the regular, have a goose egg sized fistula in my left arm, pretty much a permanent RB face due to being unable to move my muscles from my MG but those are all my norms. I’d pay a serious buck to go back to that normalcy.
I’ve got a million questions and no answers. I’m trying to give myself grace and take each day by day, one step in front of the other and know these experiences are going to help me be better along the way. My social life has halted to a very slow crawl as I navigate how to tackle these obstacles. To this point in my life, I’ve been successful in using humor to guide me through stressful mishaps and my health. Thus humor has been a bit harder to find this go round. The level of severity, a little more severe this time. A serious debate with my own mortality stares at me in the mirror. Where is this disease going?
Here is where this post has me stumped, not quite able to tie it all together and wrap it up. Honestly, I’m not really sure of the purpose of sharing all this but as my days stuck at home grow longer, I know I’m also desperate for a creative outlet and if you saw my attempts at sewing you’d beg me not to restart any of those projects!
So maybe it is a gentle reminder to others about what it is like to face adversity with your health, which seems to have come to the forefront over these last few days over what has happened in our nation. Whether that be a chronic illness, rare disease or a women’s issue, the next time somebody shares with you how they are feeling or what is going on in their life with their health, validate them. It’s not about you. It’s about the person feeling safe, being able to vent and make choices from where they sit. Unless you’ve lived with health adversity, please don’t make judgements on others on how they navigate their future.
Lastly, I guess I share this to be real. I do not need sympathy or prayers. If you can do anything, take action. Hug your loved ones tighter. Be kind. Be less judgmental. Hold open the door. Make amends. Give the kudos and tell people what they mean to you. Rescue a dog (preferably one that doesn’t leave nuggets near your pillow, ahem), donate to your favorite charity, buy somebody’s lunch. If you are thinking about somebody, text them and tell them. I will not be deterred from using these times of challenge from finding the silver linings and know it could be so much worse!
Until then, I look forward to the day when I can karate kick this machine right back to where it came from…….


Wednesday, January 26, 2022

Keep on washing..............

The soap on my sink caught my eye this morning and I smiled.  In the olden days of COVID-19, you know somewhere around March 2020, I remember watching the soap containers in what seemed like forever, go slowly down as I was home day after day.  I remember ordering soap from friends who were getting my groceries or through my grocery pick ups.  And sometimes soap was so hard to come by.  Also, you should know I'm picky about my soap, if it's not Mrs. Meyer's Iowa Pine, it needs to be in a pink or purple bottle or have that color of a label.  

As somebody with a malfunctioning immune system and very vulnerable to illness, I am not ashamed to say I hoarded soap and probably still qualify as a soap hoarder.  Please don't look in my mudroom cabinet.

But this morning I smiled as I pumped the soap into my hands.  I have basically been contained to my house, besides going out for work since December 22nd.  A little over a month. I can count on my hands the number of people I have gotten to encounter and had interactions with.  For me, pre COVID, this is very rare. I am a social person. I thrive in social situations. I love people but this go round, when omicron beared down on us, something hit me differently and I knew I could isolate at home and be actually ok.  Well let me rephrase, that, it hit me differently after I spent the darn Christmas holiday by myself because we decided I shouldn't fly on the busiest day of the year.   

I am calm. I'm happy and I am as healthy as I can be while I manage my MG. I have a roof over my head, a great job, some family who love me and care about me 🤣, an amazing support system including friends who I consider my family and a dog who might poo in my bed tonight but that's a whole other blog post.  And I've got enough soap to keep washing my hands and making the most of it.

Cherish what you got friends.  Life is short. Over 5 million people are dead because of this virus.  And let me remind you, this virus doesn't care who you vote for or what religion you think might save you.  Get your vaccinations. Get your boosters AND keep washing your hands. 
 



Saturday, June 26, 2021

The Perfect Mistake

 


If you follow me on social media, you likely already know this story! When I got home after the MGA celebration last week, I had an email from Union Station that said they would be unable to do the lighting due to an electrical issue. I replied to my contact the next morning and said how amazing the lighting was in person and that I had seen some great pictures. She responded this afternoon that the electrical issue was that some of the lighting kept going PINK. Of course I noticed that last night because if you know me you know PINK if my favorite color, in fact my house is quite obnoxious with PINK. What they thought was a mistake could not have turned out more perfect……

Let Your Light Shine

I wrote this piece for the MGA blog but wanted to share it here also.  My wheels have been turning for revitalizing this blog as I truly do enjoy writing.  I just haven't had a lot of time over the last few years but I hope that will change!

