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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!!!!
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.!
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.
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.
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.
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?
For the members of team DC
Place to discuss lung transplant issues.
Been there, done that? Thinking about doing it? Join us for discussion and comeraderie around the living kidney donor and living liver donor experience.
Aqui los Hispanoparlantes hablamos de todos aspectos de nuestros transplantes!
Heart Recipients can get to know one another. Discuss medication, issues, blessings, concerns, etc.
Sandimmune (Cyclosporine) is old school drug...if anyone is one it, feel free to come chat, rant or rave about it :)
LifeSharers - Organs for Organ Donors
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.
A group of Liver Transplant Recipients who received their transplants at New York Presbyterian Hospital - Columbia Medical Center.
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.
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?
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.”
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