Gunnar Bratland Fund

Gunnar Bratland was born on 12/7/2016. He was diagnosed with Cystic Fibrosis. He has had a tough road with this disease and we are still learning and growing as a family helping him with it. Gunnar has multiple medications that he has to take by IV, Nebulizer, and orally to maintain his health and prevent Cystic Fibrosis from damaging his lungs. He has two genetic mutations that cause the disease. This was a hard reality to hear when he was diagnosed, but we trust the Lord and are grateful for everyday. He is a beautiful strong little boy that we love dearly. My wife Angela had to leave work early in November a month before he was due as she was borderline pre-clampsia and was put on bed rest. From November until today she has only worked very little and part time. His disease has now put us in a position where she will need to stop working as soon as we can due to his level of care needs and treatments. The cost of her loss of wages, traveling to the University hospital, his specialist, medications, equipment, and more have put us in a tough spot financially. We were introduced to go fund me by a dear friend, and we took their wisdom to create this account. We are believing the Lord for 20,000 dollars to cover all of the bills and expenses we have occured and to cover lost wages that have already happened and that are still coming. We ask if you are able to give to Gunnar's cause please do. Thank you for your support, love, prayers and financial contribution.