Craig’s Story

Site created on June 2, 2018

Welcome to our CaringBridge website. We are using it to keep family and friends updated in one place. We appreciate your support and words of hope and encouragement. Thank you for visiting.


Saturday June 2nd 10:30pm
Its been officially 24 hours since we first thought we were going in for migraine medication for Craig, where we learned that the headaches he has had for 4-5 days were much more serious than we thought. Its pretty crazy when you receive that news, it doesn't feel real and when the Physician Assistant said those words, "I have bad news, we are seeing a mass in your brain on your CT Scan". I can tell you, nothing prepares you for that moment. These things are not supposed to happen, especially not to Craig, not to my husband and the father of our son. Time doesn't stop because your not ready for that moment - luckily the staff at Essentia were great and let us know we needed to proceed with a MRI and get Craig admitted to the hospital. 


During this time our good friends Alicia and Al had already stepped in to take care of our dog and our 2 year old son Reeve. Thank you. Thank you. 


The next few hours ticked by slowly, but by 6:00am Craig's parents and sister were in route to Fargo and my parents shortly after. 


Now today, Saturday around 3:00pm we met with the Neurologist and discussed the MRI that was taken the previous night. The mass or left frontal lobe tumor is approximately the size of a lime. Which more than explains the pain he's had this week. The Neurologist let us know our next step is surgery and to remove as much of the tumor as possible. The surgery is this followingThursday. Craig will be in ICU for at least 2 days, and then moved to the hospital for 2 more days before returning home. We won't know much about our road to recovery until about 10-14 days  after surgery. We are told the tumor has to be tested to tell us about it, and to see if its benign, or the other 100+ other possibilities. Then we will know if we will need Chemo or Radiation as well.  


In these short 24 hours we have had a rush of emotions and are still processing the news ourselves. We have lots to pray for, lots to be thankful for, and appreciate all the kind words we've received thus far. Craig is a champ, strong as hell, heck - he ran the 10K just 2 weeks ago with me (and he didn't train!), he has limited symptoms, and the tumor seems to be secluded to a singular area and no where else in his body. Plus on top of that we have a wonderful network of friends/family and tons of prayer warriors. Thank you all for praying and caring for Craig. We love you all and will keep you updated as we learn more each day. 


- Candice 



Newest Update

Journal entry by Candice Ahmann

October 20th will mark 1 year since Craig’s death. This month has been grueling but also good in so many ways. The fact that its only halfway over is a little fatiguing to just think about though. I was told by someone recently that there are times in our life we thrive and sometimes in our life we just need to survive.

Earlier this year, I thought with time possibly my grief might fade or go away, but I am realizing now that grief will always be a part of who I am. I will always grieve the father of my children and the dreams I had of growing old with him. I am sure that my grief will shape and change over time, but I have concluded that this will never go away.

If anyone has heard me talk about my children, they may have heard me say – that without them I may have not made it through this year. Shortly after Craig passed away, I remember laying in bed. I was hoping that I could shut my eyes and sleep through the day. That morning Reeve sat on my chest. I was pregnant so in all reality there wasn’t much room there in the first place, but anyway he reminded me that I had to get up.

A few days later, we buried Craig’s ashes. At the cemetery Reeve made a leaf nest and ran around like the crazy toddler he was. He laughed and played with his friends.

Then 2 days later, the crowd dispersed, and people had to leave and go back to their lives. We were alone. Reeve and I had to figure out how to be a family together. He has challenged me. Asked questions. Both of us have had big feelings. He has taught me how to talk about the tough stuff. He has been the constant reminder to keep pushing forward because life doesn’t halt even if you feel like it should. 

Then in February on the 14th, my 2nd son was born. Kellen Adrian Ahmann. To say that light can come from darkness is a true understatement when it comes to this child. The smile he shares each morning with me, the way his eyes light up --- this is him truly to his core in most hours of the day. I dare anyone to try and not smile back at him. Happy 8 months Kellen. You are a true gift from GOD.

Craig Michael Ahmann will be forever missed. Thank  you for giving me the best reminders to keep going, to keep laughing, to live without fear, and to keep hoping for a better future. I am forever grateful for the life that I had, the life that I have now, and the future I have with our babies.

Love Always.

 

 

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