My mother (in her mid 50's) had a kidney transplant approximatly 8 years ago. This kidney failed about a year ago and she has been on kidney
dialysisDialysis
Kidney diet - dialysis patients (hemo) since that time. In the process to be cleared for her next transplant (to be donated by her brother) they have discovered a "leaking heart valve". Doctors feel that the damage has possibly been caused by her being on kidney
dialysisDialysis
Kidney diet - dialysis patients. (At times her blood
pressurePressure ulcer would go as high as 240 over 160-170). Oddly enough her name has come up on the transplant list
twiceTwice-a-day in the last 3 weeks, around the same time we heard about the heart valve problem.
Obviously she and my
familyBirth control and family planning
Choosing a primary care provider
Ewing’s sarcoma
Family troubles - resources are disheartened by this new set-back. Doctors refuse to transplant until she has the heart valve replacement. She was informed today that they would like to schedule surgery as soon as next week. She is fearful to ask many questions, yet I am more afraid of not asking.
My
majorMajor tears
Major-gesic questions and concerns are how risky is this procedure, and what type of valve will most likey used? The little research I have done shows that mechanical valves generally last the lifetime of the individual but the person has to be on anticoagulants. If she does recieve a mechanical valve, could there be conflicting problems either now or later after she recieves the kidney transplant?
She has already had to go through so much that I would hate for her to get a stentless or stented valve, and need it replaced in the future.
A reply as soon as possible is greatly appreciated due to the surgery being called for so quickly. Replys from others in similar circumstances is apprecated as well. Thank you for providing this service. The news I recieve will certainly help to releive my anxiety!