PLEASE HELP DANIEL WRIGHT DONATE A DOLLAR TODAY

I was diagnosed with Multiple Sclerosis (MS) in 2012. After several failed medications, I received a Hematopoetic Stem Cell Transplant (HSCT) in 2016 and unfortunately, quickly started progressing. Within 6 months to a year, post transplant, I relied on a cane and scooter. I then pushed to get properly tested for Lyme disease through a Lyme literate lab and I received a positive diagnoses for both Lyme disease and Bartonella.

Treatments are limited for me as all the MS meds make my disease worse and disability continues to progress. Ozone therapy seems to check all the boxes for what I need to focus on, but the cost of going to a clinic for multiple treatments on top of the other therapies I’m needing, make Ozone nearly impossible to obtain, unless I have my own unit in my house that I can self administer.

As I was developing my 2025 treatment plan, Ozone was added as a dream, but I believe in writing it down, praying over it and letting the dream work itself out. The Ozone Foundation popped up as a suggested group on Facebook, to which I found out that they help people like me, obtain their own unit. My heart raced as I anticipated this part of my 2025 protocol becoming a reality.

I’m quite excited to begin using Ozone to help kill pathogens and give my body the chance to do what it was created to do— heal itself!