Support for Brad Andrews: A Battle Against ALS
Hello, my name is Jaden, and I am reaching out to you with a heavy heart and an urgent plea for help. In the end of May 2024, my husband, Brad Andrews, who is just 39 years old, was diagnosed with rapidly progressing ALS (Amyotrophic Lateral Sclerosis). This devastating news has turned our world upside down, and we are now facing challenges we never imagined.
**About Brad:**
Brad has always loved being active, whether it was 4x4ing through rugged terrains, exploring the great outdoors, or hiking with his wife. His zest for life, boundless love, and energy are truly infectious. He brings joy to everyone who knows him.
**Understanding ALS:**
ALS, also known as Lou Gehrig's disease, is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. Over time, individuals with ALS lose the ability to control muscle movement, leading to complete paralysis while the mind remains alert and aware. It is a cruel and relentless disease with no known cure.
**Impact on Our Family:**
The diagnosis has been a tremendous emotional and financial burden on our family. Watching Brad's condition and independence to do the things he loves deteriorate has been heart-wrenching, and the medical expenses continue to mount. We are determined to provide Brad with the best care possible, ensuring his comfort and dignity throughout this journey. However, the cost of specialized equipment, treatments, and home modifications is overwhelming.
**How You Can Help:**
We are humbly asking for your support to help cover these expenses and provide Brad with the quality of life he deserves. Your generous contributions will go towards medical bills, mobility aids, and essential home adaptations. Every donation, no matter how small, brings us one step closer to ensuring Brad's comfort and care.
Thank you from the bottom of our hearts for your kindness, generosity, and support during this incredibly difficult time.
With gratitude,
Brad's family