It has been six-months since my kidney transplant. So far, so good! My doctors’ visits have been good, and my lab work has been normal. Hopefully, there will be no changes in my medication levels for a while.
It’s been three months since I posted a personal note. What’s going on with me since then?
1. I have been cleared to start some core abdominal exercises. Hooray! I started Yoga this week. Well, I learned that I have a long way to go to get back into shape! LOL
2. I am still posting to my blog. Please check it out!
3. I have been trying to help my parents get situated from a few states away. My mother can’t stay in the house anymore and my dad can’t really help her. They have an aide during the day — but this week, her doctors upped that to 24 hour care. I think they are going to move into a senior care facility in my hometown. I tried to move to nearer to me, but my mother is being stubborn. Oh well, what can you do? When they get ready to move, I will have to travel back to Alabama to help clear out the house.
4. I am finishing up my first novel. An editor friend of mine is editing it. Again, so far, so good.
5. I am still publicizing stories from people looking for donors or people who donated. Just email me through the site.
My donor is doing well, and we text each other at least once a week.
Send in your stories about people who need a kidney and please share the posts with your friends– remember more eyes, more exposure!
My name is Cindy Elrod. I am a wife, a mother, and I need a kidney. I was diagnosed with Polycystic Kidney Disease in December 2013. I have been on the waiting list since then. I am on two waiting lists, actually, in hopes that I will be able to receive a transplant sooner rather than later. The most certain and expeditious way for me to receive a transplant is to reach out to potential living donors. I am sharing my plea and hope that you will make the call to be tested should you feel compelled to do so.
Since being diagnosed with PKD and renal failure, I have been on peritoneal dialysis. For 9 hours each night, I am hooked to a machine designed to rid my body of toxins since my kidneys can no longer function as they should. I visit the doctor as least twice each month, have monthly labs drawn, and went from taking no medications to taking ten pills daily. Needless to say, it is a lot to keep up with and can be physically exhausting. I am limited in my ability to travel to spend time with family and friends, as the equipment and supplies required for peritoneal dialysis are bulky and numerous. I also have diet restrictions to include no chocolate, ice cream, or sodas.
Receiving a transplant would change my life in so many ways. I would have the time and energy to be the active mom I would like to be. I would be free from dialysis, allowing me more freedom to travel and visit family and friends. I would feel better and be able to enjoy the things I am currently missing.
If you would like to be tested as my potential donor, I could never thank you enough. My blood type is O. I can receive a direct transplant from all Type O blood types but anyone could potentially help me, as both of my transplant centers participate in the Paired Exchange Program.
This is a post of another person looking for a donor. Please share!
My name is Manjinder Singh and I was diagnosed with kidney failure in 2013. The exact disease that I have is known as IgA Nephropathy. I had always lived a simple and clean life, so to have heard from the doctor’s mouth that I have kidney disease was surprising to say the least. My initial response was that of disbelief and quite frankly I thought someone surely must have made a mistake in the diagnosis process. I thought to myself how could someone who has never drank alcohol, smoked, or done any other drugs be hit with kidney failure at age 23. Surely this was a bad dream and I would wake up from it.
Unfortunately this was reality and for the next several years I would live with the idea that I will one day end up on dialysis and need a transplant. That day arrived in June of 2016. I received a call from my nephrologist telling me that I need to go to ER right away. I was in end stage renal failure and would need dialysis to sustain my life. As one can imagine it was a traumatic moment in my life. Here I was sitting in a hospital waiting to be dialyzed for the very first time thinking in my mind that I was supposed to be the one taking care of patients not becoming a patient myself. You see, I had high aspirations of becoming a physician. I had finished my Bachelor’s degree, taken the necessary tests and obtained the proper experience to enable myself to apply for medical school.
Unfortunately it wasn’t meant to be as my condition wouldn’t allow me to handle the ever so demanding coursework of medical school. Though this was a hard pill to swallow, I stayed positive and moved forward. Dialysis became part of my life, in fact it became the reason I have a life. I currently attend Hemo- dialysis three days a week for 3.5 hours each treatment. I have had significant changes to my life ever since I started dialysis. For example, I am always on a fluid restriction, which is absolutely horrible for someone who loved drinking water and juice. Besides controlling fluid intake, I have to always watch what I eat as well. Avoiding foods high in certain nutrients is key to sustaining longevity while on dialysis. Besides the drinking and eating component, your overall lifestyle changes as well. I haven’t been able to work out since starting dialysis, nor do I have the same energy level as before.
Being in kidney failure has not just impacted my life, but it has also drastically impacted the lives of my family members. They have struggled right along with me for that past several years now. My family has left no stone unturned in an effort to find a solution to my problem. My mother in particular has been an angel for me through this process. She takes care of me on a daily basis, and continues to believe that her son will be healthy and thriving very soon. My brother and sister-in-law have done everything possible to help get through this difficult period in my life. My father, who is an exceptionally hardworking individual, makes sure that I stay positive even when things get really difficult. I know my reality now more than ever before. I am in end stage renal failure and I have accepted that truth. My only solution to have a normal life again is to receive a kidney transplant.
I am highly convinced that upon receiving a kidney I will have a completely different outlook on life, in fact I already do. A second chance at life will mean everything to me and my family. A chance to live out my dreams again, a chance to attend medical school and most important a chance to help others in need. My inspiration remains the same as before. I have always sought ways of helping those that are less fortunate. Community service is a huge concept in my religion and it is something that I value very much. If I am given a second chance at life, I will make sure it doesn’t go to waste, but rather I become an example of someone who did the right thing.
If after reading my brief story you feel like having yourself tested to be a potential donor, please contact the following transplant center and/or visit the following link to fill out a kidney donor questionnaire using my DOB of 10/07/1988 and full name of Manjinder Singh. I thank you for reading about my struggle and possibly considering to be a donor.
My Transplant center participates in paired donor exchanges, so any blood type will work, however, blood types A+\- and O+\- are most likely to match.
California Pacific Medical Center (CPMC): 415-600-1700