I was diagnosed with myasthenia gravis at age 5. The depth and severity of my disease did not become apparent to me, I don’t think, until I was a teenager. Over the course of the last many years, there have been lots of times where I felt very little hope and that my light had been dimmed. As I have grown older and more seasoned in my journey with a rare disease, I know it is just part of the roller coaster.



However, last week with the help of many dedicated partners, we were able to let our light shine a little brighter when Union Station in Kansas City was lit teal in honor of myasthenia gravis awareness month. Coming off the heels of celebrating our organization’s 60th birthday, the skyline of Kansas City was capitalized with the iconic building standing teal.
As I stood at the Liberty Memorial and gazed out over the skyline, I couldn’t feel prouder of my journey and of the impact the Myasthenia Gravis Association has had on the rare disease community. There are 60 years of rich history intertwined throughout the heartland of dedicated staff, board of directors, medical advisory committee members, professionals, patients, and families who have all worked to lay the foundation to keep the glimmer of hope going.
While the light didn’t shine bright for a lot of people in 2020, a lot of pieces are coming back together as a re-emergence from COVID-19 begins. I hope this glimmer of light is a reminder of all the amazing things that are happening in our MG community right now. There are a handful of clinical trials of new potential treatments. There is one in fact, in the FDA pipeline for hopeful approval by the end of the year, and there are numerous ways to connect with groups across Kansas, Missouri, and NW Arkansas both in-person and virtually. Remember, when your light starts to flicker and you feel you are losing hope, think of the community that surrounds you. It takes a village to fight myasthenia gravis and we are all on this journey together. Keep shining, friends.

Friday, March 12, 2021

Rosé

Not every day will be Rosé but there is Rosé in every day. Might be the cheesiest thing I ever wrote, but goes with the picture! Reflecting on time I got to spend last week in St. Martin. 2020 was hard. It aged me. It changed me. And 2021 has been hard and hectic. But the warmth and the sunshine reminded me that there is change with every season and hope. Cheers to spring, vaccinations and future glasses of Rosé shared with others......



Tuesday, February 16, 2021

Hardships?

As I was talking on the phone this morning, I noticed a chip out of my brand new wood floor, and then two other small scratches.  A pit grew in my stomach.  How could something like that happen on something so new that I've taken such good care of?!

I've been pretty MIA from this blog for many reasons, but one being because I completely renovated my house.  Someday, a blog post will follow all about that! For nearly 8 weeks, I was living a crazy, chaotic life and am finally just resettling. So you can see how those discoveries would be upsetting.  End that call and get on another when it was abruptly stopped due to a rolling power outage.  (My work phone runs through the computer)

I was irate.  I have stuff to do! My to do list never ends.  For the last 3 years of my life, I cannot seem to get ahead or tackle things like I used to and I am plagued with this feeling of never being complete.  It keeps me up at night!  But as quick as I got mad, I got calm.  We've been living in this frozen tundra for the last 2 days and rolling power outages were predicted as a part of the energy management.  I should also add, we've been surviving COVID-19 for the last 11.5 months and flexibility is the KEY.  I scooped up my ever-not-so- friendly rescue dog and got some blankets and went to the couch.

That ever -not-so friendly rescue dog who LOVES to cuddle under a blanket, refused. She was too concerned in the quiet, with all the sounds you don't normally hear to sit still. So she perched on my leg and growled and snarled and growled some more.  Isn't it so funny how we are desperate for quiet moments and for life to slow down, then it happens and we growl about it?

It wasn't the most comfortable 75 minutes of my life.  I drafted this blog post in my head while we waited.  The house got progressively colder and darker.  And there I sat watching it all unfold.  Luckily for Ries and I, the power switched back on. While we continue to wait for the shower to turn back on, it's a small bump in the road in the big picture of life.  2020 changed our lives, changed our relationships, changed our outlooks. What can't we handle today? So whatever you are facing, keep your face to the sun and remember these days of hardship.  

Adversity builds character.

Saturday, November 21, 2020

Watermelon Mules

I know summer has long gone but it's 2020 so why not bend the rules!  I had actually planned to make these in the summer and got the supplies and just never did. Anyway, these are amazing and so refreshing! I'll definitely be making them next summer!

Watermelon Mules

(measure to your preference)

watermelon juice

Vodka

Ginger Beer (I use diet)

Garnish with watermelon



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