Polycystic Kidney Disease affects kidney tissue by changing the basic structure filling kidneys with multiples of cysts. Cystic cells replace normal functioning kidney tissue. The cystic kidney cells die and are not capable of being replaced. Eventually for some, polycystic kidneys can start a path toward decreased kidney functioning, eventually culminating with dialysis and/or organ transplant. However, polycystic Liver cells can regenerate new liver cysts. This regeneration produces an expansive liver. Both conditions are inherited, passed within families through the genes. By maintaining the integrity of ones own personal DNA, this can squelch the second hit mechanism that causes an increase in cyst numbers and symptoms.
40% PKD'rs never require dialysis or transplant. Many of us are striving to be included with these healthy individuals. Among our personal choices, are which foods do we eat? Do we smoke? Do we exercise? Do we drink sufficient water? Some have been successful by adjusting these items.
We can modify our exposure to chemicals and kidney toxins. We can adjust how much exercise we do. We can self monitor and record blood pressure readings. We can maintain a running record of past blood pressure readings. We can decide how much water to drink. We can choose to eat foods low in salt. We can adjust our diet so we eat more alkaline plant based foods. We can find the means to lower our stress, enhance relaxation, and increase the blood flow to our kidneys.
With much guided attention from our personal physicians to these many details, we can exert some influence in maintaining health especially the health of polycystic kidneys. This can all begin to incline us toward the lucky 40% of PKD'rs who have healthy PKD polycystic kidneys throughout their lifetime.
We are unable to influence certain things in our lives. We cannot decide which gene we inherited: PKD2, or the more common PKD1 gene, a more aggressive form with an earlier onset of symptoms.
We have no control if we are born male or female. Males with PKD have a higher incidence of cardiac problems and proceed earlier to left ventricular heart failure. If we are born female, and have liver cysts, there is a increased chance of developing severe PLD Polycystic Liver Disease. In both instances these symptoms are hormone related. We can continue to take special care with our overall health. For it is generally our hearts not our kidneys that leads to our eventual demise.
For various reasons, sometimes family members hesitate to get tested for PKD with an MRI until they reach 30. ADPKD has been discovered as early as in utero. A screening test could be a combination of blood pressure checks and a check for protein in the urine. These are two early symptoms that can indicate some type of kidney disease. With a family history of PKD, it is likely to be PKD. These tests can often be found at health fares at a minimal cost.
Definition of ADPKD
There are two genes known to be associated with ADKPD. PKD1 is found in approximately 85 percent of individuals who have ADPKD. This is the more aggressive gene; diminished kidney functioning can occur in the 40's. PKD2 is found in about 15 percent of individuals who have ADPKD. Symptoms do not usually appear until the 60's.
|Stage 1 CKD||Slight kidney damage||> 90|
|Stage 2 CKD||Mildly ↓ kidney function||60-89|
|Stage 3 CKD||Moderately ↓ kidney function||30-59|
|Stage 4 CKD||Severely ↓ kidney function||15-29|
|Stage 5 CKD||Kidney failure||< 15 (or dialysis)|
- Maintain alkalinity
- Correct anemia
- Lower blood pressure
- Increase kidney blood flow
- Decrease proteinuria
- Eliminate kidney toxins
- Drink more water
- Diminish Cyst Growth
- Eliminate Animal Proteins
- Essential Amino Acids
- Use of essential amino acids from Calwood a formula designed for kidney patients. A newspaper article from Malaysian Times, Saving Failing Kidneys, explains how some countries are managing declining kidney functioning without the resources to pay for dialysis or organ transplants. A few PKD'rs have had limited success by working with their nephrologists and following the recommendations of Dr. Mackenzie Walser's book called Coping with Kidney Disease