Hey everyone, I am not one to ask for help, but here I go. Back in January 2024, my wife Amanda was diagnosed with Systemic Sclerosis, a rare autoimmune disease that most doctors don’t know much about. It was a shock for both of us, and we’ve been learning to navigate the challenges that come with her diagnosis.
Then, in August 2024, I was diagnosed with Multiple Sclerosis after losing feeling in my legs, experiencing mental issues, and dealing with extreme exhaustion. Since July, I have been unable to work. I took enough from my retirement to cover our short-term expenses, but unfortunately, my job was posted and I am now battling with long-term disability and applying for SSDI benefits.
We are doing everything we can to stay afloat, but the financial strain is overwhelming. We are reaching out to our community for any help or support you can offer. Your generosity would mean the world to us as we face these health and financial challenges together. Thank you for considering helping us during this difficult time.
Then, in August 2024, I was diagnosed with Multiple Sclerosis after losing feeling in my legs, experiencing mental issues, and dealing with extreme exhaustion. Since July, I have been unable to work. I took enough from my retirement to cover our short-term expenses, but unfortunately, my job was posted and I am now battling with long-term disability and applying for SSDI benefits.
We are doing everything we can to stay afloat, but the financial strain is overwhelming. We are reaching out to our community for any help or support you can offer. Your generosity would mean the world to us as we face these health and financial challenges together. Thank you for considering helping us during this difficult time.

