With Gratitude & Hope: Standing Strong in My ALS Journey

Hi friends, family, and kind-hearted supporters. My name is Carol and I'm reaching out for help as I navigate life with ALS (Amyotrophic Lateral Sclerosis) and also known as Lou Gehrig’s Disease, is a progressive neurodegenerative disease that has profoundly impacted my daily life.

I was diagnosed with bulbar ALS, which affects my speech, swallowing, and breathing. I now rely on a feeding tube for nutrition, breathing support, and regular medical appointments to manage symptoms and slow progression. Due to the severity of this disease, I’m no longer able to work, leaving me with mounting medical expenses and everyday costs I can no longer cover on my own.

ALS is a relentless and expensive disease. One of my medications alone costs nearly $800 a month — even with insurance. There are also medical supplies, equipment, transportation to specialist appointments, and home adjustments to help me stay safe and comfortable.

Your generosity will help cover:

• Critical medications and treatments

• Medical equipment and supplies

• Transportation to and from appointments

• Home modifications to ensure safety and accessibility

• Basic living expenses as I can no longer work

I am incredibly grateful for the love and support of my family, friends, and community. Every donation, no matter the size, helps ease the financial stress and allows me to focus on what matters most — living each day with dignity, comfort, and hope.

If you’re unable to donate, sharing this page is also a huge help. Thank you for your kindness, compassion, and support during this challenging time.

With much gratitude

Carol