Here's my occasional reminder...
Please remember that the things I write about in this blog are a direct reference to my personal experience with polycystic kidney disease. How my body reacts to medicines, treatments and care plans are mine alone.
How I progress through this disease is solely about my body. How any other patient might react to similar treatments and circumstances is a purely individual thing. I am simply relating to others my singular experience.
Any other PCKD patient could have a wholly different experience that in no way resembles the journey I am taking.
Please, always consult with a specialist to determine the treatment that is right for YOU! Only your doctor can determine what your body needs to best fight this disease and lead you to the best possible outcome.
Thank You!
ScottW
Helpful Renal Websites
- American Journal of Kidney Disease
- Davita Dialysis
- Intermountain Donor Services
- National Kidney Disease Education Program
- National Kidney Foundation
- Natl. Kidney Foundation of UT & ID
- Renal Support Network
- Slide Show: Drug Therapy in CKD
- The Transplant Experience
- United Network for Organ Sharing (UNOS)
About Me
- It's As I See It
- I am an amateur historian who loves to study early US history and the founding of our Country. I also delve into Greek, Roman, Egyptian, Scandinavian and Mongolian histories, and occasionally dabble with Japanese and Chinese histories, as well as the archaeology of the pre-Columbian Americas. Besides history,I love to study Astronomy, Political Science, Medicine, and many other areas besides. Amongst my personal activities of interest are Hiking, Outdoor Photography, Golf, Baseball, and Writing.
No comments:
Post a Comment