Jackee Austerman gets real about PKU
Back to Blog · May 11, 2017 · Fundraising Ideas
This post was written recently by Jackee Austerman, and I asked her if I could share. It is wonderful, so truthful and incredibly heart-felt. Jackee and her family have a fund that they promote here at One Mission. Their goal is simple. They want to raise awareness about PKU and help fund raise for a cure. See what she has to say about having two kiddos with PKU.
Written by: Jackee Austerman
Well that hit me like a ton of bricks! Shane happened to call me and thought something crazy had happened! So many tears! I was completely sobbing! Two of my friends posted about PKU Awareness Month today. Totally unexpected. Totally out-of-the-blue. For our kids. For our family. For me.
PKU Month is something I have totally championed the last couple years. I post pictures and videos. Fundraisers. Thoughtful stories of my kids. PKU Month is so IMPORTANT for spreading awareness!
But this year, I’ve just felt overwhelming guilt. I haven’t been creative. I haven’t been vocal. I haven’t had great ideas or posts. I haven’t even shared last year’s awesome videos, pictures, and awareness spreading!
Like every other Mom, I really want to do this job right. I’m confident that I can mess up a lot of things in my life, but I do not want to mess this ‘mom thing’ up. I will try my hardest to give absolutely everything I have to my kids.
But I have to tell you.
I’m so tired.
Not like ‘I’m tired today’ or ‘I’m tired this week’ …I’m like 7.5 years tired.
I remember the exact moment when Zay was 6 days old and I held him at UofI Pediatric Specialty Clinic. I tear up every time I recall my exact thoughts…I looked at my brand new baby and thought…’We made a broken baby…this baby, that is ours, is broken’ Do you even realize how hard it is for me to admit that I had those thoughts? I described my own son as ‘broken’ when he was only DAYS old. Newborns are flawless and innocent and perfect. How in the world could the word broken come to my mind. But all I knew was what the doctors were telling us and we couldn’t fix this problem with our baby. We just had to learn to live with it. A reality that I still wrestle with 7.5 years later.
I’ve spent so many days since that moment trying to help everyone else in our world understand what I didn’t understand that day. What PKU is. What it means for our family. What it means for Zay and Ellie. The research. The setbacks. The hope. The struggles.
From the moment I became a Mom, I became a PKU Mom. I know nothing different. But I think most Moms are tired. I’m just going to throw it out there that sometimes PKU Moms are reeeally tired. And then we cry a lot…or maybe that’s just me. 😉 (Anyone feel free to tell my husband that it’s not just me)
And Shane… Shane feels the pressure to provide…not in a normal way, but in the way that his job provides health insurance. It’s never just a job and you can find a new one anywhere…it’s undeniably our kid’s lives and health. Our kids would be in an institution without these things. (I will spare you the videos of untreated PKU). I seriously get concerned about the stress Shane endures for our family. He is our kid’s biggest advocate!
There is absolutely nothing I would change about our life. PKU or not, we are so blessed. But today I realized more than ever that I really do need the help of others on this journey. And God blessed us in great big ways in the friend department. I am literally brought to tears that others remember and post and spread awareness for us…especially when I am exhausted and don’t feel like I can do it all on my own. There is no better feeling than a friend loving on your kids.
My heart is so thankful if you are still reading this. If you feel called to help us spread awareness, feel free to share this little part of our story to spread awareness. If you feel called to support, we would be so grateful if you wanted to make a One Mission Purchase through Zay & Ellie’s Fundraiser…everything goes to the National PKU Alliance for Research.