10th Annual Walk/Run in Memory of Sonia
Pamela Thompson • June 30, 2020
Help us reach our goal of $100,000 raised from this event!

The tenth (and final) Walk/Run in Memory of Sonia Balliet-Heidenreich is scheduled for Saturday, September 5 at Oak Grove Park in Fargo. The walk/run will kick off at 10 am and will be followed by a lunch (details on lunch to be determined pending current COVID status.)
The Balliet family has some lofty fundraising goals for this tenth and final event. Over the course of this event $85,000 has been raised in memory of Sonia in hopes that people living with cystic fibrosis can #BreatheEasier. The Balliet family is hoping to raise $15,000 at this walk to meet the $100,000 mark.
If you have not joined us for this event before, this would be a great chance to see, first-hand, the love and connection CF families have for each other.
The “Sonia Walk” is great fun for people of all ages and athletic ability. It is a wonderful way to spend a Saturday morning to celebrate a life well lived and to support families that are living with the very harsh realities of Cystic Fibrosis.
Register today at bit.ly/SBH5K10

I was able to surpass the limitations that used to hinder me and discover the joy of taking my
life back. By refusing to let my cystic fibrosis diagnosis impede me, I have made an entirely new
definition of “running for my life” and can happily say I no longer meet the requirements of
“Failure to Thrive”.

CFA of ND makes it so much easier for us to travel back and for to Minneapolis for my appointments. I had to make many trips this past year and I hate missing school! We would fly down in the morning and back the same day. CFA provided financial assistance to make this easier for us. I have also been on some amazing medications that have helped me stay healthy and many of those came with a big price tag! Again. CFA helped ease the cost of those meds and helped me stay healthy.

Logan was born in 2005, luckily in the state of Colorado, a state that thankfully had newborn screening for CF at the time (North Dakota does now!). She was monitored with 2 blood tests and she had her first sweat test and cystic fibrosis diagnosis at 28 days of Life. After the whirlwind of emotions and doctors at the Children’s Hospital of Denver, Logan's family learned how to take care of their little girl and then also made the decision to move back to Nikki’s home state of Minnesota to be closer to family and the University of Minnesota!

Molly is our only child and with in days of her birth she was having eye surgery in both eyes to correct congenital cataracts. She had both lenses removed and had to wear contacts as a tiny baby. She had glasses as well that did the same thing as her contacts but only would wear them at home due to the large thick lenses. We called them her "big eyes" as they magnified her eyes so much. Kids can be so unkind to anyone who is different so we made sure that Molly was comfortable and happy with her contacts and glasses. She didn't go to daycare, so my husband would take her with him to work and she was always pleasant and happy.