A Beautiful Distraction
I took this photo the day after we launched Being Positioned – the nonprofit.
Exactly one day after the greatest accomplishment of my life became a reality.
We had planned on celebrating, but through a series of unfortunate events, including an incorrect test result, I ended up having to spend it in yet another infusion chair.
Launching a business at the same time as dealing with my condition has been unexpectedly difficult for me.
Thankfully the side effects from my treatment are minimal, but the fatigue it causes has made it hard for me to keep up. Repeatedly working until 10 pm isn’t great for someone in my position, and my late nights quickly took a toll on my body.
The more tired I am, the worse my hearing gets. That’s what caused the false decline on my hearing test – and that’s why I ended up having treatment the day after we launched.
On it’s own, an extra infusion isn’t a big deal. But, the emotional roller coaster of getting bad news and having to redo my appointments all while trying to launch Being Positioned was extremely defeating.
I did what I could to show up every day, but honestly, it was some of the hardest weeks of my life. I was so proud of everything we were accomplishing but incredibly frustrated that I couldn’t just be normal for a bit and get through everything without the drain of being a patient.
It’s hard to ignore that heavy feeling of disappointment each time NF2 taints another life event.
My condition has stolen a lot from us in the last four years. But at the same time – it’s added just as much. After all, if it weren’t for this disorder, I never would have created Being Positioned.
I feel like I’m stuck in a strange reality. One minute I’m on the phone with our trademark lawyer, the next I’m calling the cancer center. Bouncing back and forth between running a business and being a patient – like I’m living two completely separate lives.
But Being Positioned has been a beautiful distraction for me.
It’s given me something to hope for during an otherwise hopeless situation. And having my health temporarily decline while launching reminded us why we’re doing this and how much people living with these conditions need a break.
I know how it feels to be desperate for an escape.
When starting a business or taking any big risk, it’s easy to feel like you’re making a terrible mistake. I couldn’t help, but think I was crazy for doing this and doubt whether people would care about what we’re trying to do.
The weeks leading up to our launch, I started feeling more insecure about the process and worried that people wouldn’t think this is a worthy cause.
So, maybe I needed the reminder.
Maybe the reason I had to go through all of those extra tests and appointments at such an important time was that I needed to remember that I’m not doing this for other people’s opinions.
I’m doing this to help adults suffering the same reality that I am.
I’m doing this for everyone fighting to live a normal life despite the battle going on inside their bodies. I’m doing this for everyone feeling like there is no chance of escaping their reality, even if just for a week. I’m doing this for everyone living the same double life and needing something to hope for again.
And despite my fears about sharing Being Positioned with the world – you did an incredible job of proving me wrong.
Thank you to everyone who wrote such meaningful messages about Cardin and me when you shared our video. We read every single post, and your words of love and encouragement were so healing for us both. And thank you to everyone who donated this last month. Your support and trust mean the world to us.
Don’t forget to subscribe to our newsletter here, so we can let you know when new blogs are posted!
Want to keep up with us daily? Follow us on Instagram at @beingpositioned, @christinamenkemeller, and on Facebook at Being Positioned.
darold adami
A moving testament to what you are going through. Seeing the thoughtful, cheerful, beautiful person we see in our times together, it is easy to overlook the inner struggles you face. My prayers are always with you and Cardin and I look forward to some time together over Christmas.
Christina Menkemeller
Aww thank you Darold! Your constant encouragement and continued prayers mean so much to us. We can’t wait to see you soon!!
Michelle Gage
Perspective is everything in life!! You are a constant encouragement to me to keep the right perspective! We are being positioned. We each have a purpose! Thank you for fighting so hard and being a hero to so many! Love you!
Christina Menkemeller
Thank you so much Michelle!! We love you too and are so grateful for your friendship and support through everything! You guys have been such a blessing to us this year.
Lauren
So proud of you! You’re doing amazing things! You inspire so many people! ❤️
Christina Menkemeller
Aww thank you Lauren!! I can’t wait to finally meet you in January!
Dee Ann Homan
Thank you for sharing the real part of this. As my daughter, age 17, deals with this for almost 5 years, it doesn’t get easier. She has lost her hearing and continues to develop more side effects. She is looking at her first brain surgery this summer. As she wonders what she is going to do for a job, college, life, it breaks my heart as I don’t know how to help or answer her questions. What should be an exciting girls time, (prom, graduation, senior pictures), only brings her sadness and uncertainty. She remains strong and wants to give college a try. We are working on taking a class beginning in January, hopeful surgery recovery will be do-able and she will be able to.
As we pray for more advances for all those with NF2, we continue to take one day at a time and enjoy all we can. Thanks for your story and sharing “the real”.
Christina Menkemeller
Aww I’m so sorry to hear about your daughter’s situation Dee Ann. I can’t imagine how hard it must be to have to watch your young daughter go through life like this and not be able to fix it. Like you said, life with NF2 only gets harder, but your daughter is so lucky to have such an incredible mom standing by her side. Thank you for sharing her story with me and let me know if your daughter ever needs someone to talk to – I’m happy to help in anyway that I can.
Beth Gilbert
I found your blog today through the CFT website. It gives me so much hope. My daughter was diagnosed 3 years ago with NF2. She had just turned 3 when we found the tumor on her optic nerve. It took 6 months for us to learn what she had only after 2 biopsies, 10 weeks of crazy infusions of steroids that didn’t help, and genetic testing to learn she is spontaneous, mosaic.
It has been a whirlwind of emotion as her mom. She is too young to understand what has transpired and how this will be a life long impact. She knows why we do the MRIs every few months but until she is older I do not think it will sink in.
My faith has been tested to its core during these 3 years. Just yesterday our sermon was over mourning through the help of our Lord. In my time of solitude, he spoke to me that I have not come to terms and properly mourned what this means for my daughter and how it will impact her for the remainder of her life. She currently has 5 brain tumors. One on her optic nerve causing complete blindness in her right eye, one on hear cochlear nerve causing slight hearing loss, and 2 on her trigeminal causing extreme facial pain and discomfort.
Thank you for your story!! I needed to find this today to know that there is hope and she will lead an amazing life.