Hi, my name is Regina, and I want to thank you from the bottom of my heart for taking the time to hear my story.
Last year, I was diagnosed with ALS, also known as Amyotrophic Lateral Sclerosis. ALS is a progressive and devastating disease that affects the nerves in the brain and spinal cord. Over time, it weakens the muscles needed to walk, speak, eat, and breathe. There is no cure, and each day brings new challenges.
Since my diagnosis, life has changed in many ways. Some days are harder than others, but I am doing everything I can to keep moving forward with strength, purpose, and hope. Staying connected to my friends, family, and the community means the world to me. It helps me feel alive, encouraged, and supported.
One of the most important tools that allows me to stay mobile and active is my wheelchair-accessible van. This van helps me get to doctor’s appointments, therapy, social events, and family gatherings. It gives me the freedom to be present in the moments that matter most. Paying off this van would lift a major financial burden and allow me to focus on my health and well-being.
In addition to helping with the van, I am also raising funds to cover essential needs that are growing with each passing month. These include medical expenses, rehabilitation services, medications, accessible technology, and food delivery services that support my daily life and independence.
If you are able, I kindly ask for your support. Every donation makes a difference, no matter the amount. I also invite you to join us for the upcoming ALS 5K this August, where we will run, walk, and roll together in honor of all those affected by this disease.
If you are not comfortable donating here, you can still make a powerful impact by donating directly to the ALS Association. Their work has brought hope and support to many families like mine. You can visit the ALS website to give directly.
Thank you for walking beside me on this journey. Your generosity, love, and encouragement mean more than words can say.
