Blayke's quest to control MS

Hello my name is Blayke. Over the past six years I have had a long tumultuous battle just to get a proper diagnosis of Multiple Sclerosis. After years of gritting my teeth and working through increasingly bad symptoms, in September of 2019 I got the official call from my neurologist. Relapsing Remitting MS, aka stage 1. Sixteenth months on disability, six rounds of IV steroids, two rounds of immune system depleting MS medication and near financial ruin later, I feel I am not much further along, if at all. With the help of my doctors, we have made a new plan - oxygen therapy to super-oxygenate my blood in order to decrease the inflammation causing nerve degeneration and increase angiogenesis (blood and oxygen profusion). This will cover 1 year of oxygenation (hyperbaric chamber), and also a supplement regimen to restart mitochondrial cell function. Unfortunately, this is expensive specialized therapy. My family and I have run out of money to fund it. Without your support, I will not be able to get these specialized treatments. Anything you can give is greatly appreciated. Thank you so much. Sincerely, Blayke