Reminder

To My Readers:

Please keep in mind that this blog reflects my journey through the process of PCKD advancement, dialysis, transplant and post-transplant life.

My journey is in no way indicative of the typical or average PCKD experience. Any treatments, procedures, meds, etc have been cleared by my doctors.

How your body reacts to the disease, any medications and associated S/S's (Signs and Symptoms) is a purely individual experience. Always follow your doctors advice. Discuss any variations from your treatment with your doctor before starting.

Thank you for your continued support, and for following me on this journey.

ScottW