For the past 14 years, It was presumed that I had IGA Nephropathy. Just recently, I was diagnosed with a rare genetic kidney disease called Alport Syndrome. It’s hereditary and 3 of my 4 children have kidney disease. My youngest child also has Alport Syndrome based on genetic testing. Alport Syndrome is an autoimmune disease, no cure but the progression can be slowed down through medications, diet and lifestyle. In the past years, I was on a low protein diet but a year ago I switched to go low carb diet, low protein and high in fats. I also follow Intermittent Fasting Lifestyle.
After 14 years, my Egfr is at 9 and I’m doing Peritoneal Dialysis. My videos show the adapting and evolving that I’ve gone through in terms of diet and food that I eat. Currently, I’m also on Rapid Cellular Balancing Treatment and it’s helping my overall health and wellness together with the low carb diet intermittent fasting lifestyle. I hope to inspire everyone with the same condition.