TransplantCafe.com - The Gift of E-Life!

Featured Groups

Most Active Groups

  • Stop Copper! Support Wilson's Disease!

    Stop Copper! Support Wilson's Disease!

    7 members
    Latest Activity: Jul 15

    This group is looking for the small percentage of people who have lived undiagnosed their whole life until going into Acute Liver Failure as a result of Wilson's Disease. WE WANT TO MEET YOU!!!!

  • Team Southern California - U.S. Transplant Games!

    Team Southern California - U.S. Transplant Games!

    16 members
    Latest Activity: May 6

    This group is for all Members of US Transplant Games Team Southern California. Join up to discuss everything related to the games, find teammates, set up practice meets, etc.!

  • Team Prograf

    Team Prograf

    38 members
    Latest Activity: 16 hours ago

    This is for those of us who take Prograf as a main immune suppressive drug. We can discuss side effects, etc. Or, we can just keep a head count of how many in the community take Prograf.

  • Team Maine

    Team Maine

    4 members
    Latest Activity: May 28

    This group is primarily for Team Maine members to discuss upcoming events, meetings and of course the Transplant Games. But we welcome everyone to join our on-line community.

  • Team Ohio

    Team Ohio

    12 members
    Latest Activity: Jul 20

    This group is mainly for Team Ohio members to discuss upcoming events, fundraisers, the U.S. Transplant Games, etc. Of course, we will be sharing our stories as well. However, we welcome all of our Transplant Games friends to join as well.

  • Liver Transplants

    Liver Transplants

    35 members
    Latest Activity: Jul 16

    This is a group for all people who have had liver transplants. Feel free to say how long you have been a recipient and what medication you are on. Some doctors hope to have their patients off all medications, any thoughts?

  • Living Organ Donors

    Living Organ Donors

    12 members
    Latest Activity: 1 day ago

    Been there, done that? Thinking about doing it? Join us for discussion and comeraderie around the living kidney donor and living liver donor experience.

  • Hispanos con transplantes

    Hispanos con transplantes

    5 members
    Latest Activity: 1 day ago

    Aqui los Hispanoparlantes hablamos de todos aspectos de nuestros transplantes!

  • Heart Transplants

    Heart Transplants

    19 members
    Latest Activity: Jul 6

    Heart Recipients can get to know one another. Discuss medication, issues, blessings, concerns, etc.

  • Team Cyclosporine

    Team Cyclosporine

    13 members
    Latest Activity: Jul 11

    Sandimmune (Cyclosporine) is old school drug...if anyone is one it, feel free to come chat, rant or rave about it :)

  • LifeSharers

    LifeSharers

    2 members
    Latest Activity: May 8

    LifeSharers - Organs for Organ Donors

  • Team MO-KAN

    Team MO-KAN

    10 members
    Latest Activity: Jul 3
  • :: Team Gratitude ::

    :: Team Gratitude ::

    7 members
    Latest Activity: May 28

    On Sunday, June 8th, we will be walking with the American Liver Foundation's Greater New York Chapter in the annual Liver Walk in Battery Park, New York City.

  • NYP Post-Liver Transplant Support Group

    NYP Post-Liver Transplant Support Group

    5 members
    Latest Activity: Jun 16

    A group of Liver Transplant Recipients who received their transplants at New York Presbyterian Hospital - Columbia Medical Center.

  • Team Rapamune

    Team Rapamune

    4 members
    Latest Activity: Jul 6

    This is for those of us who take Rapamune as a main immune suppressive drug. We can discuss side effects, etc. Or, we can just keep a head count of how many in the community take Rapamune.

  • Team Kidney

    Team Kidney

    10 members
    Latest Activity: 16 hours ago

    This group is for all people involved with kidney transplants. Please discuss how you are involved... donor, recipient, family member? What caused the renal failure that led to transplant. What medicines do you take? Do you experience side effects?

  • Polycystic Kidney Disease

    Polycystic Kidney Disease

    1 member
    Latest Activity: Jul 15

    The PKD Foundation is the only organization dedicated to promoting research to find a cure for polycystic kidney disease (PKD),improving the care and treatment of those it affects. Our vision “no one suffers the full effects of PKD.”

  • Team Florida

    Team Florida

    1 member
    Latest Activity: Apr 26
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