A day I will never forget. I was practicing yoga when I collapsed in a high plank pose. It was not more than 24 hours after I lost my mom Nona to lung cancer. My right arm gave out. The weakness was something I had never experienced before We thought (my Dr. and I) it was due too a long battle with several spine issues. But we were wrong. During the first visit with a Neurosurgeon they noticed constant muscle twitching and atrophy starting in the right arm. When the Neurologist told me I had Motor Neuron Disease aka ALS I froze. I think I’m still in shock! It was September of 2022. There is no cure. They said I had no more than a year of being able to get around on my own. Most people describe this disease as the most evil disease a person can go through. The survival rate is zero and most people die within 2-5 years from the start of symptoms.
My mind stays sharp but it attacks all the muscles that we use with out even thinking about it. Breathing, eating, talking, walking, writing, speaking, swallowing etc.
But there’s no way I was going to just sit around and except what these doctors were telling me. So I started doing my own research, and I always knew that Peptide therapy was something that could possibly assist in slowing the progression or finding a way to keep strength. And I am so grateful that I have continued to go down that path because I have now had the disease for 2 1/2 years but I am now at a point where I can no longer use my arms. I have what they call head drop syndrome my walking is extremely laboring, and I now find it easier to get around places in a Wheelchair.
Through all of my research and working with specialists, I have found a Neuro specialist (link below) that, for the first time ever, is seeing some results with their unique mixture of Plasmalogen therapy, peptide therapy, ozone dialysis and extensive blood analysis. It’s going to require me to be in a facility for three months.
My biggest fear is that I’m going to wake up and not be able to breathe on my own, needing to have a breathing tube inserted. At this point I just refuse to live like that. I feel like this is my last chance at life and I’m praying that I can raise enough to make it there in time.
Please reach out if you have any questions and I will try to update everyone as much as possible, especially if I’m able to get to the facility in time.
Thank you so much for taking the time to read this.
Corey
https://www.theepochtimes.com/epochtv/how-toxins-could-cause-als-the-disease-sandra-bullocks-partners-died-from-5478755
