Help Becky Get Stem Cell Therapy for MS

Hi, my name is Becky. I’m 45 years old, and I’m living with primary progressive multiple sclerosis (PPMS). I was diagnosed in April 2017, and by 2018, I had lost the ability to walk and became fully wheelchair-bound. Today, I am considered a quadriplegic.

I’m raising $25,000 to receive stem cell therapy at Giostar Mexico, a clinic that offers cutting-edge regenerative treatments that could give me a chance to regain even a small part of what I’ve lost. Traditional treatments have done little to stop the progression of my condition. This therapy gives me hope—not for a cure, but for a better quality of life, greater independence, and relief from the daily struggle.

Primary progressive MS is a less common form of multiple sclerosis—affecting only about 10–15% of those diagnosed. Unlike relapsing-remitting MS, PPMS progresses steadily without distinct relapses or remissions. It’s typically more aggressive and more disabling, and unfortunately, has fewer treatment options.

I’m still me—my personality, my heart, my sense of humor—but my body has become a shell of what it used to be. I wake up every day and fight with everything I’ve got, but I’m reaching a point where I can’t do it alone.

Things most people do without thinking—scratching an itch, brushing their hair, repositioning when uncomfortable—are things I need help with. Imagine needing assistance with everything, even the tiniest of tasks. It’s humbling, it’s frustrating, and it’s exhausting.

Stem cell therapy gives me the possibility of reclaiming even a small piece of my independence. I would give anything to gain back a fraction of the mobility I’ve lost.

If you can donate, no amount is too small. And if you can’t, please share my story. Every dollar, every message, every share gets me one step closer to this treatment—and to the hope I’ve been holding onto for years.

Any funds raised beyond the initial $25,000 goal will be placed into a dedicated medical account to help cover future stem cell treatments or medical needs related to my MS journey.

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

With love,

Becky