Shawna Broadbent is my daughter-in-law diagnosed with ALS on January 17 2025. She is selfless, courageous, and keeps a smile on her face. Shawna is a fighter and I am very fortunate to have her as my daughter-in-law. Unfortunately her ALS is a rare genetic mutation.She has the opportunity to receive treatments from Columbia University in New York to slow the progression or reverse her cells. She has TDP-43 mutation. We desperately need help right away. She has an appointment set for May 28, 2026 for genetic testing, lumbar puncture in her spine, skin samples, blood tests, and nerve tests. The results are going to take at least 4 months. Their hope is to replace bad cells with healthy cells. This could be the breakthrough she needs to survive longer or reverse the mutation. Her goal is to help other people with life threatening conditions get the research they desperately need as well. Shawna’s need for donations are crucial and needed as soon as possible. So please donate if you can. God bless