Stand by Naomi in Her MS Battle

Hi everyone,

I’m reaching out with something I never thought I’d have to write—but life with multiple sclerosis (MS) has humbled me in more ways than I can count. I’m asking for your support during one of the most difficult chapters of my life.

After living with undiagnosed MS symptoms for over 15 years, I finally received the correct diagnosis—but the damage was already widespread. I have lesions throughout my brain and spine, affecting my mobility, coordination, and cognitive abilities. My executive function is impaired. I can’t walk or stand without help, and I rely on a large upright walker that’s almost as tall as I am (I’m 5’10”). Traveling with it is difficult, but necessary, as I attend multiple weekly appointments for physical therapy, occupational therapy, specialist visits, and soon, neurological therapy.

MS is an invisible disease, but it impacts every part of my day. I fight to remain independent, focused, and positive—but the truth is, I’m suffering. I recently moved back to New York City, not for free or without cost, but because I needed to be closer to family and friends while I navigate this complicated and life-altering disease.

I am months behind on rent. A predatory loan company calls and emails constantly. I applied for both SSI and disability benefits but was rejected—both are currently in appeal, a slow and uncertain process. Meanwhile, I’m trying to restart my career in screenwriting, but that path is made harder by a body and brain that don’t always cooperate.

Despite everything, I’m still fighting. I’m still here. I’m still hoping.

Any amount you can contribute will go directly to basic living expenses—housing, transportation to medical appointments, and survival while I continue to seek the support I need. If you can’t give, please consider sharing this with someone who might be able to help.

Thank you for reading, for caring, and for believing in me.

With love and gratitude,

Naomi