The Noding Family

Westbrook, MN
$6,785.00 raised of $11,371.63
Utilities – Electric $600.00
108%
3 months
Utilities – Gas $900.00
103%
3 months
Mortgage/Rent $3,600.00
0%
2 months
Utilities – Water $540.00
113%
3 months
Utilities - Phone $638.25
106%
5 months
Insurance - Auto $1,460.20
80%
4 months
Insurance - Renter's $3,633.18
76%
3 months
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    Name
    "Peanut" Noding
    Injury/Illness
    Spina Bifida

    Our little family of four has been impatiently anticipating the arrival of our newest member, whom our 2 year old daughter and 4 year old son have dubbed "Peanut". We found out at 20 weeks GA that Peanut has spina bifida, a genetic condition that causes a deformity in the spine and comes with an array of potential other issues. We also learned that there is a prental surgery that could stop any further damage to Peanut's nerves and spinal cord, and could potentially decrease the necessity of some future surgeries, along with increasing the chance for greater mobility in her extremities.

    This surgery is truly a miracle! It also comes with extended bedrest near the hospital for Mom (3 hours from home), healing from the prenatal surgery and taking care not to go into preterm labor. This also means that Mom cannot work, and will be taking a dramatic pay cut in her teaching salary. Mom will be renting a place for the duration of bedrest, along with the 2 year old daughter. Big brother will join them during non-preschool days. Because of bedrest, Mom will not be able to care for the children. Family and friends have been exhausted for helping out with caring for Mom and the kids during this time, so Mom will need to hire a nanny during the time of bedrest, lasting up to 6 weeks or more depending on recovery and Peanut's stability. We hope to follow doctors orders as closely as possible in order to keep Peanut in and healthy for as long as possible, so she can come join us in this big, beautiful world!!

    November 6, 2020
    Fixing Peanut

    Hello! Thank you all for your wonderful support! This is a new, wonderfully awful journey we are on, and it would have been nearly impossible without all of your support. We are learning and growing with every day, every appointment, every update.

    Luckily, even with a diagnosis as difficult as the one we received, overall Peanut is doing well. She has some fluid buildup on her brain (roughly 11mm), which does not put us out of the danger of her getting shunts after she is born but is better of an outlook than we would have gotten had the surgery been post-delivery. The surgery hopefully corrected the brain herniation. They were able to use her own skin instead of a patch to close up her back, which was wonderful news!

    Peanut has been very active in the last couple of weeks! This is not nearly as comfortable for mom as when the first two were active, but a mobile baby is a blessing worth every ache. We are still waiting for her to be active during an ultrasound to see how her legs are moving, but this is probably something we need to remember is low priority, in all honesty.

    Mom is doing well with healing, Dad is doing his best to keep everyone sane and happy, and the two older siblings (it is crazy to call my 2 and 4 year olds "older"!) are very understanding and careful around Mom. They, like Mom and Dad, are so excited to meet Peanut!