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  • #16
    Yes, the cost and number of anti-rejection meds has caused me to re-examine whether I want or do not want a transplant (as well as the 3+ months recovery period-just long enough that no employer is required to hold your job for you...). My mother had 2 cadaver transplants, and neither lasted more than 7 years. Plus, medication interaction problems made her unable to try certain cancer medications when she developed lung cancer, so it is entirely possible that having a transplant was at least a contributing factor in her death at age 76.

    It's like leaving one master for another, plus it will make you ineligible for disability after 1 year. Unless I am GAINFULLY employed, I'm not going to even consider a transplant until I'm 64; that way, when my disability runs out, I'll be old enough for straight social security.

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    • #17
      Sorry Patricia. I have had the same thoughts about transplant. I supposedly am on the list at Cedars Sinai, but alas, as I pointed out to my DaVita Social Worker a few weeks back, I have had no contact with them since I made the list in 2013. Supposedly I am still listed. With my other health issues and my lifestyle, I can honestly say that when I was 21 I never thought I would live past 25; then when I was 40, I was facing that my Mom passed at 41; and now I just turned 50 and have been been on pd for 3 years. I am about to start some in depth research on the subject, but my plans would involve completing grad school (thanks DOR!!!) before I would want to consider the aggressive pursuit.

      As you speak of Patricia, I have lived a very full and rewarding life in my few short years. The fact one doctor told me on Monday that if he did not know already that from my blood work he sees, he would never even be able to tell that I was a dialysis patient or that type II diabetes I recently developed as a result of all the dextrose in pd is even possible based on my labs.

      Short version, I need to really examine a transplant and the issues you present and my own thoughts and desires related to how I want to wind down my life. I have heard stories (I think it was on an episode of Undercover Boss - Wast Management) of one gentleman who has been on dialysis for 20 years. I could totally live a happy and satisfying life if that is truly possible in my current circumstance.

      Thanks for sharing everyone. You definitely make the stress of our shared situations much more bearable and manageable.

      TTFN-

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      • #18
        Originally posted by richolquin View Post
        The fact one doctor told me on Monday that if he did not know already that from my blood work he sees, he would never even be able to tell that I was a dialysis patient or that type II diabetes I recently developed as a result of all the dextrose in pd is even possible based on my labs.

        TTFN-
        Rich did your family have a history of diabetes? Was wondering if you getting diabetes was because of PD or a predisposition to it. With getting Diabetes do you still feel the PD was the right choice for you?

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        • #19
          Originally posted by 1scaredycat View Post
          Patricia when did you learn about the anti-rejection drugs? Did the doctors inform you or did you do your investigation on your own?
          I was sent to the Mayo clinic in jacksonville FL for 5 days right after I started PD, for evaluation for transplant. there they tell you everything you do (and do not) want to know about transplants including the anti-rejection drugs that are so strong they cause cancer all by themselves...seemed like a no-win situation for me.

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