Having hypertension means having to take mutiple medications so that I can function day to day.
I have to do dialysis every day at home for 9 hours. Sometimes its hard since I am on cycler and it pulls my insides so hard to the point in which I want to stop doing dialysis but I know that I cant, my life means to much.
This is the most difficult thing that I have every had to write. I am in need of a kidney transplant. I need to let my family and friends know about my condition. I am currently on the transplant list and I have been on it for the last 9 months. I am on dialysis every night for 9 hours in my home on a machine, which I am thankful for, which keeps me alive and I am thankful to God for that. I still work as a Patient Care Tech taking care of clients who need me. By the time I get off I am exhausted but I know that I have to set up my machine which takes awhile to do, then I get on my machine to begin my dialysis. This is EVERY DAY FOR 9 HOURS! I am pursing a living donor for two main reasons, ( but there are nany others), kidneys from living donors last, on average, twice as long as kidneys from deceased donors and the waiting list for a deceased donor kidney could be more than 5 years. If you feel like you are that person that can help me please feel free to contact my Live Donor Coordinator:
Ashley Sauers 410-502-6102
Asuers1@jhmi.edu
Or you can go to
WWW.hopkinsmedicine.org/transplant to learn more about Live Donors.
If you are considering being a living donor please use links below to contact Betty Moore's Transplant Center. Begin by completing the donor questionnaire
Did you know?
Medical expenses for living organ donors are 100% covered, and inquires from potential donors are 100% confidential! Contact the Transplant Center to learn more about living donation.
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