Every time someone sees me since my transplant, they always ask me how I am feeling now. I guess its a valid question. Everyone says I look so different so it makes sense that they would want to know if I feel any different. There are good things that have changed and there are some… Continue reading So what has changed?
Ah, the transplant games. I remember when I was diagnosed initially and I was doing my work-up for the transplant list, my transplant co-ordinator mentioned the transplant games. I didn’t think much of it then. I had just been diagnosed and all I knew is that I wanted a new kidney. Lets go back in… Continue reading Fitness + The Transplant Games
In my last post transplant blog post (here) I was on Day 5 of my recovery and I was peeing on myself. This resulted in the nurses having to put a bedpan next to my bed as I could not make it to the bathroom in time. My days literally consisted of me getting up… Continue reading General Isolation- Post Transplant Part 2 + going home
The last two weeks have been a roller coaster. I have been struggling to find the motivation to actually write a blog post because I am adjusting to an overactive kidney and a ton of medication. So now I am taking some time to myself and I am going to write an honest post about… Continue reading ICU- Post Transplant Part 1
I get asked a lot of random and sometimes silly questions about my illness. If you have any additional questions, please feel free to ask! What caused your kidneys to fail? I have no idea. The doctors ran 13 different tests on me and they still have no idea what caused them to fail. How… Continue reading Frequently asked questions
Its been a while since I actually did an update on my health. If you follow my blog, you will know that I am on peritoneal dialysis. This means I have a port in my stomach, which allows me to do my dialysis at home. This port is roughly by my bladder. About a month… Continue reading An update
Its been exactly 4 months today since I went to my doctor and told him that I think I have diabetes because my hypochondriac sister said my sleeping habits and memory problems were not normal. Here are few things I have been grateful for over the last four months Taking my sisters advice and going to the… Continue reading Count your blessings
About 10 days ago, I went for my peritoneal catheter placement. The word catheter sounds scary, I know. I have watched enough Greys Anatomy to know that they use a catheter when you can’t urinate. LUCKILY this is not the case with the peritoneal dialysis. Your catheter is placed in your stomach. I am not… Continue reading Peritoneal Dialysis Operation