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Joe M.
Re: Life after transplant
Sun Oct 31, 2010 1:47pm
164.47.8.55

Jodi and Amy,

It is so wonderful to read all this.

I will try to make a Facebook page soon!

- Joe

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  • Life after transplantAmy Hillis, Wed Oct 27 7:09am
    Hello! It's been a long time since I've posted out here. Life always gets the better of us! I've had 4 children born with citrullinemia. We lost one, the other 3 have all had liver transplants. yes,... more
    • Re: Life after transplantJodi Phelan, Thu Oct 28 10:23pm
      Oh Amy,I am praying that things will improve. That statement speaks volumes to any parent considering it after all you have had to deal with.If it was not for this web site I dont think McKayla would ... more
      • Re: Life after transplantJoe M., Fri Oct 29 8:46am
        Jodi. . .you made my day! I keep wondering if I should migrate this 10 year old site over to Facebook - but I sure like the discussion board here. Maybe I should create a presence over there but... more
        • Re: Life after transplantAmy Hillis, Sun Oct 31 8:11am
          Absolutely go to Facebook!! I think you may be able to reach more people there! I agree with Jodi, this site has made a difference - I may not always respond to posts, but I read them all and have... more
        • Re: Life after transplantJodi Phelan, Fri Oct 29 9:28pm
          Good Joe cause this site changed our life! I am glad it is true I remember the very day I found this site. I said I am thinking about transplant,and I got the response whats to think about and at... more
          • Re: Life after transplant — Joe M., Sun Oct 31 1:47pm
    • Praying for u!Kelly Corby, Thu Oct 28 4:32pm
      Amy, I'm hoping that your little boy gets better, alot of prayers and support help! I have talked to or gi dr in Philadelphia she told me to talk to my daughters metabolic drs about my decision of a... more
      • Re: Praying for u!Joe M., Fri Oct 29 8:45am
        Kelly, Pub Med has lots of good research. Also, you can befriend the ASA Kids group on facebook and ask parents questions. I'm assuming you've already been to nucdf.org - thank God for them! - Joe
        • Thank you!!Joe, Fri Oct 29 9:33am
          I have contacted NUCDF since Alysa was born they have been so helpful, now facebook is hard bc I don't know where to look for parents, I found a few from other parents but if you know any please let... more
    • Re: Life after transplantJoe Marquez, Wed Oct 27 9:54am
      God Bless you Amy. Losing a child and another stuck in the ICU after his transplant. My son Justin has had his fair share of complications - including time in critical care (the only place where care ... more
      • Life After TransplantMichelle Ping, Fri Oct 29 12:49pm
        My daughter Katy is the exception to the rule on transplantation. She is 14 and 1/2 years post liver transplant and has never had a rejection episode nor has she ever been in the hospital since she... more
        • Life After TransplantJodi Phelan, Fri Oct 29 9:42pm
          McKayla as well she is 13 and Transplanted January 5,2004 and has never returned to the hospital she only spent 12 days in and I spent 7. I was asked to go and speak at a conference in Vancouver,... more
          • Re: Life After TransplantJoe M., Sun Oct 31 2:04pm
            I love reading these stories about Katy and McKayla. I know Justin has had an infinitely better life than the trajectory he was on before his transplant. Before TRUE Kids existed - the Ping and... more
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