It’s been over 2 years since my diagnosis, and I still don’t have the words to really explain all that has changed. It’s been 2 years of struggle, questions, tears, denial, achievement, difficulty, love, sadness, and so much more. I feel like a completely different person most days. But through it all, I try to remind myself, “Today, you get to keep living.”

In June 2023, I was diagnosed with ALS. It has taken a lot from me physically and I am constantly learning and adapting to my every day struggles. But, mentally it has given me a deep sense of gratitude for the life I have and the people who are by my side in it (especially Garrett, who has been my angel through all of this). I choose to wake up every day with perseverance, hope for a cure, and a desire to find joy in the life I get to continue to live.

I am making this post because I would love my community’s support as I join the 2025 Walk ALS Georgia on September 20, 2025. We are walking to support ALS United of Georgia, which has been a program that has helped navigate this journey for me and my family. ALS United of Georgia and Walk ALS Georgia raises money to provide Georgians living with ALS the support they need to live a full life post-diagnosis. We are also walking to support research efforts into treatments and a cure so that an ALS diagnosis is not fatal.

I hope you will Join my team to walk with me on September 20, 2025 at Center Parc Stadium at Georgia State (old Turner Field), and support me and my team by fundraising below.

Every dollar donated supports the programs and services families with ALS right here in Georgia need. From equipment rental and transportation to respite care and financial assistance, families can access the programs free of cost thanks to generous supporters like you.

Melissa