Welcoem to posts!!
in the future - u will be able to do some more stuff here,,,!! like pat catgirl- i mean um yeah... for now u can only see others's posts :c
Hey KIDNEY WARRIORS! I’m going LIVE at 8pm on Sunday June 30 . Let’s chat and answer some questions from the community. Please support my LIVE!!! Thank you! ❤️❤️❤️
14 - 1
I eat Chicken Skin as source of fats. But I make sure to fry it in its own oil. Just to remind everyone that my diet is low carb low protein moderate in fats. What’s your specific diet? Leave a comment 👇
14 - 4
Be brave cause everything will be alright 👍
31 - 4
40 - 7
Happy new year to everyone🎈🎆💥 I hope for a healthy and prosperous year 2024. Thank you for all your love and support. Let’s continue the FIGHT👍🙌💪
10 - 4
Happy New Year 🎆 wherever you are in the world. Wishing everyone the best of healthy.Keep the fight!
20 - 11
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.